Molecular Profiling in Non-Small-Cell Lung Cancer: A Single-Center Study on Prevalence and Prognosis.

IF 2.8 4区 医学 Q2 ONCOLOGY
Mustafa Özgür Arıcı, Bora Demirkan, Ebru Taştekin, Derya Kıvrak Salim
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引用次数: 0

Abstract

The aim of this study is to evaluate the prognostic value of molecular profiling in patients with metastatic non-small-cell lung cancer (NSCLC). This single-center study included patients diagnosed and treated between July 2020 and April 2024. The molecular profiles of patients detected by either next-generation sequencing or conventional methods were reviewed retrospectively. Survival analyses were conducted based on the targetable alterations and treatments received. Seventy patients were included, with a median age of 65 years and a median overall survival (OS) of 13 months. Of all patients, 56 (80%) had at least one molecular alteration, and the most frequent alteration was TP53 (52.9%), followed by KRAS (20%) and EGFR (8.6%). Eighteen patients (25.7%) had an alteration amenable to targeted therapy. Patients who could reach a matched targeted therapy at any treatment line exhibited a longer median OS compared to those who could not (not reached vs. 6.9 months, p = 0.042). Patients with a targetable alteration for first-line treatment demonstrated a longer progression-free survival compared to those without a targetable alteration (not reached vs. 4.9 months, p = 0.006). According to current guidelines, conducting molecular testing to identify all potential targetable alterations in NSCLC is the cornerstone of the treatment decision process. The survival analysis in this study emphasized the impact of the use of targeted therapies on the survival outcomes.

非小细胞肺癌的分子分析:患病率和预后的单中心研究。
本研究的目的是评估分子谱分析在转移性非小细胞肺癌(NSCLC)患者中的预后价值。这项单中心研究纳入了2020年7月至2024年4月期间诊断和治疗的患者。回顾性回顾了采用新一代测序或传统方法检测的患者的分子谱。生存分析基于可靶向的改变和接受的治疗。纳入70例患者,中位年龄为65岁,中位总生存期(OS)为13个月。在所有患者中,56例(80%)至少有一种分子改变,最常见的改变是TP53(52.9%),其次是KRAS(20%)和EGFR(8.6%)。18例患者(25.7%)有可适应靶向治疗的改变。能够在任何治疗线上达到匹配靶向治疗的患者比无法达到的患者表现出更长的中位OS(未达到vs. 6.9个月,p = 0.042)。与没有靶向性改变的患者相比,接受一线治疗的靶向性改变患者的无进展生存期更长(未达到vs. 4.9个月,p = 0.006)。根据目前的指南,进行分子检测以确定NSCLC中所有潜在的可靶向改变是治疗决策过程的基石。本研究的生存分析强调了靶向治疗对生存结果的影响。
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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来源期刊
Current oncology
Current oncology ONCOLOGY-
CiteScore
3.30
自引率
7.70%
发文量
664
审稿时长
1 months
期刊介绍: Current Oncology is a peer-reviewed, Canadian-based and internationally respected journal. Current Oncology represents a multidisciplinary medium encompassing health care workers in the field of cancer therapy in Canada to report upon and to review progress in the management of this disease. We encourage submissions from all fields of cancer medicine, including radiation oncology, surgical oncology, medical oncology, pediatric oncology, pathology, and cancer rehabilitation and survivorship. Articles published in the journal typically contain information that is relevant directly to clinical oncology practice, and have clear potential for application to the current or future practice of cancer medicine.
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