Ontology highlight
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.
SUBMITTER: Nie X
PROVIDER: S-EPMC10428614 | biostudies-literature | 2023 Aug
REPOSITORIES: biostudies-literature
Nie Xin X Zhang Ping P Bie Zhixin Z Song Chenhui C Zhang Min M Ma Di D Cui Di D Cheng Gang G Li Hui H Lei Yan Y Su Xiaoxing X Wu Wendy W Li Lin L
World journal of surgical oncology 20230816 1
<h4>Background</h4>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.<h4>Case presentation</h4>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 diag ...[more]