Literature DB >> 26381515

Erlotinib versus carboplatin and paclitaxel in advanced lepidic adenocarcinoma: IFCT-0504.

Jacques Cadranel1, Radj Gervais2, Patrick Merle3, Denis Moro-Sibilot4, Virginie Westeel5, Laurence Bigay-Game6, Elisabeth Quoix7, Sylvie Friard8, Fabrice Barlesi9, Claire Lethrosne10, Lionel Moreau11, Isabelle Monnet12, Mathieu Salaun13, Gérard Oliviero14, Pierre-Jean Souquet15, Martine Antoine16, Alexandra Langlais17, Franck Morin17, Marie Wislez18, Gérard Zalcman19.   

Abstract

The IFCT-0504 phase II trial evaluated the efficacy of erlotinib versus carboplatin-paclitaxel (CP) as first-line treatment in 130 cases of advanced lepidic-predominant adenocarcinoma (ADC).The primary objective of the study was treatment efficacy, evaluated based on an end-point of disease control at 16 weeks.The primary objective was met, with a disease control in 35 (53%) out of 66 patients treated with CP and in 25 (39.1%) out of 64 patients treated with erlotinib. Median progression-free survival (PFS) for the total population was 3.6 months. The disease control rate did not differ between either the therapeutic arms or pathological subtypes, whereas there was a strong interaction between treatment arms and tumour pathological subtypes for PFS (p=0.009). Mucinous tumour patients treated with erlotinib exhibited an increased progression risk (hazard ratio 3.4, 95% CI 1.7-6.5; p≤0.001). The PFS for nonmucinous tumour patients was similar in both arms. Median overall survival was 20.1 months and did not differ between therapeutic arms. These findings were not further elucidated by molecular analyses and the toxicity profiles were as expected.Our study demonstrated the dominant role of CP alongside erlotinib in the management of advanced lepidic ADC. Based on these findings, erlotinib should not be administered in first-line therapy to patients with lepidic ADC in the absence of an epidermal growth factor receptor mutation.
Copyright ©ERS 2015.

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Year:  2015        PMID: 26381515     DOI: 10.1183/13993003.02358-2014

Source DB:  PubMed          Journal:  Eur Respir J        ISSN: 0903-1936            Impact factor:   16.671


  3 in total

1.  Osteopontin improves sensitivity to tyrosine kinase inhibitor in lung adenocarcinoma in vitro by promoting epidermal growth factor receptor phosphorylation.

Authors:  Yu-Jin Wang; Qing-Wen Wang; Dong-Hu Yu; Cong-Kuan Song; Zi-Xin Guo; Xiao-Ping Liu; Chen Chen; Jie Yao; Ai-Fen Wang; Wei-Dong Hu
Journal:  J Cancer Res Clin Oncol       Date:  2021-07-13       Impact factor: 4.553

2.  Fatal toxic effects related to EGFR tyrosine kinase inhibitors based on 53 cohorts with 9,569 participants.

Authors:  Xianhe Xie; Xuewen Wang; Sumei Wu; Haitao Yang; Junjin Liu; Huijuan Chen; Yin Ding; Liting Ling; Heng Lin
Journal:  J Thorac Dis       Date:  2020-08       Impact factor: 2.895

3.  Characteristics and Prognostic Nomogram for Primary Lung Lepidic Adenocarcinoma.

Authors:  Hui Tang; Caixia Qiao; Yingyi Wang; Chunmei Bai
Journal:  Can Respir J       Date:  2022-08-31       Impact factor: 2.130

  3 in total

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