Ensartinib targeted conversion surgery for ALK-positive unresectable locally advanced non-small cell lung cancer: a case report.
[UNLABELLED] Currently, there is limited evidence supporting ensartinib’s efficacy as a neoadjuvant treatment for locally advanced anaplastic lymphoma kinase (ALK)-positive non–small cell lung cancer
APA
Huang S, Yuan C, et al. (2026). Ensartinib targeted conversion surgery for ALK-positive unresectable locally advanced non-small cell lung cancer: a case report.. Journal of cardiothoracic surgery, 21(1). https://doi.org/10.1186/s13019-026-03940-1
MLA
Huang S, et al.. "Ensartinib targeted conversion surgery for ALK-positive unresectable locally advanced non-small cell lung cancer: a case report.." Journal of cardiothoracic surgery, vol. 21, no. 1, 2026.
PMID
41776641
Abstract
[UNLABELLED] Currently, there is limited evidence supporting ensartinib’s efficacy as a neoadjuvant treatment for locally advanced anaplastic lymphoma kinase (ALK)-positive non–small cell lung cancer (NSCLC). This case study describes a 65-year-old female who presented with an incidental pulmonary lesion and was diagnosed with unresectable locally advanced stage IIIB (cT3N2M0) ALK-positive NSCLC. After multidisciplinary evaluation, she underwent 12 weeks of neoadjuvant ensartinib therapy (225 mg/day, later reduced to 175 mg/day), achieving a 78.4% reduction in tumor volume and reassessment as resectable. Subsequently, video-assisted thoracoscopic surgery (VATS) comprising a right upper lobectomy and systematic lymph node dissection resulted in R0 resection. Postoperative pathological analysis confirmed pathological complete response (pCR). During an fifteen-month follow-up, no recurrence of the disease was detected. These results indicate that ensartinib may provide potential benefit for patients with locally advanced ALK-positive NSCLC by optimizing surgical feasibility and survival outcomes.
[SUPPLEMENTARY INFORMATION] The online version contains supplementary material available at 10.1186/s13019-026-03940-1.
[SUPPLEMENTARY INFORMATION] The online version contains supplementary material available at 10.1186/s13019-026-03940-1.
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