Treatment of Pancreatic Neuroendocrine Tumors: Beyond Traditional Surgery and Targeted Therapy
- PMID: 40429384
- PMCID: PMC12112752
- DOI: 10.3390/jcm14103389
Treatment of Pancreatic Neuroendocrine Tumors: Beyond Traditional Surgery and Targeted Therapy
Abstract
Pancreatic neuroendocrine tumors (PNETs) are a rare subset of pancreatic neoplasms with diverse biological behavior and clinical presentations. Traditional treatment approaches, such as surgery and targeted therapies, have significantly improved outcomes. However, advancements in molecular biology, immunotherapy, and minimally invasive techniques have ushered in a new era of treatment possibilities. This manuscript explores the emerging modalities in PNET management, emphasizing the need for a multidisciplinary approach tailored to individual patient profiles.
Keywords: EUS-guided ablation; conversion surgery; immunotherapy advancements; microwave ablation; minimally invasive techniques; molecular; neoadjuvant and adjuvant therapy; pancreatic neuroendocrine tumors (PNETs); peptide receptor radionuclide therapy (PRRT); radiofrequency ablation; somatostatin analogs; targeted therapy.
Conflict of interest statement
The authors declare no conflicts of interest.
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