Abstract
The emergence of human intratumoural immunotherapy (HIT-IT) is a major step forward in the management of unresectable melanoma. The direct injection of treatments into melanoma lesions can cause cell lysis and induce a local immune response, and might be associated with a systemic immune response. Directly injecting immunotherapies into tumours achieves a high local concentration of immunostimulatory agent while minimising systemic exposure and, as such, HIT-IT agents are associated with lower toxicity than systemic immune checkpoint inhibitors (CPIs), enabling their potential use in combination with other therapies. Consequently, multiple HIT-IT agents, including oncolytic viruses, pattern-recognition receptor agonists, injected CPIs, cytokines and immune glycolipids, are under investigation. This review considers the current clinical development status of HIT-IT agents as monotherapy and in combination with systemic CPIs, and the practical aspects of administering and assessing the response to these agents. The future of HIT-IT probably lies in its use in combination with systemic CPIs; data from Phase 2 trials indicate a synergy between HIT-IT and CPIs. Data also suggest that the addition of HIT-IT to a CPI might generate responses in CPI-refractory tumours, thereby overcoming resistance and addressing a current unmet need in unresectable and metastatic melanoma for treatment options following progression after CPI treatment.
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Background
The standard of care for patients with melanoma whose tumour burden is limited and disease spread is confined comprises surgical resection with the intention to cure. In approximately two-thirds of all cases of primary cutaneous melanoma, disease spread begins with locoregional metastasis, with about 50% of patients developing the first metastasis in regional lymph nodes.1 Satellite or in-transit metastases also frequently occur at readily accessible cutaneous or subcutaneous locations.1,2,3,4 Although resection still, theoretically, remains an option in such cases, repeated surgery for locoregional disease might not be the best approach for patients with disease affecting a large anatomic area, for those in whom relapse occurs rapidly following repeated surgery, or for those in whom the morbidity of surgery might outweigh the benefits.5 In these, and other, patients with unresectable melanoma, the approval of targeted therapies (such as inhibitors of BRAF and mitogen-activated protein kinase [MEK]) and immune checkpoint inhibitors (CPIs; such as anti-programmed death receptor 1 [PD-1] and anti-cytotoxic T-lymphocyte-associated protein 4 [CTLA-4] agents) has revolutionised outcomes—with CPI treatment, around one-third of patients survive at least 5 years.6,7,8,9,10 However, the treatments can result in severe and long-lasting toxicities, and primary or acquired resistance are common.8,9,10,11,12 Furthermore, because most Phase 3 trials assessing targeted therapies or CPIs have predominately enrolled patients with stage IV disease, limited efficacy data are available for these agents in the treatment of unresectable stage IIIB–C locoregional melanoma.13,14,15,16,17
The need for additional treatment options for unresectable locoregional disease coupled with the accessibility of this type of metastasis has led to increased interest in immunostimulatory agents that can be injected directly into the tumour.5 These intratumoural immunotherapies can cause cell lysis, either directly or indirectly, and promote the induction of a local immune response, and might also be associated with the generation of a systemic immune response.18,19 Importantly, direct injection of a therapeutic agent into the tumour maximises its concentration at the disease site, promoting a tumour-specific immune response while reducing systemic exposure.2 There are anticipated benefits of combining intratumoural therapy with systemic immunotherapies such as CPIs. Not only do they offer different modes of action, but they also have non-overlapping toxicity profiles.20
Here, we review the latest data on the development of human intratumoural immunotherapy (HIT-IT), as a single-agent strategy and in combination with CPIs, for unresectable melanoma, alongside practical aspects involved in administering and assessing the response to this therapeutic approach. Although some chemical and local physical and radiation strategies might be defined as intratumoural therapies (e.g. PV-10 [a 10% solution of Rose Bengal], electrochemotherapy, cryotherapy, high-intensity focused ultrasound, irradiation and liposomal and nano-delivery systems) these therapeutic options are not immunotherapies and are thus considered to be outside the scope of this review.21
Ideal characteristics for an intratumoural immunotherapy
An ideal HIT-IT should elicit a measurable biological effect, reflective of the mechanism of action, that should lead to an objective response in the injected tumour.21 The ability to generate a local complete response and a durable response (i.e. lasting several months) is important to enable its use as a monotherapy, since it demonstrates the agent’s effectiveness when used on its own.21,22,23 Likewise, local disease control should translate into clinical benefit (e.g. symptom control, delayed disease progression, improved survival).22 Ideally, HIT-IT should stimulate a systemic immune response leading to regression of uninjected tumours at locoregional and distant metastatic sites.18,19,21 The initiation of a systemic immune response can occur through a variety of mechanisms, including the enhanced release and presentation of tumour antigens, immune cell trafficking and activation and inhibition of immunosuppressive pathways.24,25,26,27 It is anticipated that HIT-ITs will reach high concentrations in injected lesions, increasing the local bioavailability.21,28 Furthermore, by minimising systemic exposure, HIT-IT should be associated with low toxicity compared with systemic immunotherapies.22,25,29,30 Moreover, HIT-ITs might be able to reverse resistance to systemic immunotherapies.31,32,33 These attributes indicate that HIT-ITs could be used both as monotherapies and as part of a combination strategy,28 and data from the past 5 years suggest synergy between intratumoural and systemic immunotherapies (as described in more detail below).19,20,34,35,36,37,38,39
Currently available HIT-ITs for unresectable and metastatic melanoma
Talimogene laherparepvec (T-VEC) is the only treatment with regulatory approval for intratumoural administration in unresectable metastatic melanoma, and is recommended in current clinical practice guidelines.40,41,42,43,44 Interleukin-2 (IL-2) is included in guidelines as a systemic treatment for unresectable metastatic melanoma,43,44 and intratumoural administration has also been investigated.45,46,47
T-VEC
T-VEC is a genetically modified oncolytic virus that expresses granulocyte-macrophage colony-stimulating factor (GM-CSF).48,49 It selectively infects and replicates in tumour cells, which not only leads to cell lysis but also to the release of GM-CSF. This recruits dendritic cells, which, in turn, process and present tumour antigens to cytotoxic T lymphocytes (CTLs), thereby inducing a systemic tumour-specific immune response.48,49 T-VEC is approved in Europe for the treatment of adults with stage IIIB, IIIC and IVM1a unresectable melanoma with no bone, brain, lung or other visceral disease, and in the USA for the local treatment of unresectable cutaneous, subcutaneous and nodal lesions in patients with melanoma recurrent after initial surgery.
The approval of T-VEC was based on data from the OPTiM Phase 3 trial (n = 436), which demonstrated that the durable response rate (objective response lasting ≥6 months) and overall response rate were significantly higher following treatment with intralesional T-VEC than with subcutaneous GM-CSF in patients with unresectable and/or metastatic stage IIIB–IV melanoma (Table 1).22 Efficacy was highest in patients with stage IIIB–IVM1a disease; in this group, T-VEC led to a survival benefit22 and demonstrated a tolerable safety profile.22 A systemic immune response is suggested by observed reductions in the size of uninjected lesions associated with T-VEC treatment (≥50% reduction in 15–34% of uninjected lesions).18,22 This implication is also supported by a prospective Phase 2 trial in which T-VEC led to a significant increase in the number of CD8+ T cells, effector and memory cytotoxic lymphocytes (CTLs), natural killer cells, and CTLs expressing PD-1 and CTLA-4 (indicative of immune activation) in uninjected lesions.50
IL-2
IL-2 is a proinflammatory cytokine that can activate CD8+ T cells, regulatory T cells, B cells, macrophages and natural killer cells.45,51 Systemically administered IL-2 is approved for the treatment of metastatic melanoma in the USA,52 but not in Europe.53 To date, intratumoural treatment with IL-2 has only been studied in single-arm trials involving a limited number of patients.45,46,47 Although responses with intratumoural IL-2 appear to be durable (lasting ≥ 6 months), they are largely limited to injected lesions, which suggests that intratumoural IL-2 does not elicit a strong systemic effect—at least, not at the doses and regimens that have been studied.30 Intratumoural IL-2 is generally well tolerated.
Novel agents in development for unresectable and metastatic melanoma
Many agents are being developed for intratumoural use, including other oncolytic viruses and peptides, pattern-recognition receptor (PRR) agonists, immune CPIs and cytokines (see Table 1 and below for further details).21 Figure 1 shows how these agents might interact with the cancer-immunity cycle, the process by which cancer cells are effectively killed by an immune response.
Other oncolytic viruses
Given that the only currently approved HIT-IT is an oncolytic virus, it is not surprising that other oncolytic viruses are undergoing development for the treatment of unresectable and metastatic melanoma.54 Coxsackievirus A21 (CVA21) is an enterovirus that preferentially infects tumour cells, leading to cell lysis, which appears to provoke a systemic antitumour immune response even in the absence of the virus encoding an immune component such as GM-CSF or IL-2.55 In a single-arm Phase 2 trial, CVA21 led to durable responses lasting 6 months or more.56 No Phase 3 trials are currently planned for CVA21 monotherapy in melanoma since the future of these agents is most likely in combination, particularly with immunotherapies. In this regard, trials are ongoing with CVA21 in combination with other therapies (see below). Canerpaturev (formerly HF-10) is a spontaneously occurring, replication-competent mutant strain of herpes simplex virus type 1 that causes lysis of infected cells.34,57 Similar to CVA21, canerpaturev is being assessed in combination therapy; no monotherapy trials are ongoing. Other oncolytic viruses are in early clinical development as monotherapy and/or in combination therapy: RP1 and RP2, engineered strains of the herpes simplex virus; ONCOS102, an adenovirus engineered to express GM-CSF; JX-594 (Pexa-Vec), a GM-CSF-expressing poxvirus; and CF33-hNIS, a chimeric poxvirus encoding a human sodium iodide symporter (hNIS).58,59,60,61
PRR agonists
Another class of HIT-IT in development comprises the PRR agonists, which include Toll-like receptor (TLR) agonists, stimulator of interferon genes (STING) agonists and retinoic acid-inducible gene I (RIG-I)-like receptor agonists.21,62 PRRs are costimulatory molecules that recognise pathogen-associated molecular patterns (PAMPs), such as lipopolysaccharide and other bacterial and viral components, as well as damage-associated molecular patterns (DAMPs) resulting from cellular stress, apoptosis and necrosis.62 Recognition of PAMPs/DAMPs leads to upregulation of the transcription of genes involved in inflammatory responses, which encode proinflammatory cytokines, type-I interferons, chemokines and, antimicrobial proteins.63 Activation of TLR-9 signalling in plasmacytoid dendritic cells induces production of interferon-α and tumour necrosis factor (TNF)-α, which promotes leucocyte migration and induces synthesis of antimicrobial peptides and cytokines, and promotes phagocytosis in macrophages.64 Three TLR-9 agonists (SD-101, IMO-2125 and CMP-001) are in clinical development in combination therapy (see below).31,32,65,66 RIG-I-like receptors are cytosolic PRRs that detect viral and endogenous RNA, triggering binding to the mitochondrial antiviral signalling protein (MAVS) and resulting in type-I interferon production.62 MK4621 (formerly RGT-100), a synthetic RNA agonist of the RIG-I pathway, has been shown to have antitumour activity in mouse models.67 STING is an endoplasmic reticulum transmembrane protein involved in recognition of cytosolic DNA. In tumours, STING pathway activation leads to interferon-β production and T-cell response.62 Cyclic dinucleotides have been found to act as immune adjuvants by activating STING, in turn stimulating a proinflammatory immune response;68 Phase 1 trials of two intratumoural STING agonists, ADU-S100 and MK-1454, are ongoing.69,70,71
CPIs
Immune CPIs, such as TNF receptor superfamily agonists (e.g. CD40) and immunoglobulin superfamily antagonists (e.g. PD-1 and CTLA-4), are also in development as intratumoural agents.21 The activation of CD40 on antigen-presenting cells initiates their maturation and ability to activate CD8+ T cells. Modulation of this pathway in melanoma is being evaluated in a Phase 1/2 trial of an intratumoural CD40 agonist, APX005M.72 The feasibility of utilising approved anti-PD-1 systemic therapies as intratumoural agents was demonstrated in a 2018 pilot study; further studies are needed to determine the efficacy of this approach.73 Similarly, intratumoural administration of the anti-CTLA-4 antibody ipilimumab plus IL-2 demonstrated the induction of both local and systemic immune responses in a Phase 1 trial; no dose-limiting toxicities were reported.27 A Phase 1/2 trial assessing intratumoural ipilimumab plus systemic nivolumab, an anti-PD-1 antibody, is currently recruiting patients.74
Cytokines
Cytokines (e.g. IL-2 and GM-CSF) were among the first HIT-ITs to be assessed in melanoma.5 Subsequently, cytokine fusion proteins and plasmids expressing cytokines have been developed with the aim of increasing efficacy.75,76 For example, the immunocytokine fusion protein L19–IL-2 (Darleukin) is a targeted form of IL-2 that recognises the extra domain B of fibronectin, which is expressed in cancer-associated blood vessels and extracellular matrix but absent from almost all healthy tissue.75 In a single-arm Phase 2 trial, L19–IL-2 resulted in local responses, including local complete responses.75 Daromun, another investigational treatment, combines L19–IL-2 and L19–TNF. In a single-arm Phase 2 trial, Daromun led to objective responses in both injected and uninjected lesions. A pivotal trial of Daromun is being conducted in the neoadjuvant setting.77
Tavokinogene telseplasmid (also called pIL-12) is a synthetic plasmid encoding the cytokine IL-12, which, when delivered to melanomas in a highly localised manner, leads to a proinflammatory response, resulting in T-cell recruitment and activation. In a Phase 2 trial, tavokinogene telseplasmid demonstrated induction of an antitumour immune response and a high disease control rate in melanoma.78 Tavokinogene telseplasmid was given orphan drug status by the US Food and Drug Administration (FDA) in 2017 for the treatment of unresectable metastatic melanoma.76
Other promising HIT-ITs
Several other novel HIT-ITs have shown promising preclinical antitumour activity and are entering clinical trials. AGI-134 is a glycolipid that recruits pre-existing endogenous anti-Gal antibodies to the injected lesion, leading to complement activation and enhanced tumour antigen processing, whereas IMM60 is a non-glycolipid that activates invariant natural killer cells, leading to an antitumour immune response. A Phase 1/2 trial of AGI-134 is currently recruiting patients, and trials of IMM60 are anticipated.79,80,81 IFx-Hu2.0 is a plasmid DNA encoding the streptococcal membrane protein, Emm55, and the first in human Phase 1 study of intratumoural use in melanoma is in progress.82 Preliminary laboratory data from the first three patients in the trial suggest the treatment may be associated with decreases in tumour cells and formation of an immune response.83 mRNA-2416 is a novel lipid nanoparticle therapeutic agent encoding the TNF receptor ligand OX40L. Results so far delivered from an ongoing Phase 1/2 study indicate that intratumoural mRNA-2416 monotherapy is well tolerated and elevates PD-L1 levels and proinflammatory activity.84
Going forward
Although many HIT-ITs have been investigated, most data at present originate from Phase 2 trials only. Such data are difficult to interpret, because early-stage efficacy might not reflect the results of Phase 3 trials:85,86,87 for example, despite promising efficacy in Phase 2 trials, the plasmid-DNA-based intratumoural immunotherapy velimogene aliplasmid (a plasmid–lipid complex comprising the DNA sequences encoding HLA-B7 and β2 microglobulin) either provided no benefit or reduced survival compared with standard of care in Phase 3 trials.86 This result highlights the need for caution when interpreting data from single-arm, non-randomised trials in small and highly selected patient populations, as well as emphasising the importance of mechanistic tumour biology research to enable rational drug and clinical trial design.
Combining intratumoural and systemic immunotherapies
As noted, many intratumoural agents in development are being assessed in combination with systemic CPIs, reflecting the likely future clinical application of intratumoural therapy.
HIT-ITs might enhance the response to CPIs...
Although CPIs provide an effective therapeutic approach as monotherapy in melanoma,6,7 only a subset of patients initially respond, and a substantial proportion of responders subsequently develop resistance and relapse.88 Data suggest that therapeutic responses to immunotherapy can, to some extent, be predicted by the presence of tumour immune cell infiltration. Three tumour immune profiles correlate with response to CPIs: inflamed or ‘hot’ tumours exhibiting immune cell infiltration are likely to respond, whereas ‘cold’ immune-excluded tumours with immune cells surrounding, but not infiltrating, the tumour, and immune desert tumours, characterised by a complete lack of immune cells, are less likely to respond. HIT-ITs that elicit a local immune response have been shown to promote immune cell infiltration into the tumour in both injected and uninjected lesions.26,37,50 Consequently, by altering the tumour microenvironment and converting a non-responsive ‘cold’ tumour into a responsive ‘hot’ tumour, HIT-IT might enhance response to systemic immunotherapies.26,37,38
…and CPIs might enhance the response to HIT-ITs
On the other hand, CPIs might also enhance the response to HIT-IT. Cancer cells can activate immune checkpoint pathways to downregulate the response to local immunostimulation, thus limiting the response to intratumoural monotherapy.89,90 Indeed, a 2018 Phase 2 trial of T-VEC showed that this therapy leads to an increase in the number of CTLs expressing PD-1 and CTLA-4.50 Blocking PD-1 or CTLA-4 might restore suppressed antitumour immune responses and enhance the ability of T cells (which have been primed by intratumoural injection) to recognise and kill tumour cells.35,91 CPIs might also enhance the systemic effects of some HIT-ITs.35,37,38,50 Therefore, combination therapy might result in improved clinical activity beyond what would be expected with either agent alone. Additionally, owing to the low toxicity of HIT-IT, combination therapy has the potential to be tolerated at effective doses.
Combination trials of HIT-ITs with pembrolizumab or ipilimumab
Given the therapeutic promise of combining intratumoural and systemic immunotherapies, several combination trials have been conducted or are ongoing (Table 2). Data indicating the synergistic activity of such combinations are available from the Phase 1b/3 MASTERKEY-265/KEYNOTE-034 trial of T-VEC plus the anti-PD-1 agent pembrolizumab versus pembrolizumab alone. In the combination arm, two injections of T-VEC were given before pembrolizumab was initiated. Although single-agent T-VEC increased CD8+ T-cell infiltration into the tumour, in both injected and uninjected lesions, and increased the numbers of systemic circulating CD4+ and CD8+ T cells, combination therapy was associated with greater clinical benefit than that seen previously with either agent alone, with no additional toxicity.37,92 Longer-term follow-up (median 36.8 months) of the Phase 1b part of the trial suggests that this combination induces a high rate of complete responses (43%), with a 3-year survival rate of ~70%.93 The same combination is currently being evaluated in the large randomised Phase 3 MASTERKEY-265/KEYNOTE-034 trial.94
Systemic pembrolizumab is being assessed in combination with various other HIT-ITs, with promising early results. Interim data from a Phase 1b/2 trial combining the intratumoural TLR-9 agonist SD-101 with pembrolizumab demonstrated that the combination is well tolerated and leads to increased tumour immune cell infiltration, as well as inducing tumour shrinkage, in injected and uninjected lesions—including those in distant metastases.65,66 Pembrolizumab is also being investigated in a Phase 2 trial with intratumoural tavokinogene telseplasmid78,95 and in a Phase 1b trial with the oncolytic virus CVA21. A Phase 2 trial is also planned to investigate pembrolizumab with CVA21.96 Apart from T-VEC plus pembrolizumab, none of these combinations is currently being assessed in Phase 3 trials.
T-VEC has also been assessed in a randomised Phase 1b/2 trial in combination with ipilimumab versus ipilimumab alone;97 the results suggest that this combination is tolerable and might have greater efficacy than either agent alone.39,98,99 Other ipilimumab and intratumoural combinations have shown efficacy in Phase 1b or 2 trials, including with the oncolytic viruses CVA21 and canerpaturev.34,100 However, a Phase 2 trial of ipilimumab combined with intratumoural IL-2 reported no objective responses.2 Currently there are no ongoing or planned Phase 3 trials of any of these combinations.
Use of HIT-IT following anti-PD-1 therapy
For patients who have previously received an anti-PD-1 agent, treatment options are limited.88 Data from the past 3 years—particularly from studies using TLR-9 agonists—indicate that treatment regimens incorporating a HIT-IT can lead to responses in patients who have previously received, or who have progressed following, anti-PD-1 therapy (Table 2).31,32,33,101 Limited data are available on the efficacy of HIT-IT as monotherapy in patients who have previously received an anti-PD-1 therapy.
Several studies are investigating whether combining a HIT-IT with ipilimumab can provide additional activity. In a Phase 1/2 trial, addition of the TLR-9 agonist IMO-2125 (tilsotolimod) to ipilimumab revived the immune response in injected and uninjected anti-PD-1-resistant tumours.31 A randomised Phase 3 trial assessing IMO-2125 plus ipilimumab in patients who have progressed on previous anti-PD-1 therapy is ongoing.102 Phase 2 data show that the addition of canerpaturev to ipilimumab can lead to responses in a minority of patients previously treated with anti-PD-1 therapy.101
Early phase data indicate that the addition of a HIT-IT to an anti-PD-1 agent might restore response and fundamentally overcome resistance to anti-PD-1 therapy. In a Phase 1b trial, the TLR-9 agonist CMP-001 was able to overcome resistance to PD-1 inhibition when combined with pembrolizumab.32 Likewise, in a Phase 1b/2 trial, addition of the TLR-9 agonist SD-101 to pembrolizumab restored tumour sensitivity to PD-1 inhibition in refractory tumours; responses were seen in both injected and uninjected lesions.33 A Phase 2 trial of T-VEC plus pembrolizumab is ongoing in patients with advanced melanoma whose disease progressed following anti-PD-1 therapy.103
For future analyses on the sequence of HIT-ITs, it will be important to ascertain if the response to these agents differs among patients who progress following initial response to CPI treatment compared with those who never respond to CPI treatment and/or patients who have previously received a CPI and discontinued for other reasons (e.g. poor tolerability). This will help to identify the most appropriate HIT-IT to use in different clinical situations. Another interesting area for future research is the potential to give HIT-IT to patients who experience progression despite adjuvant CPI therapy, as many of these patients progress with accessible locoregional disease only.104
HIT-ITs in combination with targeted therapies
There is also interest in combining HIT-ITs with BRAF and MEK inhibitors such as dabrafenib and trametinib. This approach aims to specifically target the BRAF driver mutation, which is present in around 50% of malignant melanomas.105 The combination of MEK inhibition and T-VEC has shown increased melanoma tumour cell death in vitro106 and a Phase 1 trial of dabrafenib, trametinib and T-VEC is ongoing.107
Practical implications of HIT-IT for the clinical management of unresectable and metastatic melanoma
Patient selection
From a practical perspective, HIT-IT can only be administered to patients with lesions that are visible, palpable or detectable by ultrasound or other imaging techniques. Key considerations for the selection of patients for HIT-IT monotherapy are described in Box 1. The decision to select a patient for HIT-IT should result from discussions within a multidisciplinary team. These considerations will change if a HIT-IT is approved in combination with a systemic CPI. Similarly, a better understanding of the chances of obtaining a response will help to weigh the risk:benefit consideration in the case of less accessible lesions (e.g. lung metastases).
Lesion mapping and injection
To ensure accurate drug delivery, response and evaluation, lesion mapping using clinical evaluation (i.e. palpation and imaging) should be conducted to identify and measure lesions for injection. Lesions that will not be injected should also be mapped to enable the assessment of systemic responses. Ultrasound provides an accessible option for the mapping of most lesions (including subcutaneous and nodal), as well as allowing the measurement of 3D tumour volume, and can be more accurate than palpation for the determination of lesion size. Computed tomography (CT), positron emission tomography (PET-CT) and, in rare cases, magnetic resonance imaging can also be considered for mapping deep lesions or those located in the extremities. Before initiating HIT-IT, it is important to record the tumour load throughout the patient, the tumour volume available for injection and the total volume of agent injected before response evaluation. Both injected and uninjected lesions (including visceral lesions) should be measured before treatment and compared with previous measurements: a lesion tracking sheet and high-resolution photographs could facilitate lesion tracking.
It is beyond the scope of this review to detail handling and administration for HIT-IT; these topics have been covered extensively by Marabelle et al.,21 Gutzmer et al.108 and Harrington et al.109. Briefly, most cutaneous, subcutaneous and superficial lymph node lesions can be injected under ultrasound guidance.21 Multiple injections can be administered to a single lesion, and multiple lesions can be injected at the same visit.21 The choice of whether to use the same needle for all lesions or individual needles for each lesion might depend on the type of HIT-IT used and the risk of drug exposure to the patient or healthcare professional.21,41 Intratumoural injections should be performed by a trained healthcare professional (e.g. a nurse, physician, radiologist, interventional radiologist or surgeon).21
Electroporation is sometimes employed for delivery of tavokinogene telseplasmid and other plasmids. After injection of the plasmid into the lesion, application of electroporation pulses locally permeabilise and transduce the cells.110 The precision of the technique is an advantage. Only cells that are exposed to both the plasmid and the electrical field will undergo transfection, enabling local, targeted delivery.110
Safety and tolerability of intratumoural injections
As mentioned, most reported adverse events associated with HIT-IT have generally been mild and might not require active treatment. Injection-site reactions are frequent, but they tend to resolve within 24–48 h and can be helped with ice and pain relief. Local anaesthetic can be given ~30 min before the procedure. Careful wound care is important to help to avoid skin infections. In the event of cellulitis, oral or intravenous antibiotics should be administered as required and blood samples taken for culture.111 Although HIT-IT is generally associated with low toxicity, adverse events such as fatigue, chills and pyrexia have been reported in clinical trials and it is important to manage the patient’s expectations of tolerability to ensure that they remain on treatment.18,22,112
Assessment of response
Current trials of HIT-ITs have used a range of response criteria. Thorough and consistent assessments of response will be required in future clinical trials to properly evaluate the plethora of HIT-ITs in development. The Response Evaluation Criteria in Solid Tumors (RECIST v1.1) were designed to measure responses to cytotoxic agents, and might not be suitable for evaluating HIT-ITs: according to RECIST v1.1, new lesions define progressive disease, but the appearance of new lesions can precede prolonged disease stabilisation in response to immune checkpoint blockade.113 Indeed, pseudoprogression, in which a tumour appears to grow as a result of a treatment effect rather than true disease progression, has been reported to occur in patients receiving HIT-IT;18 in such cases, discontinuing treatment at the point of apparent initial disease progression might not be appropriate. The immune-related response criteria (irRC) and immune-related (ir)RECIST partially ameliorate these issues by requiring confirmation of progressive disease by consecutive imaging assessment at least 4 weeks from the date of the first documentation and by incorporating the measurement of new lesions into the sum of lesions.114,115,116 irRECIST further attempts to harmonise data collection and to clarify response measurement that allows for pseudoprogression. New lesions are assessed separately. Importantly, the progressive disease thresholds for irRECIST are aligned with RECIST v1.1, allowing comparisons to be made between trials and historical data.
European Society for Medical Oncology (ESMO) recommendations on the development of HIT-ITs propose that, for clinical trials, RECIST v1.1 is used for the overall assessment of tumour response, iRECIST is used for assessing responses of injected and uninjected tumours, and the duration of response for both injected and uninjected lesions should be reported.21 We are in agreement with the ESMO recommendations that injected lesions are evaluated separately from uninjected lesions, to characterise systemic effects in clinical trials.21 As a result, the evaluation of HIT-IT in clinical trials is more complex than for conventional therapies, due to the need to differentiate lesions (e.g. ‘target injected’, ‘target non-injected’, ‘non-target’, ‘new target’ and ‘new non-target’). Furthermore, visceral lesions must be considered in the response criteria; responses to HIT-IT have been reported in uninjected visceral lesions, and advances in imaging guidance techniques now allow visceral lesions to be directly injected.31 Such complexity in response assessment requires specially trained radiologists.
These assessment criteria are currently likely to be too complicated and not relevant for real-world practice, in which treatment decisions are based on patient-level responses, and harmonisation on how to evaluate tumour response to HIT-IT is still awaited. As HIT-IT becomes more widely used, the link between formal response evaluation, clinical benefit and decision-making in practice will evolve further.
Conclusions
The efficacy and tolerability of HIT-IT for the treatment of melanoma provide proof-of-concept for this modality. Early data indicate the existence of a synergy between HIT-IT and CPIs, and it is likely that future clinical use will focus on the combined use of these agents; indeed strategies that combine treatments that have different modes of action without overlapping toxicities are likely to feature in future research. Furthermore, there is a high unmet need in unresectable and metastatic melanoma for treatment options following progression after PD-1 inhibition, and data indicate that adding HIT-IT to systemic agents can lead to responses in anti-PD-1-refractory tumours, thereby overcoming resistance.
The development of HIT-IT has focused on unresectable disease; however, there is now interest in the efficacy of this approach in the neoadjuvant setting, and early data suggest that neoadjuvant HIT-IT could prevent recurrence following surgery in patients with resectable melanoma.117,118 Additionally, although it has been widely assessed in melanoma, HIT-IT could be considered for use in any tumour that is injectable (including under image guidance).21 Consequently, a plethora of HIT-ITs are in early-stage clinical development for the treatment of a range of solid tumour types and lymphoma.
References
Meier, F., Will, S., Ellwanger, U., Schlagenhauff, B., Schittek, B., Rassner, G. et al. Metastatic pathways and time courses in the orderly progression of cutaneous melanoma. Br. J. Dermatol. 147, 62–70 (2002).
Weide, B., Martens, A., Wistuba-Hamprecht, K., Zelba, H., Maier, L., Lipp, H. P. et al. Combined treatment with ipilimumab and intratumoral interleukin-2 in pretreated patients with stage IV melanoma-safety and efficacy in a phase II study. Cancer Immunol. Immunother. 66, 441–449 (2017).
Balch, C. M., Gershenwald, J. E., Soong, S.-J., Thompson, J. F., Atkins, M. B., Byrd, D. R. et al. Final version of 2009 AJCC melanoma staging and classification. J. Clin. Oncol. 27, 6199–6206 (2009).
Abbott, A. M. & Zager, J. S. Locoregional therapies in melanoma. Surg. Clin. North Am. 94, 1003–1015 (2014).
Weide, B., Neri, D. & Elia, G. Intralesional treatment of metastatic melanoma: a review of therapeutic options. Cancer Immunol. Immunother. 66, 647–656 (2017).
Wolchok, J. D., Chiarion-Sileni, V., Gonzalez, R., Rutkowski, P., Grob, J.-J., Cowey, C. L. et al. Overall survival with combined nivolumab and ipilimumab in advanced melanoma. N. Engl. J. Med. 377, 1345–1356 (2017).
Maio, M., Grob, J. J., Aamdal, S., Bondarenko, I., Robert, C., Thomas, L. et al. Five-year survival rates for treatment-naive patients with advanced melanoma who received ipilimumab plus dacarbazine in a phase III trial. J. Clin. Oncol. 33, 1191–1196 (2015).
Hamid, O., Hersey, P., Wolchok, J. D., Dronca, R., Joseph, R., Weber, J. S. et al. Five-year survival outcomes for patients with advanced melanoma treated with pembrolizumab in KEYNOTE-001. Ann. Oncol. 30, 528–588 (2019).
Mackiewicz, J. & Mackiewicz, A. BRAF and MEK inhibitors in the era of immunotherapy in melanoma patients. Contemp. Oncol. (Pozn., Pol.) 22, 68–72 (2018).
Sharma, P., Hu-Lieskovan, S., Wargo, J. A. & Ribas, A. Primary, adaptive, and acquired resistance to cancer immunotherapy. Cell 168, 707–723 (2017).
Bristol-Myers Squibb. Yervoy (ipilimumab): summary of product characteristics. https://www.ema.europa.eu/en/documents/product-information/yervoy-epar-product-information_en.pdf (2019).
Merck. KEYTRUDA (pembrolizumab): summary of product characteristics. https://www.ema.europa.eu/en/documents/product-information/keytruda-epar-product-information_en.pdf (2019).
Robert, C., Schachter, J., Long, G. V., Arance, A., Grob, J. J., Mortier, L. et al. Pembrolizumab versus ipilimumab in advanced melanoma. N. Engl. J. Med. 372, 2521–2532 (2015).
McArthur, G. A., Chapman, P. B., Robert, C., Larkin, J., Haanen, J. B., Dummer, R. et al. Safety and efficacy of vemurafenib in BRAF(V600E) and BRAF(V600K) mutation-positive melanoma (BRIM-3): extended follow-up of a phase 3, randomised, open-label study. Lancet Oncol. 15, 323–332 (2014).
Larkin, J., Ascierto, P. A., Dréno, B., Atkinson, V., Liszkay, G., Maio, M. et al. Combined vemurafenib and cobimetinib in BRAF-mutated melanoma. N. Engl. J. Med. 371, 1867–1876 (2014).
Robert, C., Long, G. V., Brady, B., Dutriaux, C., Maio, M., Mortier, L. et al. Nivolumab in previously untreated melanoma without BRAF mutation. N. Engl. J. Med. 372, 320–330 (2015).
Hauschild, A., Grob, J. J., Demidov, L. V., Jouary, T., Gutzmer, R., Millward, M. et al. Dabrafenib in BRAF-mutated metastatic melanoma: a multicentre, open-label, phase 3 randomised controlled trial. Lancet 380, 358–365 (2012).
Andtbacka, R. H., Ross, M., Puzanov, I., Milhem, M., Collichio, F., Delman, K. A. et al. Patterns of clinical response with talimogene laherparepvec (T-VEC) in patients with melanoma treated in the OPTiM phase III clinical trial. Ann. Surg. Oncol. 23, 4169–4177 (2016).
Thompson, J. F., Agarwala, S. S., Smithers, B. M., Ross, M. I., Scoggins, C. R., Coventry, B. J. et al. Phase 2 study of intralesional PV-10 in refractory metastatic melanoma. Ann. Surg. Oncol. 22, 2135–2142 (2015).
Agarwala, S. S. The role of intralesional therapies in melanoma. Oncol. (Williston Park) 30, 436–441 (2016).
Marabelle, A., Andtbacka, R., Harrington, K., Melero, I., Leidner, R., de Baere, T. et al. Starting the fight in the tumor: expert recommendations for the development of human intratumoral immunotherapy (HIT-IT). Ann. Oncol. 29, 2163–2174 (2018).
Andtbacka, R. H., Kaufman, H. L., Collichio, F., Amatruda, T., Senzer, N., Chesney, J. et al. Talimogene laherparepvec improves durable response rate in patients with advanced melanoma. J. Clin. Oncol. 33, 2780–2788 (2015).
Perez, M. C., Miura, J. T., Naqvi, S. M. H., Kim, Y., Holstein, A., Lee, D. et al. Talimogene laherparepvec (TVEC) for the treatment of advanced melanoma: a single-institution experience. Ann. Surg. Oncol. 25, 3960–3965 (2018).
Toomey, P., Kodumudi, K., Weber, A., Kuhn, L., Moore, E., Sarnaik, A. A. et al. Intralesional injection of rose bengal induces a systemic tumor-specific immune response in murine models of melanoma and breast cancer. PLoS ONE 8, e68561 (2013).
Malvehy, J., Samoylenko, I., Schadendorf, D., Gutzmer, R., Grob, J. J., Sacco, J. et al. Relationship between talimogene laherparepvec and intratumoral CD8+ density in patients with unresectable stage IIIB-IVM1c melanoma: Interim efficacy, safety and biomarker results of a Phase 2 study. J. Eur. Acad. Dermatol. 31, 39–40 (2017).
Wang, D., Jiang, W., Zhu, F., Mao, X. & Agrawal, S. Modulation of the tumor microenvironment by intratumoral administration of IMO-2125, a novel TLR9 agonist, for cancer immunotherapy. Int. J. Oncol. 53, 1193–1203 (2018).
Ray, A., Williams, M. A., Meek, S. M., Bowen, R. C., Grossmann, K. F., Andtbacka, R. H. I. et al. A phase I study of intratumoral ipilimumab and interleukin-2 in patients with advanced melanoma. Oncotarget 7, 64390–64399 (2016).
Marabelle, A., Tselikas, L., de Baere, T. & Houot, R. Intratumoral immunotherapy: using the tumor as the remedy. Ann. Oncol. 28, xii33–xii43 (2017).
Danielli, R., Patuzzo, R., Di Giacomo, A. M., Gallino, G., Maurichi, A., Di Florio, A. et al. Intralesional administration of L19-IL2/L19-TNF in stage III or stage IVM1a melanoma patients: results of a phase II study. Cancer Immunol. Immunother. 64, 999–1009 (2015).
Weide, B., Derhovanessian, E., Pflugfelder, A., Eigentler, T. K., Radny, P., Zelba, H. et al. High response rate after intratumoral treatment with interleukin-2: results from a phase 2 study in 51 patients with metastasized melanoma. Cancer 116, 4139–4146 (2010).
Diab, A., Haymaker, C., Bernatchez, C., Andtbacka, R., Shaheen, M., Johnson, D. H. et al. Intratumoral (IT) Injection of the TLR9 agonist tilsotolimod (IMO-2125) in combination with ipilimumab (ipi) triggers durable responses in PD-1 inhibitor refractory metastatic melanoma (rMM): Results from a multicenter, phase I/II study. Ann. Oncol. 29(Suppl 8), viii442 (2018).
Milhem, M., Gonzales, R., Medina, T., Kirkwood, J. M., Buchbinder, E., Mehmi, I. et al. Intratumoral toll-like receptor 9 (TLR9) agonist, CMP-001, in combination with pembrolizumab can reverse resistance to PD-1 inhibition in a phase Ib trial in subjects with advanced melanoma. Cancer Res. 78(Suppl 1), CT144 (2018).
Ribas, A., Mehmi, I., Medina, D., Lao, C., Kummar, S., Amin, A. et al. Phase Ib/II study of the combination of SD-101 and pembrolizumab in patients with advanced melanoma who had progressive disease on or after prior anti-PD-1 therapy. Ann. Oncol. 29(Suppl 8), viii451–viii452 (2018).
Curti, B., Richards, J., Faries, M. B., Andtbacka, R. H., Grose, M., Karpathy, R. et al. The MITCI (phase 1b) study: novel immunotherapy combination of coxsackievirus A21 and ipilimumab in patients with advanced melanoma. Ann. Oncol. 27(Suppl 6), vi360 (2016).
Dummer, R., Hoeller, C., Gruter, I. P. & Michielin, O. Combining talimogene laherparepvec with immunotherapies in melanoma and other solid tumors. Cancer Immunol. Immunother. 66, 683–695 (2017).
Silk, A. W., Kaufman, H. L., Gabrail, N., Faries, M. B., Mehnert, J., Bryan, J. et al. Phase Ib study of intratumoral oncolytic Coxsackievirus A21 (CVA21) and systemic pembrolizumab in subjects with advanced melanoma: interim results of the CAPRA clinical trial. Cancer Res. 77(Suppl 13), CT026 (2017).
Ribas, A., Dummer, R., Puzanov, I., VanderWalde, A., Andtbacka, R. H., Michielin, O. et al. Oncolytic virotherapy promotes intratumoral T cell infiltration and improves anti-PD-1 immunotherapy. Cell 170, 1109–1119 (2017).
Moesta, A. K., Cooke, K., Piasecki, J., Mitchell, P., Rottman, J. B., Fitzgerald, K. et al. Local delivery of OncoVEXmGM-CSF generates systemic antitumor immune responses enhanced by cytotoxic T-lymphocyte-associated protein blockade. Clin. Cancer Res. 23, 6190–6202 (2017).
Chesney, J., Puzanov, I., Collichio, F., Singh, P., Milhem, M. M., Glaspy, J. et al. Randomized, open-label phase II study evaluating the efficacy and safety of talimogene laherparepvec in combination with ipilimumab versus ipilimumab alone in patients with advanced, unresectable melanoma. J. Clin. Oncol. 36, 1658–1667 (2018).
Amgen. Imlygic (T-VEC): prescribing information. https://www.fda.gov/media/94129/download (2015).
Amgen. Imlygic (T-VEC): summary of product characteristics. https://www.ema.europa.eu/en/documents/product-information/imlygic-epar-product-information_en.pdf (2019).
Michielin, O., van Akkooi, A. C. J., Ascierto, P. A., Dummer, R. & Keilholz, U. Cutaneous melanoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 30, 1884–1901 (2019).
Garbe, C., Peris, K., Hauschild, A., Saiag, P., Middleton, M., Bastholt, L. et al. Diagnosis and treatment of melanoma. European consensus-based interdisciplinary guideline—update 2016. Eur. J. Cancer 63, 201–217 (2016).
National Comprehensive Cancer Network. NCCN Guidelines version 2. 2019 Melanoma. 2019. https://www.nccn.org/professionals/physician_gls/pdf/cutaneous_melanoma.pdf
Temple-Oberle, C. F., Byers, B. A., Hurdle, V., Fyfe, A. & McKinnon, J. G. Intra-lesional interleukin-2 therapy for in transit melanoma. J. Surg. Oncol. 109, 327–331 (2014).
Byers, B. A., Temple-Oberle, C. F., Hurdle, V. & McKinnon, J. G. Treatment of in-transit melanoma with intra-lesional interleukin-2: a systematic review. J. Surg. Oncol. 110, 770–775 (2014).
Weide, B., Eigentler, T. K., Pflugfelder, A., Leiter, U., Meier, F., Bauer, J. et al. Survival after intratumoral interleukin-2 treatment of 72 melanoma patients and response upon the first chemotherapy during follow-up. Cancer Immunol. Immunother. 60, 487–493 (2011).
Kaufman, H. L., Ruby, C. E., Hughes, T. & Slingluff, C. L. Jr. Current status of granulocyte-macrophage colony-stimulating factor in the immunotherapy of melanoma. J. Immunother. Cancer 2, 11 (2014).
Liu, B. L., Robinson, M., Han, Z. Q., Branston, R. H., English, C., Reay, P. et al. ICP34.5 deleted herpes simplex virus with enhanced oncolytic, immune stimulating, and anti-tumour properties. Gene Ther. 10, 292–303 (2003).
Gogas, H., Samoylenko, I., Schadendorf, D., Gutzmer, R., Grob, J. J., Sacco, J. et al. Talimogene laherparepvec treatment increases intratumoural effector T-cell and natural killer (NK) cell density in noninjected tumours in patients with stage IIIB–IVM1c melanoma: evidence for systemic effects in a phase 2, single-arm study. Ann. Oncol. 29(Suppl 8), viii443 (2018).
Alì, G., Boldrini, L., Lucchi, M., Picchi, A., Dell’Omodarme, M., Prati, M. C. et al. Treatment with interleukin-2 in malignant pleural mesothelioma: immunological and angiogenetic assessment and prognostic impact. Br. J. Cancer 101, 1869–1875 (2009).
Novartis. Proleukin (aldesleukin): prescribing information. https://www.proleukin.com/downloads/proleukin-pi.pdf (2015).
Novartis. Proleukin (adesleukin): summary of product characteristics. https://www.medicines.org.uk/emc/product/291/smpc (2019).
Twumasi-Boateng, K., Pettigrew, J. L., Kwok, Y. Y. E., Bell, J. C. & Nelson, B. H. Oncolytic viruses as engineering platforms for combination immunotherapy. Nat. Rev. Cancer 18, 419–432 (2018).
Bradley, S., Jakes, A. D., Harrington, K., Pandha, H., Melcher, A. & Errington-Mais, F. Applications of coxsackievirus A21 in oncology. Oncol. Virother. 3, 47–55 (2014).
Andtbacka, R. H., Curti, B. D., Hallmeyer, S., Feng, Z., Paustian, C., Bifulco, C. et al. Phase II CALM extension study: Coxsackievirus A21 delivered intratumorally to patients with advanced melanoma induces immune-cell infiltration in the tumor microenvironment. J. Immunother. Cancer 3(Suppl 2), P343 (2015).
Eissa, I. R., Naoe, Y., Bustos-Villalobos, I., Ichinose, T., Tanaka, M., Zhiwen, W. et al. Genomic signature of the natural oncolytic herpes simplex virus HF10 and its therapeutic role in preclinical and clinical trials. Front. Oncol. 7, 149 (2017).
Fein, S., Guttman, L., Marino, M.T. & Fong, Y. A first-in-human phase 1 ascending, multiple dose, safety and tolerance study of Vaxinia (CF33-hNIS), a novel chimeric oncolytic poxvirus, administered intratumorally or intravenously in adult patients with mixed advanced solid tumors (MAST) (American Association for Cancer Research Annual Meeting, Washington, DC, 2020).
ClinicalTrials.gov. Immunization strategy with intra-tumoral injections of Pexa-Vec with ipilimumab in metastatic/advanced solid tumors. (ISI-JX). https://clinicaltrials.gov/ct2/show/NCT02977156?intr=JX-594&draw=2&rank=17 (2019).
ClinicalTrials.gov. A pilot study of sequential ONCOS-102, an engineered oncolytic adenovirus expressing GM-CSF, and pembrolizumab in patients with advanced or unresectable melanoma progressing after programmed cell death protein 1 (PD1) blockade. https://clinicaltrials.gov/ct2/show/NCT03003676?cond=Melanoma&intr=ONCOS102&rank=1 (2019).
Middleton, M., Sacco, J., Merchan, J., Thomassen, A., Curti, B., VanderWalde, A. et al. Initial results of the phase 1 portion of an ongoing phase 1/2 study of RP1 as a single agent and in combination with nivolumab in patients with solid tumors. J. Immunother. Cancer 7(Suppl 1), 236 (2019).
Shekarian, T., Valsesia-Wittmann, S., Brody, J., Michallet, M. C., Depil, S., Caux, C. et al. Pattern recognition receptors: immune targets to enhance cancer immunotherapy. Ann. Oncol. 28, 1756–1766 (2017).
Takeuchi, O. & Akira, S. Pattern recognition receptors and inflammation. Cell 140, 805–820 (2010).
Melisi, D., Frizziero, M., Tamburrino, A., Zanotto, M., Carbone, C., Piro, G. et al. Toll-like receptor 9 agonists for cancer therapy. Biomedicines 2, 211–228 (2014).
Long, G. V., Milhem, M., Amin, A., Hoimes, C. J., Medina, D., Conry, R. et al. Phase Ib/II, open label, multicenter, study of the combination of SD-101 and pembrolizumab in patients with advanced melanoma who are naïve to anti-PD-1/L1 therapy. Ann. Oncol. 29(Suppl 8), viii736 (2018).
Ribas, A., Medina, T., Kummar, S., Amin, A., Kalbasi, A., Drabick, J. J. et al. SD-101 in combination with pembrolizumab in advanced melanoma: results of a phase Ib, multicenter study. Cancer Disco. 8, 1250–1257 (2018).
Barsoum, J., Renn, M., Schuberth, C., Jakobs, C., Schwickart, A., Schlee, M. et al. Selective stimulation of RIG-I with a novel synthetic RNA induces strong anti-tumor immunity in mouse tumor models. Cancer Immunol. Res. 5(Suppl 1), B44 (2017).
Fu, J., Kanne, D. B., Leong, M., Glickman, L. H., McWhirter, S. M., Lemmens, E. et al. STING agonist formulated cancer vaccines can cure established tumors resistant to PD-1 blockade. Sci. Transl. Med. 7, 283ra252 (2015).
ClinicalTrials.gov. Study of the safety and efficacy of MIW815 (ADU-S100) in patients with advanced/metastatic solid tumors or lymphomas. https://clinicaltrials.gov/ct2/show/NCT02675439 (2017).
ClinicalTrials.gov. Study of the safety and efficacy of MIW815 with PDR001 to patients with advanced/metastatic solid tumors or lymphomas. https://clinicaltrials.gov/ct2/show/NCT03172936?intr=ADU-S100&rank=2 (2019).
ClinicalTrials.gov. Study of MK-1454 alone or in combination with pembrolizumab in participants with advanced/metastatic solid tumors or lymphomas (MK-1454-001). https://clinicaltrials.gov/ct2/show/NCT03010176?intr=MK-1454&rank=1 (2019).
Johnson, D. H., Lecagoonporn, S., Beratchez, C., Haymaker, C., Bentebibel, S., Uemura, M. et al. Phase I/II safety and efficacy study of image guided intratumoral CD40 agonistic monoclonal antibody APX005M in combination with systemic pembrolizumab in metastatic melanoma patients. J. Immunother. Cancer 5(Suppl 2), 122 (2017).
Samoylenko, I., Korotkova, O. V., Zabotina, T. & Demidov, L. V. Intralesional anti-PD1 treatment in patients with metastatic melanoma: the pilot study. J. Clin. Oncol. 36(Suppl 1), 188 (2018).
ClinicalTrials.gov. A trial evaluating the safety & efficacy of intra-tumoral ipilimumab in combination with intra-venous nivolumab in patients with metastatic melanoma (NIVIPIT). https://clinicaltrials.gov/ct2/show/NCT02857569?term=nivolumab&cond=melanoma&draw=5&rank=44 (2016).
Weide, B., Eigentler, T. K., Pflugfelder, A., Zelba, H., Martens, A., Pawelec, G. et al. Intralesional treatment of stage III metastatic melanoma patients with L19-IL2 results in sustained clinical and systemic immunologic responses. Cancer Immunol. Res. 2, 668–678 (2014).
Canton, D. A., Shirley, S., Wright, J., Connolly, R., Burkart, C., Mukhopadhyay, A. et al. Melanoma treatment with intratumoral electroporation of tavokinogene telseplasmid (pIL-12, tavokinogene telseplasmid). Immunotherapy 9, 1309–1321 (2017).
Philogen S.p.A. Neoadjuvant L19IL2/L19TNF- Pivotal Study (Pivotal). https://clinicaltrials.gov/ct2/show/NCT02938299?term=NCT02938299&rank=1 (2016).
Algazi, A., Tsai, K.K., Bannavong, D., Shainsky, V., Talia, R., Browning, E., et al. Clinical immune monitoring and biomarker data of tavo monotherapy compared to tavo with pembrolizumab in metastatic melanoma supports the rationale for combination therapy. https://oncosec.com/wp-content/uploads/2018/06/Algazi-SMR-10-19-17-FINAL.pdf (2017).
Bedard, M., Salio, M. & Cerundolo, V. Harnessing the power of invariant natural killer T cells in cancer immunotherapy. Front. Immunol. 8, 1829 (2017).
ClinicalTrials.gov. Study to evaluate safety & tolerability of AGI-134 in solid tumour. https://clinicaltrials.gov/ct2/show/NCT03593226?intr=AGI-134&rank=1 (2019).
Shaw, S. M., Middleton, J., Wigglesworth, K., Charlemagne, A., Schulz, O., Glossop, M. S. et al. AGI-134: a fully synthetic alpha-Gal glycolipid that converts tumors into in situ autologous vaccines, induces anti-tumor immunity and is synergistic with an anti-PD-1 antibody in mouse melanoma models. Cancer Cell Int. 19, 346 (2019).
ClinicalTrials.gov. pDNA intralesional cancer vaccine for cutaneous melanoma. https://clinicaltrials.gov/ct2/show/NCT03655756 (2018).
Markowitz, J., Brohl, A., Sarnaik, A.A., Eroglu, Z., De Aquino, D.B., Khushalani, N., et al. Trial in progress: IFx-Hu2.0 (plasmid DNA coding for Emm55 streptococcal antigen in a cationic polymer) phase I first in human study for unresectable stage III or stage IV cutaneous melanoma. (American Association for Cancer Research Annual Meeting, Washington, DC, 2020).
Jimeno, A., Gupta, S., Sullivan, R., Do, J. T., Akerley, W. L., Wang, D., et al. A phase 1/2, open-label, multicenter, dose escalation and efficacy study of mRNA-2416, a lipid nanoparticle encapsulated mRNA encoding human OX40L, for intratumoral injection alone or in combination with durvalumab for patients with advanced malignancies. (American Association for Cancer Research Annual Meeting, Washington, DC, 2020).
Hoeller, C., Michielin, O., Ascierto, P. A., Szabo, Z. & Blank, C. U. Systematic review of the use of granulocyte–macrophage colony-stimulating factor in patients with advanced melanoma. Cancer Immunol. Immunother. 65, 1015–1034 (2016).
Andtbacka, R.H., Gonzalez, R., Wloch, M.K., Strause, L., Stardal, K., Chu, A., et al. A phase 3 clinical trial to evaluate the safety and efficacy of treatment with 2 mg intralesional Allovectin-7 compared to dacarbazine or temozolomide in subjects with recurrent metastatic melanoma. (10th International Meeting of the Society for Melanoma Research, Philadelphia, 2013).
Sciencemag. A promising new cancer drug has hit a major setback, raising questions about whether the field is moving too fast. http://www.sciencemag.org/news/2018/05/promising-new-cancer-drug-has-hit-major-setback-raising-questions-about-whether-field (2018).
Syn, N. L., Teng, M. W. L., Mok, T. S. K. & Soo, R. A. De-novo and acquired resistance to immune checkpoint targeting. Lancet Oncol. 18, e731–e741 (2017).
Chen, D. S. & Mellman, I. Elements of cancer immunity and the cancer–immune set point. Nature 541, 321 (2017).
Muenst, S., Laubli, H., Soysal, S. D., Zippelius, A., Tzankov, A. & Hoeller, S. The immune system and cancer evasion strategies: therapeutic concepts. J. Intern Med. 279, 541–562 (2016).
Marconcini, R., Spagnolo, F., Stucci, L. S., Ribero, S., Marra, E., Rosa, F. et al. Current status and perspectives in immunotherapy for metastatic melanoma. Oncotarget 9, 12452–12470 (2018).
Long, G. V., Dummer, R., Ribas, A., Puzanov, I., VanderWalde, A., Andtbacka, R. H., et al. Efficacy analysis of MASTERKEY-265 phase 1b study of talimogene laherparepvec and pembrolizumab for unresectable stage IIIB–IV melanoma. J. Clin. Oncol. 15(Suppl), abstract 9568 (2016).
Long, G. V., Dummer, R., Andtbacka, R., Johnson, D., Michielin, O., Martin-Algarra, S. et al. Follow-up analysis of MASTERKEY-265 phase 1b (ph1b) study of talimogene laherparepvec (T-VEC) in combination (combo) with pembrolizumab (pembro) in patients (pts) with unresectable stage IIIB–IVM1c melanoma (MEL). Pigment Cell Melanoma Res. 32, 133–134 (2019).
ClinicalTrials.gov. Pembrolizumab with or without talimogene laherparepvec or talimogene laherparepvec placebo in unresected melanoma (KEYNOTE-034). https://clinicaltrials.gov/ct2/show/NCT02263508?cond=Melanoma&intr=talimogene+laherparepvec&phase=2&rank=3 (2018).
Algazi, A., Tsai, K. K., Rosenblum, M. D., Andtbacka, R. H., Ballesteros-Merino, C., Jensen, S. et al. Clinical and biomarker analyses of a phase II study of intratumoral tavokinogene telseplasmid (Pil-12) plus pembrolizumab in stage III/IV melanoma patients predicted to not respond to anti-PD-1. J. Immunother. Cancer 5(Suppl 3), 14 (2017).
ClinicalTrials.gov. Efficacy, safety, and tolerability of V937 administered intravenously or intratumorally with pembrolizumab (MK-3475) versus pembrolizumab alone in participants with advanced/metastatic melanoma (V937-011). https://clinicaltrials.gov/ct2/show/NCT04152863 (2019).
Puzanov, I., Milhem, M. M., Minor, D., Hamid, O., Li, A., Chen, L. et al. Talimogene laherparepvec in combination with ipilimumab in previously untreated, unresectable stage IIIB-IV melanoma. J. Clin. Oncol. 34, 2619–2626 (2016).
Chesney, J., Puzanov, I., Ross, M., Collichio, F., Milhem, M., Chen, L. et al. Primary results from a randomized (1:1), open-label phase II study of talimogene laherparepvec (T) and ipilimumab (I) vs I alone in unresected stage IIIB–IV melanoma. J. Clin. Oncol. 35(Suppl 1), 9509 (2017).
Chesney, J. A., Puzanov, I., Collichio, F., Singh, P., Milhem, M., Glaspy, J. et al. Talimogene laherparepvec (T-VEC) in combination (combo) with ipilimumab (ipi) versus ipi alone for advanced melanoma: 3-year landmark analysis of a randomized, open-label, phase II trial. Ann. Oncol. 30(Suppl 5), v906–v907 (2019).
Andtbacka, R. H., Ross, M., Agarwala, S. S., Taylor, M., Vetto, J., Neves, R. I. et al. Final results of a phase II multicenter trial of HF10, a replication-competent HSV-1 oncolytic virus, and ipilimumab combination treatment in patients with stage IIIB-IV unresectable or metastatic melanoma. J. Clin. Oncol. 35(Suppl 1), 9510 (2017).
Yokota, K., Isei, T., Uhara, H., Fujisawa, Y., Takenouchi, T., Kiyohara, Y. et al. Final results from phase II of combination with canerpaturev (formerly HF10), an oncolytic viral immunotherapy, and ipilimumab in unresectable or metastatic melanoma in second-or later line treatment. Ann. Oncol. 30(Suppl 5), v557 (2019).
ClinicalTrials.gov. A study of IMO-2125 in combination with ipilimumab versus ipilimumab alone in subjects with anti-PD-1 refractory melanoma (ILLUMINATE-301). https://clinicaltrials.gov/ct2/show/NCT03445533?cond=Melanoma&intr=Ipilimumab&phase=2&rank=1 (2018).
Hu-Lieskovan, S., Moon, J., Campos, D., Grossmann, K. F., Sosman, J. A., Ryan, C. W. et al. Reversing resistance to PD-1 blockade by combination of talimogene laherparepvec (T-VEC) with pembrolizumab (pembro) in advanced melanoma patients following progression on a prior PD-1 inhibitor: SWOG S1607 (NCT#02965716). J. Clin. Oncol. 36(Suppl 1), TPS9603 (2018).
Eggermont, A. M. M., Blank, C. U., Mandala, M., Long, G. V., Atkinson, V., Dalle, S. et al. Adjuvant pembrolizumab versus placebo in resected stage III melanoma. N. Engl. J. Med. 378, 1789–1801 (2018).
Alqathama, A. BRAF in malignant melanoma progression and metastasis: potentials and challenges. Am. J. Cancer Res. 10, 1103–1114 (2020).
Bommareddy, P. K., Aspromonte, S., Zloza, A., Rabkin, S. D. & Kaufman, H. L. MEK inhibition enhances oncolytic virus immunotherapy through increased tumor cell killing and T cell activation. Sci. Transl. Med. 10, eaau0417 (2018).
ClinicalTrials.gov. Combining talimogene laherparepvec with BRAF and MEK inhibitors in BRAF mutated advanced melanoma. https://clinicaltrials.gov/ct2/show/NCT03088176 (2017).
Gutzmer, R., Harrington, K., Hoeller, C., Lebbe, C., Malvehy, J., Ohrling, K. et al. Practical clinical guide for the use of talimogene laherparepvec monotherapy in patients with unresectable melanoma in Europe. Eur. J. Dermatol. 28, 736–749 (2018).
Harrington, K. J., Michielin, O., Malvehy, J., Pezzani Gruter, I., Grove, L., Frauchiger, A. L. et al. A practical guide to the handling and administration of talimogene laherparepvec in Europe. Onco Targets Ther. 10, 3867–3880 (2017).
Canton, D. A., Shirley, S., Wright, J., Connolly, R., Burkart, C., Mukhopadhyay, A. et al. Melanoma treatment with intratumoral electroporation of tavokinogene telseplasmid (pIL-12, tavokinogene telseplasmid). Immunotherapy 9, 1309–1321 (2017).
Seery, V. Intralesional therapy: consensus statements for best practices in administration from the melanoma nursing initiative. Clin. J. Oncol. Nurs. 21, 76–86 (2017).
Andtbacka, R. H., Ross, M., Agarwala, S. S., Taylor, M., Vetto, J., Neves, R. I. et al. Tumour response from phase II study of combination treatment with intratumoral HF10, a replication competent HSV-1 oncolytic virus, and ipilimumab in patients with stage IIIB, IIIC, or IV unresectable or metastatic melanoma. Ann. Oncol. 27(Suppl 6), vi393 (2016).
Hodi, F. S., Hwu, W. J., Kefford, R., Weber, J. S., Daud, A., Hamid, O. et al. Evaluation of immune-related response criteria and RECIST v1.1 in patients with advanced melanoma treated with pembrolizumab. J. Clin. Oncol. 34, 1510–1517 (2016).
Seymour, L., Bogaerts, J., Perrone, A., Ford, R., Schwartz, L. H., Mandrekar, S. et al. iRECIST: guidelines for response criteria for use in trials testing immunotherapeutics. Lancet Oncol. 18, e143–e152 (2017).
Wolchok, J. D., Hoos, A., O’Day, S., Weber, J. S., Hamid, O., Lebbe, C. et al. Guidelines for the evaluation of immune therapy activity in solid tumors: immune-related response criteria. Clin. Cancer Res. 15, 7412–7420 (2009).
Nishino, M., Giobbie-Hurder, A., Gargano, M., Suda, M., Ramaiya, N. H. & Hodi, F. S. Developing a common language for tumor response to immunotherapy: immune-related response criteria using unidimensional measurements. Clin. Cancer Res. 19, 3936–3943 (2013).
Andtbacka, R. H. I., Dummer, R., Gyorki, D. E., Berger, A. C., Conry, R. M., Demidov, L. V. et al. Interim analysis of a randomized, open-label phase 2 study of talimogene laherparepvec (T-VEC) neoadjuvant treatment (neotx) plus surgery (surgx) vs surgx for resectable stage IIIB-IVM1a melanoma (MEL). J. Clin. Oncol. 36(Suppl 1), 9508 (2018).
Aznar, M. A., Tinari, N., Rullan, A. J., Sanchez-Paulete, A. R., Rodriguez-Ruiz, M. E. & Melero, I. Intratumoral delivery of immunotherapy-act locally, think globally. J. Immunol. 198, 31–39 (2017).
Harrington, K. J., Andtbacka, R. H., Collichio, F., Downey, G., Chen, L., Szabo, Z. et al. Efficacy and safety of talimogene laherparepvec versus granulocyte-macrophage colony-stimulating factor in patients with stage IIIB/C and IVM1a melanoma: subanalysis of the Phase III OPTiM trial. Onco Targets Ther. 9, 7081–7093 (2016).
Curti, B., Richards, J., Hallmeyer, S., Faries, M. B., Andtbacka, R. H. I., Daniels, G. et al. Activity of a novel immunotherapy combination of intralesional Coxsackievirus A21 and systemic ipilimumab in advanced melanoma patients previously treated with anti-PD1 blockade therapy. J. Clin. Oncol. 35(Suppl 1), 3014 (2017).
Isei, T., Yokota, K., Uhara, H., Fujisawa, Y., Takenouchi, T., Kiyohara, Y. et al. Topline results from phase II of combination treatment with canerpaturev (HF10), an oncolytic viral immunotherapy, and ipilimumab in patients with unresectable or metastatic melanoma after anti-PD-1 therapy. Ann. Oncol. 29(Suppl 8), viii452–viii453 (2018).
Chen, D. S. & Mellman, I. Oncology meets immunology: the cancer-immunity cycle. Immunity 39, 1–10 (2013).
Andtbacka, R. H., Agarwala, S. S., Ollila, D. W., Hallmeyer, S., Milhem, M., Amatruda, T. et al. Cutaneous head and neck melanoma in OPTiM, a randomized phase 3 trial of talimogene laherparepvec versus granulocyte-macrophage colony-stimulating factor for the treatment of unresected stage IIIB/IIIC/IV melanoma. Head Neck 38, 1752–1758 (2016).
Rehman, H., Silk, A. W., Kane, M. P. & Kaufman, H. L. Into the clinic: Talimogene laherparepvec (T-VEC), a first-in-class intratumoral oncolytic viral therapy. J. Immunother. Cancer 4, 53 (2016).
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Medical writing support, funded by Amgen (Europe) GmbH, was provided by Kelly Soady PhD from Oxford PharmaGenesis, Oxford, UK and Ryan Woodrow from Aspire Scientific, Bollington, UK.
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M.R.M., C.H., O.M., C.R., C.C., K.Ö. and A.H. helped to write the manuscript, reviewed all versions of the manuscript and provided final approval.
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M.R.M. has acted as an advisor for Alkermes, Amgen, Astellas (was OSI), Bioline, Boehringer Ingelheim, Bristol-Myers Squibb, Codiak, CytomX, Eisai, GSK, Kineta, Merck, Novartis, Roche, Silicon Therapeutics and Valo Therapeutics; has received grants from AstraZeneca, GSK and Roche; and has received other types of support from Immunocore, Pfizer, Regeneron, Replimune, TC Biopharma, and Vertex. C.H. has acted as a speaker or advisor for Amgen, Bristol-Myers Squibb, Incyte, Merck Sharp & Dohme, Novartis, Pierre Fabre and Roche. O.M. has received honoraria for advisory roles from Amgen, Bristol-Myers Squibb, Novartis and Roche, and research funding from MSD. Caroline Robert has participated in advisory boards for Amgen, Biothera, Bristol-Myers Squibb, Merck Sharp & Dohme, Novartis and Roche. C.C. has received honoraria for advisory roles from Amgen, AstraZeneca, Bristol-Myers Squibb and Roche. K.Ö. is an employee of Amgen (Europe) GmbH and is a stockholder in Amgen. A.H. has received grants and honoraria from Amgen, Bristol-Myers Squibb, Merck Serono, Merck Sharp & Dohme, Philogen, Pierre Fabre, Provectus, Regeneron and Roche, and has received honoraria from OncoSec.
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Middleton, M.R., Hoeller, C., Michielin, O. et al. Intratumoural immunotherapies for unresectable and metastatic melanoma: current status and future perspectives. Br J Cancer 123, 885–897 (2020). https://doi.org/10.1038/s41416-020-0994-4
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DOI: https://doi.org/10.1038/s41416-020-0994-4
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