Literature DB >> 28623122

A Randomized Phase II Study Comparing Nivolumab With Carboplatin-Pemetrexed for Patients With EGFR Mutation-Positive Nonsquamous Non-Small-Cell Lung Cancer Who Acquire Resistance to Tyrosine Kinase Inhibitors Not Due to a Secondary T790M Mutation: Rationale and Protocol Design for the WJOG8515L Study.

Hidetoshi Hayashi1, Yasutaka Chiba2, Kazuko Sakai3, Tomonobu Fujita4, Hiroshige Yoshioka5, Daisuke Sakai6, Chiyoe Kitagawa7, Tateaki Naito8, Koji Takeda9, Isamu Okamoto10, Tetsuya Mitsudomi11, Yutaka Kawakami4, Kazuto Nishio3, Shinichiro Nakamura12, Nobuyuki Yamamoto13, Kazuhiko Nakagawa14.   

Abstract

Antibodies to programmed cell death-1 (PD-1), such as nivolumab, have shown promising clinical activity in patients with advanced non-small-cell lung cancer (NSCLC), but their efficacy appears to be less pronounced in patients with such tumors harboring epidermal growth factor receptor gene (EGFR) mutations. Recent findings suggest that patients with EGFR mutation-positive NSCLC who develop resistance to tyrosine kinase inhibitors (TKIs) due to mechanisms other than acquisition of the secondary T790M mutation of EGFR are more likely to benefit from nivolumab treatment, possibly as a result of a higher level of expression of the PD-1 ligand PD-L1, than are patients who are T790M-positive. The WJOG8515L study (UMIN ID: 000021133) is a randomized phase II trial to compare nivolumab with the combination of carboplatin and pemetrexed in patients with EGFR mutation-positive nonsquamous NSCLC who have developed resistance to EGFR-TKIs due to mechanisms other than T790M. Eligible patients are those with stage IV or recurrent EGFR mutation-positive NSCLC who experience disease progression after therapy with more than 1 EGFR-TKI, including gefitinib, erlotinib, or afatinib; they must show no evidence of the T790M mutation on analysis of a tumor biopsy specimen obtained after progression on such EGFR-TKI therapy, or, if T790M is detected, they must again experience progression on subsequent treatment with a third-generation EGFR-TKI. The primary endpoint is progression-free survival (PFS), and secondary end points include overall survival (OS), objective response rate, duration of response, safety, and OS and PFS according to PD-L1 expression level. Recruitment started in May 2016 and is ongoing.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Chemotherapy; Epidermal growth factor receptor (EGFR); Programmed cell death ligand 1 (PD-L1); Programmed cell death–1 (PD-1); Survival

Mesh:

Substances:

Year:  2017        PMID: 28623122     DOI: 10.1016/j.cllc.2017.05.012

Source DB:  PubMed          Journal:  Clin Lung Cancer        ISSN: 1525-7304            Impact factor:   4.785


  4 in total

Review 1.  Treatment Strategies for Non-Small Cell Lung Cancer Harboring Common and Uncommon EGFR Mutations: Drug Sensitivity Based on Exon Classification, and Structure-Function Analysis.

Authors:  Rui Kitadai; Yusuke Okuma
Journal:  Cancers (Basel)       Date:  2022-05-20       Impact factor: 6.575

Review 2.  Role of Immunotherapy for Oncogene-Driven Non-Small Cell Lung Cancer.

Authors:  Yosuke Miura; Noriaki Sunaga
Journal:  Cancers (Basel)       Date:  2018-07-27       Impact factor: 6.639

Review 3.  Immunotherapy for EGFR-mutant advanced non-small-cell lung cancer: Current status, possible mechanisms and application prospects.

Authors:  Chunyan Shi; Yan Wang; Jianxin Xue; Xiaojuan Zhou
Journal:  Front Immunol       Date:  2022-07-22       Impact factor: 8.786

Review 4.  Efficacy of pemetrexed-based regimens in advanced non-small cell lung cancer patients with activating epidermal growth factor receptor mutations after tyrosine kinase inhibitor failure: a systematic review.

Authors:  BaoHui Han; LuLu Yang; Xin Wang; LuanDi Yao
Journal:  Onco Targets Ther       Date:  2018-04-12       Impact factor: 4.147

  4 in total

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