日本一线奥希替尼和其他表皮生长因子受体酪氨酸激酶抑制剂对未经治疗的晚期表皮生长因子受体突变非小细胞肺癌患者总生存期的影响:TREAD项目01的最新数据。

IF 4.4 3区 医学 Q2 ONCOLOGY
Makoto Hibino, Yoshinori Imamura, Rai Shimoyama, Tomoya Fukui, Ryuta Fukai, Akihiko Iwase, Yukihiro Tamura, Yusuke Chihara, Takafumi Okabe, Kiyoaki Uryu, Tadahisa Okuda, Masataka Taguri, Hironobu Minami
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引用次数: 0

摘要

背景:与第一代表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂(TKIs)相比,奥希替尼在表皮生长因子受体突变的非小细胞肺癌的初始治疗中显示出更高的有效性。然而,在亚洲人群(尤其是日本患者)中,该药在总生存期方面的优越性仍不确定:目的:利用真实世界的数据,评估在日本患者中,奥希替尼与其他 EGFR-TKIs 相比的生存获益。方法 :作为 Tokushukai REAl-world Data 项目的一部分,在日本 46 家医院开展了一项多机构回顾性研究,采用倾向评分匹配法评估晚期 EGFR 突变非小细胞肺癌患者的总生存期。研究涉及2010年4月至2022年12月期间接受奥希替尼一线治疗的患者(1L-Osi)、最初接受其他EGFR-TKIs治疗的患者(1L-non-Osi)以及最初接受EGFR-TKIs治疗后接受奥希替尼治疗的患者(2L/later-Osi),并随访至2023年4月:在1062名EGFR突变非小细胞肺癌日本患者中,416人(39.2%)接受了1L-奥希治疗,646人(60.8%)接受了1L-非奥希治疗,其中139人(13.1%)接受了2L/later-奥希治疗。在这些组别中,分别有 416 例(39.2%)、293 例(27.6%)和 75 例(7.1%)患者在日本(2016 年 3 月)批准osimertinib 作为晚线治疗后接受了 EGFR-TKI 一线治疗。经过倾向评分匹配后,在2016年3月后的子集中,1L-Osi组的总生存期与1L-Non-Osi组相当(n = 283,42.0个月 vs 42.4个月)。在 Del19 和 L858R 亚组中也观察到类似的趋势。2L/later-Osi 组的中位总生存期明显较长:2016 年 3 月后为 60.2 个月(n = 75)。基于1L-non-Osi组和2L/later-Osi组初始EGFR-TKI治疗的亚组分析显示,吉非替尼组、厄洛替尼组和阿法替尼组之间无显著差异:基于真实世界的数据,在日本(亚洲)人群中,奥希替尼作为EGFR突变晚期非小细胞肺癌的一线治疗药物,与其他EGFR-TKIs相比,总生存期没有明显改善:本研究于2023年3月9日在美国大学医院医学信息网临床试验注册处注册(编号UMIN000050552)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of First-Line Osimertinib and Other EGFR-Tyrosine Kinase Inhibitors on Overall Survival in Untreated Advanced EGFR-Mutated Non-small Cell Lung Cancer in Japan: Updated Data from TREAD Project 01.

Background: Osimertinib shows higher effectiveness than first-generation epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) in the initial treatment of EGFR-mutated non-small cell lung cancer. However, its superiority in terms of overall survival in the Asian population, especially Japanese patients, remains uncertain.

Objective: To evaluate the survival benefit of osimertinib over other EGFR-TKIs in Japanese patients, using real-world data. METHODS : As part of the Tokushukai REAl-world Data project, a retrospective multi-institutional study across 46 hospitals in Japan was conducted to evaluate the overall survival of patients with advanced EGFR-mutated non-small cell lung cancer using propensity score matching. The study involved patients receiving osimertinib as the first-line treatment (1L-Osi), those initially treated with other EGFR-TKIs (1L-non-Osi), and those receiving osimertinib after initial EGFR-TKI treatment (2L/later-Osi) between April 2010 and December 2022 and followed up until April 2023.

Results: Among 1062 Japanese patients with EGFR-mutated non-small cell lung cancer, 416 (39.2%) received 1L-Osi, while 646 (60.8%) received 1L-non-Osi, including 139 (13.1%) who received 2L/later-Osi. Within these groups, 416 (39.2%), 293 (27.6%), and 75 (7.1%) patients received first-line EGFR-TKI treatment post-osimertinib approval as a later-line treatment in Japan (March 2016). After propensity score matching, the overall survival of the 1L-Osi group was comparable to that of the 1L-non-Osi group in the post-March 2016 subset (n = 283, 42.0 vs 42.4 months). Similar trends were observed in the Del19 and L858R subgroups. The median overall survival of the 2L/later-Osi group was notably long: 60.2 months post-March 2016 (n = 75). A subgroup analysis based on initial EGFR-TKI treatment in the 1L-non-Osi and 2L/later-Osi groups revealed no significant differences among the gefitinib, erlotinib, and afatinib groups.

Conclusions: Based on real-world data, osimertinib did not show a significant improvement in overall survival compared to other EGFR-TKIs as a first-line treatment for EGFR-mutated advanced non-small cell lung cancer in the Japanese (Asian) population.

Clinical trial registration: This study was registered at the University Hospital Medical Information Network Clinical Trials Registry on 9 March, 2023 (identification UMIN000050552).

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来源期刊
Targeted Oncology
Targeted Oncology 医学-肿瘤学
CiteScore
8.40
自引率
3.70%
发文量
64
审稿时长
>12 weeks
期刊介绍: Targeted Oncology addresses physicians and scientists committed to oncology and cancer research by providing a programme of articles on molecularly targeted pharmacotherapy in oncology. The journal includes: Original Research Articles on all aspects of molecularly targeted agents for the treatment of cancer, including immune checkpoint inhibitors and related approaches. Comprehensive narrative Review Articles and shorter Leading Articles discussing relevant clinically established as well as emerging agents and pathways. Current Opinion articles that place interesting areas in perspective. Therapy in Practice articles that provide a guide to the optimum management of a condition and highlight practical, clinically relevant considerations and recommendations. Systematic Reviews that use explicit, systematic methods as outlined by the PRISMA statement. Adis Drug Reviews of the properties and place in therapy of both newer and established targeted drugs in oncology.
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