Abstract
BackgroundAlthough a toxic regimen, FOLFIRINOX is one of the most efficient chemotherapy regimens in advanced pancreatic adenocarcinoma. There is no standard number of cycles in locally advanced or metastatic stages.Materials and methodThe present retrospective study reports the experience of a single center with this regimen administered until disease progression or unacceptable toxicity. The authors of this retrospective study analyzed the data on patients with this diagnosis treated in our clinic during 2017-2021. Forty-two patients were included in the study, 21 who received six courses or less and 21 who received more than six courses. Progression-free survival (PFS) and overall survival (OS) were analyzed according to this stratification. The oncological response was also reported according to dose reduction and treatment delay, irrespective of the number of courses administered.ResultsMedian PFS was 7.5 months, and median OS was 13.6 months in the entire studied population. When patients were compared according to the number of courses received (under six vs. over six), there were obvious differences (PFS: 5.17 months vs. 11.2, p = 0.8, OS: 8 months vs. 17.3 months, p = 0.6). However, when stratifying survival by treatment delay and the presence or absence of dose reduction, better results were seen with lower doses (p<0.001) and treatment temporization (p=0.03). The general incidence of hematologic and neurologic toxicity was higher than the ones reported in the literature.ConclusionThe study revealed that patients benefit from the administration of FOLFIRINOX for more than six months, but that the administration of full dose and the maintaining dose intensity does not necessarily favor the patient.
Highlights
Pancreatic cancer is a disease with high mortality, causing over 400,000 deaths annually [1], with median survival in the advanced stages of about 12 months and for the metastatic stage of about six months
When patients were compared according to the number of courses received, there were obvious differences (PFS: 5.17 months vs. 11.2, p = 0.8, overall survival (OS): 8 months vs. 17.3 months, p = 0.6)
The present study reports experience with this regimen administered up to unacceptable toxicity or disease progression, with a follow-up period of four years, quantifying the benefit of survival, and the impact of maintaining dose
Summary
Pancreatic cancer is a disease with high mortality, causing over 400,000 deaths annually [1], with median survival in the advanced stages of about 12 months and for the metastatic stage of about six months. FOLFIRINOX is a reference regimen extremely effective in advanced pancreatic adenocarcinoma Better survival with this type of chemotherapy, when compared with gemcitabine monotherapy, has been demonstrated in the pivotal PRODIGE trial (11.1 vs 6.8 months, hazard ratio (HR) for death 0.57; 95% confidence interval (CI); p
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