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Pathologic complete response to pralsetinib in stage IV RET-positive non-small cell lung cancer: A case report
Xinxin Chen1, Guoxin Wang1, Jianfeng Zhang2
1Department of Respiratory Medicine, Jinling Hospital, Nanjing University School of Medicine, Nanjing, 210002, China.
Abstract:
Neoadjuvant therapy with tyrosine kinase inhibitors has been proposed as a feasible approach for downstaging potential resectable non-small cell lung cancer (NSCLC). Pralsetinib is a paradigm of precision medicine for cancers driven by mutant RET (rearranged during transfection). In this case, we reported dramatic response to Pralsetinib in a stage IV NSCLC patient with RET rearrangement. Strikingly, treatment with 10 months of Pralsetinib impended downstaging of the N2 lymph node and metastatic pleural disease. Histological examination of the surgically resected specimen indicated a pathologic complete response (pCR). The patient was recommended to continue Pralsetinib as an adjuvant therapy. This case highlighted potential application of Pralsetinib in locally advanced RET-positive NSCLC to prime surgical resection. Postoperative Pralsetinib adjuvant therapy should also be considered.
Insights
Pralsetinib demonstrated significant effectiveness in downstaging advanced non-small cell lung cancer (NSCLC) with RET rearrangement, achieving a pathologic complete response. This suggests Pralsetinib
Area of Science:
- Oncology
- Medical Genetics
- Thoracic Surgery
Background:
- Neoadjuvant tyrosine kinase inhibitors (TKIs) are explored for downstaging non-small cell lung cancer (NSCLC).
- Pralsetinib targets cancers with rearranged during transfection (RET) gene fusions, a key aspect of precision medicine.
- RET rearrangements are an actionable driver mutation in a subset of NSCLC.
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