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化疗与针对 EGFR 突变肺腺癌对 EGFR 酪氨酸激酶抑制剂耐药的个体化治疗:一项回顾性双中心研究。

Chemotherapy versus personalized therapy for EGFR mutant lung adenocarcinoma resistance to EGFR-tyrosine kinase inhibitors: a retrospective dual-center study.

机构信息

Department of Thoracic Oncology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.

The Second Department of Thoracic Oncology, the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Hunan Cancer Hospital, Changsha, China.

出版信息

BMC Pulm Med. 2024 Feb 24;24(1):96. doi: 10.1186/s12890-024-02905-1.

Abstract

BACKGROUND

Advanced lung adenocarcinoma patients often develop resistance to EGFR tyrosine kinase inhibitors (EGFR-TKIs), leaving uncertainties regarding subsequent treatment strategies. Although personalized therapy targeting individual acquired resistances (ARs) shows promise, its efficacy has not been systematically compared with platinum-containing doublet chemotherapy, a widely accepted treatment after EGFR-TKIs failure.

METHODS

A retrospective dual-center study was conducted involving patients with advanced lung adenocarcinoma and EGFR mutations who developed resistance to EGFR-TKIs between January 2017 and December 2022. Eligible patients were adults aged 18 years or older with an Eastern Cooperative Oncology Group score of 0-1, normal organ function, and no prior chemotherapy. Patients were divided into the chemotherapy group (CG) or personalized therapy group (PG) based on the treatment received after disease progression. The primary endpoints were progression-free survival (PFS) and objective response rate (ORR).

RESULTS

Of the 144 patients enrolled, there were 53 patients in the PG and 91 patients in the CG. The PG acquired resistance to EGFR-TKIs through the MET amplification (27, 50%) and small cell lung cancer transformation (16, 30%) and 18% of them reported multiple resistance mechanisms. The ORR of the PG was similar to that of the CG (34% vs. 33%, P = 1.0) and the PFS of the PG patients was not statistically different from that of their CG counterparts [4.2 months (95% CI: 3.6-4.8 months) vs. 5.3 months (95% CI: 4.6-6.0 months), P = 0.77].

CONCLUSIONS

These findings suggest that the therapeutic efficacy of chemotherapy approximates to that of personalized therapy, which signifies that chemotherapy is still a reliable choice for patients who develop resistance to EGFR-TKIs and that further research is awaited to explore the benefit of personalized treatment.

摘要

背景

晚期肺腺癌患者常对表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)产生耐药性,这给后续治疗策略带来了不确定性。虽然针对个体获得性耐药(ARs)的个体化治疗具有一定前景,但与 EGFR-TKIs 失败后的广泛接受的铂类双联化疗相比,其疗效尚未得到系统比较。

方法

这是一项回顾性的双中心研究,纳入了 2017 年 1 月至 2022 年 12 月期间接受 EGFR-TKIs 治疗后发生耐药的晚期肺腺癌和 EGFR 突变的患者。符合条件的患者为年龄在 18 岁或以上、东部肿瘤协作组评分 0-1 分、器官功能正常且无既往化疗史的成年人。根据疾病进展后接受的治疗,将患者分为化疗组(CG)或个体化治疗组(PG)。主要终点为无进展生存期(PFS)和客观缓解率(ORR)。

结果

在纳入的 144 例患者中,PG 组有 53 例患者,CG 组有 91 例患者。PG 组通过 MET 扩增(27 例,50%)和小细胞肺癌转化(16 例,30%)获得 EGFR-TKIs 耐药,其中 18%的患者报告存在多种耐药机制。PG 组的 ORR 与 CG 组相似(34%比 33%,P=1.0),PG 组患者的 PFS 与 CG 组无统计学差异[4.2 个月(95%CI:3.6-4.8 个月)比 5.3 个月(95%CI:4.6-6.0 个月),P=0.77]。

结论

这些发现表明,化疗的疗效与个体化治疗相当,这表明化疗仍然是 EGFR-TKIs 耐药患者的可靠选择,需要进一步研究来探索个体化治疗的获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99d5/10893690/1c898626a4d7/12890_2024_2905_Fig1_HTML.jpg

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