Propensity score analysis of overall survival between first‐ and second‐generation EGFR‐TKIs using real‐world data
Autor: | Kazuhiro Asada, Joe Shindoh, Kazuyoshi Imaizumi, Masato Karayama, Akihito Kubo, Yuko Oya, Kenta Murotani, Eiji Kunii, Takafumi Suda, Sayako Morikawa, Tatsuya Yoshida, Toyoaki Hida, Takeshi Tsuda, Kentaro Ito, Kosuke Takahashi, Teppei Yamagichi, Tomoki Kimura, Shunsaku Hayai, Osamu Hataji, Hirokazu Taniguchi, Takashi Abe, Naoki Inui, Motoyasu Okuno |
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Rok vydání: | 2020 |
Předmět: |
Adult
Male 0301 basic medicine Oncology Cancer Research medicine.medical_specialty non–small‐cell lung cancer Afatinib Disease-Free Survival Erlotinib Hydrochloride 03 medical and health sciences 0302 clinical medicine Gefitinib Japan Clinical Research Carcinoma Non-Small-Cell Lung Internal medicine Antineoplastic Combined Chemotherapy Protocols Clinical endpoint Humans Medicine Osimertinib Protein Kinase Inhibitors EGFR‐TKI Aged Aged 80 and over Acrylamides Aniline Compounds business.industry Hazard ratio General Medicine Middle Aged propensity scoring analysis real‐world data respiratory tract diseases ErbB Receptors Clinical trial 030104 developmental biology 030220 oncology & carcinogenesis Mutation Propensity score matching Female Original Article Erlotinib business medicine.drug |
Zdroj: | Cancer Science |
ISSN: | 1349-7006 1347-9032 |
DOI: | 10.1111/cas.14560 |
Popis: | We constructed a data set of EGFR‐mutant non–small‐cell lung carcinoma (NSCLC) patients, and compared the overall survival of first‐generation (1G), and second‐generation (2G) EGFR‐tyrosine kinase inhibitors (TKIs) in clinical practice using a propensity score. We reviewed the clinical data of consecutive EGFR‐mutated NSCLC patients who received EGFR‐TKI therapy between January 2008 and August 2017 at 11 institutions in Japan. The primary endpoint was overall survival (OS). When comparing OS between 1G and 2G EGFR‐TKIs, propensity score analyses were performed using 2 methods: matching and inverse probability of treatment weighting (IPTW). (Clinical Trial information: UMIN000030121) In total, 1400 patients from 11 institutions were enrolled in this study, and the data from the 1366 patients who received only EGFR‐TKI therapy were analyzed (gefitinib [GEF], N = 732; erlotinib [ERL], N = 416; afatinib, N = 218). Median OS times (months [95%CI]) were 29.7 [27.5‐33.5] in the 1G group (gefitinib, 32.0 [28.1‐35.8]; erlotinib, 27.5 [23.9‐31.7]), and 38.6 [32.2‐NR] in the 2G group (afatinib), respectively. The trend of longer OS for afatinib against 1G EGFR‐TKIs remained, even after adjusted by propensity score. (unadjusted, hazard ratio [HR] 0.676, P = .0023; adjusted by IPTW, HR 0.685 P |
Databáze: | OpenAIRE |
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