Hotta Katsuyuki, Saeki Sho, Sakata Shinya, Yamaguchi Masafumi, Harada Daijiro, Bessho Akihiro, Tanaka Kentaro, Inoue Koji, Inoue Koji, Gemba Kenichi, Kubo Toshio, Sato Akiko, Ichihara Eiki, Watanabe Hiromi, Kishimoto Junji, Shioyama Yoshiyuki, Katsui Kuniaki, Sugio Kenji, Kiura Katsuyuki
Center for Innovative Clinical Medicine, Okayama University Hospital, 2-5-1, Shikata-cho, Okayama, 700-8558, Japan.
Department of Respiratory Medicine, Kumamoto University Hospital, Kumamoto, Japan.
Int J Clin Oncol. 2025 Mar;30(3):497-503. doi: 10.1007/s10147-025-02696-3. Epub 2025 Feb 5.
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 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.
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.
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.
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.
我们之前在一项II期试验中显示,对于不可切除的III期表皮生长因子受体(EGFR)突变型非小细胞肺癌(NSCLC)患者,先使用吉非替尼诱导治疗,然后进行放化疗(CRT),其主要终点2年总生存率(OS)为90%。然而,尚未公布长期生存数据和晚期不良事件情况。
对不可切除的EGFR突变型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天给予顺铂和多西他赛,并同时进行总剂量为60 Gy的放疗。
在入组的20例患者中,5年总生存率和中位生存时间分别为70.0%[95%置信区间:45.1 - 85.3]和5.5年[4.91 - 无上限(NE)],而5年无进展生存率(PFS)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治疗的效果重新规划放疗野,疗效似乎也未受影响。至于晚期不良事件,7例患者(35%)发生了肺纤维化。从放化疗结束到事件发生的中位时间为245天。所有病例均为1级,且在病程中没有病变空洞形成或曲霉菌感染等慢性感染的证据。在此期间发生了1例小细胞肺癌。
随着随访时间延长,我们证明了在EGFR突变型III期NSCLC患者中,先进行EGFR酪氨酸激酶抑制剂(TKI)诱导治疗,然后进行标准CRT,疗效良好且毒性可耐受。
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。