吉非替尼诱导和放化疗治疗egfr突变III期非小细胞肺癌的5年预后:LOGIK0902/OLCSG0905 II期研究

IF 2.4 3区 医学 Q3 ONCOLOGY
Katsuyuki Hotta, Sho Saeki, Shinya Sakata, Masafumi Yamaguchi, Daijiro Harada, Akihiro Bessho, Kentaro Tanaka, Koji Inoue, Koji Inoue, Kenichi Gemba, Toshio Kubo, Akiko Sato, Eiki Ichihara, Hiromi Watanabe, Junji Kishimoto, Yoshiyuki Shioyama, Kuniaki Katsui, Kenji Sugio, Katsuyuki Kiura
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引用次数: 0

摘要

背景:我们之前显示,在一项II期试验中,吉非替尼诱导后放化疗(CRT)治疗不可切除的III期egfr突变非小细胞肺癌(NSCLC)的2年总生存率(主要终点)为90%。然而,既没有长期生存数据,也没有晚期不良事件概况。患者和方法:不可切除的egfr突变III期NSCLC患者给予吉非替尼单药治疗8周。在诱导治疗期间确认无疾病进展后,随后在第1、8、29和36天给予顺铂和多西紫杉醇,同时进行总剂量为60 Gy的放射治疗。结果:入选的20例患者,5年OS率和中位生存时间分别为70.0%[95%可信区间:45.1-85.3]和5.5年[4.91-NE], 5年PFS率和中位PFS时间分别为15.0%(3.7-33.5)和1.4年[0.69-2.29]。即使根据吉非替尼诱导的效果重新规划辐射场,疗效似乎也不受影响。至于晚期不良事件,7例(35%)患者发生肺纤维化。从CRT完成到事件发生的中位时间为245天。所有病例均为1级,在疾病过程中没有病变空化或曲霉感染等慢性感染的证据。期间发生1例小细胞肺癌。结论:通过更长的随访时间,我们证明了EGFR-TKI诱导后标准CRT治疗egfr突变III期NSCLC的良好疗效和可耐受的毒性。试验注册号:UMIN00005086。https://upload.umin.ac.jp/cgi-open-bin/ctr/ctr.cgi?function=brows&action=brows&recptno=R000006047&type=summary&language=EjRCTs071180036。https://jrct.niph.go.jp/latest-detail/jRCTs071180036。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Five-year outcomes with gefitinib induction and chemoradiotherapy in EGFR-mutant stage III non-small-cell lung cancer: LOGIK0902/OLCSG0905 phase II study.

Background: We previously showed the 2-year OS rate, the primary endpoint, of 90% in a phase II trial of gefitinib induction followed by chemoradiotherapy (CRT) in unresectable, stage III, EGFR-mutant, non-small-cell lung cancer (NSCLC). However, neither long-term survival data nor late-phase adverse event profiles have been presented.

Patients and methods: Patients with unresectable, EGFR-mutant, stage III NSCLC were administered gefitinib monotherapy for 8 weeks. After confirming no disease progression during induction therapy, cisplatin and docetaxel on days 1, 8, 29, and 36 with concurrent radiotherapy at a total dose of 60 Gy were subsequently administered.

Results: In the enrolled twenty patients, the 5-year OS rate and median survival time were 70.0% [95% confidence interval: 45.1-85.3] and 5.5 years [4.91-NE], respectively, whereas 5-year PFS rate and median PFS time were 15.0% (3.7-33.5) and 1.4 years [0.69-2.29], respectively. Efficacy did not seem influenced even if radiation field was re-planed in response to the effect of gefitinib induction. As for late adverse events, pulmonary fibrosis occurred in 7 patients (35%). The median time from completion of CRT to the occurrence of the event was 245 days. All were grade 1, and there was no evidence of cavitation of the lesions or chronic infections such as Aspergillus infection during the course of the disease. One case of small cell lung cancer occurred during the period.

Conclusions: With longer follow-up time, we demonstrated favorable efficacy with tolerable toxicity profiles in the EGFR-TKI induction followed by standard CRT in EGFR-mutant, stage III, NSCLC.

Trial registration numbers: UMIN00005086. https://upload.umin.ac.jp/cgi-open-bin/ctr/ctr.cgi?function=brows&action=brows&recptno=R000006047&type=summary&language=EjRCTs071180036 . https://jrct.niph.go.jp/latest-detail/jRCTs071180036.

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来源期刊
CiteScore
6.80
自引率
3.00%
发文量
175
审稿时长
2 months
期刊介绍: The International Journal of Clinical Oncology (IJCO) welcomes original research papers on all aspects of clinical oncology that report the results of novel and timely investigations. Reports on clinical trials are encouraged. Experimental studies will also be accepted if they have obvious relevance to clinical oncology. Membership in the Japan Society of Clinical Oncology is not a prerequisite for submission to the journal. Papers are received on the understanding that: their contents have not been published in whole or in part elsewhere; that they are subject to peer review by at least two referees and the Editors, and to editorial revision of the language and contents; and that the Editors are responsible for their acceptance, rejection, and order of publication.
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