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西班牙裔表皮生长因子受体突变型非小细胞肺癌患者一线奥希替尼耐药的机制(FRESTON-CLICaP)。

Mechanisms of Resistance to First-Line Osimertinib in Hispanic Patients With EGFR Mutant Non-Small Cell Lung Cancer (FRESTON-CLICaP).

机构信息

Direction of Research and Education, Luis Carlos Sarmiento Angulo Cancer Treatment and Research Center (CTIC), Bogotá, Colombia; Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia.

Foundation for Clinical and Applied Cancer Research (FICMAC), Bogotá, Colombia; Molecular Oncology and Biology Systems Research Group (Fox-G/ONCOLGroup), Universidad El Bosque, Bogotá, Colombia.

出版信息

Clin Lung Cancer. 2022 Sep;23(6):522-531. doi: 10.1016/j.cllc.2022.06.001. Epub 2022 Jun 6.

Abstract

INTRODUCTION

Osimertinib is a third generation EGFR-TKI inhibitor approved in the first-line setting for patients with advanced non-small cell lung cancer (NSCLC). Additionally, it represents the treatment of choice in patients who present with T790M mutations and evidence of relapse of the disease. Effectiveness and safety of this drug have been studied in multiple clinical trials and observational studies, however, information regarding outcomes among Hispanic patients treated with Osimertinib is scarce. The objective of this study was to examine real-world effectiveness and safety of first-line Osimertinib in a cohort of Hispanic patients with NSCLC, emphasizing post-progression outcomes.

METHODS

This is a multicenter, multinational, retrospective cohort study of Hispanic patients treated with Osimertinib as first-line for EGFR-mutated NSCLC. Patients with a confirmed diagnosis of metastatic EGFR-mutated NSCLC who received Osimertinib (80mg/day until evidence of disease progression or presence of intolerable adverse effects) were identified and included. NGS was performed in tumor samples or liquid biopsies among patients who had disease progression. The primary outcome was progression-free survival, and the secondary outcome was post-progression survival.

RESULTS

A total of 94 patients from Mexico, Argentina, Costa Rica, Colombia, Panama, Chile and the USA were included, with a median age of 59 years. Identified mutations included EGFR Exon 19 deletions and EGFR pL858R point mutations. Median progression-free survival (PFS) was 14.4 months (95%CI 12.4-18.2 months). Lung/pleura and lymph nodes were the most common sites of progression. Median post-progression survival was 7.73 months (95%CI 4.07 months-Not reached). Factors which negatively affected PFS included presence of liver metastases at diagnosis and a tumor mutational burden > 5 mut/Mb.

CONCLUSION

Treatment with first line osimertinib represents an effective and safe option for Hispanic patients with metastatic NSCLC. Liver metastases and a higher tumor mutation burden were associated with a lower PFS. Despite effectiveness, different mechanisms of resistance were identified among the patients in this cohort, including mutations which can be targeted by other therapeutic options.

摘要

介绍

奥希替尼是第三代 EGFR-TKI 抑制剂,适用于晚期非小细胞肺癌(NSCLC)患者的一线治疗。此外,对于存在 T790M 突变且疾病复发证据的患者,奥希替尼也是首选治疗方法。该药物的有效性和安全性已在多项临床试验和观察性研究中进行了研究,但关于接受奥希替尼治疗的西班牙裔患者的结果信息却很少。本研究的目的是研究一线奥希替尼在西班牙裔 NSCLC 患者中的真实世界疗效和安全性,重点关注疾病进展后的结果。

方法

这是一项多中心、多国、回顾性队列研究,纳入了接受奥希替尼一线治疗 EGFR 突变型 NSCLC 的西班牙裔患者。纳入了经组织学或液体活检确诊为转移性 EGFR 突变型 NSCLC 且接受奥希替尼(80mg/天,直至疾病进展或出现无法耐受的不良反应)治疗的患者。对疾病进展的患者进行了下一代测序(NGS)。主要结局是无进展生存期(PFS),次要结局是疾病进展后的生存期(post-progression survival)。

结果

共纳入了来自墨西哥、阿根廷、哥斯达黎加、哥伦比亚、巴拿马、智利和美国的 94 例患者,中位年龄为 59 岁。鉴定出的突变包括 EGFR 外显子 19 缺失和 EGFR pL858R 点突变。中位无进展生存期(PFS)为 14.4 个月(95%CI 12.4-18.2 个月)。肺部/胸膜和淋巴结是最常见的进展部位。中位疾病进展后生存期为 7.73 个月(95%CI 4.07 个月-未达到)。影响 PFS 的因素包括诊断时存在肝转移和肿瘤突变负担(TMB)>5 mut/Mb。

结论

一线奥希替尼治疗对于转移性 NSCLC 的西班牙裔患者是一种有效且安全的选择。肝转移和更高的 TMB 与较低的 PFS 相关。尽管有效,但在该队列患者中确定了不同的耐药机制,包括可以通过其他治疗选择靶向的突变。

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