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  4. Experience from Asian centers in a named-patient-use program for afatinib in patients with advanced non-small-cell lung cancer who had progressed following prior therapies, including patients with uncommon EGFR mutations
 
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Experience from Asian centers in a named-patient-use program for afatinib in patients with advanced non-small-cell lung cancer who had progressed following prior therapies, including patients with uncommon EGFR mutations

Journal
International Journal of Clinical Oncology
Journal Volume
26
Journal Issue
5
Pages
841-850
Date Issued
2021
Author(s)
Chang G.-C.
Lam D.C.-L.
Tsai C.-M.
Chen Y.-M.
JIN-YUAN SHIH  
Aggarwal S.
Wang S.
Kim S.-W.
Kim Y.-C.
Wahid I.
Li R.
Lim D.W.-T.
Sriuranpong V.
Chan R.T.-T.
Lorence R.M.
Carriere P.
Raabe C.
Cseh A.
Park K.
DOI
10.1007/s10147-021-01869-0
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85103394339&doi=10.1007%2fs10147-021-01869-0&partnerID=40&md5=6a085927da5a6e0f7dc0bef8db9b9e4d
https://scholars.lib.ntu.edu.tw/handle/123456789/558527
Abstract
Background: This study evaluated outcomes among patients with advanced/metastatic non-small-cell lung cancer (NSCLC) treated at Asian centers participating in the global named-patient-use (NPU) program for afatinib. Methods: Patients had progressed after initial benefit with erlotinib or gefitinib, and/or had an EGFR or HER2 mutation, had no other treatment options, and were ineligible for afatinib trials. The recommended starting dose of afatinib was 50?mg/day. Dose modifications were allowed, and afatinib was continued as long as deemed beneficial. Response and survival information was provided voluntarily. Safety reporting was mandatory. Results: 2242 patients (26% aged ? 70?years, 96% with adenocarcinoma) received afatinib at centers in 10 Asian countries. Most were heavily pre-treated, including prior treatment with erlotinib or gefitinib. Of 1281 patients tested, 1240 had EGFR mutations (common: 1034/1101; uncommon: 117/1101). There were no new safety signals, the most common adverse events being rash and diarrhea. Objective response rate (ORR) was 24% overall (n = 431 with data available), 27% for patients with common EGFR mutations (n = 230) and 28% for those with uncommon mutations (n = 32); median time to treatment failure (TTF) in these groups was 7.6?months (n = 1550), 6.4?months (n = 692) and 8.4?months (n = 83), respectively. In patients with EGFR exon 20 insertions (n = 23) and HER2 mutations (n = 12), median TTF exceeded 12?months. Conclusions: Patient outcomes in this study were similar to those reported in the analysis of the global NPU. Afatinib achieved clinical benefits in patients with refractory NSCLC. ORR and TTF were similar between patients with tumors harboring uncommon and common EGFR mutations. ? 2021, The Author(s).
Subjects
Afatinib; HER2 mutations; Lung cancer; Named patient use; NSCLC; Uncommon EGFR mutations
SDGs

[SDGs]SDG3

Publisher
Springer Japan
Type
journal article

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