Survival Outcomes Following Discontinuation of Ipilimumab and Nivolumab for Advanced Melanoma in a Population-based Cohort

被引:7
作者
Ksienski, D. [1 ,2 ]
Truong, P. T. [1 ,2 ]
Wai, E. S. [1 ,2 ]
Croteau, N. S. [3 ]
Chan, A. [2 ,4 ]
Patterson, T. [1 ]
Clarkson, M. [1 ]
Hackett, S. [1 ]
Irons, S. [1 ]
Lesperance, M. [5 ]
机构
[1] BC Canc Victoria, Victoria, BC, Canada
[2] Univ British Columbia, Vancouver, BC, Canada
[3] Univ British Columbia, Dept Anesthesiol Pharmacol & Therapeut, Vancouver, BC, Canada
[4] BC Canc Surrey, Victoria, BC, Canada
[5] Univ Victoria, Dept Math & Stat, Victoria, BC, Canada
关键词
Adverse events; ipilimumab; melanoma; nivolumab; METASTATIC MELANOMA; ADVERSE EVENTS; TREATMENT FAILURE; ASSOCIATION; SAFETY; TIME;
D O I
10.1016/j.clon.2021.06.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: Induction ipilimumab and nivolumab followed by maintenance nivolumab improve overall survival compared with ipilimumab alone in patients with advanced melanoma, but immune-related adverse events (irAE) occur commonly. The need for induction discontinuation because of irAE and the relationship between irAE and survival in non-trials patients are unclear. Materials and methods: Patients with unresectable stage III-IV melanoma receiving first-line combination immunotherapy at one of six centres between December 2017 and February 2020 outside of trials were identified retrospectively. Landmark 12-week Kaplan-Meier analyses and log-rank tests were used to evaluate associations between discontinuation of induction therapy on overall survival and time to treatment failure (TTF). Multivariable analysis of factors influencing overall survival and TTF was undertaken. Results: Among 95 patients, the median age was 62 years, 38.9% had Eastern Cooperative Oncology Group performance status >= 1 and 22.1% had brain metastases. The median follow-up for the whole cohort was 19.8 months by the reverse Kaplan-Meier method. Any grade and grade 3-4 irAE were noted in 78.9% and 44.2% of the cohort, respectively. 44.2% of patients completed induction immunotherapy, whereas 41.1% did not due to irAE. Twelve-week landmark overall survival and TTF were similar in patients who completed induction versus those who did not due to irAE. On multivariable analysis, any grade irAE (versus none) was associated with longer overall survival (hazard ratio = 0.35, 95% confidence interval 0.15-0.82, P = 0.02) and TTF (hazard ratio = 0.38, 95% confidence interval = 0.17-0.81, P = 0.01). Grade 3-4 irAE correlated with longer TTF (hazard ratio = 0.45, 95% confidence interval = 0.20-1.01, P = 0.05). Conclusion: In this population-based cohort, discontinuation of induction immunotherapy as a result of irAE did not adversely affect overall survival or TTF. irAE observed during ipilimumab and nivolumab induction were associated with improved survival outcomes. (C) 2021 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:E561 / E569
页数:9
相关论文
共 25 条
  • [1] [Anonymous], 2019, Tableone: Create "Table 1"to. Describe Baseline Characteristics
  • [2] [Anonymous], PACKAGE SURVIVAL ANA
  • [3] Real World Outcomes of Ipilimumab and Nivolumab in Patients with Metastatic Melanoma
    Asher, Nethanel
    Ben-Betzalel, Guy
    Lev-Ari, Shaked
    Shapira-Frommer, Ronnie
    Steinberg-Silman, Yael
    Gochman, Neta
    Schachter, Jacob
    Meirson, Tomer
    Markel, Gal
    [J]. CANCERS, 2020, 12 (08) : 1 - 18
  • [4] BC, CANC PROTOCOL SUMMAR
  • [5] Landmark Analysis at the 25-Year Landmark Point
    Dafni, Urania
    [J]. CIRCULATION-CARDIOVASCULAR QUALITY AND OUTCOMES, 2011, 4 (03) : 363 - U216
  • [6] Immortal Time Bias Question in the Association Between Toxicity and Outcome of Immune Checkpoint Inhibitors
    Dall'Olio, Filippo G.
    Di Nunno, Vincenzo
    Massari, Francesco
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2020, 38 (01) : 105 - +
  • [7] The majority of patients with metastatic melanoma are not represented in pivotal phase III immunotherapy trials
    Donia, Marco
    Kimper-Karl, Marie Louise
    Hoyer, Katrine Lundby
    Bastholt, Lars
    Schmidt, Henrik
    Svane, Inge Marie
    [J]. EUROPEAN JOURNAL OF CANCER, 2017, 74 : 89 - 95
  • [8] Prognostic factors related to clinical response in patients with metastatic melanoma treated by CTL-associated antigen-4 blockade
    Downey, Stephanie G.
    Klapper, Jacob A.
    Smith, Franz O.
    Yang, James C.
    Sherry, Richard M.
    Royal, Richard E.
    Kammula, Udai S.
    Hughes, Marybeth S.
    Allen, Tamika E.
    Levy, Catherine L.
    Yellin, Michael
    Nich, Geoffrey
    White, Donald E.
    Steinberg, Seth M.
    Rosenberg, Steven A.
    [J]. CLINICAL CANCER RESEARCH, 2007, 13 (22) : 6681 - 6688
  • [9] Nivolumab in Resected and Unresectable Metastatic Melanoma: Characteristics of Immune-Related Adverse Events and Association with Outcomes
    Freeman-Keller, Morganna
    Kim, Youngchul
    Cronin, Heather
    Richards, Allison
    Gibney, Geoffrey
    Weber, Jeffrey S.
    [J]. CLINICAL CANCER RESEARCH, 2016, 22 (04) : 886 - 894
  • [10] Combined nivolumab and ipilimumab versus ipilimumab alone in patients with advanced melanoma: 2-year overall survival outcomes in a multicentre, randomised, controlled, phase 2 trial
    Hodi, F. Stephen
    Chesney, Jason
    Pavlick, Anna C.
    Robert, Caroline
    Grossmann, Kenneth F.
    McDermott, David F.
    Linette, Gerald P.
    Meyer, Nicolas
    Giguere, Jeff Rey K.
    Agarwala, Sanjiv S.
    Shaheen, Montaser
    Ernstoff, Marc S.
    Minor, David R.
    Salama, April K.
    Taylor, Matthew H.
    Ott, Patrick A.
    Horak, Christine
    Gagnier, Paul
    Jiang, Joel
    Wolchok, Jedd D.
    Postow, Michael A.
    [J]. LANCET ONCOLOGY, 2016, 17 (11) : 1558 - 1568