一项关于非小细胞肺癌和表皮生长因子受体 20 外显子插入突变患者的临床特征、治疗顺序和疗效的真实世界研究。

IF 2.8 3区 医学 Q2 ONCOLOGY
Guillermo Suay, Paloma Martín-Martorell, Francisco Aparisi, María Arnal, María Guirado, Aitor Azkárate, Javier Garde-Noguera, José David Cumplido-Burón, Amelia Insa, José Francisco González-Muñoz, Sarai Palanca, María Díaz, Alfredo Sánchez-Hernández, Óscar Juan-Vidal
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引用次数: 0

摘要

研究目的在所有非小细胞肺癌(NSCLC)患者中,高达 4% 的患者存在表皮生长因子受体外显子 20 插入(EGFRex20ins)突变。这些患者通常对表皮生长因子受体酪氨酸激酶抑制剂(TKIs)不敏感,预后比表皮生长因子受体更常见突变的患者更差。在这项多中心、回顾性、真实世界研究中,我们试图确定最近批准的专门针对表皮生长因子受体ex20ins突变的治疗是否能显著改善这类患者的预后:我们评估了西班牙巴伦西亚大区 7 家医院在 2012 年 12 月 31 日至 2022 年 12 月 31 日期间确诊为 NSCLC 和 EGFRex20ins 基因突变的 41 例患者的临床特征、病情发展以及对治疗的反应:32名患者(72%)出现转移性疾病,其中29人(71%)接受了肿瘤治疗。我们发现,在治疗过程中的某个阶段使用针对表皮生长因子受体ex20ins突变的靶向疗法(阿米万他单抗、莫伯替尼和/或舒伐他尼),可显著提高转移性患者的中位生存期,从8个月(95% CI 0-21.7)提高到30个月(95% CI 11.1-48.8;危险比=0.297,P=0.02):我们的研究结果为这一特殊人群不断发展的治疗标准做出了贡献,并凸显了癌症靶向疗法的临床优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A real‑world study of clinical characteristics, treatment sequence and outcomes of patients with non-small cell lung cancer and EGFR exon 20 insertion mutations.

Objectives: EGFR exon 20 insertion (EGFRex20ins) mutations are found in up to 4% of all patients with non-small cell lung cancer (NSCLC). These patients are often insensitive to EGFR-tyrosine kinase inhibitors (TKIs) and have worse prognosis than patients with more common EGFR mutations. In this multicenter, retrospective, real-world study, we sought to determine whether the administration of recently approved treatments that specifically target EGFRex20ins mutations could significantly improve outcomes in this patient population.

Materials and methods: We evaluated the clinical features of 41 patients diagnosed with NSCLC and EGFRex20ins mutations, their evolution, and response to treatments received across 7 hospitals in the Valencian Community, Spain, between 31st December 2012 and 31st December 2022.

Results: 32 patients (72%) developed metastatic disease, and 29 (71%) of them received oncological treatment. We found that administering a targeted therapy against EGFRex20ins mutations (amivantamab, mobocertinib and/or sunvozertinib) at some point during the course of treatment, significantly increased the median OS of metastatic patients from 8 months (95% CI 0-21.7) to 30 months (95% CI 11.1-48.8; Hazard ratio = 0.297, p = 0.02).

Conclusion: Our findings contribute to the evolving standard of care for this specific population and highlight the clinical benefits of targeted cancer therapies.

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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
240
审稿时长
1 months
期刊介绍: Clinical and Translational Oncology is an international journal devoted to fostering interaction between experimental and clinical oncology. It covers all aspects of research on cancer, from the more basic discoveries dealing with both cell and molecular biology of tumour cells, to the most advanced clinical assays of conventional and new drugs. In addition, the journal has a strong commitment to facilitating the transfer of knowledge from the basic laboratory to the clinical practice, with the publication of educational series devoted to closing the gap between molecular and clinical oncologists. Molecular biology of tumours, identification of new targets for cancer therapy, and new technologies for research and treatment of cancer are the major themes covered by the educational series. Full research articles on a broad spectrum of subjects, including the molecular and cellular bases of disease, aetiology, pathophysiology, pathology, epidemiology, clinical features, and the diagnosis, prognosis and treatment of cancer, will be considered for publication.
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