Neo-adjuvant FOLFIRINOX in borderline resectable and locally advanced pancreatic adenocarcinoma
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John Wiley and Sons Inc
Abstract
Background: Surgery and systemic therapy provide the best option for long-term cancer control in localized resectable pancreas cancer. The present study assessed the efficacy and safety of neoadjuvant treatment with FOLFIRINOX in patients with borderline resectable (BR) and locally advanced (LA) pancreas cancer (PDAC). Methods: This was a prospective noninterventional observational trial of neoadjuvant FOLFIRINOX in BR and LA PDAC. The primary objective was the R0/R1 surgical resection rate. Secondary objectives included progression free survival (PFS) and overall survival (OS), tolerability, and toxicity. Results: Forty-nine patients were enrolled between 2013 and 2019; the majority had LA disease (59.2%). Median age was 61 years, and median Ca 19-9 level pretreatment was 523.4 μmol/L. Following neoadjuvant FOLFIRINOX, 11 patients (22.5%) underwent surgical resection, the majority of which were BR at diagnosis (72.7%). Median OS and PFS for the entire group were 25 (95% CI: 17.2–32.8) and 12 months (95% CI: 9.7–13.3), respectively. Median PFS in BR patients was 14 (95% CI: 10.5–17.5) compared to 12 months (95% CI: 5.2–18.8) in patients with LA patients. Median OS and PFS were not reached in patients who underwent surgical resection as compared to 22 (95% CI: 18.6–25.4) and 9 months (95% CI: 4.2–13.9) in those who did not, respectively. Grade 3/4 neutropenia, leukopenia, neuropathy, nausea/vomiting, and diarrhea occurred in 6.3%, 2.1%, 10.4%, 4.2%, and 8.3%, respectively. Conclusion: Neoadjuvant FOLFIRINOX is an active regimen for patients with LA/BR PDAC with a resection rate of 22.5%. These results are in line with prior data. © 2022 John Wiley & Sons Australia, Ltd.
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Folfirinox, Neoadjuvant therapy, Pancreatic neoplasm, Resectability, Survival, Adenocarcinoma, Antineoplastic combined chemotherapy protocols, Fluorouracil, Humans, Leucovorin, Middle aged, Pancreatic neoplasms, Prospective studies, Ca 19-9 antigen, Folinic acid, Granulocyte colony stimulating factor, Irinotecan, Oxaliplatin, Antineoplastic agent, Adjuvant therapy, Adult, Advanced cancer, Aged, Article, Body weight loss, Cancer localization, Cancer surgery, Clinical article, Clinical outcome, Cohort analysis, Confidence interval, Continuous infusion, Controlled clinical trial, Controlled study, Device safety, Diarrhea, Drug dose reduction, Drug efficacy, Drug tolerability, Fatigue, Female, Human, Human tissue, Infection, Leukopenia, Liver toxicity, Loss of appetite, Male, Mucosa inflammation, Multiple cycle treatment, Nausea, Neoadjuvant chemotherapy, Neuropathy, Neutropenia, Observational study, Overall survival, Pancreas adenocarcinoma, Progression free survival, Prospective study, Side effect, Therapy delay, Thrombocytopenia, Vomiting, Adverse event, Pancreas tumor, Pathology, Procedures