Clinicopathologic Features of NRG1 Fusion-Positive Non-Small Cell Lung Cancer

IF 2.3 2区 医学 Q2 GENETICS & HEREDITY
Bahadır Köylü, Nur İlayda Genç, Mehmet Haluk Yücel, Anıl Yıldız, Esra Aşık, Cevat İlteriş Kıkılı, Fatih Kemik, Nazan Demir, Pınar Bulutay, Ömer Fatih Ölmez, Fatih Selçukbiricik
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Abstract

Data on the clinicopathological features of NRG1 fusion-positive non-small cell lung cancer (NSCLC) are limited. We conducted a retrospective, multicenter study and included patients with NRG1 fusion-positive NSCLC diagnosed between January 2018 and February 2025. Six patients were identified; five were female (83.3%), two were never-smokers (33.3%), and four were former smokers (66.7%). Adenocarcinoma was the predominant histology (n = 5), comprising mucinous (n = 2), enteric (n = 2), and not otherwise specified (n = 1) variants, while one patient had squamous cell carcinoma. All were PD-L1–negative, and CD74-NRG1 was the most common fusion (50%). Three patients received afatinib; only one achieved a partial response with a progression-free survival of 8.7 months. Median overall survival was 6.7 months. Our study demonstrates the histologic and molecular heterogeneity of NRG1 fusion-positive NSCLC, encompassing mucinous and enteric variants of adenocarcinoma. Responses to afatinib were variable, underscoring the need for more effective therapies, including zenocutuzumab and emerging agents.

NRG1融合阳性非小细胞肺癌的临床病理特征。
NRG1融合阳性非小细胞肺癌(NSCLC)的临床病理特征资料有限。我们进行了一项回顾性、多中心研究,纳入了2018年1月至2025年2月诊断为NRG1融合阳性的NSCLC患者。确定了6例患者;女性5人(83.3%),从不吸烟者2人(33.3%),戒烟者4人(66.7%)。腺癌是主要的组织学(n = 5),包括黏液癌(n = 2),肠癌(n = 2)和其他未指定的(n = 1)变异,而1例患者为鳞状细胞癌。所有患者均为pd - l1阴性,CD74-NRG1是最常见的融合(50%)。3例患者接受阿法替尼治疗;只有1例获得部分缓解,无进展生存期为8.7个月。中位总生存期为6.7个月。我们的研究证明了NRG1融合阳性NSCLC的组织学和分子异质性,包括粘液和肠腺癌变体。对阿法替尼的反应是可变的,强调需要更有效的治疗,包括zenocutuzumab和新兴药物。
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来源期刊
Genes, Chromosomes & Cancer
Genes, Chromosomes & Cancer 医学-遗传学
CiteScore
7.00
自引率
8.10%
发文量
94
审稿时长
4-8 weeks
期刊介绍: Genes, Chromosomes & Cancer will offer rapid publication of original full-length research articles, perspectives, reviews and letters to the editors on genetic analysis as related to the study of neoplasia. The main scope of the journal is to communicate new insights into the etiology and/or pathogenesis of neoplasia, as well as molecular and cellular findings of relevance for the management of cancer patients. While preference will be given to research utilizing analytical and functional approaches, descriptive studies and case reports will also be welcomed when they offer insights regarding basic biological mechanisms or the clinical management of neoplastic disorders.
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