The treatment of multiple myeloma (MM) continues to evolve rapidly with arrival of multiple new drugs, and emerging data from randomized trials to guide therapy. Along the disease course, the choice of specific therapy is affected by many variables including age, performance status, comorbidities, and eligibility for stem cell transplantation. In addition, another key variable that affects treatment strategy is risk stratification of patients into standard and high-risk MM. High-risk MM is defined by the presence of t(4;14), t(14;16), t(14;20), gain 1q, del(17p), or p53 mutation. In this paper, we provide algorithms for the treatment of newly diagnosed and relapsed MM based on the best available evidence. We have relied on data from randomized controlled trials whenever possible, and when appropriate trials to guide therapy are not available, our recommendations reflect best practices based on non-randomized data, and expert opinion. Each algorithm has been designed to facilitate easy decision-making for practicing clinicians. In all patients, clinical trials should be considered first, prior to resorting to the standard of care algorithms we outline.
Major changes have occurred in the diagnostic criteria, staging system, response criteria, and treatment for multiple myeloma (MM) in the last decade1. The International Myeloma Working Group (IMWG) diagnostic criteria for MM require 10% or more clonal plasma cells in the bone marrow (and/or a biopsy proven plasmacytoma) plus any one or more myeloma defining events (MDE): end-organ damage (hypercalcemia, renal insufficiency, anemia, or bone lesions) attributable to the underlying plasma-cell disorder, bone marrow clonal plasma cells ≥60%, serum involved to uninvolved free light chain (FLC) ratio ≥100 (provided involved FLC level is ≥100 mg/L), or more than 1 focal lesion (5 mm or more in size) on magnetic resonance imaging (MRI)2. The current IMWG staging system for MM incorporates tumor burden and high-risk cytogenetics, and is referred to as the Revised International Staging System3. Updated IMWG response criteria include definitions for minimal residual disease (MRD) negativity4. These changes in diagnosis, staging, and response assessment have been made necessary by the rapid advances in treatment of the MM, with the arrival of several new drugs (carfilzomib, pomalidomide, daratumumab, elotuzumab, panobinostat, ixazomib, and selinexor). Numerous clinical trials provide data on best practices along the spectrum of the disease. The purpose of this current treatment algorithm is to synthesize the available data in the field and provide an evidence-based approach to the current treatment of newly diagnosed and relapsed MM.
Classification and risk stratification
There are four major subtypes of MM that account for more than 80% of patients with the disease. They include trisomic MM, t(11;14) MM, t(4;14) MM, and MM with translocations of t(14;16) or t(14;20) referred to as MAF MM (Table 1)5. Secondary cytogenetic abnormalities such as deletion 17p, gain 1q, deletion 1p, deletion 13q, or monosomy 13 can occur in any of the primary cytogenetic types of myeloma, and can further modify disease course, response to therapy, and prognosis.
High-risk MM is defined by the presence of t(4;14), t(14;16), t(14;20), deletion 17p, gain 1q, or p53 mutation1. Double-hit MM refers to the presence of any two or more high-risk abnormalities. Triple-hit MM refers to the presence of three or more high-risk abnormalities.
Bone marrow studies must be performed in all patients and must include fluorescent in situ hybridization or other more sensitive means to detect cytogenetic abnormalities. Whole-body low-dose computed tomography (CT) or positron emission tomography–CT studies are preferred over conventional skeletal surveys for bone imaging6. MRI scans are indicated in patients felt to have clinical smoldering multiple myeloma (SMM) to rule out focal bone marrow lesions. In patients who are in CR, MRD assessment by next-generation flow cytometry or next-generation sequencing is recommended7,8.
Several drugs have shown activity in MM and are available for clinical use. As a result, there are numerous regimens that use two or more of these active drugs available for the treatment of MM in various settings. The major classes include alkylating agents (melphalan, cyclophosphamide) corticosteroids (dexamethasone, prednisone), immunomodulatory drugs (thalidomide, lenalidomide, pomalidomide), and proteasome inhibitors (bortezomib, carfilzomib, ixazomib). Daratumumab and isatuximab are monoclonal (M) antibodies targeting CD38, and are playing an increasingly important role in the treatment of MM. Other active approved agents include elotuzumab, a M antibody targeting the SLAMF7 antigen; panobinostat, a histone deacetylase inhibitor; and selinexor, an inhibitor of exportin-1 (XPO1). Elotuzumab, panobinostat, and selinexor do not seem to have significant single-agent activity, but appear to exert their therapeutic effect in combination with other active drugs. Anthracyclines (doxorubicin and liposomal doxorubicin) have minimal single-agent activity in MM. They are used infrequently used in the treatment of MM given availability of other active agents. However, doxorubicin is incorporated into some multi-agent combination regimens for aggressive or refractory MM.
Treatment of newly diagnosed myeloma
The two main factors that drive our approach to newly diagnosed MM are eligibility for autologous stem cell transplantation (ASCT) and risk stratification. The current algorithms for the treatment of symptomatic newly diagnosed MM based on these two factors is shown in Fig. 1. In general, eligibility for ASCT is affected by age, performance status, and comorbidities. Modern treatments can produce deep responses, and some patients can achieve MRD negative state. Although MRD negative status is associated with improved progression-free survival (PFS) and overall survival (OS), it is not the goal of therapy. There are no data from randomized trials that modifying therapy in MRD positive patients in an attempt to make them MRD negative will lead to better outcomes. Ongoing randomized trials are investigating if changing therapy based on MRD results can improve survival in MM. In the absence such data, modifying therapy based on MRD results is not recommended for clinical practice, except young patients with high-risk MM, especially double or triple-hit MM.
Initial therapy in patients eligible for transplantation
As outlined in Fig. 1, patients who candidates for ASCT are treated with 3–4 cycles of induction therapy followed by stem cell harvest. After stem cell harvest, most patients should proceed to ASCT followed by maintenance. However in selected patients who have standard-risk MM, ASCT can be delayed until relapse. Such patients who have deferred ASCT until relapse should resume induction therapy following stem cell harvest, for a few more cycles followed by maintenance.
The preferred initial therapy for patients who are candidates for ASCT is bortezomib, lenalidomide, dexamethasone (VRd). VRd is a well-tolerated regimen with a long track record. It is associated with high overall and complete response (CR) rates. In a Southwest Oncology Group (SWOG) randomized trial, treatment with VRd led to superior PFS and OS compared with lenalidomide plus dexamethasone (Rd)9. A subsequent randomized trial by the Intergroupe Francophone du Myelome found that the 4-year OS rate with VRd was >80% with or without early ASCT10.
An important alternative to VRd in newly diagnosed MM is daratumumab, lenalidomide, and dexamethasone (DRd). DRd has shown significant efficacy in a randomized trial conducted in transplant-ineligible patients, with improved PFS compared with Rd11. Based on overall cost, and strength of long-term data, we prefer VRd over DRd for most patients12. However, DRd is a suitable alternative for patients with preexisting neuropathy or for patients who have intolerance to VRd. In high-risk patients, especially those with double-hit MM or triple-hit MM, we recommend addition of daratumumab to the standard VRd regimen (Dara-VRd). In a randomized phase II trial, Dara-VRd has shown better and deeper responses compared to VRd13. Another quadruplet regimen that has shown promise is daratumumab, bortezomib, thalidomide, dexamethasone (Dara-VTd). In a randomized trial, Dara-VTd was associated with improved PFS, and a trend to better OS compared to bortezomib, thalidomide, dexamethasone (VTd)14. Further data from phase III trials are awaited.
We do not recommend carfilzomib, lenalidomide, dexamethasone (KRd) as initial therapy. In a recent randomized trial by the Eastern Cooperative Oncology Group (ECOG), there was no significant benefit with KRd over VRd in newly diagnosed patients with standard-risk MM15. KRd is more expensive, and is associated with a higher risk of serious cardiac, renal, and pulmonary toxicity than VRd.
In certain settings, the treatment regimens for newly diagnosed MM have to be modified. For example, bortezomib, cyclophosphamide, dexamethasone (VCd) is our preferred regimen in patients presenting with acute renal failure due to light-chain cast nephropathy16. Similarly, VTd is used instead of VRd as initial therapy in countries where lenalidomide is not approved for frontline therapy17. In patients with primary plasma-cell leukemia or significant extramedullary disease, multi-agent combination chemotherapy such as bortezomib/dexamethasone/thalidomide/cisplatin/doxorubicin/cyclophosphamide/etoposide (VDT-PACE) may be needed initially to achieve rapid disease control18.
Initial therapy in patients ineligible for transplantation
The two main options for initial therapy in patients ineligible for ASCT are VRd and DRd (Fig. 1). Melphalan-based regimens are no longer recommended due to concerns about stem cell damage, secondary myelodysplastic syndrome, and acute leukemia. VRd has shown improved OS compared with Rd, and is our preferred choice for initial therapy9. VRd is administered for ~8–12 cycles, followed by maintenance therapy. In frail elderly patients, a lower dose of lenalidomide and dexamethasone should be used. If therapy with VRd is not possible due to inability to travel for parenteral administration, ixazomib can be considered in place of bortezomib.
The main alternative to VRd for initial therapy in transplant-ineligible patients is DRd. DRd is approved for patients with newly diagnosed MM in the United States based on the results of a randomized trial in which PFS was found to be significantly superior to Rd11. MRD negative rates with DRd were also superior. The main disadvantage of DRd, is that unlike VRd where the triplet regimen is only used for a limited duration (8–12 cycles), therapy with DRd requires treatment with all three drugs until disease progression, resulting in a much more expensive and cumbersome regimen in the long term12. Subcutaneous availability of daratumumab may reduce the inconvenience but it still retains many of the disadvantages compared to VRd19.
Dosage and supportive care considerations
There is a significant risk of peripheral neuropathy with VRd and other bortezomib-containing regimens. This can be minimized by using bortezomib in a once-weekly schedule20,21, and by administering the drug through subcutaneously22. For all regimens, dexamethasone should be used once-weekly (low-dose dexamethasone)23. One exception is the first 4 days of therapy in patients with acute light-chain cast nephropathy when dexamethasone can be administered daily, and then switched to once-weekly. In patients who have received prolonged lenalidomide therapy, plerixafor may be needed for adequate stem cell mobilization24.
All patients treated with lenalidomide need deep vein thrombosis and pulmonary embolism prophylaxis. Aspirin is adequate for most patients, but patients at higher risk of thrombosis should receive low-molecular weight heparin, warfarin, or direct thrombin inhibitors25,26,27. All patients receiving proteasome inhibitors need herpes zoster prophylaxis. We recommend prophylaxis against pneumocystis jiroveci for all patients on dexamethasone. We also recommend levofloxacin daily for the first two cycles in all patients with newly diagnosed MM28.
Stem cell transplantation
Autologous stem cell transplantation (ASCT)
ASCT is not curative in MM, but improves median OS by ~12 months29,30,31,32,33,34,35,36. The treatment-related mortality rate is 1–2%. In ~50% of patients, ASCT can be done on an outpatient basis37. The preferred conditioning regimen for ASCT is melphalan, 200 mg/m2. As discussed earlier, the early use of ASCT is preferred, but in some patients with standard-risk MM, ASCT can be delayed until first relapse, primarily based on patient choice38. Three randomized trials conducted prior to the introduction of the VRd regimen showed that OS was similar whether ASCT is done early (after 3–4 cycles of initial therapy) or delayed (at the time of relapse as salvage therapy)32,39,40. A recent randomized trial using VRd as initial therapy found improved PFS but no difference in OS with early ASCT compared to delayed ASCT at the time of first relapse10. Thus, patient and physician preference plays an important role in deciding the timing of ASCT, especially in standard-risk patients. We still prefer early ASCT in most patients since it can be done with low risk, is logistically easier, and provides the longest duration of remission. There is a small risk of therapy-related secondary myelodysplastic syndrome and acute leukemia associated with ASCT.
Tandem (double) ASCT refers to a second planned ASCT after recovery from the first transplantation. The role of tandem ASCT in myeloma is limited. A randomized trial conducted in the United States by the Bone Marrow Transplantation Clinical Trials Network (BMT-CTN) has found no benefit with tandem ASCT41. However, a survival benefit has been found in a randomized trial conducted by the European Myeloma Network42,43. It is likely that the contradictory outcomes in these trials reflect access and availability of new treatment options in the salvage setting. In the US, where multiple options for salvage therapy are available, there seems to be no benefit with tandem ASCT. At present, outside of a clinical trial setting, we consider tandem ASCT only in selected young patients with del 17p.
Allogeneic transplantation remains investigational in MM. Its use should be restricted primarily to clinical trials, and to young patients (<60 years of age) with high-risk MM that is in first relapse. These patients must be counseled about the high treatment-related mortality rate associated with the procedure and the lack of definitive proof of benefit.
A randomized trial by the BMT-CTN found no benefit with administering consolidation therapy post ASCT41. As a result, we do not recommend additional cycles of VRd chemotherapy or other forms of consolidation following ASCT. Post ASCT, we prefer to move straight to maintenance therapy in the absence of significant residual disease.
Lenalidomide has been shown to improve PFS and OS following ASCT, and is the recommended form of maintenance for most patients33,44,45,46,47,48. Based on the results of the SWOG trial we also recommend lenalidomide maintenance to patients who have not undergone ASCT, but have completed initial therapy with a triplet such as VRd9. There is a two- to threefold increase in the risk of second cancers, including therapy-related myelodysplastic syndrome, with lenalidomide and this must be discussed with the patient44,45.
In high-risk patients, bortezomib-based maintenance is preferable. In one randomized trial, bortezomib administered every other week as posttransplant maintenance produced better OS than thalidomide maintenance46. Bortezomib can be given alone given every other week, or as part of low-intensity VRd, to combine the beneficial effects of bortezomib and lenalidomide49. In patients unable to access or tolerate bortezomib, ixazomib is a reasonable alternative that has shown benefit in a placebo controlled randomized trial50.
A present data on optimal duration of maintenance are lacking. Long-term indefinite maintenance is associated with cost, toxicity, and inconvenience. Many patients can benefit from a drug-free interval. Currently an ECOG randomized trial is comparing lenalidomide maintenance given until progression versus a limited duration of 2 years. Trials are also examining if the duration of maintenance can be modified based on MRD results. At present we continue maintenance until progression in the absence of toxicity.
Treatment of relapsed MM
Almost all patients with MM eventually relapse. In fact, MM is a disease characterized by multiple remissions and relapses. With modern therapy, the first relapse of MM occurs after ~3–4 years following initial diagnosis. Each subsequent remission is of shorter duration. Many patients with MM receive five or more lines of therapy in a sequential manner over several years. The remission duration in relapsed MM decreases with each regimen51. The choice of treatment at each relapse is affected by many factors. These include the timing of the relapse, response to prior therapy, aggressiveness of the relapse, and performance status. Patients eligible for ASCT should be considered for transplantation if they had elected to delay the procedure, or if they achieved excellent remission duration with the first ASCT, defined as a remission of 36 months or longer with maintenance.
In general, a triplet regimen is preferred. At each relapse, a regimen that contains at least two new drugs that the patient is not refractory to should be considered. Our algorithm for the treatment of relapsed MM is given in Fig. 2. These recommendations are based on the results of several major randomized trials52,53,54,55,56,57,58,59,60,61,62. Unfortunately in many of these trials, lenalidomide-containing regimens were tested mainly in patient populations who were not previously exposed to lenalidomide. But in current clinical practice most patients have received lenalidomide as initial therapy, which limits the generalizability of these data to some extent.
Treatment of first relapse
Patients who are eligible for ASCT should consider ASCT as salvage therapy at first relapse if they have never had a transplant before, or if they have had a prolonged remission with the first ASCT. If relapse occurs more than 6 months after stopping all therapy, the initial treatment regimen that successfully controlled the MM initially can be reinstituted when possible. For all other patients, the strategy for therapy at first relapse is described below. Treatment for relapsed MM is typically continued until disease progression. However, based on tolerability and response, we do consider increasing the interval between cycles, as well as treatment-free intervals. In general, triplet regimens are preferred, but in some elderly frail patients with indolent relapse, doublet regimens such as pomalidomide, dexamethasone can be considered.
At first relapse, for patients who are not refractory to lenalidomide, multiple triplet regimens can be considered, including DRd, KRd, ixazomib, lenalidomide, dexamethasone (IRd), and elotuzumab, lenalidomide, dexamethasone. Each of these regimens has shown superiority over Rd in randomized trials53,55,56,63. However, none of them have been compared head-to-head with each other to determine the most effective combination for clinical practice64. In the absence of such data, we have to rely on non-randomized comparisons of efficacy and tolerability. Our preferred option is DRd, since it has produced the best reduction in risk of progression compared to Rd, and based on its tolerability. Daratumumab is also available now as a subcutaneous formulation, which reduces infusion-related side effects and reduces the time for administration. KRd is our preferred alternative if daratumumab is not available, or if the patient has been previously treated with daratumumab. For patients who are frail, oral IRd would be a reasonable first choice for relapse.
In patients who are refractory to lenalidomide, options for therapy at first relapse consist of several pomalidomide-based or bortezomib-based combinations. Pomalidomide-based combinations include daratumumab, pomalidomide, dexamethasone, carfilzomib, pomalidomide, dexamethasone (KPd), isatuximab, pomalidomide, dexamethasone, KPd, and elotuzumab, pomalidomide, dexamethasone62,65,66,67. Bortezomib-based combinations include daratumumab, bortezomib, dexamethasone (DVd), VCd, and bortezomib, pomalidomide, dexamethasone57,68,69. Daratumumab, carfilzomib, and dexamethasone can also be considered. Unfortunately none of these regimens have been compared head-to-head in randomized trials. Our preferred choice based on non-randomized comparisons of efficacy data is DVd. However, in patients who have been previously treated with daratumumab, KPd would be our preferred option. Any of the other regimens would also be reasonable alternatives depending on availability and comorbidities. As in newly diagnosed MM, VRd and VTd are also active regimens available for use in relapsed disease70,71.
Although patients refractory to a drug are likely to be refractory to different drug in the same class, two important exceptions do exist. Pomalidomide has clinical activity in patients who are refractory to lenalidomide72, and carfilzomib has activity in patients who are refractory to bortezomib73. Carfilzomib is typically administered twice-weekly at a dose of 27 mg/m2, but a once-weekly schedule of 56–70 mg/m2 may be equally effective and safe, and more convenient74. Carfilzomib has a lower risk of neurotoxicity than bortezomib, but ~5% of patients can experience serious cardiac side effects.
Treatment of second and subsequent relapses
The algorithm for second and subsequent relapses is given in Fig. 2. At each relapse, any of the regimens that were mentioned for use in first relapse can be considered, with the goal of having at least two new drugs that the patient is not refractory two, and preferably from a different drug class. In many instances this may mean the necessity of adding a M antibody to one of the triplets to create a quadruplet regimen. Importantly, alkylator-containing regimens must be considered at this stage. Additional options for second or higher relapses include adding panobinostat to a proteasome-inhibitor containing regimen58, or using a selinexor-containing regimen such as selinexor, bortezomib, dexamethasone75,76. Bendamustine- or anthracycline-containing regimens are used in refractory settings77,78 or the addition of panobinostat to a proteasome-inhibitor containing regimen58. For young high-risk patients with a suitable donor, allogeneic transplantation is an option as well79.
Venetoclax is not approved for use in MM, but is commercially available, and appears to have single-agent activity in patients with t(11;14) subtype of MM80. However, the results of a recent randomized trial found significantly higher mortality with venetoclax in relapsed myeloma despite producing deeper responses and better PFS81. Therefore, venetoclax is best considered investigational, and its use should be restricted to patients with t(11;14) who have relapsed disease.
Each remission is likely to be shorter than the previous one. However, with careful analysis of the various options and combinations possible, we can induce remissions multiple times with creative strategies, provided the patient remains in good performance status and is willing and interested in continuing therapy82. One strategy we have used in selected patients is one to two cycles of a multi-drug regimen such as VDT-PACE to induce a remission, and then try and maintain it with a more manageable triplet regimen. At each step opportunities for clinical trials may open up and should be considered. Allogeneic transplantation can be considered in selected young patients with relapsed or refractory MM in whom a suitable donor cells are available.
Investigational treatment approaches
Several promising treatments are under investigation for MM. One of the most exciting options is chimeric antigen receptor T cells targeting B-cell maturation antigen (BCMA) such as bb212183. In studies so far more than 80% of patients appear to respond, with median response duration of ~12 months. Another promising treatment that has been recently approved in the United States is belantamab mafodotin, a humanized anti-BCMA antibody that is conjugated to monomethyl auristatin-F, a microtubule disrupting agent84. A third promising new strategy is the use of bispecific T-cell engager, such as AMG 70185,86. Cereblon E3 ligase modulators also appear promising87.
Treatment of SMM
SMM is defined by the presence of a serum M protein of ≥3 g/dl (or urine M protein ≥500 mg/24 h) and/or 10–60% BMPCs with no evidence of end-organ damage or other MDE (Table 1)2,88. SMM is a clinically defined heterogeneous entity with some patients having biological premalignancy and some with biologic malignancy. Thus some patients behave like M gammopathy of undetermined significance with very low rate of progression (low-risk SMM), while others develop clinical symptoms and end-organ damage within a few years (high-risk SMM)89. Although no single pathologic or molecular feature that reliably can be used to distinguish these two groups of patients, we can use a combination of factors to differentiate the two groups (Table 2)90. In addition, patients with t(4;14), gain 1q, and del(17p) are at high risk of progression91,92.
The approach to treatment of SMM is shown on Fig. 3. High-risk patients should be offered therapy with lenalidomide or Rd, or enrollment in a clinical trial. In contrast, patients with low-risk SMM should be observed without therapy every 3–4 months, on an indefinite basis. If during follow up, low-risk SMM patients develop an evolving change in M protein level (defined as 10% increase in M protein within the first 6 months of diagnosis if M-protein 3 g/dl and/or 25% increase in M protein within the first 12 months, with a minimum required increase of 0.5 gm/dl) accompanied by an evolving change in hemoglobin (defined as 0.5 g/dl or greater decrease within 12 months of diagnosis), treatment for MM should be considered according to Fig. 1 or 3. These recommendations are based on data showing that such increase is associated with >90% risk of progression within 2 years93
Therapy for high-risk SMM is recommended based on the results of two randomized trials. The first one conducted in Spain found improved PFS and OS with Rd compared with observation in patients with high-risk SMM94. In a subsequent ECOG trial, a significant improvement in time to end-organ damage was found with lenalidomide compared with observation95. Further studies are comparing a preventive approach (lenalidomide or Rd) as we recommend with treatment with a triplet as in newly diagnosed MM96.
Bisphosphonates have been studied in SMM in an attempt to delay bone disease. In a randomized trial, a reduction in skeletal-related events (SRE) has been seen with pamidronate (60–90 mg once a month for 12 months) compared with observation97. In a separate randomized trial, zoledronic acid (4 mg once a month for 12 months) reduced SREs compared to versus observation98. We feel once-yearly bisphosphonate used for the treatment of osteoporosis is appropriate for most low-risk SMM, but based on data from these two randomized trials, more frequent dosing every 3–4 months can be considered for selected high-risk SMM patients.
Rajkumar, S. V. Multiple myeloma: 2020 update on diagnosis, risk-stratification and management. Am. J. Hematol. 95, 548–67 (2020).
Rajkumar, S. V. et al. International Myeloma Working Group updated criteria for the diagnosis of multiple myeloma. Lancet Oncol. 15, e538–e548 (2014).
Palumbo, A. et al. Revised international staging system for multiple myeloma: a report from International Myeloma Working Group. J. Clin. Oncol. Off. J. Am. Soc. Clin. Oncol. 33, 2863–2869 (2015).
Kumar, S. et al. International Myeloma Working Group consensus criteria for response and minimal residual disease assessment in multiple myeloma. Lancet Oncol. 17, e328–e346 (2016).
Kumar, S. & Rajkumar, S. V. The multiple myelomas—current concepts in cytogenetic classification and therapy. Nat. Rev. Clin. Oncol. 15, 409–21 (2018).
Hillengass, J. et al. International myeloma working group consensus recommendations on imaging in monoclonal plasma cell disorders. Lancet Oncol. 20, e302–e312 (2019).
Flores-Montero, J. et al. Next generation flow (NGF) for highly sensitive and standardized detection of minimal residual disease in multiple myeloma. Leukemia 31, 2094–2103 (2017).
Martinez-Lopez, J. et al. Prognostic value of deep sequencing method for minimal residual disease detection in multiple myeloma. Blood 123, 3073–3079 (2014).
Durie, B. G. M. et al. Bortezomib, lenalidomide and dexamethasone vs. lenalidomide and dexamethasone induction followed by lenalidomide and dexamethasone maintenance in patients with newly diagnosed myeloma without intent for immediate autologous stem cell transplant: results of the Randomised Phase III SWOG Trial S0777. Lancet 389, 519–527 (2017).
Attal, M. et al. Autologous transplantation for multiple myeloma in the era of new drugs: a phase III study of the Intergroupe Francophone Du Myelome (IFM/DFCI 2009 Trial). Blood 126, 391 (2015).
Facon, T. et al. Daratumumab plus lenalidomide and dexamethasone for untreated myeloma. N. Engl. J. Med. 380, 2104–2115 (2019).
Kapoor, P. & Rajkumar, S. V. MAIA under the microscope—bringing trial design into focus. Nat. Rev. Clin. Oncol. 16, 339–40 (2019).
Voorhees, P. M. et al. Daratumumab, lenalidomide, bortezomib, & dexamethasone for transplant-eligible newly diagnosed multiple myeloma: GRIFFIN. Blood 136, 936–945 (2020).
Moreau, P. et al. Bortezomib, thalidomide, and dexamethasone with or without daratumumab before and after autologous stem-cell transplantation for newly diagnosed multiple myeloma (CASSIOPEIA): a randomised, open-label, phase 3 study. Lancet 394, 29–38 (2019).
Kumar, S. K. et al. Carfilzomib or bortezomib in combination with lenalidomide and dexamethasone for newly diagnosed myeloma without intent for immediate autologous stem-cell transplant (E1A11): a multicenter, open label, phase 3, randomised, controlled trial. Lancet Oncol. https://doi.org/10.1016/S1470-2045(20)30452-6 (2020).
Burnette, B. L., Leung, N. & Rajkumar, S. V. Renal improvement in myeloma with bortezomib plus plasma exchange. N. Engl. J. Med. 364, 2365–2366 (2011).
Moreau, P. et al. Bortezomib, thalidomide and dexamethasone (VTD) is superior to bortezomib, cyclophosphamide and dexamethasone (VCD) prior to autologous stem cell transplantation for patients with de novo multiple myeloma. Results of the prospective IFM 2013-04 trial. Proc. ASH Annual Meeting (2015).
Barlogie, B. et al. Incorporating bortezomib into upfront treatment for multiple myeloma: early results of total therapy 3. Br. J. Haematol. 138, 176–85 (2007).
Mateos, M. V. et al. Subcutaneous versus intravenous daratumumab in patients with relapsed or refractory multiple myeloma (COLUMBA): a multicentre, open-label, non-inferiority, randomised, phase 3 trial. Lancet Haematol. 7, e370–e380 (2020).
Mateos, M. V., Oriol, A. & Martinez-Lopez, J. Bortezomib/melphalan/prednisone (VMP) versus bortezomib/thalidomide/prednisone (VTP) as induction therapy followed by maintenance treatment with bortezomib/thalidomide (VT) versus bortezomib/prednisone (VP): a randomised trial in elderly untreated patients with multiple myeloma older than 65 years. Lancet Oncol. 11, 934–941 (2010).
Palumbo, A. et al. Bortezomib-melphalan-prednisone-thalidomide followed by maintenance with bortezomib-thalidomide compared with bortezomib-melphalan-prednisone for initial treatment of multiple myeloma: a randomized controlled trial. J. Clin. Oncol. 28, 5101–5109 (2010).
Moreau, P. et al. Subcutaneous versus intravenous administration of bortezomib in patients with relapsed multiple myeloma: a randomised, phase 3, non-inferiority study. Lancet Oncol. 12, 431–40 (2011).
Rajkumar, S. V. et al. Lenalidomide plus high-dose dexamethasone versus lenalidomide plus low-dose dexamethasone as initial therapy for newly diagnosed multiple myeloma: an open-label randomised controlled trial. Lancet Oncol. 11, 29–37 (2010).
Kumar, S. et al. Mobilization in myeloma revisited: IMWG consensus perspectives on stem cell collection following initial therapy with thalidomide-, lenalidomide-, or bortezomib-containing regimens. Blood 114, 1729–1735 (2009).
Palumbo, A. et al. Aspirin, warfarin, or enoxaparin thromboprophylaxis in patients with multiple myeloma treated with thalidomide: a phase III, open-label, randomized trial. J. Clin. Oncol. 29, 986–993 (2011).
Larocca, A. et al. Aspirin or enoxaparin thromboprophylaxis for newly-diagnosed multiple myeloma patients treated with lenalidomide. Blood 119, 933–939 (2011).
Palumbo, A. et al. Prevention of thalidomide- and lenalidomide-associated thrombosis in myeloma. Leukemia 22, 414–423 (2008).
Drayson, M. T. et al. Levofloxacin prophylaxis in patients with newly diagnosed myeloma (TEAMM): a multicentre, double-blind, placebo-controlled, randomised, phase 3 trial. Lancet Oncol. 20, 1760–72 (2019).
Attal, M. et al. A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma. Intergroupe Francais du Myelome. N. Engl. J. Med. 335, 91–97 (1996).
Child, J. A. et al. High-dose chemotherapy with hematopoietic stem-cell rescue for multiple myeloma. N. Engl. J. Med. 348, 1875–83 (2003).
Fermand, J. P. et al. High-dose therapy and autologous blood stem-cell transplantation compared with conventional treatment in myeloma patients aged 55 to 65 years: long-term results of a randomized control trial from the Group Myelome-Autogreffe. J. Clin. Oncol. 23, 9227–33 (2005).
Barlogie, B. et al. Standard chemotherapy compared with high-dose chemoradiotherapy for multiple myeloma: final results of phase III US Intergroup Trial S9321. J. Clin. Oncol. 24, 929–936 (2006).
Palumbo, A. et al. Autologous transplantation and maintenance therapy in multiple myeloma. N. Engl. J. Med. 371, 895–905 (2014).
Gay, F. et al. Chemotherapy plus lenalidomide versus autologous transplantation, followed by lenalidomide plus prednisone versus lenalidomide maintenance, in patients with multiple myeloma: a randomised, multicentre, phase 3 trial. Lancet Oncol. 16, 1617–1629 (2015).
Cavo, M. et al. Autologous stem cell transplantation versus bortezomib-melphalan-prednisone for newly diagnosed multiple myeloma: second interim analysis of the phase 3 EMN02/HO95 study. Blood 130, 397 (2017).
Attal, M. et al. Lenalidomide, bortezomib, and dexamethasone with transplantation for myeloma. N. Engl. J. Med. 376, 1311–1320 (2017).
Gertz, M. A. et al. Autologous stem cell transplantation in 716 patients with multiple myeloma: low treatment-related mortality, feasibility of outpatient transplantation, and impact of a multidisciplinary quality initiative. Mayo Clin. Proc. 83, 1131–1135 (2008).
Kumar, S. K., Buadi, F. K. & Rajkumar, S. V. Pros and cons of frontline autologous transplant in multiple myeloma: the debate over timing. Blood 133, 652–659 (2019).
Fermand, J. P. et al. High-dose therapy and autologous peripheral blood stem cell transplantation in multiple myeloma: up-front or rescue treatment? Results of a multicenter sequential randomized clinical trial. Blood 92, 3131–3136 (1998).
Facon, T. et al. Front-line or rescue autologous bone marrow transplantation (ABMT) following a first course of high dose melphalan (HDM) in multiple myeloma (MM). Preliminary results of a prospective randomized trial (CIAM) protocol. Blood 88, 685a (1996).
Stadtmauer, E. A. et al. Comparison of autologous hematopoietic cell transplant (autoHCT), bortezomib, lenalidomide (Len) and dexamethasone (RVD) consolidation with len maintenance (ACM), tandem autohct with len maintenance (TAM) and autohct with len maintenance (AM) for up-front treatment of patients with multiple myeloma (MM): primary results from the randomized phase III trial of the blood and marrow transplant clinical trials network (BMT CTN 0702-StaMINA Trial). Blood 2016;128:LBA-1-LBA-1.
Cavo, M. et al. Double autologous stem cell transplantation significantly prolongs progression-free survival and overall survival in comparison with single autotransplantation in newly diagnosed multiple myeloma: an analysis of phase 3 EMN02/HO95 study. Blood 130, 401 (2017).
Cavo, M. et al. Autologous haematopoietic stem-cell transplantation versus bortezomib-melphalan-prednisone, with or without bortezomib-lenalidomide-dexamethasone consolidation therapy, and lenalidomide maintenance for newly diagnosed multiple myeloma (EMN02/HO95): a multicentre, randomised, open-label, phase 3 study. Lancet Haematol. 7, e456–e468 (2020).
Attal, M. et al. Lenalidomide maintenance after stem-cell transplantation for multiple myeloma. N. Engl. J. Med. 366, 1782–1791 (2012).
McCarthy, P. L. et al. Lenalidomide after stem-cell transplantation for multiple myeloma. N. Engl. J. Med. 366, 1770–1781 (2012).
Sonneveld, P. et al. Bortezomib induction and maintenance treatment in patients with newly diagnosed multiple myeloma: results of the randomized phase III HOVON-65/ GMMG-HD4 trial. J. Clin. Oncol. 30, 2946–2955 (2012).
Palumbo, A. et al. Continuous lenalidomide treatment for newly diagnosed multiple myeloma. N. Engl. J. Med. 366, 1759–1769 (2012).
Benboubker, L. et al. Lenalidomide and dexamethasone in transplant-ineligible patients with myeloma. N. Engl. J. Med. 371, 906–917 (2014).
Nooka, A. K. et al. Consolidation and maintenance therapy with lenalidomide, bortezomib and dexamethasone (RVD) in high-risk myeloma patients. Leukemia 28, 690–693 (2014).
Dimopoulos, M. A. et al. Oral ixazomib maintenance following autologous stem cell transplantation (TOURMALINE-MM3): a double-blind, randomised, placebo-controlled phase 3 trial. Lancet 393, 253–264 (2019).
Kumar, S. K. et al. Clinical course of patients with relapsed multiple myeloma. Mayo Clin. Proc. 79, 867–874 (2004).
Lonial, S. et al. Elotuzumab therapy for relapsed or refractory multiple myeloma. N. Engl. J. Med. 373, 621–631 (2015).
Stewart, A. K. et al. Carfilzomib, lenalidomide, and dexamethasone for relapsed multiple myeloma. N. Engl. J. Med. 372, 142–152 (2015).
Siegel, D. S. et al. Improvement in overall survival with carfilzomib, lenalidomide, and dexamethasone in patients with relapsed or refractory multiple myeloma. J. Clin. Oncol. 36, 728–734 (2018).
Moreau, P. et al. Oral ixazomib, lenalidomide, and dexamethasone for multiple myeloma. N. Engl. J. Med. 374, 1621–1634 (2016).
Dimopoulos, M. A. et al. Daratumumab, lenalidomide, and dexamethasone for multiple myeloma. N. Engl. J. Med. 375, 1319–1331 (2016).
Palumbo, A. et al. Daratumumab, bortezomib, and dexamethasone for multiple myeloma. N. Engl. J. Med. 375, 754–766 (2016).
San-Miguel, M. D. J. F., Hungria, V. T. M. & Yoon, M. D. S. Randomized phase 3 trial of the deacetylase inhibitor panobinostat plus bortezomib and dexamethasone versus placebo plus bortezomib and dexamethasone in relapsed or relapsed and refractory multiple myeloma. Lancet Oncol. 15, 1195–1206 (2014).
San Miguel, J. et al. Pomalidomide plus low-dose dexamethasone versus high-dose dexamethasone alone for patients with relapsed and refractory multiple myeloma (MM-003): a randomised, open-label, phase 3 trial. Lancet Oncol. 14, 1055–1066 (2013).
Dimopoulos, M. A. et al. Carfilzomib and dexamethasone versus bortezomib and dexamethasone for patients with relapsed or refractory multiple myeloma (ENDEAVOR): a randomised, phase 3, open-label, multicentre study. Lancet Oncol. 17, 27–38 (2016).
Dimopoulos, M. A. et al. Carfilzomib or bortezomib in relapsed or refractory multiple myeloma (ENDEAVOR): an interim overall survival analysis of an open-label, randomised, phase 3 trial. Lancet Oncol. 18, 1327–1337 (2017).
Attal, M. et al. Isatuximab plus pomalidomide and low-dose dexamethasone versus pomalidomide and low-dose dexamethasone in patients with relapsed and refractory multiple myeloma (ICARIA-MM): a randomised, multicentre, open-label, phase 3 study. Lancet 394, 2096–2107 (2019).
Dimopoulos, M. A. et al. Elotuzumab plus lenalidomide/dexamethasone for relapsed or refractory multiple myeloma: ELOQUENT-2 follow-up and post-hoc analyses on progression-free survival and tumour growth. Br. J. Haematol. 178, 896–905 (2017).
Rajkumar, S. V. & Kyle, R. A. Progress in myeloma—a monoclonal breakthrough. N. Engl. J. Med. 375, 1390–1392 (2016).
Chari, A. et al. Daratumumab plus pomalidomide and dexamethasone in relapsed and/or refractory multiple myeloma. Blood 130, 974–981 (2017).
Bringhen, S. et al. Once-weekly carfilzomib, pomalidomide, and low-dose dexamethasone for relapsed/refractory myeloma: a phase I/II study. Leukemia 32, 1803–1807 (2018).
Dimopoulos, M. A. et al. Elotuzumab plus pomalidomide and dexamethasone for multiple myeloma. N. Engl. J. Med. 379, 1811–1822 (2018).
Kropff, M. et al. Bortezomib and low-dose dexamethasone with or without continuous low-dose oral cyclophosphamide for primary refractory or relapsed multiple myeloma: a randomized phase III study. Ann. Hematol. 96, 1857–1866 (2017).
Richardson, P. G. et al. Pomalidomide, bortezomib, and dexamethasone for patients with relapsed or refractory multiple myeloma previously treated with lenalidomide (OPTIMISMM): a randomised, open-label, phase 3 trial. Lancet Oncol. 20, 781–794 (2019).
Pineda-Roman, M. et al. VTD combination therapy with bortezomib-thalidomide-dexamethasone is highly effective in advanced and refractory multiple myeloma. Leukemia 22, 1419–1427 (2008).
Richardson, P. G. et al. Multicenter, phase I, dose-escalation trial of lenalidomide plus bortezomib for relapsed and relapsed/refractory multiple myeloma. J. Clin. Oncol. 27, 5713–5719 (2009).
Richardson, P. G. et al. Pomalidomide alone or in combination with low-dose dexamethasone in relapsed and refractory multiple myeloma: a randomized phase 2 study. Blood 123, 1826–1832 (2014).
Siegel, D. S. et al. A phase 2 study of single-agent carfilzomib (PX-171-003-A1) in patients with relapsed and refractory multiple myeloma. Blood 120, 2817–2825 (2012).
Bringhen, S. et al. Once-weekly versus twice-weekly carfilzomib in patients with newly diagnosed multiple myeloma: a pooled analysis of two phase I/II studies. Haematologica 104, 1640–1647 (2019).
Chari, A. et al. Oral selinexor-dexamethasone for triple-class refractory multiple myeloma. N. Engl. J. Med. 381, 727–738 (2019).
Dimopoulos M. A., et al. Weekly selinexor, bortezomib, and dexamethasone (SVd) versus twice weekly bortezomib and dexamethasone (Vd) in patients with multiple myeloma (MM) after one to three prior therapies: initial results of the phase III BOSTON study. Proc. ASCO Annual Meeting Abstracts, A8501(2020).
Mey, U. J. et al. Bendamustine, lenalidomide and dexamethasone (BRd) has high activity as 2(nd) -line therapy for relapsed and refractory multiple myeloma - a phase II trial. Br. J. Haematol. 176, 770–82 (2017).
Rodon, P. et al. Phase II study of bendamustine, bortezomib and dexamethasone as second-line treatment for elderly patients with multiple myeloma: the Intergroupe Francophone du Myelome 2009-01 trial. Haematologica 100, e56–e59 (2015).
Laubach, J. et al. Management of relapsed multiple myeloma: recommendations of the International Myeloma Working Group. Leukemia 30, 1005–1017 (2016).
Kumar, S. et al. Efficacy of venetoclax as targeted therapy for relapsed/refractory t(11;14) multiple myeloma. Blood 130, 2401–2409 (2017).
Kumar, S. & Rajkumar, S. V. Surrogate endpoints in randomised controlled trials: a reality check. Lancet 394, 281–283 (2019).
Rajan, A. M., Buadi, F. K. & Rajkumar, V. Effective use of panobinostat in combination with other active agents in myeloma in a novel five-drug combination: case report and interesting observations. Am. J. Hematol. 91, E5–E6 (2016).
Raje, N. et al. Anti-BCMA CAR T-cell therapy bb2121 in relapsed or refractory multiple myeloma. N. Engl. J. Med. 380, 1726–1737 (2019).
Lonial, S. et al. Belantamab mafodotin for relapsed or refractory multiple myeloma (DREAMM-2): a two-arm, randomised, open-label, phase 2 study. Lancet Oncol. 21, 207–221 (2020).
Topp, M. S. et al. Anti-B-cell maturation antigen BiTE molecule AMG 420 induces responses in multiple myeloma. J. Clin. Oncol. 38, 775–783 (2020).
Kumar, S. & Rajkumar, S. V. BiTEing the tumor. J. Clin. Oncol. 38, 2077–2079 (2020).
Bjorklund, C. C. et al. Iberdomide (CC-220) is a potent cereblon E3 ligase modulator with antitumor and immunostimulatory activities in lenalidomide- and pomalidomide-resistant multiple myeloma cells with dysregulated CRBN. Leukemia 34, 1197–1201 (2020).
Kyle, R. A. et al. Clinical course and prognosis of smoldering (Asymptomatic) multiple myeloma. N. Engl. J. Med. 356, 2582–2590 (2007).
Rajkumar, S. V., Landgren, O. & Mateos, M. V. Smoldering multiple myeloma. Blood 125, 3069–3075 (2015).
Lakshman, A. et al. Risk stratification of smoldering multiple myeloma incorporating revised IMWG diagnostic criteria. Blood Cancer J. 8, 59 (2018).
Rajkumar, S. V. et al. Impact of primary molecular cytogenetic abnormalities and risk of progression in smoldering multiple myeloma. Leukemia 27, 1738–1744 (2013).
Neben, K. et al. Progression in smoldering myeloma is independently determined by the chromosomal abnormalities del(17p), t(4;14), gain 1q, hyperdiploidy, and tumor load. J. Clin. Oncol. Off. J. Am. Soc. Clin. Oncol. 31, 4325–4332 (2013).
Ravi, P. et al. Evolving changes in disease biomarkers and risk of early progression in smoldering multiple myeloma. Blood Cancer J. 6, e454 (2016).
Mateos, M.-V. et al. Lenalidomide plus dexamethasone for high-risk smoldering multiple myeloma. N. Engl. J. Med. 369, 438–447 (2013).
Lonial, S. et al. Randomized trial of lenalidomide versus observation in smoldering multiple myeloma. J. Clin. Oncol. 38, 1126–1137 (2020).
Lonial, S., Dhodapkar, M. V., Rajkumar, S. V. Smoldering myeloma and the art of war. J. Clin. Oncol. https://doi.org/10.1200/JCO.20.00875 (2020).
D’Arena, G. et al. Pamidronate versus observation in asymptomatic myeloma: final results with long-term follow-up of a randomized study. Leuk. Lymphoma 52, 771–775 (2011).
Musto, P. et al. A multicenter, randomized clinical trial comparing zoledronic acid versus observation in patients with asymptomatic myeloma. Cancer 113, 1588–1595 (2008).
Supported in part by Grants CA107476, CA168762, and CA186781 from the National Cancer Institute, Rockville, MD, USA.
Conflict of interest
S.K. reports consultancy (BMS/Celgene, Takeda, and Janssen), and research funding (BMS/Celgene, Takeda, Novartis, AbbVie, Janssen, and Amgen). The other author declares that he has no conflict of interest.
Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Rajkumar, S.V., Kumar, S. Multiple myeloma current treatment algorithms. Blood Cancer J. 10, 94 (2020). https://doi.org/10.1038/s41408-020-00359-2
This article is cited by
Integrative analysis of the prognostic value and immune microenvironment of mitophagy-related signature for multiple myeloma
BMC Cancer (2023)
Patient perspectives on considerations, tradeoffs, and experiences with multiple myeloma treatment selection: a qualitative descriptive study
BMC Cancer (2023)
Characterization and application of a lactate and branched chain amino acid metabolism related gene signature in a prognosis risk model for multiple myeloma
Cancer Cell International (2023)
PRMT1 methylation of WTAP promotes multiple myeloma tumorigenesis by activating oxidative phosphorylation via m6A modification of NDUFS6
Cell Death & Disease (2023)
Clinical evidence for immune-based strategies in early-line multiple myeloma: current challenges in decision-making for subsequent therapy
Blood Cancer Journal (2023)