Literature DB >> 28854067

Phase III Trial of Ipilimumab Combined With Paclitaxel and Carboplatin in Advanced Squamous Non-Small-Cell Lung Cancer.

Ramaswamy Govindan1, Aleksandra Szczesna1, Myung-Ju Ahn1, Claus-Peter Schneider1, Pablo Fernando Gonzalez Mella1, Fabrice Barlesi1, Baohui Han1, Doina Elena Ganea1, Joachim Von Pawel1, Vladimir Vladimirov1, Natalia Fadeeva1, Ki Hyeong Lee1, Takayasu Kurata1, Li Zhang1, Tomohide Tamura1, Pieter E Postmus1, Jacek Jassem1, Kenneth O'Byrne1, Justin Kopit1, Mingshun Li1, Marina Tschaika1, Martin Reck1.   

Abstract

Purpose Patients with squamous non-small-cell lung cancer (NSCLC) have poor prognosis and limited treatment options. This randomized, double-blind, phase III study investigated the efficacy and safety of first-line ipilimumab or placebo plus paclitaxel and carboplatin in advanced squamous NSCLC. Patients and Methods Patients with stage IV or recurrent chemotherapy-naïve squamous NSCLC were randomly assigned (1:1) to receive paclitaxel and carboplatin plus blinded ipilimumab 10 mg/kg or placebo every 3 weeks on a phased induction schedule comprising six chemotherapy cycles, with ipilimumab or placebo from cycles 3 to 6 and then, after induction treatment, ipilimumab or placebo maintenance every 12 weeks for patients with stable disease or better. The primary end point was overall survival (OS) in patients receiving at least one dose of blinded study therapy. Results Of 956 randomly assigned patients, 749 received at least one dose of blinded study therapy (chemotherapy plus ipilimumab, n = 388; chemotherapy plus placebo, n = 361). Median OS was 13.4 months for chemotherapy plus ipilimumab and 12.4 months for chemotherapy plus placebo (hazard ratio, 0.91; 95% CI, 0.77 to 1.07; P = .25). Median progression-free survival was 5.6 months for both groups (hazard ratio, 0.87; 95% CI, 0.75 to 1.01). Rates of grade 3 or 4 treatment-related adverse events (TRAEs), any-grade serious TRAEs, and TRAEs leading to discontinuation were numerically higher with chemotherapy plus ipilimumab (51%, 33%, and 28%, respectively) than with chemotherapy plus placebo (35%, 10%, and 7%, respectively). Seven treatment-related deaths occurred with chemotherapy plus ipilimumab, and one occurred with chemotherapy plus placebo. Conclusion The addition of ipilimumab to first-line chemotherapy did not prolong OS compared with chemotherapy alone in patients with advanced squamous NSCLC. The safety profile of chemotherapy plus ipilimumab was consistent with that observed in previous lung and melanoma studies. Ongoing studies are evaluating ipilimumab in combination with nivolumab in this population.

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Year:  2017        PMID: 28854067     DOI: 10.1200/JCO.2016.71.7629

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  137 in total

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Authors:  Ugo Testa; Germana Castelli; Elvira Pelosi
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Review 9.  Recent treatment strategy for advanced squamous cell carcinoma of the lung in Japan.

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Journal:  Int J Clin Oncol       Date:  2019-03-07       Impact factor: 3.402

Review 10.  Ipilimumab-Induced Enterocolitis: A Systematic Review and Meta-Analysis.

Authors:  Kelcie Witges; Leigh Anne Shafer; Ryan Zarychanski; Ahmed M Abou-Setta; Rasheda Rabbani; Orvie Dingwall; Charles N Bernstein
Journal:  Drug Saf       Date:  2020-12       Impact factor: 5.606

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