Second-line palliative chemotherapy, survival, and prognostic factors in patients with advanced pancreatic cancer.

Acta Oncol

Department of Clinical Sciences Lund, Oncology and Pathology, Institute for Palliative Care, Faculty of Medicine, Lund University, Lund, Sweden.

Published: December 2021

AI Article Synopsis

  • Pancreatic cancer is a deadly disease, with first-line chemotherapy extending survival but second-line treatments showing uncertain benefits; identifying prognostic factors is crucial.
  • A study of 170 patients revealed that those with better performance status or normal albumin levels had higher median survival rates after second-line therapy, while poor status and low albumin suggested worse outcomes.
  • The findings suggest that poor performance status and hypoalbuminemia are significant negative prognostic factors for survival on second-line treatment, emphasizing the need for careful consideration before administering such therapies.

Article Abstract

Introduction: Pancreatic cancer is a highly lethal disease with a close association between incidence and mortality. First-line (FL) palliative chemotherapy prolongs survival and alleviates cancer-related symptoms. However, the survival benefit of second-line (SL) treatment is uncertain, as studies fail to consistently show prolonged survival for any given SL treatment, and in the absence of prognostic factors patients will receive a futile treatment. The aim of this study was to examine prognostic factors and survival in patients with pancreatic cancer, with special reference to SL therapy.

Material And Methods: This retrospective study included all patients with histopathologically verified pancreatic adenocarcinoma who received palliative chemotherapy at Skåne University Hospital and died between 1 Feb 2015 and 31 Dec 2017.

Results: During the study period, a total of 170 patients with pancreatic cancer died after receiving palliative chemotherapy. Of these, 72 had received SL treatment after progression on FL treatment. Median overall survival (OS) from the start of SL treatment was 5.0 months (95% CI: 4.0-6.1). Median OS was 2.9 months for patients with performance status 2 at start of SL treatment compared to 5.3 months for patients with performance status 0-1 ( = .03), and 3.5 months (95% CI: 3.0-5.4) in patients with hypoalbuminemia (<36 g/L) at the start of SL therapy compared to 8.0 months (95% CI: 5.3-11.1) for patients with normal albumin levels ( = .009). Weight loss during FL therapy, a doubling of CA 19-9 after FL therapy, and length of progression-free survival during FL treatment were not associated with survival following SL therapy.

Conclusion: Poor performance status and hypoalbuminemia are negative prognostic factors for survival on SL palliative treatment in patients with advanced pancreatic cancer. Possible gain in survival should be carefully considered before initiating SL chemotherapy.

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Source
http://dx.doi.org/10.1080/0284186X.2021.1973680DOI Listing

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