Neoadjuvant targeted therapy versus targeted combined with chemotherapy for resectable EGFR-mutant non–small cell lung cancer: a retrospective controlled real-world study

Weipeng Shao, Zhan Liu, Bobo Li, Feng Chen, J. Liu, Hui Li, Hongbo Guo
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Abstract

This study aimed to assess the role and effect of neoadjuvant targeted therapy (TT) versus targeted combined with chemotherapy (TC) for resectable EGFR-mutant non–small cell lung cancer (NSCLC).Between March 2021 and June 2023, 20 patients with stage IA3-IIIB NSCLC were enrolled in the study. Eleven patients received EGFR-TKIs in the TT group, while nine patients received EGFR-TKIs and two cycles of cisplatin-based doublet chemotherapy (TC group). We compare the differences between the two groups through the following variables, including age, sex, surgical approach, postoperative complications, neoadjuvant therapy adverse events, complete response (CR), partial response (PR), stable disease (SD), progressive disease (PD), objective response rate (ORR), major pathologic response (MPR), and pathologic complete response (pCR).Patients were predominantly female (75%) and never-smokers (95%). The average age was 59.2 years (range 46-79 years). Fifty-five percent harbored an exon 19 EGFR mutation and 45% an exon 21 mutation. The average targeted drug dosing time was 2.91 ± 1.7 (range 1-6) months in the TT group and 3.56 ± 3.54 (range 1-12) months in the TC group (P=0.598). The most common side effects were rash and diarrhea. No grade 5 events with neoadjuvant therapy were observed. The rate of R0 resection was 100% in all patients. Among the 11 patients in the TT group, 6 achieved a PR and 5 had SD, resulting in an ORR of 54.5%. Among the 9 patients in the TC group, 6 had PR and the remaining 3 had SD, resulting in an ORR of 66.6%. one patient (11.1%) in the TC group achieved pCR, while no patients in the TT group achieved pCR (P = 0.142). Two patients (18.2%) in the TT group reached MPR, and 2 patients (22.2%) in the TC group reached MPR (P = 0.257). The overall clinical downstage rate is 60%. Only 9 (45%) cases of yield clinical TNM (ycTNM) were consistent with yield pathologic TNM (ypTNM).Results from this retrospective controlled research indicate that the neoadjuvant TT group is likely to be more effective outcomes and has safer profile in patients with EGFR-positive NSCLC than the neoadjuvant TC group. However, our results need to be validated in a multicenter, large sample prospective study.
可切除表皮生长因子受体突变非小细胞肺癌的新辅助靶向治疗与靶向治疗联合化疗:一项回顾性对照真实世界研究
这项研究旨在评估新辅助靶向治疗(TT)与靶向联合化疗(TC)在可切除的表皮生长因子受体突变非小细胞肺癌(NSCLC)中的作用和效果。2021年3月至2023年6月期间,20名IA3-IIIB期NSCLC患者被纳入研究。在TT组中,11名患者接受了EGFR-TKIs治疗,而在TC组中,9名患者接受了EGFR-TKIs和两个周期的顺铂双联化疗。我们通过年龄、性别、手术方式、术后并发症、新辅助治疗不良事件、完全反应(CR)、部分反应(PR)、疾病稳定(SD)、疾病进展(PD)、客观反应率(ORR)、主要病理反应(MPR)和病理完全反应(pCR)等变量来比较两组之间的差异。患者平均年龄为 59.2 岁(46-79 岁不等)。55%的患者存在表皮生长因子受体19外显子突变,45%的患者存在表皮生长因子受体21外显子突变。TT组平均靶向药物用药时间为2.91 ± 1.7(范围1-6)个月,TC组平均靶向药物用药时间为3.56 ± 3.54(范围1-12)个月(P=0.598)。最常见的副作用是皮疹和腹泻。新辅助治疗未出现5级副作用。所有患者的R0切除率均为100%。在TT组的11名患者中,6人达到PR,5人达到SD,ORR为54.5%。在 TC 组的 9 名患者中,6 人获得 PR,其余 3 人获得 SD,ORR 为 66.6%。TC 组有一名患者(11.1%)获得 pCR,而 TT 组没有患者获得 pCR(P = 0.142)。TT组有两名患者(18.2%)达到MPR,TC组有两名患者(22.2%)达到MPR(P = 0.257)。总体临床下阶段率为 60%。这项回顾性对照研究的结果表明,对于表皮生长因子受体(EGFR)阳性的NSCLC患者,新辅助TT组可能比新辅助TC组的疗效更好、更安全。然而,我们的结果还需要在多中心、大样本的前瞻性研究中得到验证。
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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