At the MONARCH 3 interim analysis, abemaciclib plus a nonsteroidal aromatase inhibitor (AI) significantly improved progression-free survival (PFS) and objective response rate (ORR) with a tolerable safety profile as initial treatment for hormone receptor-positive (HR+), human epidermal growth factor receptor 2-negative (HER2−) advanced breast cancer (ABC). MONARCH 3 is a randomized, phase III, double-blind study of abemaciclib/placebo (150 mg twice daily, continuous) plus nonsteroidal AI (1 mg anastrozole or 2.5 mg letrozole, daily). A total of 493 postmenopausal women with HR+, HER2− ABC with no prior systemic therapy in this setting were enrolled. The primary endpoint was investigator-assessed PFS (final analysis after 240 events); other endpoints included response and safety evaluations. Here we analyze the final PFS data and update secondary endpoints. The abemaciclib arm had a significantly longer median PFS than the placebo arm (28.18 versus 14.76 months; hazard ratio [95% confidence interval], 0.540 [0.418–0.698]; p = .000002). The ORR was 61.0% in the abemaciclib arm versus 45.5% in the placebo arm (measurable disease, p = .003). The median duration of response was longer in the abemaciclib arm (27.39 months) compared to the placebo arm (17.46 months). The safety profile was consistent with previous reports. The most frequent grade ≥ 3 adverse events in the abemaciclib versus placebo arms were neutropenia (23.9% versus 1.2%), diarrhea (9.5% versus 1.2%), and leukopenia (8.6% versus 0.6%). Abemaciclib plus a nonsteroidal AI was an effective initial treatment with an acceptable safety profile for HR+, HER2− ABC.
Sequential endocrine therapy regimens comprise the standard of care for hormone receptor-positive (HR+) advanced breast cancer.1,2 However, endocrine therapy resistance remains a major clinical challenge, as patients ultimately succumb to progressive disease.3,4 New therapeutic strategies that synergize with endocrine therapies are needed to overcome resistance and potentially prolong patient survival. The primary clinical endpoint to measure resistance to endocrine therapies is progression-free survival (PFS), and improvements in PFS can be associated with overall survival in advanced breast cancer.5,6 However, tumor shrinkage, specifically objective response rate (ORR), is also associated with overall survival in this disease.7,8 Thus, improving the frequency, depth, and duration of response of endocrine-based therapies while overcoming resistance to endocrine therapy may ultimately translate into prolonged survival.
Inhibition of cyclin dependent kinase 4 (CDK4) and cyclin dependent kinase 6 (CDK6) has shown considerable promise in attenuating endocrine therapy resistance.9,10 CDK4 and CDK6 are not only essential for the G1 to S phase cell cycle transition, but also play a central role in the growth of HR+ breast cancer cells.11,12,13,14 Thus, in the clinic, CDK4 and CDK6 inhibition has been an effective means to treat HR+, HER2− advanced breast cancer; currently, three CDK4 and CDK6 inhibitors (palbociclib, ribociclib, and abemaciclib) have been approved in combination with endocrine therapy for the treatment of this disease, based on improvements in PFS and ORR.15,16,17
Abemaciclib is an orally administered CDK4 and CDK6 inhibitor that is 14 times more potent against CDK4/cyclin D1 than CDK6/cyclin D3 (based on enzymatic assays) and, unlike other currently approved CDK4 and CDK6 inhibitors, is dosed on a twice daily continuous schedule.13,15,16,17 In preclinical models, continuous inhibition by abemaciclib was essential for promoting sustained cell cycle arrest, leading to apoptosis or senescence, while short-term inhibition led to a rebound effect upon withdrawal.13,18 Furthermore, preclinical evidence has demonstrated a potential novel role for abemaciclib in promoting anti-tumor immunity through increased antigen presentation and selective inhibition of regulatory T-cell proliferation, possibly suggesting that abemaciclib may be operating through multiple mechanisms to induce tumor shrinkage.19
Abemaciclib was approved in September 2017 by the U.S. Food and Drug Administration (FDA) in combination with fulvestrant for women with HR+, HER2− advanced or metastatic breast cancer that progressed following endocrine therapy, based on significant improvements in PFS and ORR observed in the MONARCH 2 trial.9,17 In addition, abemaciclib is the only CDK4 and CDK6 inhibitor currently approved by the FDA as monotherapy for patients with heavily pretreated HR+, HER2− metastatic breast cancer based on single agent ORR observed in the MONARCH 1 trial.17,20 Abemaciclib has now been approved by the FDA (February 2018) in combination with a nonsteroidal aromatase inhibitor (AI) based on the MONARCH 3 trial (NCT02246621). At the preplanned interim analysis of the MONARCH 3 trial, abemaciclib in combination with a nonsteroidal AI demonstrated significant improvements in PFS and ORR with a generally tolerable safety profile as initial therapy for patients with HR+, HER2− advanced breast cancer.21
Here we present the preplanned final analysis of PFS for the MONARCH 3 trial along with detailed analyses of endpoints associated with objective response, including tumor shrinkage and duration of response. Overall, these analyses demonstrate that abemaciclib in combination with a nonsteroidal AI prolonged PFS; improved the frequency, depth, and duration of response; and provided a tolerability profile consistent with other breast cancer studies of abemaciclib.
Patients and treatment
From November 18, 2014 to November 11, 2015, a total of 493 patients were randomly assigned to abemaciclib plus a nonsteroidal AI (n = 328) or placebo plus a nonsteroidal AI (n = 165) (Supplementary Fig. S1). Baseline patient and disease characteristics were similar between treatment arms and were previously described.21 Briefly, approximatively 80% of patients presented with measurable disease at baseline and 196 (39.8%) patients had de novo metastatic breast cancer. A total of 230 (46.7%) patients had received prior neoadjuvant or adjuvant endocrine therapy, and 191 (38.7%) had received prior neoadjuvant or adjuvant chemotherapy.
At the final PFS cutoff on November 3, 2017, a total of 125 (38.1%) patients in the abemaciclib arm and 35 (21.2%) patients in the placebo arm remained on treatment (Supplementary Fig. S1). The median number of cycles received was 19 in the abemaciclib arm and 15 in the placebo arm. The median relative dose intensity was 85.25% for abemaciclib compared to 98.25% for placebo.
At the final data cutoff, 246 PFS events had occurred, of which 138 (42.1%) were in the abemaciclib arm and 108 (65.5%) were in the placebo arm. The median follow-up was 26.73 months. The median investigator-assessed PFS was 28.18 months in the abemaciclib arm versus 14.76 months in the placebo arm (hazard ratio [HR] [95% confidence interval (CI)]: 0.540 [0.418 to 0.698]; p = .000002) (Fig. 1a). These PFS results were consistent with the independent central review assessment of PFS (HR [95% CI]: 0.465 [0.339 to 0.636]; p < .000001) (Fig. 1b). Analysis of PFS across patient subgroups demonstrated that all patient subgroups benefited from the addition of abemaciclib to nonsteroidal AI (Fig. 2).
For the intent-to-treat (ITT) population, the ORR was 49.7% (95% CI 44.3–55.1%) in the abemaciclib arm and 37.0% (95% CI 29.6–44.3%) in the placebo arm (p = .005) (Table 1). Patients with bone-only non-measurable disease cannot have a best response of partial response; thus, the remaining analyses focus on a subset of 399 patients (80.9%) with measurable disease. In patients with measurable disease, the ORR was 61.0% (95% CI 55.2–66.9%) in the abemaciclib arm versus 45.5% (95% CI 37.0–53.9%) in the placebo arm (p = .003), including 9 (3.4%) complete responses in the abemaciclib arm and none in the placebo arm (Table 1). The best percentage change in tumor size for patients with measurable disease was greater for those in the abemaciclib arm than in the placebo arm (Fig. 3a). The median time to initial response was similar between arms (3.58 months in the abemaciclib arm and 3.65 months in the placebo arm). However, an exploratory analysis of mean change in tumor size demonstrated that after 2 cycles, tumor size in the abemaciclib arm decreased by 27.7% compared to 16.6% in the placebo arm. Tumor shrinkage in the abemaciclib arm continued for at least 24 cycles (approximately 22 months), whereas tumor shrinkage in the placebo arm plateaued after approximately 10–12 cycles of treatment (Fig. 3b). Following 24 cycles of treatment, the mean decrease in tumor size was 76.1% in the abemaciclib arm and 50.0% in the placebo arm.
For patients who responded to abemaciclib, the response typically occurred within the first 8 months of treatment (Fig. 4a). Median duration of response was considerably longer in the abemaciclib arm (27.39 months) than in the placebo arm (17.46 months) (Fig. 4b). Duration of response curves cannot be directly compared by traditional statistical methods, and thus were compared by the probability of being in response function (PBRF) and expected duration of response (EDoR) methods.22 The PBRF provides an estimate of the proportion of patients in response over time, presenting simultaneously the time to response and the duration of response for patients with measurable disease. The rate at which the curve initially rises corresponds to the time it takes to obtain a response, confirming a similar time to response in both treatment arms (Fig. 4c). The maximum probability of being in response was reached at approximately 9 months after randomization in the abemaciclib arm and approximately 11 months after randomization in the placebo arm; at these times, the maximum probability of being in response was 53.4% in the abemaciclib arm and 38.1% in the placebo arm. Finally, the rate of decrease of the curve was slower in the abemaciclib arm compared to the placebo arm, suggesting more durable responses in the abemaciclib arm. Approximately two years after randomization, out of 112 patients with measurable disease, almost twice as many patients in the abemaciclib arm were in a responding state compared to placebo, 45.5% versus 23.5%, respectively, a difference considerably larger than the observed difference in the ORR. The EDoR were estimated to 21.4 months in the abemaciclib arm and 9.0 months in the placebo arm. The EDoR ratio for abemaciclib compared to placebo was 2.39 (p < 0.001), indicating that the EDoR was significantly higher for patients receiving abemaciclib.
The safety profile was consistent with the interim analysis (Table 2). In the abemaciclib and placebo arms, 15 deaths (4.6%) (11 due to adverse events) and 3 (1.9%) (2 due to adverse events), respectively, occurred either while patients were receiving therapy or within 30 days of treatment discontinuation. Of these, 3 occurred in the abemaciclib arm after the interim analysis cutoff (lung infection [n = 1], respiratory failure [n = 1], cerebrovascular accident [n = 1]) (Table 2).
In the abemaciclib arm, longer follow-up confirmed that diarrhea was typically of low grade (72.8% grade 1 or 2) and often occurred early (69.1% of patients experienced diarrhea in cycle 1). The management of diarrhea appeared generally successful with the incidence dropping below 10% (grade 2) and 1% (grade 3) by cycle 4 (Supplementary Fig. S2). Of the patients who had diarrhea, 74.3% in abemaciclib arm received antidiarrheal medications compared to 30.8% in placebo arm. Diarrhea was managed with dose adjustments: 16.7% of patients in abemaciclib arm had a dose reduction and 19% had a dose omission due to diarrhea. Treatment duration was typically not limited by diarrhea, with 6 (1.8%) of the patients in the abemaciclib arm discontinuing treatment for this event (Supplementary table S1). Of note, 4 of these patients were not given a dose reduction prior to discontinuation. The final analysis confirmed that 43.7% of patients had an adverse event of neutropenia, and grade 3 or 4 neutropenia occurred in 23.9% of patients. While one patient experienced an adverse event of febrile neutropenia at the interim analysis, no new cases were observed at this final analysis.
In this study, there was an imbalance of venous thromboembolic events (VTEs) (abemaciclib arm, n = 20 [6.1%]; placebo arm, n = 1 [0.6%]). Of these, 4 were reported after the interim analysis (all non-serious grade 2 deep vein thromboses).
As would be expected with longer follow-up and the continuous dosing schedule of abemaciclib, dose modification rates were slightly higher compared to the interim analysis. In the abemaciclib versus placebo arms, 152 (46.5%) patients versus 10 (6.2%) patients, respectively, had at least one dose reduction of abemaciclib/placebo due to an adverse event. A total of 82 (25.1%) patients in abemaciclib arm and 7 (4.3%) patients in placebo arm discontinued any study drug as the result of AE. Discontinuation was not due to any specific single adverse event or group of adverse events (Supplementary table S1). Discontinuation of all study treatment due to an adverse event occurred in 54 (16.5%) patients in the abemaciclib arm and 5 (3.1%) in the placebo arm (Supplementary table S1). Furthermore, discontinuation of abemaciclib/placebo (with continuation of nonsteroidal AI) due to an adverse event occurred in 31 (9.5%) patients in the abemaciclib arm and none in the placebo arm. Notably, half of the patients in the abemaciclib arm who discontinued due to an adverse event did not first have a dose reduction (Supplementary Table S2). Conversely, in the abemaciclib arm, 112 (74%) of 152 patients who had a dose reduction due to an adverse event did not discontinue due to toxicity.
Relationship between early diarrhea and PFS
An exploratory analysis was performed to examine the potential relationship between early toxicities associated with abemaciclib and PFS of patients. Compared to the placebo arm, patients treated with abemaciclib who had diarrhea within the first 7 days (HR [95% CI]: 0.49 [0.35–0.67]) or who did not have diarrhea within the first 7 days (HR [95% CI]: 0.58 [0.43–0.78]) had an improvement in PFS (Supplementary Fig. S3). A time-dependent covariate analysis was performed to examine the association between current dose level (150, 100, and 50 mg) and PFS. Compared to being treated at the 150 mg dose level, there was no apparent difference in PFS for patients reduced to 100 mg (HR [95% CI]: 0.764 [0.467–1.251]; p = 0.2849) or to 50 mg (HR [95% CI]: 0.985 [0.511–1.902]; p = 0.9650) (Supplementary Table S3).
Analysis from the preplanned final data cutoff of the MONARCH 3 trial provided efficacy and safety results consistent with the interim analysis. The final PFS data confirmed that abemaciclib dosed on a continuous schedule in combination with a nonsteroidal AI provided statistically significant increases in median PFS and ORR as an initial treatment for postmenopausal women with HR+, HER2− advanced breast cancer. The addition of abemaciclib to a nonsteroidal AI provided PFS benefit across all pre-specified subgroups. Importantly, the responses observed in patients who received abemaciclib generally occurred early, were maintained over time, and led to substantial tumor shrinkage. This activity could be relevant for patients with a large tumor burden.
The addition of abemaciclib to a nonsteroidal AI significantly increased the frequency, depth, and duration of tumor response. However, it is difficult to statistically interpret comparisons of duration of response, which considers the length of response only for the responders in each arm, and thus leads to a potential imbalance of clinical characteristics.22 To address the bias of this approach, the PBRF method can be used to assess the probability of a patient in each arm being in a responding state at any given time after randomization. This methodology was previously shown to be a useful way of comparing response duration of endocrine therapy for advanced breast cancer.23 Here, we found that patients in the abemaciclib arm had an expected duration of response of 21.4 months compared to 9.0 months in the placebo arm. The duration of response in patients treated with abemaciclib was substantiated by the greater than 75% reduction in tumor size observed after 24 cycles.
The safety profile observed at the final PFS cutoff was largely consistent with the interim analysis and with other abemaciclib studies.9,20,21 Although discontinuations due to adverse events were higher in the abemaciclib arm compared to the placebo arm, there was not any single adverse event or group of adverse events responsible for the increased number of discontinuations during the preplanned final PFS analysis. Furthermore, half of the discontinuations occurred without first having a dose reduction. Of note, the majority of patients who had a dose reduction due to an adverse event did not discontinue therapy. Importantly, in the exploratory analysis, there was no apparent loss of efficacy in patients who had a dose reduction due to an adverse event, thus highlighting the importance of finding the optimal dose for each patient experiencing an adverse event, such that toxicities can be managed while seeking to preserve efficacy.
Recently, a systematic review and meta-analysis of randomized controlled trials demonstrated that the combination of CDK4 and 6 inhibitors to endocrine therapy (letrozole or fulvestrant) was associated with a higher incidence of VTE.24 An increase of VTE was observed in the abemaciclib arm in the registration trials MONARCH 29 and MONARCH 3.21 In the abemaciclib arm of MONARCH 3, most of the patients who experienced a VTE were treated with standard anticoagulant medication (17 out of 20). Of the patients who had a VTE, 15 were able to continue therapy.
As reported in the interim analysis, three patients experienced a VTE with a fatal outcome, in one of which the diagnosis was confirmed by CT scan—this patient who underwent a surgery two months prior to starting study treatment, had a pulmonary embolism (PE) and deep vein thrombosis (DVT). One patient with a prior history of PE, hypertension, diabetes, and multiple metastatic lesions experienced respiratory failure, and the cause of death was reported as PE, respiratory failure, and breast cancer. A third patient who was a current tobacco user with history of hypertension, sinus tachycardia, and coronary heart disease experienced a thromboembolism with no further information provided.
As previously reported, diarrhea was generally low grade, typically occurred early in the course of treatment, and in most cases could be effectively managed with antidiarrheal medication and/or dose adjustment if needed.21 No difference in efficacy was observed in patients who experienced diarrhea within the first seven days of treatment compared to those who did not.
Abemaciclib in combination with a nonsteroidal AI had a generally predictable and acceptable tolerability profile. When toxicities are experienced by patients, “one size fits all dosing” often is not an optimal way to administer anticancer medicines. Therefore, it is important to tailor the dose of any medicine to the individual patient by observing early toxicities and making the appropriate dose adjustments at that time. When adopting this approach it is beneficial when the toxicities tend to manifest early and are typically rapidly reversible. The diarrhea induced by abemaciclib is such a toxicity. This analysis suggests that patients who received appropriate early dose reductions of abemaciclib could generally remain on therapy and achieved similar benefit to those who did not require dose reduction.
The results of this trial come in light of recent studies demonstrating a mechanism for CDK4/cyclin D in the regulation of cancer immune surveillance.25 In addition, the role of abemaciclib in promoting immunogenicity of tumor cells was recently proposed.19 Of note, abemaciclib can induce intra-tumor immune inflammation, and the combination of abemaciclib with anti-PD-L1 immunotherapy increased tumor regression in various murine models.19,26 These novel findings suggest that CDK4 and CDK6 inhibitors may be operating via additional mechanisms rather than simply inhibiting cell cycle proliferation and could potentially be playing a critical role in the robust tumor response achieved with abemaciclib in this and other studies. Future studies will be necessary to understand how the implications of these findings may affect treatment strategies.
Overall, this preplanned final PFS analysis of MONARCH 3 confirmed that abemaciclib dosed on a continuous schedule in combination with a nonsteroidal AI significantly improved PFS and ORR compared to placebo plus a nonsteroidal AI as initial therapy for patients with HR+, HER2- advanced breast cancer. Patients treated with abemaciclib plus a nonsteroidal AI experienced a longer duration of response. The safety profile was consistent with other abemaciclib studies, indicating that the combination was generally tolerable and manageable.1,9,20 Thus, abemaciclib in combination with a nonsteroidal AI was an effective treatment option for patients in this disease setting.
Materials and methods
Study design and patients
MONARCH 3 is a randomized, double-blind, phase III trial of abemaciclib or placebo with a nonsteroidal AI (anastrozole or letrozole, per physician’s choice) in postmenopausal women with HR+, HER2− locoregionally recurrent breast cancer not amenable to surgical resection or radiotherapy with curative intent or metastatic disease who have not received prior systemic therapy in the advanced setting. Endocrine therapy in the neoadjuvant or adjuvant setting was permitted if the disease-free interval was greater than 12 months from the completion of endocrine therapy. Detailed inclusion and exclusion criteria were previously described.21 Eligible patients were enrolled at 158 sites in 22 countries.
The MONARCH 3 study was approved by the ethical and local institutional review boards for the sites participating in the clinical trial, and was conducted according to the Declaration of Helsinki. Patients provided written informed consent before enrollment. This study was overseen by a steering committee, and safety data were evaluated quarterly by an independent data monitoring committee.
Eligible patients were randomly assigned to receive abemaciclib on a continuous schedule (150 mg, twice daily) plus nonsteroidal AI (1 mg anastrozole or 2.5 mg letrozole, physician’s choice, daily) or placebo plus nonsteroidal AI in a 2:1 ratio using an interactive, web-based randomization scheme. All drugs were orally administrated during each 28-day cycle. Patients were randomly assigned based on stratification factors: metastatic site (visceral, bone-only, or other) and prior neoadjuvant or adjuvant endocrine therapy (AI, no endocrine therapy, or other). Other treatment procedures were previously described.21
Efficacy and safety assessments
Tumors were assessed by computed tomography or magnetic resonance imaging according to RECIST version 1.1 at baseline (within 28 days before randomization) and every second cycle during cycles 2–18, every third cycle thereafter, and within 2 weeks of clinical progression.
Safety analysis was performed on the safety population defined as all enrolled patients receiving at least one dose of study treatment. Adverse events were graded according to National Cancer Institute Common Terminology Criteria version 4.0 and were evaluated at every patient visit from baseline to follow-up. Laboratory analyses schedules were previously described.21
The primary endpoint was investigator-assessed PFS as defined by RECIST version 1.1, and measured from the time of randomized assignment until progressive disease or death from any cause. Secondary endpoints included ORR (percentage of patients with complete response [CR] or partial response [PR]), disease control rate (percentage of patients with CR, PR, or stable disease [SD]), clinical benefit rate (the percentage of patients with CR, PR, or SD ≥ 6 months), duration of response (time from a confirmed CR or PR until disease progression or death), overall survival (time of randomized assignment until death), and safety.
The MONARCH 3 study was designed to compare the investigator-assessed PFS of patients treated with abemaciclib plus a nonsteroidal AI versus placebo plus a nonsteroidal AI. The primary statistical analysis of PFS was performed on the intent-to-treat (ITT) population defined as all patients randomized to study treatment. A sensitivity analysis was planned to assess the PFS based on a fully blinded, independent central review. Power calculations and methods for analyzing the primary and secondary endpoints were previously reported.21 Subgroup analyses were assessed on subgroups pre-specified in the protocol.
Exploratory analyses of duration of response and change in tumor size were performed. PBRF which incorporates duration of response and ORR, was calculated using the method of Temkin.27 Using the method of Ellis et al.22, EDoR was calculated as the product of the fraction of patients with a response and the mean duration of response in responding patients for each arm assuming a Weibull distribution. The treatments were formally compared based on the ratio of EDoR, which follows a standard normal distribution on the log scale. Change in tumor size over time was compared using a mixed model with an unstructured covariance matrix.
To evaluate the association between early toxicity and efficacy, a landmark analysis was performed for diarrhea. A landmark was selected based on the median time to onset for diarrhea. Patients were stratified by whether diarrhea had or had not been observed by the landmark, and PFS was compared between each of these groups and the placebo arm using a Cox model.
To examine the impact of dose reductions on efficacy, a time-dependent covariate analysis of dose level versus PFS was performed. The dose covariate for all patients was initially set at the study starting dose of 150 mg for all patients and was adjusted at a patient level as physician-directed dose modifications were reported. For patients who discontinued abemaciclib completely prior to progression, the covariate was set to 0 mg from discontinuation to progression.
Lilly makes patient-level data available from Lilly-sponsored studies on marketed drugs for approved uses following acceptance for publication. Lilly is one of several companies that provide this access through the website clinicalstudydatarequest.com. Qualified researchers can submit research proposals and request anonymized data to test new hypotheses. Lilly’s data sharing policies are provided on the clinicalstudydatarequest.com site under the Study Sponsors page.
Cardoso, F. et al. ESO-ESMO international consensus guidelines for Advanced Breast Cancer (ABC 3). Breast 31, 244–259 (2017).
Cardoso, F. et al. ESO-ESMO international consensus guidelines for Advanced Breast Cancer (ABC 3). Ann. Oncol. 28, 16–33 (2017).
Milani, A., Geuna, E., Mittica, G. & Valabrega, G. Overcoming endocrine resistance in metastatic breast cancer: current evidence and future directions. World J. Clin. Oncol. 5, 990–1001 (2014).
Castrellon, A. B. Novel strategies to improve the endocrine therapy of breast cancer. Oncol. Rev. 11, 323 (2017).
Sherrill, B. et al. Relationship between effects on time-to-disease progression and overall survival in studies of metastatic breast cancer. Br. J. Cancer 99, 1572–1578 (2008).
Beauchemin, C., Cooper, D., Lapierre, M. E., Yelle, L. & Lachaine, J. Progression-free survival as a potential surrogate for overall survival in metastatic breast cancer. OncoTargets Ther. 7, 1101–1110 (2014).
Bruzzi, P. et al. Objective response to chemotherapy as a potential surrogate end point of survival in metastatic breast cancer patients. J. Clin. Oncol. 23, 5117–5125 (2005).
Burzykowski, T. et al. Evaluation of tumor response, disease control, progression-free survival, and time to progression as potential surrogate end points in metastatic breast cancer. J. Clin. Oncol. 26, 1987–1992 (2008).
Sledge, G. W. et al. MONARCH 2: abemaciclib in combination with fulvestrant in women with HR+/HER2- advanced breast cancer who had progressed while receiving endocrine therapy. J. Clin. Oncol. 35, 2875–2884 (2017).
Cristofanilli, M. et al. Fulvestrant plus palbociclib versus fulvestrant plus placebo for treatment of hormone-receptor-positive, HER2-negative metastatic breast cancer that progressed on previous endocrine therapy (PALOMA-3): final analysis of the multicentre, double-blind, phase 3 randomised controlled trial. Lancet Oncol. 17, 425–439 (2016).
Knudsen, E. S. & Knudsen, K. E. Tailoring to RB: tumour suppressor status and therapeutic response. Nat. Rev. Cancer 8, 714–724 (2008).
VanArsdale, T., Boshoff, C., Arndt, K. T. & Abraham, R. T. Molecular pathways: targeting the cyclin D-CDK4/6 axis for cancer treatment. Clin. Cancer Res. 21, 2905–2910, (2015).
Torres-Guzman, R. et al. Preclinical characterization of abemaciclib in hormone receptor positive breast cancer. Oncotarget, https://doi.org/10.18632/oncotarget.17778 (2017).
Finn, R. S. et al. PD 0332991, a selective cyclin D kinase 4/6 inhibitor, preferentially inhibits proliferation of luminal estrogen receptor-positive human breast cancer cell lines in vitro. Breast Cancer Res. 11, R77 (2009).
Caldon, C. E., Swarbrick, A., Lee, C. S., Sutherland, R. L. & Musgrove, E. A. The helix-loop-helix protein Id1 requires cyclin D1 to promote the proliferation of mammary epithelial cell acini. Cancer Res. 68, 3026–3036 (2008).
Timpson, P. et al. Aberrant expression of cortactin in head and neck squamous cell carcinoma cells is associated with enhanced cell proliferation and resistance to the epidermal growth factor receptor inhibitor gefitinib. Cancer Res. 67, 9304–9314 (2007).
van Dam, P. A. et al. Neoadjuvant endocrine treatment in early breast cancer: an overlooked alternative? Eur. J. Surg. Oncol. 42, 333–342 (2016).
Gelbert, L. M. et al. Preclinical characterization of the CDK4/6 inhibitor LY2835219: in-vivo cell cycle-dependent/independent anti-tumor activities alone/in combination with gemcitabine. Invest. New Drugs 32, 825–837 (2014).
Goel, S. et al. CDK4/6 inhibition triggers anti-tumour immunity. Nature 548, 471–475 (2017).
Dickler, M. N. et al. MONARCH 1, a phase 2 study of abemaciclib, a CDK4 and CDK6 inhibitor, as a single agent, in patients with refractory HR+/HER2- metastatic breast cancer. Clin. Cancer Res. 23, 5218–5224 (2017).
Goetz, M. P. et al. MONARCH 3: abemaciclib as initial therapy for advanced breast cancer. J. Clin. Oncol. 35, 3638–3646 (2017).
Ellis, S., Carroll, K. J. & Pemberton, K. Analysis of duration of response in oncology trials. Contemp. Clin. Trials 29, 456–465 (2008).
Garnett, S. A. et al. Comparing duration of response and duration of clinical benefit between fulvestrant treatment groups in the CONFIRM trial: application of new methodology. Breast Cancer Res. Treat. 138, 149–155 (2013).
Thein, K. et al. Abstract P3-14-02: incidence of venous thromboembolism in patients with hormone receptor-positive HER2-negative metastatic breast cancer treated with CDK 4/6 inhibitors: a systematic review and meta-analysis of randomized controlled trials. Cancer Res. 78, P3-14-02-P13-14-02 (2018).
Zhang, J. et al. Cyclin D-CDK4 kinase destabilizes PD-L1 via cullin 3-SPOP to control cancer immune surveillance. Nature 553, 91–95 (2018).
Schaer, D. A. et al. The CDK4/6 inhibitor abemaciclib induces a T cell inflamed tumor microenvironment and enhances the efficacy of PD-L1 checkpoint blockade. Cell Rep. 22, 2978–2994 (2018).
Temkin, N. R. An analysis for transient states with application to tumor shrinkage. Biometrics 34, 571–580 (1978).
We extend our gratitude to the patients and their families and caregivers for participating in the MONARCH 3 trial. We thank the MONARCH study steering committee, in addition to the investigators and their support staff, who generously participated in the MONARCH 3 trial. This trial was funded by Eli Lilly and Company. Writing and editorial support were funded by Eli Lilly and Company: Annie-Carole Trampont (Eli Lilly and Company, Indianapolis, IN) provided medical writing assistance and Cynthia Bush, ELS (Syneos Health, Raleigh, NC) provided editorial assistance.
S.J. is a consultant/independent contractor for AstraZeneca, Novartis, Pfizer, OBI, and Eli Lilly and Company; receives grants/research support from Pfizer; and is on the Speaker’s Bureau for OBI and Puma. M.M. is a consultant/independent contractor AstraZeneca, Novartis, Roche-Genentech, Pfizer, Glaxo, Pharmamar, Taiho Oncology and Eli Lilly and Company; and have received research grants from Novartis and Roche. D.L. has been a consultant/independent contractor for Amgen, Roche, Novartis, Pfizer, AstraZeneca, Eli Lilly and Company, Pierre Fabre, Bayer, Celgene, Puma Biotechnology, and Daichii-Sankyo; has received grant/research support from Novartis, Pfizer, and AstraZeneca; honorarium from Roche, Novartis, Pfizer, AstraZeneca, Genomic Health, Eisai, Eli Lilly and Company, Pierre Fabre, Bayer, Celgene, and Daichii-Sankyo; and received travel/accommodations/expenses from Roche, Novartis, Pfizer, AstraZeneca, Eisai, Eli Lilly and Company, Pierre Fabre, Bayer, Celgene, Puma Biotechnology, and Daichii-Sankyo. S.I. receives grants/research support from AstraZeneca and is an advisory/board member for AstraZeneca, Eisai, Hanmi, Novartis, Pfizer and Roche. A.A. is an advisor/board member for Roche, Pfizer, Eli Lilly and Company, Eisai, Novartis, MSD, and BMS. T.F. is a full-time employee and stock shareholder of Eli Lilly and Company. M.F. is a full-time employee and stock shareholder of Eli Lilly and Company. M.C.H. is a full-time employee and stock shareholder of Eli Lilly and Company. J.C. is a full-time employee of Eli Lilly and Company. S.B. is a full-time employee of Eli Lilly and Company. M.T. is a consultant/independent contractor for Kyowa-Hakko Kirin; received grant/research support from Novartis, AstraZeneca, Taiho Pharma, Chugai Pharmaceutical Co. Ltd., Pfizer, and Eli Lilly and Company; served on an advisory board for Genomic Health Inst; received honorarium from Novartis, MSD, Takeda, AstraZeneca, Taiho Pharma, Chugai Pharmaceutical Co. Ltd., Pfizer, Eisai, Eli Lilly and Company, Kyowa-Hakko Kirin, and Genomic Health Inst.; and received travel funds/accommodations/expenses from Genomic Health Inst. and Eli Lilly and Company. H.I. is a consultant/independent contractor for Pfizer, Daiichi-Sankyo, and AstraZeneca; received grants/research support from Eli Lilly and Company, Chugai, Pfizer, Daiichi-Sankyo, AstraZeneca, Novartis, Bayer, and MSD; is an advisor/board member for Eli Lilly and Company, Chugai, and Daiichi-Sankyo; and received honorarium from Chugai, Pfizer, Eisai, Daiichi-Sankyo, and AstraZeneca. M.P.G. has been a consultant for Eli Lilly and Company, bioTheranostics, Novartis, Genomic Health, Eisai, Biovica, and Sermonix; and received research funding from Eli Lilly and Company, and Pfizer.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Johnston, S., Martin, M., Di Leo, A. et al. MONARCH 3 final PFS: a randomized study of abemaciclib as initial therapy for advanced breast cancer. npj Breast Cancer 5, 5 (2019). https://doi.org/10.1038/s41523-018-0097-z
This article is cited by
The dilemma of selecting a first line CDK4/6 inhibitor for hormone receptor-positive/HER2-negative metastatic breast cancer
npj Breast Cancer (2023)
Position paper on CDK4/6 inhibitors in early breast cancer
memo - Magazine of European Medical Oncology (2023)
Patient characteristics, treatment patterns, and outcomes of hormone receptor-positive, human epidermal growth factor receptor 2-negative advanced breast cancer patients prescribed cyclin-dependent kinase 4 and 6 inhibitors: large-scale data analysis using a Japanese claims database
Breast Cancer Research and Treatment (2023)
The effects of Abemaciclib on cell cycle and apoptosis regulation in anaplastic thyroid cancer cells
Molecular Biology Reports (2023)
Real-world treatment patterns and outcomes of abemaciclib for the treatment of HR + , HER2- metastatic breast cancer patients in Japan
Breast Cancer (2023)