A Locally Advanced NSCLC Patient Harboring a Rare KIF13A-RET Fusion Benefited from Pralsetinib: A Case Report
Zenghao Chang, Tengfei Zhu, Hao Jiang, Wei Ou, Siyu Wang

TL;DR
A lung cancer patient with a rare gene fusion responded well to a targeted drug and early detection through blood tests.
Contribution
Demonstrates the efficacy of pralsetinib and ctDNA monitoring in a rare RET fusion NSCLC case.
Findings
Pralsetinib as adjuvant therapy achieved 27 months of disease-free survival.
ctDNA detected tumor recurrence 4 months earlier than imaging techniques.
Adding bevacizumab upon recurrence continued to benefit the patient.
Abstract
The application of adjuvant treatment has significantly enhanced the survival of patients with resectable non-small cell lung cancer (NSCLC) carrying driver gene mutations. However, adjuvant-targeted therapy remains controversial for some NSCLC patients carrying rare gene mutations such as RET, as there is currently a lack of confirmed randomized controlled trials demonstrating efficacy. In this report, we describe the case of a 58-year-old man with stage IIIA NSCLC who underwent complete lobectomy with selective lymph node dissection. Postoperative next-generation sequencing revealed that the patient harbored a rare KIF13A-RET fusion. The patient elected to receive adjuvant treatment with pralsetinib monotherapy and underwent serial circulating tumor DNA (ctDNA) monitoring after surgery. During follow-up, despite experiencing dose reduction and irregular medication adherence, the…
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Taxonomy
TopicsCancer Genomics and Diagnostics · Lung Cancer Treatments and Mutations · Pancreatic and Hepatic Oncology Research
