非小细胞肺癌的真实生存结果:基因组检测和靶向治疗在拉丁美洲中等收入国家的影响

IF 3.2 Q2 ONCOLOGY
JCO Global Oncology Pub Date : 2024-12-01 Epub Date: 2024-12-05 DOI:10.1200/GO-24-00338
Juan-Manuel Hernandez-Martinez, Alberto Guijosa, Diana Flores-Estrada, Graciela Cruz-Rico, Jenny Turcott, Norma Hernández-Pedro, Enrique Caballé-Perez, Andrés F Cardona, Oscar Arrieta
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引用次数: 0

摘要

目的:针对非小细胞肺癌(NSCLC)和驱动性肿瘤突变患者进行靶向治疗。然而,关于这些药物的生存益处的实际研究是有限的。本研究旨在评估与基因组改变相匹配的靶向治疗对非小细胞肺癌患者生存的影响。方法:这项回顾性研究包括446例晚期NSCLC患者,这些患者在2016年至2023年期间在墨西哥国立Cancerología研究所接受了下一代测序。主要结局为无进展生存期(PFS)和总生存期(OS)。结果:对于整个队列,PFS和OS分别为10.71个月(95% CI, 9.35至12.06)和47.77个月(95% CI, 29.67至65.86)。接受靶向治疗的可操作突变患者的PFS明显更长(19.41个月[95% CI, 14.27至24.55];P < 0.001),比没有可操作突变的患者(6.4个月[95% CI, 4.4至8.4])或未接受靶向治疗的患者(6.6个月[95% CI, 5.3至7.89])。同样,接受靶向治疗的具有可操作突变的患者的OS明显更长(89.69个月[95% CI, 45.54至133.84];P < 0.001),而没有可操作突变的患者(17.11个月[95% CI, 8.65至25.57])或未接受靶向治疗的患者(22.3个月[95% CI, 12.48至32.1])。EGFR和ALK突变患者PFS和OS的显著改善推动了生存期的增加。结论:现实世界的数据分析表明,靶向治疗提高了具有可操作突变的非小细胞肺癌患者的生存率,这支持了扩大广泛基因组检测和靶向治疗的建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Real-World Survival Outcomes in Non-Small Cell Lung Cancer: The Impact of Genomic Testing and Targeted Therapies in a Latin American Middle-Income Country.

Purpose: Targeted therapies are indicated for patients with non-small cell lung cancer (NSCLC) and driver tumor mutations. However, real-world studies on the survival benefits of these agents are limited. This study aimed to evaluate the effect of targeted therapies matched to a genomic alteration on the survival of patients with NSCLC.

Methods: This retrospective study included 446 patients with advanced NSCLC who underwent next-generation sequencing between 2016 and 2023 at the Instituto Nacional de Cancerología in Mexico. The primary outcomes were progression-free survival (PFS) and overall survival (OS).

Results: For the entire cohort, the PFS and OS were 10.71 months (95% CI, 9.35 to 12.06) and 47.77 months (95% CI, 29.67 to 65.86). PFS was significantly longer in patients with actionable mutations treated with targeted therapies (19.41 months [95% CI, 14.27 to 24.55]; P < .001) than in patients without actionable mutations (6.4 months [95% CI, 4.4 to 8.4]) or not treated with targeted therapies (6.6 months [95% CI, 5.3 to 7.89]). Similarly, OS was significantly longer in patients with actionable mutations treated with targeted therapies (89.69 months [95% CI, 45.54 to 133.84]; P < .001) than in patients without actionable mutations (17.11 months [95% CI, 8.65 to 25.57]) or not treated with targeted therapies (22.3 months [95% CI, 12.48 to 32.1]). Survival gains were driven by significant improvements in PFS and OS in patients with EGFR and ALK mutations.

Conclusion: This real-world data analysis demonstrated that targeted therapies improve the survival of patients with NSCLC with actionable mutations, which supports a recommendation for widening access to broad-based genomic testing and targeted therapies.

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来源期刊
JCO Global Oncology
JCO Global Oncology Medicine-Oncology
CiteScore
6.70
自引率
6.70%
发文量
310
审稿时长
7 weeks
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