Comparison of efficacy of gefitinib and osimertinib for untreated EGFR mutation-positive non-small-cell lung cancer in patients with poor performance status

IF 2.4 Q2 RESPIRATORY SYSTEM
Kazuhisa Nakashima , Hiroaki Kodama , Haruyasu Murakami , Toshiaki Takahashi , Keita Kawakado , Takashi Yanagawa , Kashu Kitani , Takamasa Hottta , Masaaki Abe , Kosuke Hamai , Takuya Tanimoto , Nobuhisa Ishikawa , Tomoki Tamura , Shoichi Kuyama , Takeshi Isobe , Yukari Tsubata
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引用次数: 0

Abstract

Background

There is a dearth of studies on the efficacy and safety of the tyrosine kinase inhibitors osimertinib (OSI) and gefitinib (GEF) in treating epidermal growth factor receptor (EGFR) mutation-positive non-small cell lung cancer (NSCLC), even in patients with poor performance status (PS).

Methods

We retrospectively reviewed and compared data of 113 patients with EGFR mutation-positive NSCLC with Eastern Cooperative Oncology Group PS 2–4 who were administered OSI 80 mg/day or GEF 250 mg/day from May 2016 to March 2022.

Results

The GEF group (39 patients; median age: 74 years) included 20 patients with a PS of 2, 17 with a PS of 3, and 2 with a PS of 4. The OSI group (74 patients; median age: 76 years) included 48 patients with a PS of 2, 24 with a PS of 3, and 2 with a PS of 4. The overall response rates were 69% and 66% in the GEF and OSI groups, respectively. The disease control and PS improvement rates were 89% and 51% in both groups, respectively. The median progression-free survival in the GEF and OSI groups was 6.9 and 9.2 months, respectively (p = 0.15). The OSI group experienced better overall survival than the GEF group (median: 20.9 vs. 13.0 months, p = 0.0031). The incidence of pneumonitis was 10% and 11% in the GEF and OSI groups, respectively. One treatment-related death owing to pneumonitis occurred in the GEF group.

Conclusions

OSI may be a useful treatment for untreated EGFR mutation-positive NSCLC with poor PS.
比较吉非替尼和奥希替尼对表现状态不佳的未经治疗的表皮生长因子受体突变阳性非小细胞肺癌患者的疗效。
背景:关于酪氨酸激酶抑制剂osimertinib(OSI)和吉非替尼(GEF)治疗表皮生长因子受体(EGFR)突变阳性非小细胞肺癌(NSCLC)的疗效和安全性的研究很少,即使是对表现状态(PS)较差的患者也是如此:我们回顾并比较了东部合作肿瘤学组 PS 2-4 的 113 例 EGFR 突变阳性 NSCLC 患者的数据,这些患者在 2016 年 5 月至 2022 年 3 月期间接受了 OSI 80 毫克/天或 GEF 250 毫克/天的治疗:GEF组(39名患者;中位年龄:74岁)包括20名PS为2的患者、17名PS为3的患者和2名PS为4的患者;OSI组(74名患者;中位年龄:76岁)包括48名PS为2的患者、24名PS为3的患者和2名PS为4的患者。两组的疾病控制率和PS改善率分别为89%和51%。GEF组和OSI组的中位无进展生存期分别为6.9个月和9.2个月(P = 0.15)。OSI 组的总生存期优于 GEF 组(中位数:20.9 个月对 13.0 个月,p = 0.0031)。GEF组和OSI组的肺炎发生率分别为10%和11%。GEF组出现了一起因肺炎导致的治疗相关死亡病例:OSI可能是一种有效的治疗方法,适用于未经治疗且PS较差的表皮生长因子受体突变阳性NSCLC。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Respiratory investigation
Respiratory investigation RESPIRATORY SYSTEM-
CiteScore
4.90
自引率
6.50%
发文量
114
审稿时长
64 days
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