Author:
Nie Xin,Zhang Ping,Bie Zhixin,Song Chenhui,Zhang Min,Ma Di,Cui Di,Cheng Gang,Li Hui,Lei Yan,Su Xiaoxing,Wu Wendy,Li Lin
Abstract
Abstract
Background
NRG1 fusions are rare oncogenic drivers in solid tumors, and the incidence of NRG1 fusions in non-small cell lung cancer (NSCLC) was 0.26%. It is essential to explore potential therapeutic strategies and efficacy predictors for NRG1 fusion-positive cancers.
Case presentation
We report an advanced lung adenocarcinoma patient harboring a novel NPTN-NRG1 fusion identified by RNA-based next-generation sequencing (NGS), which was not detected by DNA-based NGS at initial diagnosis. Transcriptomics data of the tissue biopsy showed NRG1α isoform accounted for 30% of total NRG1 reads, and NRG1β isoform was undetectable. The patient received afatinib as fourth-line treatment and received a progression-free survival (PFS) of 14 months.
Conclusions
This report supports afatinib can provide potential benefit for NRG1 fusion patients, and RNA-based NGS is an accurate and cost-effective strategy for fusion detection and isoform identification.
Funder
Chinese Academy of Medical Sciences(CAMS) Innovation Fund for Medical Sciences
Publisher
Springer Science and Business Media LLC
Cited by
3 articles.
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