Evidence map›Paper›PMID 42137140›Full record

ArticleFrontiers in oncology2026

Identification of a novel ALK intergenic fusion in a resected high‑recurrence‑risk lung adenocarcinoma and adjuvant treatment with ensartinib: a case report.

Jing Li, Bo Ma, Ruiqing Mian, Yifan Wang, Lei Zhang, Na Yan, Jinxi He

Abstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2026. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Jing LiDepartment of General Thoracic Surgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Bo MaDepartment of General Thoracic Surgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Ruiqing MianDepartment of General Thoracic Surgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Yifan WangDepartment of General Thoracic Surgery, General Hospital of Ningxia Medical University, Yinchuan, China.
Lei ZhangKey Laboratory of Digital Technology in Medical Diagnostics of Zhejiang Province, Dian Diagnostics Group Co. Ltd., Hangzhou, Zhejiang, China.
Na Yan *Key Laboratory of Digital Technology in Medical Diagnostics of Zhejiang Province, Dian Diagnostics Group Co. Ltd., Hangzhou, Zhejiang, China.
Jinxi He *Department of General Thoracic Surgery, General Hospital of Ningxia Medical University, Yinchuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report a novel intergenic anaplastic lymphoma kinase (ALK) fusion identified in a patient with resected stage IIIA lung adenocarcinoma. A 75-year-old woman underwent lobectomy for a left lower lobe tumor, with final pathology revealing pT3N2aM0 disease with high-risk features (pleural invasion, vascular tumor thrombus, and spread through air spaces). Comprehensive next-generation sequencing (NGS) of the surgical specimen identified a previously unreported in-frame fusion between an intergenic region of chromosome 6 (between STPLC1P2 and LOC100128365) and exon 20 of ALK on chromosome 2, retaining the entire kinase domain. Immunohistochemistry confirmed strong ALK protein expression (D5F3, Ventana). Based on the high-risk pathological stage and the presence of a targetable ALK driver, adjuvant therapy with the ALK tyrosine kinase inhibitor ensartinib was initiated instead of conventional chemotherapy. The patient tolerated treatment well, and a follow-up chest CT at approximately 6 months showed no evidence of local recurrence or distant metastasis. Long-term outcomes remain to be determined. This case expands the spectrum of ALK rearrangements and highlights the critical role of molecular profiling in guiding adjuvant treatment decisions for early-stage, high-risk non-small cell lung cancer (NSCLC).

Indexed as

adjuvant therapyALK fusioncase reportensartinibintergenic regionlung adenocarcinoma

Identifiers

PMID42137140
PMCPMC13167402

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