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Pancreatic adenocarcinoma third line systemic treatments: a retrospective cohort study

Anna Gueiderikh, A. Tarabay, M. Abdelouahab, Cristina Smolenschi, M-L. Tanguy, Marine Valéry, David Malka, T. Pudlarz, Alina Fuerea, V. Boige, Antoine Hollebecque, Michel Ducreux, Alice Boilève

2024BMC Cancer12 citationsDOIOpen Access PDF

Abstract

Abstract Background Chemotherapy for metastatic pancreatic adenocarcinoma (PDAC) primarily relies on FOLFIRINOX (LV5FU- irinotecan – Oxaliplatine) and Gemcitabine – Nab-Paclitaxel in the first-line setting. However, second-lines remain less well-defined and there is limited data regarding third-line treatments. The objective of our study was to determine the proportion of patients advancing to third line chemotherapy, to outline the various third-line chemotherapy regimens used in routine practice and to evaluate their respective efficacy. Methods A retrospective single-center cohort from 2010-2022 compiled baseline characteristics, treatment outcomes and survival of PDAC patients who received at least one chemotherapy line in a French tertiary-center. Overall survivals (OS) were analyzed using a Cox multivariable model. Results In total, 676 patients were included, with a median follow-up time of 69.4 months, (Interquartile Range (IQR) = 72.1). Of these, 251 patients (37%) that proceeded to 3 rd -line chemotherapy. The median PFS in 3 rd line was 2.03 months, [CI95%: 1.83, 2.36]. The median 3 rd line overall survival was 5.5 months, [CI95%: 4.8, 6.3]. In multivariable analysis erlotinib-based chemotherapy was found to be deleterious (HR=2.38, [CI95%: 1.30, 4.34], p =0.005) compared to fluoropyrimidine-based chemotherapy in terms of 3 rd line overall survival while gemcitabine monotherapy showed a tendency towards negative outcomes. First and 2 nd line chemotherapies sequence didn’t influence 3 rd line outcome. Conclusion In our cohort, one-third of treated patients proceeded to 3 rd line chemotherapy resulting in a 5.5 months median 3 rd line OS, consistent with treatments at advanced stage. Our results argue against the use of erlotinib and gemcitabine monotherapy.

Topics & Concepts

MedicineGemcitabineFOLFIRINOXInternal medicineChemotherapyIrinotecanOncologyRetrospective cohort studyErlotinibInterquartile rangeCohortSurgeryCancerColorectal cancerEpidermal growth factor receptorPancreatic and Hepatic Oncology ResearchNeuroendocrine Tumor Research AdvancesCancer Research and Treatments