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Neoadjuvant Chemotherapy for Intraductal Papillary Mucinous Neoplasm-derived Pancreatic Cancer
Joseph R Habib1,2, Ingmar F Rompen1,3,4,5, Ammar A Javed1,4,5
1New York University Langone Health, Department of Surgery, New York, USA.
Annals of Surgery
|March 5, 2025
Summary
Neoadjuvant chemotherapy (NAT) shows value for advanced IPMN-derived pancreatic cancer, improving outcomes regardless of initial resectability stage. Its benefit in resectable disease requires further individualized assessment.
Area of Science:
- Oncology
- Gastroenterology
- Surgical Oncology
Background:
- Intraductal papillary mucinous neoplasm (IPMN)-derived pancreatic cancer management is debated, especially regarding neoadjuvant chemotherapy (NAT).
- The role of NAT in IPMN-derived pancreatic cancer remains controversial, necessitating further investigation.
Purpose of the Study:
- To evaluate the efficacy and role of neoadjuvant chemotherapy (NAT) in IPMN-derived pancreatic cancer.
- To compare outcomes between upfront surgery and NAT followed by resection.
Main Methods:
- Retrospective analysis of 1,019 patients with IPMN-derived pancreatic cancer from eight international centers (2000-2023).
- Comparison of clinicopathologic data between patients treated with upfront surgery (US) versus NAT.
- Kaplan-Meier and Cox-regression analyses for overall survival (OS) and recurrence-free survival (RFS).
Main Results:
- Of 1,019 patients, 76 (7%) received NAT, presenting with more advanced resectability stages and higher CA19-9 levels.
- Overall survival (OS) was not significantly different between US and NAT groups (38.0 vs. 27.5 months, P=0.121).
- Pathological treatment response and CA19-9 normalization post-NAT correlated with improved survival; N2 disease, elevated CA19-9, and R1 margin were independent predictors of OS after NAT.
Conclusions:
- Neoadjuvant chemotherapy (NAT) followed by resection is valuable for borderline resectable and locally advanced IPMN-derived pancreatic cancer.
- The benefit of NAT in resectable IPMN-derived pancreatic cancer is uncertain and may require personalized treatment strategies.
- CA19-9 normalization and pathological response serve as indicators of biological treatment effect in IPMN-derived pancreatic cancer.

