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.
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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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).
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