Open AccessGefitinib versus erlotinib as salvage treatment for lung adenocarcinoma patients who benefited from the initial gefitinib: A retrospective study
Author(s) -
Yu Shufei,
Wang Yan,
Li Junling,
Hao Xuezhi,
Wang Bin,
Wang Ziping,
Zhang Xiangru,
Shi Yuankai
Publication year - 2013
Publication title -
thoracic cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.823
H-Index - 28
eISSN - 1759-7714
pISSN - 1759-7706
DOI - 10.1111/j.1759-7714.2012.00152.x
Subject(s) - gefitinib , erlotinib , medicine , erlotinib hydrochloride , epidermal growth factor receptor , adenocarcinoma , lung cancer , oncology , adverse effect , gastroenterology , cancer
Background: The optimal strategy was not established for patients who initially responded to gefitinib although re‐administration of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) has been proven to be an option. Gefitinib and erlotinib were compared as salvage treatment after gefitinib failure. Methods: Thirty‐eight lung adenocarcinoma patients were analyzed retrospectively as they received the second EGFR‐TKIs treatment with either gefitinib or erlotinib. All of them had obtained disease control from initial gefitinib. Sixteen patients received gefitinib (G‐G group) and 22 patients received erlotinib (G‐E group). Results: Of all patients, progress free survival (PFS) and overall survival (OS) were three and 12 months, respectively, and the disease controlled rate (DCR) of the second EGFR‐TKIs treatment was 52.6%. One patient (6.3%) had partial remission (PR) and 10 (62.5%) had stable disease (SD), in the G‐G group, whereas, three (13.6%) had PR and six (27.2%) had SD, in the G‐E group. There was no statistical significance observed, although the DCR in the G‐G group was higher than that in G‐E group (68.8% vs. 40.8%, P = 0.09). Adverse events of both gefitinib and erlotinib were mild and administered. The median PFS and OS in G‐G and G‐E groups were similar (PFS four vs. three months; OS 22 vs. 12 months). In multivariate analysis, patients with SD in initial gefitinib treatment had significantly longer OS ( P = 0.04). Conclusions: Gefitinib as well as erlotinib could be an option for patients who benefited from prior gefitinib treatment. Patients with SD in initial gefitinib obtained a significantly longer OS than those with PR.