Evidence map›Paper›PMID 40418326›Full record

ArticleVirchows Archiv : an international journal of pathology2025

FGFR3 amplification is predictive of poor prognosis in esophageal squamous cell carcinoma patients.

Xiang Wang, Jie Huang, Chen Xu, Lili Zhang, Jieakesu Su, Jia Liu, Licheng Shen, Lijuan Luan, Yingyong Hou

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Article in Virchows Archiv : an international journal of pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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9 authors.

Xiang Wang *Department of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Jie Huang *Department of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Chen XuDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Lili ZhangDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Jieakesu SuDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Jia LiuDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Licheng ShenDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China.
Lijuan LuanDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China. luan.lijuan@zs-hospital.sh.cn.
Yingyong HouDepartment of Pathology, Zhongshan Hospital, Fudan University, Shanghai, China. houyingyong@aliyun.com.ORCID http://orcid.org/0000-0001-9156-2305

Funding

National Key Clinical Specialty Discipline Construction Program of China No.YWP2023-001Shanghai Natural Science Foundation of China No.23ZR1410000Shanghai Natural Science Foundation of China No.23ZR1410200
6 · The paper itself

Abstract

Identification and verification of clinically actionable molecular variations to refine currently adopted risk-stratified treatment strategy for esophageal squamous cell carcinoma (ESCC) is urgently needed. Here, we evaluated FGFR3 amplification status by fluorescence in situ hybridization (FISH) performed on tissue microarrays and its prognostic value in 526 ESCC patients. FGFR3 amplification was found in 3.0% (16/526) of ESCC patients enrolled in this study cohort. Intratumor heterogeneity and metastatic heterogeneity of FGFR3 amplification were found in 10% (2/20) and 40% (2/5) FGFR3 amplified ESCC cases, respectively. No statistically significant associations were found between FGFR3 amplification status and common clinicopathological features. Survival analyses demonstrated that FGFR3 amplification was associated with a worse disease-free survival (DFS) and overall survival (OS) (DFS, P = 0.008; OS, P = 0.027). Univariate and multivariate analyses revealed that invasive depth was significantly associated with DFS (P = 0.001, HR: 1.498, 95% CI: 1.172-1.914) and OS (P = 0.002, HR: 1.482, 95% CI: 1.159-1.894), and FGFR3 amplification was significantly associated with DFS (P = 0.020, HR: 2.065, 95% CI: 1.120-3.808) and tend to associate with OS (P = 0.070, HR: 1.756, 95% CI: 0.954-3.233). Furthermore, when patients were stratified into stage I-II group and stage III-IV group, the adverse effect of FGFR3 amplification on prognosis was presented in stage III-IV patients (DFS, P = 0.0047; OS, P = 0.029) rather than stage I-II patients (DFS, P = 0.46; OS, P = 0.53), indicating that the prognostic value of FGFR3 amplification may relying on clinical stage. Our findings might provide a better understanding of the FGFR3 amplification status in ESCC patients and add further insights into its potential prognostic value.

Indexed as

Biomarkers, TumorEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaGene AmplificationReceptor, Fibroblast Growth Factor, Type 3AdultAgedAged, 80 and overDisease-Free SurvivalFemaleHumansIn Situ Hybridization, FluorescenceMaleMiddle AgedPrognosisTissue Array AnalysisBiomarkers, TumorFGFR3 protein, humanReceptor, Fibroblast Growth Factor, Type 3Clinical stageEsophageal cancerEsophageal squamous cell carcinomaFGFR3 amplificationFluorescence in situ hybridizationPrognosis

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.