Background Several therapeutic options are now available in the adjuvant melanoma setting, mandating an understanding of their benefit‒risk profiles in order to make informed treatment decisions. Herein we characterize adjuvant nivolumab select (immune-related) treatment-related adverse events (TRAEs) and evaluate possible associations between safety and recurrence-free survival (RFS) in the phase III CheckMate 238 trial.
Methods Patients with resected stage IIIB–C or IV melanoma received nivolumab 3 mg/kg every 2 weeks (n=452) or ipilimumab 10 mg/kg every 3 weeks for four doses and then every 12 weeks (n=453) for up to 1 year or until disease recurrence, unacceptable toxicity, or consent withdrawal. First-occurrence and all-occurrence select TRAEs were analyzed within discrete time intervals: from 0 to 3 months of treatment, from >3–12 months of treatment, and from the last dose (regardless of early or per-protocol treatment discontinuation) to 100 days after the last dose. Possible associations between select TRAEs and RFS were investigated post randomization in 3-month landmark analyses and in Cox model analyses (including a time-varying covariate of select TRAE), within and between treatment groups.
Results From the first nivolumab dose to 100 days after the last dose, first-occurrence select TRAEs were reported in 67.7% (306/452) of patients. First-occurrence select TRAEs were reported most frequently from 0 to 3 months (48.0%), during which the most common were pruritus (15.5%) and diarrhea (15.3%). Most select TRAEs resolved within 6 months. There was no clear association between the occurrence (or not) of select TRAEs and RFS by landmark analysis or by Cox model analysis within treatment arms or comparing nivolumab to the ipilimumab comparator arm.
Conclusion Results of this safety analysis of nivolumab in adjuvant melanoma were consistent with its established safety profile. In the discrete time intervals evaluated, most first-occurrence TRAEs occurred early during treatment and resolved. No association between RFS and select TRAEs was evident.
Trial registration number NCT02388906.
- programmed cell death 1 receptor
Data availability statement
Data are available upon reasonable request. BMS policy on data sharing may be found at HYPERLINK "https://protecteu.mimecast.com/s/8tv9CyQYCWkmRytMnYgD?domain=bms.com" https://www.bms.com/researchers-and-partners/independent-research/data-sharing-request-process.html.
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There is a need for effective adjuvant treatment for patients with high-risk, stage III/IV resected melanoma given that surgical resection alone, while critical for the treatment of the primary tumor, is associated with high rates of relapse. Historically, 5-year recurrence rates in high-risk stage III melanoma after surgery were 50%‒80%1–4 and the 5-year overall survival (OS) rate was approximately 60%.5 6 Adjuvant systemic treatment of melanoma was initially limited to interferon-α and ipilimumab (which is only approved in the USA).7 8 However, new therapies have recently become available, such as the anti-programmed death 1 (PD-1) agents nivolumab and pembrolizumab, and the BRAF/MEK kinase inhibitor combination of dabrafenib plus trametinib.9 10 In the phase III CheckMate 238 trial (ClinicalTrials.gov identifier: NCT02388906), nivolumab 3 mg/kg demonstrated significantly longer recurrence-free survival (RFS) and a lower rate of grade 3–4 adverse events (AEs) than ipilimumab at 10 mg/kg in patients with completely resected stage IIIB/IIIC or stage IV melanoma.11 Based on these results, adjuvant nivolumab was approved globally. With extended follow-up, the RFS benefit with nivolumab was sustained compared with ipilimumab (estimated 48-month RFS rates, 51.7% for nivolumab vs 41.2% for ipilimumab; HR: 0.71; 95% CI: 0.60 to 0.86; p=0.0003).12
With several therapeutic options now available in the adjuvant melanoma setting, an understanding of the benefit‒risk profile of each is needed to make informed treatment decisions. Here we provide a comprehensive evaluation of nivolumab safety in the adjuvant melanoma setting and evaluate possible associations with efficacy using data from the CheckMate 238 trial.
Patients and methods
Eligible patients were age 15 years or older and had stage IIIB/IIIC or stage IV melanoma (per the 2009 classification of the American Joint Committee on Cancer (AJCC), seventh edition,13 an Eastern Cooperative Oncology Group performance status of 0 or 1, and histologically confirmed melanoma with metastases to regional lymph nodes or distant metastases that had been surgically resected. Patients were required to have had complete resection of disease within the 12 weeks before randomization. Patients with resected brain metastases were eligible to participate. Exclusion criteria included a diagnosis of ocular or uveal melanoma, active autoimmune disease, previous non-melanoma cancer without complete remission for more than 3 years, systemic glucocorticoid use, and previous systemic treatment for melanoma (prior interferon therapy was permitted).
CheckMate 238 is an ongoing phase III, randomized, double-blind trial (online supplemental appendix figure A1).11 12 Patients were enrolled from March 30, 2015, to November 30, 2015, at 130 centers in 25 countries. Patients were assigned (1:1) to receive either nivolumab 3 mg/kg every 2 weeks or ipilimumab 10 mg/kg every 3 weeks for four doses and then every 12 weeks, each for a maximum of 1 year or until disease recurrence, unacceptable toxicity, or withdrawal of consent when these occur before 1 year.
Trial endpoints and assessments
The primary endpoint was RFS assessed in the intention-to-treat population; secondary endpoints included OS and safety.11 12 Patients were assessed radiologically and clinically for recurrence every 12 weeks for the first 2 years after randomization and every 6 months thereafter for up to 5 years. RFS was defined as the time from randomization until the date of the first recurrence (local, regional, or distant metastasis), new primary melanoma, or death from any cause. AE data were collected according to Common Terminology Criteria for Adverse Events, version 4.0.14 Patients were followed for safety for up to 100 days following their last dose and select (ie, immune-related) treatment-related adverse events (TRAEs) are investigated here. Select TRAEs were determined based on a prespecified list of terms from the Medical Dictionary for Regulatory Activities. Select TRAEs are those with presumed immune-related etiology that may be mitigated by early recognition and potential management with immunosuppression and for which multiple event terms may be used to describe a single type. As in previous nivolumab reports, those included here were endocrine, gastrointestinal, hepatic, pulmonary, renal, and skin. Endpoints that involve corticosteroid use are reported for both corticosteroid use (without other immunosuppressants) and for corticosteroid use including other immunosuppressants.
Since the approval of PD-1 inhibitors, ipilimumab is no longer a standard of care for the adjuvant treatment of melanoma and therefore, nivolumab treatment is the main focus of this study. However, coordinating data for ipilimumab are included in the online supplemental appendix.
The initial 18-month minimum follow-up analysis for this trial has been previously reported and included a final safety analysis based on data up to 30 days after the last dose.11 12 This report presents the full safety analysis for the entire period for which safety data were collected (100 days after the last dose, per protocol). Select TRAE data collected during treatment and for up to 100 days from the last dose were evaluated within the following discrete time intervals: 0–3 months of treatment, >3–12 months of treatment, and from the last dose (regardless of early or per-protocol treatment discontinuation) to 100 days after the last dose. First-occurrence and all-occurrence (including repeat occurrences) select TRAEs were evaluated within these time intervals. Overall time to onset and time to resolution of select TRAEs were analyzed for events reported between first dose and 100 days after last dose of study therapy.
Association between select TRAEs and RFS
A possible association between select TRAEs and RFS was investigated using efficacy data with a minimum of 24 months of follow-up. All RFS associations were estimated using Kaplan-Meier landmark analysis accounting for guarantee-time bias15 within the first 3 months after randomization. Comparisons were made between patients with and without a select TRAE in the first 3 months, the median time to onset for most select TRAEs. In addition, a Cox model was used to evaluate the association between the occurrence of select TRAEs (or not) and RFS, both within treatment groups and comparing nivolumab to ipilimumab. The model included a time-varying covariate with a value of 0 before the AE onset and 1 after onset and was adjusted for AJCC seventh edition disease stage (stage IIIB, IIIC, IV, or other), sex, and age (<65 years or ≥65 years). The model included the treatment indicator and the product of the treatment indicator and the time-varying select TRAE category indicator. HRs (and 95% CIs) were estimated for the randomized treatment in the presence and absence of select TRAEs. The p values provided are descriptive.
A total of 906 patients were randomized to either nivolumab (n=453) or ipilimumab (n=453). Patient characteristics were reported previously (online supplemental appendix table A1).11 One patient who was randomized to the nivolumab group did not receive treatment. Patients received a median of 24 doses (range: 1–26) of nivolumab and 4 doses (range: 1–7) of ipilimumab. One year of treatment was completed by 61% of nivolumab-treated patients and 27% of ipilimumab-treated patients, with the majority of treatment discontinuations due to disease recurrence with nivolumab (121/177) and to study drug toxicity with ipilimumab (208/331).11
In the nivolumab group, first-occurrence, any-grade select TRAEs from the first dose to 100 days after the last dose were reported in 306 of 452 patients (67.7%; grade 1–2: n=285 (63.1%); grade 3–4: n=21 (4.6%); online supplemental appendix table A2). Among all first-occurrence select TRAEs with nivolumab, the most common were diarrhea (24.8%), pruritus (23.5%) and rash (20.6%). First-occurrence any-grade endocrine select TRAEs occurring in ≥1% of nivolumab-treated patients included hypothyroidism (11.3%), hyperthyroidism (8.0%), thyroiditis (2.0%), hypophysitis (1.8%), and adrenal insufficiency (1.3%). Although not reported as immune related, first-occurrence any-grade pneumonitis and diabetes mellitus occurred in 1.3% and 0.4% of nivolumab-treated patients, respectively, and first-occurrence any-grade paresthesia, peripheral neuropathy, and axonal neuropathy (neurologic TRAEs of special interest) were reported in 2.7%, 0.4%, and 0.2% of nivolumab-treated patients, respectively.
First-occurrence select TRAEs with nivolumab were reported in 48.0% of patients from 0 to 3 months of treatment (online supplemental appendix table A3), 35.0% of patients from >3 to 12 months of treatment (online supplemental appendix table A4), and 11.9% of patients from the last dose to 100 days after the last dose (online supplemental appendix table A5). First-occurrence select TRAEs reported in at least 2% of nivolumab-treated patients during any of the three time intervals evaluated are depicted in figure 1. During the time period from 0 to 3 months of treatment, the most common of these first-occurrence select TRAEs were pruritus at 15.5%, diarrhea at 15.3%, rash at 11.7% and hyperthyroidism at 7.1% (figure 1A; online supplemental appendix table A3). During the time period from >3 to 12 months on treatment, the most common first-occurrence select TRAEs were rash at 7.5%, diarrhea at 7.3%, pruritus at 7.3%, and hypothyroidism at 5.3% (figure 1A; online supplemental appendix table A4), and from the last dose to 100 days after last dose, the most common was diarrhea at 2.2% (figure 1B; online supplemental appendix table A5).
Similar safety analyses for the three time periods were also performed to evaluate the incidence of all-occurrence select TRAEs (including repeat occurrences), as well as with first occurrence and all-occurrence all-inclusive TRAEs, with similar results obtained (data not shown). In nivolumab-treated patients, 39.7% of all-occurrence, all-inclusive TRAEs (1079/2716) occurred from 0 to 3 months of treatment, 46.1% (1252/2716) occurred from >3 to 12 months of treatment, and 14.2% (385/2716) occurred from the last dose to 100 days after the last dose. Of the all-inclusive TRAEs with nivolumab, 39.9% (1084/2716) were considered select TRAEs and of those, 40.4% (438/1084) occurred from 0 to 3 months of treatment, 45.8% (496/1084) from after 3 months to 12 months of treatment, and 13.8% (150/1084) from the last dose to 100 days after the last dose. Discontinuation due to all-inclusive TRAEs and select TRAEs occurred in 7.7% (35/452) and 5.1% (23/452) of patients, respectively. All-occurrence endocrine TRAEs from first dose to 100 days following last dose are presented in online supplemental appendix table A6.
Median time to onset of select TRAEs with nivolumab was approximately 8 weeks for skin, gastrointestinal, and endocrine AEs; 13 weeks for hepatic AEs; and 19 weeks for pulmonary and renal AEs (figure 2A). Most select TRAEs with nivolumab resolved within 6 months (figure 2B), although the median time to resolution of endocrine TRAEs was more than 1 year. Endocrine AEs were not considered resolved in 50.5% (53/105) of nivolumab-treated patients.
Corticosteroids (and not other immunosuppressant agents) were administered to 31.0% (140/452) of nivolumab-treated patients for the management of select TRAEs. The median duration (range) of corticosteroid use was 1.8 months (0–18.0) and corticosteroids or other immunosuppressant agents were administered to 45.4% (205/452) of nivolumab-treated patients. The median duration (range) of use of corticosteroids or other immunosuppressant agents was 3.7 months (0–21.3).
Safety and efficacy association
In Kaplan-Meier 3-month landmark analyses, there was no clear association between the occurrence of a select TRAE in the first 3 months of nivolumab treatment and RFS (figure 3). In similar landmark analyses evaluating RFS in patients with and without select TRAEs, no clear association was observed between RFS and select skin TRAEs, select gastrointestinal TRAEs, the use of corticosteroids as the sole type of immunosuppressant agent, or the use of immunosuppressants such as corticosteroids or other agents (online supplemental appendix figure A2). Patients treated with nivolumab and with corticosteroid use had a slight numerical decrease in RFS versus those without corticosteroid use, but because of the very small number of patients available in the former group, interpretation of these data is very limited. Results of additional landmark analyses of clinical interest (ie, those evaluating the association between RFS and the occurrence of vitiligo, discontinuation of study treatment for any reason, or discontinuation of study treatment due to study drug toxicity) were inconclusive because one or both of the treatment subgroups contained 10 or fewer patients (data not shown). In a cox model analysis, the occurrence of a select TRAE reported between first study dose and 100 days after last study dose was not associated with RFS in patients treated with nivolumab (table 1). HR for RFS in patients without a select TRAE compared with patients with a select TRAE was 0.97 (95% CI: 0.70 to 1.34; p=0.858), with similar results in skin and gastrointestinal select TRAEs, and select TRAEs with or without the use of corticosteroids or immune suppressants use. In addition, compared with the ipilimumab arm, the reduction in the hazard of recurrence or death was not significant (p=0.1400) in patients treated with nivolumab with or without the onset of select TRAEs (table 2).
Coordinating analyses were performed for ipilimumab. As expected, treatment with ipilimumab led to greater toxicity than nivolumab (online supplemental appendix figure A3, tables A7–A11). In ipilimumab-treated patients, median time to both onset of select TRAEs and resolution of most select TRAEs was less than 12 weeks (online supplemental appendix figure A4). There was no clear association between RFS and a select TRAE occurring in the first 3 months of ipilimumab treatment (online supplemental appendix figure A5), or with the various other select TRAE categories analyzed (online supplemental appendix figure A6). Moreover, as with nivolumab treatment, the presence or absence of select TRAEs reported between first study dose and 100 days after last study dose (time-varying covariate) was not associated with RFS in the ipilimumab group (HR: 0.62; 95% CI: 0.41 to 0.96; p=0.0301 (to account for multiple comparisons, p≤0.01 is considered significant, although, descriptive); online supplemental appendix table A12).
Results of this safety analysis of adjuvant nivolumab or ipilimumab in patients with resected stage IIIB/IIIC or stage IV melanoma in the CheckMate 238 trial were consistent with the established safety profiles of these agents in more advanced settings. This analysis revealed that most first-occurrence select TRAEs with nivolumab took place early during treatment and that an association between the development of early TRAEs with nivolumab and RFS was not evident when the data were analyzed by two different statistical techniques.
Select TRAEs with adjuvant nivolumab and the timing of their first occurrence were consistent with the established safety profile of nivolumab monotherapy.16 Overall, 67.7% of patients had a first-occurrence select TRAE. In the discrete time periods analyzed here, 48.0% of patients reported a first-occurrence select TRAEs within the first 3 months of treatment. During this period, the most common first-occurrence, select TRAEs with nivolumab were pruritus (15.5%), diarrhea (15.3%), rash (11.7%), and hyperthyroidism (7.1%). These results were generally consistent with those of a pooled analysis of nivolumab in patients with advanced melanoma from four studies, in which the most common any-grade all-inclusive TRAEs were fatigue (24.8%), pruritus (17.2%), diarrhea (12.7%), and rash (12.7%).16 Considering total events, approximately 40% of all-occurrence (including repeat occurrences) all-inclusive TRAEs and of all-occurrence select TRAEs were reported within the first 3 months of treatment.
As a class, immune checkpoint inhibitors are associated with select (ie, immune-related) AEs.9 17 In this analysis, most select TRAEs with nivolumab occurred within approximately 3 months of treatment initiation and generally resolved within 6 months of occurrence. However, the median time to resolution of endocrine select TRAEs was more than 1 year, likely because some (eg, thyroid-related AEs)—even though medically controlled—may not have been considered resolved (even if asymptomatic) if patients continued to require medical treatment (eg, hormone replacement therapy). These results confirmed that select TRAEs with adjuvant nivolumab are manageable using established safety guidelines, as demonstrated in the advanced/metastatic melanoma setting.17
Results of some analyses have suggested an association between TRAEs and response to immune checkpoint inhibitors in patients with advanced or metastatic melanoma, although the evidence has been contradictory.16 18–21 In the pooled safety analysis with nivolumab for metastatic melanoma, objective response rate (ORR) was significantly higher in patients who experienced select TRAEs than in those who did not, but no association was noted between occurrence of select TRAEs and progression-free survival using a landmark approach.16 In a pooled analysis of two phase I studies in patients with advanced melanoma treated with nivolumab, OS was significantly longer in patients who experienced rash or vitiligo than in those who did not in a 12-week landmark analysis, although an association was not observed for the other select TRAEs evaluated.18 In an observational study in patients with metastatic melanoma treated with pembrolizumab, ORR was significantly higher in patients with vitiligo than in those without this AE, but there was no association between vitiligo and OS in landmark analyses.19 In an expanded access program with pembrolizumab in advanced melanoma, there was no significant difference in ORR between patients who experienced select TRAEs and those who did not.20 Also in advanced melanoma, disease control and OS was not statistically associated with immune-related AEs in patients treated with ipilimumab 10 mg/kg in an analysis of three phase II trials.21 These contradictory findings underscore the need for more extensive research to identify novel biological markers to predict checkpoint inhibitor-related toxicity and response to therapy in patients with melanoma presenting with early or late-stage disease.
The results of the Kaplan-Meier 3-month landmark analyses of CheckMate 238 suggested that there was no clear association between RFS and select TRAEs occurring in the first 3 months of nivolumab or ipilimumab treatment. These results contrast with those of a time-varying covariate analysis from the KEYNOTE-054 trial in patients with high-risk stage III melanoma treated with adjuvant pembrolizumab or placebo.22 In that analysis, the occurrence of an any-grade select TRAE with pembrolizumab was associated with a longer RFS (HR: 0.61; 95% CI: 0.39 to 0.95; p=0.03).22 In contrast, a similar analysis conducted here with CheckMate 238 data found no relationship for nivolumab treatment between the occurrence of select TRAEs at any time and RFS (HR: 0.97; 95% CI: 0.70 to 1.34; p=0.8583). Although CheckMate 238 and KEYNOTE-054 enrolled largely overlapping patient populations, the different outcomes noted between the two post-hoc analyses cannot be easily explained and may be partially related to unaccounted inherent differences in baseline patient characteristics. Lastly, the list of specific AEs included in the select TRAEs evaluated in CheckMate 238 differed slightly from the immune-related AEs evaluated in KEYNOTE-054, which included endocrine AEs, pneumonitis/interstitial lung disease, sarcoidosis, vitiligo, severe skin reaction, colitis, pancreatitis, hepatitis, nephritis, uveitis, myositis, or myocarditis.22 The potentially different definition used in CheckMate 238 may have partially contributed to the difference noted in the results.
Findings from this safety analysis of adjuvant nivolumab and ipilimumab in patients with resected stage IIIB–C or stage IV melanoma from the CheckMate 238 trial are consistent with the established safety profile of each agent. In the discrete time intervals evaluated, 40% of first-occurrence select TRAEs with nivolumab occurred within the first 3 months of treatment. Most select TRAEs with nivolumab resolved within 6 months of onset. There was no association between treatment-related select AEs and RFS, suggesting that the development of such immune-mediated events may not be predictive of efficacy. Limitations of this analysis included the retrospective nature and the lack of powering for these retrospective landmark and time-varying Cox model analyses. Specifically for the Kaplan-Meier analyses, adjustments required to reduce lead-time bias necessarily resulted in the removal of some patients. Overall, these findings add to the understanding of the benefit‒risk profile of adjuvant nivolumab in patients with resected high-risk melanoma and may ultimately help in guiding clinicians and patients to recognize and monitor select TRAEs in this setting.
Data availability statement
Data are available upon reasonable request. BMS policy on data sharing may be found at HYPERLINK "https://protecteu.mimecast.com/s/8tv9CyQYCWkmRytMnYgD?domain=bms.com" https://www.bms.com/researchers-and-partners/independent-research/data-sharing-request-process.html.
Patient consent for publication
This trial was approved by the institutional review board or ethics committee at each center and complied with Good Clinical Practice Guidelines, the Declaration of Helsinki, and local laws. All patients provided written informed consent before any protocol-related procedure or treatment.
We thank the patients and families who made the study possible and the clinical study teams who participated. In addition, we thank Agnes Balogh and Margarita Askelson for statistical assistance. We also acknowledge Ono Pharmaceutical Company Ltd (Osaka, Japan) for contributions to nivolumab development and Dako, an Agilent Technologies, Inc company, for collaborative development of the PD-L1 IHC 28-8 pharmDx assay. This analysis was supported by Bristol Myers Squibb. All authors contributed to and approved the manuscript; writing and editorial assistance was provided by Mark Palangio, Melissa Kirk, and Michele Salernitano at Ashfield Healthcare Communications, funded by Bristol Myers Squibb.
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Correction notice This paper has been updated to amend author details.
Contributors All authors were involved in conception and design, administrative support, provision of study material or patients, collection and assembly of data, data analysis and interpretation, and manuscript writing. All authors gave final approval of the manuscript to be published and were accountable for all aspects of the work.
Funding CheckMate 238 is supported by Bristol Myers Squibb and Ono Pharmaceutical.
Competing interests MM: Consulting or Advisory Role: Bristol Myers Squibb, Novartis, MSD Oncology, Pierre Fabre, Roche/Genentech; Honoraria: Bristol Myers Squibb, MSD Oncology, Novartis, Pierre Fabre, Roche/Genentech; Research Funding: Novartis, Roche/Genentech; JL: Grants: Achilles Therapeutics, Aveo, Bristol Myers Squibb, MSD, Nektar, Novartis, Pierre Fabre, Pfizer, Pharmacyclics, Roche/Genentech, Secarna, Vitaccess, Covance, Immunocore; Personal Fees: Achilles Therapeutics, AstraZeneca, Boston Biomedical, Bristol Myers Squibb, Eisai, EUSA Pharma, Imugen, Incyte, Ipsen, iOnctura, Kymab, Merck Serono, MSD, Nektar, Novartis, Pierre Fabre, Pfizer, Pharmacyclics, Roche/Genentech, Secarna, Vitaccess; PAA: Grant: Array, Bristol Myers Squibb, Roche/Genentech; Personal Fees: 4SC, Array, AstraZeneca, Bristol Myers Squibb, Idera, Immunocore, Incyte, Genmab, Medimmune, MSD, NewLink Genetics, Novartis, Merck Serono, Pierre Fabre, Roche/Genentech, Sandoz, Sanofi, Syndax, Sun Pharma, Ultimovacs; Advisory/consultant role and travel support: MSD; MDV: Consultant/Advisory Boards: Bristol Myers Squibb, Merck, Novartis, Pierre Fabre, Sanofi; HG: Consulting or Advisory Role: Amgen, Bristol Myers Squibb, MSD Oncology, Novartis, Roche, Pierre Fabre; Travel, Accommodations, Expenses: Bristol Myers Squibb, Roche; Honoraria: Amgen, Bristol Myers Squibb, MSD Oncology, Novartis, Roche; Research Funding: Bristol Myers Squibb, MSD Oncology, Roche, Novartis; CLC: Nothing to disclose; AA: Personal Fees: Bristol Myers Squibb, MSD, Novartis, Merck, Roche; Travel Grant: Bristol Myers Squibb, MSD, Novartis, Merck, Roche; SD: Consulting or Advisory Role: MSD; Research Funding: AstraZeneca, Bristol Myers Squibb, MSD, Roche; Travel, Accommodations, Expenses: Bristol Myers Squibb; Stock Ownership/Employment: Sanofi Pasteur (immediate family member); MS Grant: AbbVie, Amgen, AstraZeneca, Bristol Myers Squibb, Eli Lilly, Gilead, Merck Serono, MSD, Mylan, Novartis, Pfizer, Regeneron, Roche, Samsung; J-JG: Personal Fees: Amgen, Bristol Myers Squibb, MSD, Novartis, Pierre Fabre, Roche, Sanofi, SunPharma; VC-S: Advisory Board: Incyte, Merck-Sorono, MSD; Meeting Expenses: Bristol Myers Squibb, Pierre Fabre; Speaker Fee: Novartis; IM: Grant: Amgen, BionCoTech, Bristol Myers Squibb, Incyte, MSD, Roche; Personal Fees: Amgen, BionCoTech, Bristol Myers Squibb, Incyte, MSD, Regeneron, Roche, Sanofi; Non-financial Support: BionCoTech, Bristol Myers Squibb, MSD, Roche; MOB: Consulting or Advisory Role: Adaptimmune, Bristol Myers Squibb, EMD Serono, GlaxoSmithKline, Genzyme, Immunocore, Immunovaccine, Merck, Novartis; Expert Testimony: Merck; Honoraria: Bristol Myers Squibb, Merck, Novartis, Roche; Research Funding: Takara Bio, Merck; AMDG: Consulting or Advisory Role: Bristol Myers Squibb, Incyte, MSD, Pierre Fabre; JL: Consulting or Advisory Role: Array BioPharm, Bristol Myers Squibb, Novartis; Speakers’ Bureau: Array BioPharm, Novartis, Regeneron; Travel, Accommodations, and Expenses: Bristol Myers Squibb, Novartis, Pfizer; Research Funding: Amgen, AstraZeneca/MedImmune, Bristol Myers Squibb, Elios Pharmaceutical, Genentech/Roche, Incyte, Merck Seronon, Merck, Novartis, Pfizer, Viralytics; LDLC-M: Nothing to disclose; VA: Personal Fees: Bristol Myers Squibb, Merck Serono, MSD, Novartis, Pierre Fabre, Roche, Oncosec; PA: Nothing to disclose; AH: Nothing to disclose; LF: Grant: Bristol Myers Squibb, EMD Serono, Incyte, Kartos, Merck, Pfizer, Array; Consulting or Advisory Role: Elsevier/Via Oncology, Hoosier Cancer Research Network; MM: Consulting or Advisory Role: AstraZeneca, Boehringer Ingelheim, Bristol Myers Squibb, EMD Serono, MSD, Novartis, Pfizer, Roche; Travel, Accommodations, and Expenses: AstraZeneca, Bristol Myers Squibb, MSD, Roche; NIK: Consulting or Advisory Role: Array BioPharma, AstraZeneca, Bristol Myers Squibb, EMD Serono, Immunocore, HUYA Bioscience International, Genentech, Merck, Regeneron; Research Funding: Amgen, HUYA Bioscience International, GlaxoSmithKline, Merck, Novartis, Regeneron; Stock/Other Ownership Interests: Amarin Corporation, Bellicum Pharmaceuticals, Mazor Robotics, TransEnterix; VdP: Employee: Bristol Myers Squibb; Stock Ownership: Bristol Myers Squibb; ML: Employee: Bristol Myers Squibb; Stock Ownership: Advaxis Immunotherapies, Bristol Myers Squibb; JW: Consulting or Advisory Role: AbbVie Inc, Altor Bioscience, Amgen, AstraZeneca, Bristol Myers Squibb, CytomX Therapeutics, Daiichi Sankyo, Eisai, Genentech, GlaxoSmithKline, Medivation, Merck, Nektar Therapeutics, Novartis, Pieris Pharmaceuticals, Inc, Roche, SELLAS Life Sciences Group, Inc, WindMIL Therapeutics; Research Funding: Astellas Pharma, Bristol Myers Squibb, Genentech, Incyte Corporation, Merck, Novartis, Roche; Travel, Accommodations, and Expenses: Amgen, AstraZeneca, Bristol Myers Squibb, Daiichi Sankyo, Genentech, GlaxoSmithKline, Merck, Novartis, Pieris Pharmaceuticals, Inc, Roche; Honoraria: AbbVie Inc, Altor Bioscience, Amgen, AstraZeneca, Bristol Myers Squibb, CytomX Therapeutics, Daiichi Sankyo, Eisai, Genentech, GlaxoSmithKline, Medivation, Merck, Nektar Therapeutics, Novartis, Pieris Pharmaceuticals, Inc, Roche, SELLAS Life Sciences Group, Inc, WindMIL Therapeutics; Stock/Ownership Interests: Biond; Patents: Named on a patent submitted by Moffitt Cancer Center for an ipilimumab biomarker; named on a patent submitted from Biodesix for a PD-1 antibody biomarker.
Provenance and peer review Not commissioned; externally peer reviewed.
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