Abstract

Simple SummaryThe role of neoadjuvant therapy in pancreatic cancer is poorly defined. Our results show improved overall survival in patients who received neoadjuvant therapy, driven by improved chemotherapy delivery, with no apparent increase in early or late perioperative complications.The role of neoadjuvant chemoradiotherapy and/or chemotherapy (neoCHT) in patients with pancreatic ductal adenocarcinoma (PDAC) is poorly defined. We hypothesized that patients who underwent neoadjuvant therapy (NAT) would have improved systemic therapy delivery, as well as comparable perioperative complications, compared to patients undergoing upfront resection. This is an IRB-approved retrospective study of potentially resectable PDAC patients treated within an academic quaternary referral center between 2011 and 2018. Data were abstracted from the electronic medical record using an institutional cancer registry and the National Surgical Quality Improvement Program. Three hundred and fourteen patients were eligible for analysis and eighty-one patients received NAT. The median overall survival (OS) was significantly improved in patients who received NAT (28.6 vs. 20.1 months, p = 0.014). Patients receiving neoCHT had an overall increased mean duration of systemic therapy (p < 0.001), and the median OS improved with each month of chemotherapy delivered (HR = 0.81 per month CHT, 95% CI (0.76–0.86), p < 0.001). NAT was not associated with increases in early severe post-operative complications (p = 0.47), late leaks (p = 0.23), or 30–90 day readmissions (p = 0.084). Our results show improved OS in patients who received NAT, driven largely by improved chemotherapy delivery, without an apparent increase in early or late perioperative complications compared to patients undergoing upfront resection.

Highlights

  • Pancreatic cancer is estimated to cause more than 430,000 deaths per year worldwide, ranking as the seventh leading cause of cancer deaths worldwide and third in the UnitedStates [1–3]

  • A total of 314 patients underwent curative-intent resection, 71 (22.6%) of whom were classified as borderline resectable, with a median follow-up of 24.1 months

  • overall survival (OS) improved with each month of chemotherapy delivered (HR = 0.81 per month CHT, 95% CI 0.76–0.86, p < 0.001)

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Summary

Introduction

Pancreatic cancer is estimated to cause more than 430,000 deaths per year worldwide, ranking as the seventh leading cause of cancer deaths worldwide and third in the UnitedStates [1–3]. The most promising outcomes for patients with resectable disease were reported in the PRODIGE 24-ACCORD trial, in which patients who received adjuvant combination chemotherapy with modified FOLFIRINOX demonstrated a median overall survival (OS) of 54.4 months, compared to 35.0 months with gemcitabine alone [5]. This dramatic survival improvement is primarily attributed to the enhanced activity of combination chemotherapy. The benefits of adjuvant combination chemotherapy are not available to approximately half of all patients who undergo upfront surgery

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