Literature DB >> 29766492

Nivolumab versus ipilimumab in the treatment of advanced melanoma: a critical appraisal: ORIGINAL ARTICLE: Wolchok JD, Chiarion-Sileni V, Gonzalez R et al. Overall survival with combined nivolumab and ipilimumab in advanced melanoma. N Engl J Med 2017; 377:1345-56.

M T Wan1, M E Ming1.   

Abstract

AIM: To show whether either nivolumab in combination with ipilimumab or nivolumab monotherapy vs. ipilimumab monotherapy extends overall survival (OS) or progression-free survival (PFS) in adults with previously untreated, advanced melanoma. SETTING AND
DESIGN: The trial was conducted at 137 sites in 21 countries. Randomization (n = 945; 1 : 1 : 1 ratio) was stratified according to metastasis stage, BRAF mutation status and programmed death ligand 1 status. STUDY EXPOSURE: Adults were randomized to one of the following: nivolumab plus ipilimumab every 3 weeks for four doses, followed by nivolumab every 2 weeks; nivolumab every 2 weeks plus placebo; or ipilimumab every 3 weeks for four doses plus placebo. Treatment was continued until progression, unacceptable toxicity or withdrawal. OUTCOMES: OS, PFS and objective response rate were determined. Patients were also assessed for adverse events. The primary end points of interest were OS and PFS, comparing either the nivolumab plus ipilimumab group or the nivolumab-only group with the patients treated with ipilimumab only.
RESULTS: At 3 years, the OS rates were 58%, 52% and 34% for the nivolumab plus ipilimumab, the nivolumab monotherapy and the ipilimumab monotherapy groups, respectively. For the nivolumab plus ipilimumab group, the median OS was not reached at the time of analysis. For the nivolumab-only group, the median OS was 37·6 months, and the ipilimumab-only group had a median OS of 19·9 months. The hazard ratio for death was 0·55 [95% confidence interval (CI) 0·45-0·69; P < 0·001] comparing nivolumab plus ipilimumab with ipilimumab, and 0·65 (95% CI 0·53-0·80; P < 0·001) comparing nivolumab with ipilimumab. The PFS rates at 3 years were 39% for the nivolumab plus ipilimumab group, 32% for the nivolumab monotherapy group and 10% for the ipilimumab monotherapy group, with 95% CIs for the two nivolumab groups that did not overlap with that for ipilimumab alone.
CONCLUSIONS: Among patients with advanced melanoma, significantly longer OS and PFS occurred with the combination of nivolumab plus ipilimumab or with nivolumab alone compared with ipilimumab alone. Furthermore, survival outcomes favoured the nivolumab-containing groups over the ipilimumab group in subgroup analyses.
© 2018 British Association of Dermatologists.

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Year:  2018        PMID: 29766492     DOI: 10.1111/bjd.16785

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  19 in total

1.  Loss of E-Cadherin Inhibits CD103 Antitumor Activity and Reduces Checkpoint Blockade Responsiveness in Melanoma.

Authors:  Bradley D Shields; Brian Koss; Erin M Taylor; Aaron J Storey; Kirk L West; Stephanie D Byrum; Samuel G Mackintosh; Rick Edmondson; Fade Mahmoud; Sara C Shalin; Alan J Tackett
Journal:  Cancer Res       Date:  2019-01-23       Impact factor: 12.701

2.  Combined Nivolumab and Ipilimumab in Melanoma Metastatic to the Brain.

Authors:  Hussein A Tawbi; Peter A Forsyth; Alain Algazi; Omid Hamid; F Stephen Hodi; Stergios J Moschos; Nikhil I Khushalani; Karl Lewis; Christopher D Lao; Michael A Postow; Michael B Atkins; Marc S Ernstoff; David A Reardon; Igor Puzanov; Ragini R Kudchadkar; Reena P Thomas; Ahmad Tarhini; Anna C Pavlick; Joel Jiang; Alexandre Avila; Sheena Demelo; Kim Margolin
Journal:  N Engl J Med       Date:  2018-08-23       Impact factor: 91.245

Review 3.  Mechanisms of Resistance to PD-1 and PD-L1 Blockade.

Authors:  Theodore S Nowicki; Siwen Hu-Lieskovan; Antoni Ribas
Journal:  Cancer J       Date:  2018 Jan/Feb       Impact factor: 3.360

4.  Osteonecrosis of the jaw induced by treatment with anti-PD-1 immunotherapy: a case report.

Authors:  Xerxes Pundole; Amy Little Jones; Michael T Tetzlaff; Michelle D Williams; William A Murphy; Adegbenga Otun; Ryan P Goepfert; Michael A Davies
Journal:  Immunotherapy       Date:  2020-09-09       Impact factor: 4.196

5.  Synthetic DNA-Encoded Monoclonal Antibody Delivery of Anti-CTLA-4 Antibodies Induces Tumor Shrinkage In Vivo.

Authors:  Elizabeth K Duperret; Aspen Trautz; Regina Stoltz; Ami Patel; Megan C Wise; Alfredo Perales-Puchalt; Trevor Smith; Kate E Broderick; Emma Masteller; J Joseph Kim; Laurent Humeau; Kar Muthumani; David B Weiner
Journal:  Cancer Res       Date:  2018-10-04       Impact factor: 12.701

Review 6.  Trends in the treatment of advanced hepatocellular carcinoma: immune checkpoint blockade immunotherapy and related combination therapies.

Authors:  Huijuan Cheng; Guodong Sun; Hao Chen; Yu Li; Zhijian Han; Yangbing Li; Peng Zhang; Luxi Yang; Yumin Li
Journal:  Am J Cancer Res       Date:  2019-08-01       Impact factor: 6.166

7.  An Immune-Related lncRNA Signature to Predict Survival In Glioma Patients.

Authors:  Pengfei Xia; Qing Li; Guanlin Wu; Yimin Huang
Journal:  Cell Mol Neurobiol       Date:  2020-05-14       Impact factor: 5.046

8.  NCI 8628: A randomized phase 2 study of ziv-aflibercept and high-dose interleukin 2 or high-dose interleukin 2 alone for inoperable stage III or IV melanoma.

Authors:  Ahmad A Tarhini; Paul Frankel; Christopher Ruel; Marc S Ernstoff; Timothy M Kuzel; Theodore F Logan; Nikhil I Khushalani; Hussein A Tawbi; Kim A Margolin; Sanjay Awasthi; Lisa H Butterfield; David McDermott; Alice Chen; Primo N Lara; John M Kirkwood
Journal:  Cancer       Date:  2018-10-10       Impact factor: 6.860

9.  Characteristics and outcomes of patients with recurrent ovarian cancer undergoing early phase immune checkpoint inhibitor clinical trials.

Authors:  Emily Hinchcliff; David Hong; Hung Le; Gary Chisholm; Revathy Iyer; Aung Naing; Patrick Hwu; Amir Jazaeri
Journal:  Gynecol Oncol       Date:  2018-10-24       Impact factor: 5.482

10.  Immunotherapy-related hepatitis: real-world experience from a tertiary centre.

Authors:  Vincent Cheung; Tarun Gupta; Miranda Payne; Mark R Middleton; Jane D Collier; Alison Simmons; Paul Klenerman; Oliver Brain; Jeremy F Cobbold
Journal:  Frontline Gastroenterol       Date:  2019-03-22
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