دورية أكاديمية

Clinical efficacy of dacomitinib in rechallenge setting for patients with epidermal growth factor receptor mutant non–small cell lung cancer: A multicenter retrospective analysis (TOPGAN2020‐02)

التفاصيل البيبلوغرافية
العنوان: Clinical efficacy of dacomitinib in rechallenge setting for patients with epidermal growth factor receptor mutant non–small cell lung cancer: A multicenter retrospective analysis (TOPGAN2020‐02)
المؤلفون: Hisashi Tanaka, Hiroaki Sakamoto, Takahiro Akita, Fumiyoshi Ohyanagi, Yosuke Kawashima, Yuichi Tambo, Azusa Tanimoto, Atsushi Horiike, Eisaku Miyauchi, Yuko Tsuchiya‐Kawano, Noriko Yanagitani, Makoto Nishio
المصدر: Thoracic Cancer, Vol 13, Iss 10, Pp 1471-1478 (2022)
بيانات النشر: Wiley
سنة النشر: 2022
المجموعة: Directory of Open Access Journals: DOAJ Articles
مصطلحات موضوعية: dacomitinib, epidermal growth factor receptor mutation, exon 21 L858R, non‐small cell lung cancer, rechallenge, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: Background Dacomitinib is the second‐generation epidermal growth factor receptor (EGFR)‐tyrosine kinase inhibitor (TKI) for mutant non–small cell lung cancer (NSCLC). EGFR‐TKIs are often re‐administered in Japan after the disease progression prior EGFR‐TKI. There is little evidence of dacomitinib in rechallenge setting. This study evaluated clinical outcomes of dacomitinib in rechallenge setting. Methods Patients who received dacomitinib for advanced EGFR‐mutant NSCLC who had progressed after EGFR‐TKI in nine institutions in Japan were included in the analyses. Results In total, 43 patients were analyzed. The median progression‐free survival (PFS) was 4.3 months (95% confidence interval [CI], 2.5–5.6). The overall survival (OS) was 10.5 months (95% CI, 7.4–not reached). The overall response rate was 25.5% (95% CI, 13.1–33.7). Subset analysis indicated that patients with EGFR exon 21 L858R showed longer PFS than those with EGFR exon 19 deletion (5.8 vs. 4.1 months) (p = 0.018). The most common adverse events leading to dose modification were diarrhea, paronychia, rash, and oral mucositis. Conclusion In the real practice in Japan, dacomitinib showed a worthwhile treatment option for NSCLC patients with EGFR mutation after failure of previous EGFR‐TKI. The benefit was especially pronounced in patients with the exon 21 mutation.
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 1759-7714
1759-7706
العلاقة: https://doi.org/10.1111/1759-7714.14415Test; https://doaj.org/toc/1759-7706Test; https://doaj.org/toc/1759-7714Test; https://doaj.org/article/5e5f715847fd4a66aa35dd6d0e976bdaTest
DOI: 10.1111/1759-7714.14415
الإتاحة: https://doi.org/10.1111/1759-7714.14415Test
https://doaj.org/article/5e5f715847fd4a66aa35dd6d0e976bdaTest
رقم الانضمام: edsbas.1108853E
قاعدة البيانات: BASE
الوصف
تدمد:17597714
17597706
DOI:10.1111/1759-7714.14415