Abstract

Peritoneal carcinomatosis (pcm) in metastatic pancreatic ductal adenocarcinomas (mpdac) is frequently encountered in day-to-day practice, but rarely addressed in the literature. The objective of the present study was to describe the management and outcome of patients diagnosed with pcm. Data for all consecutive patients with mpdac treated in our centre between 1 January 2014 and 31 August 2015 were analyzed retrospectively. Computed tomography imaging was centrally reviewed by a dedicated radiologist to determine the date of pcm diagnosis. The analysis included 48 patients. Median age in the group was 61 years, and 41 patients had an Eastern Cooperative Oncology Group performance status (ecog ps) of 0-1. All patients presented with pcm either synchronously (group 1) or metachronously (group 2). Those groups differed significantly by baseline ecog ps and neutrophil-to-lymphocyte ratio (nlr), with ecog ps being poorer and nlr being higher in group 1. In addition to pcm, the main sites of metastasis were liver (62.5%) and lungs (31.3%). First-line chemotherapy in 36 patients (75%) was folfirinox (fluorouracil-irinotecan-leucovorin-oxaliplatin). The median overall survival for the entire population was 10.81 months [95% confidence interval (ci): 7.16 months to 14.16 months]; it was 13.17 months (95% ci: 5.9 months to 15.4 months) for patients treated with folfirinox. Median overall survival was 7.13 months (95% ci: 4.24 months to 10.41 months) for patients in group 1 and 14.34 months (95% ci: 9.79 months to 19.91 months) for patients in group 2, p = 0.1296. Compared with other metastatic sites, synchronous pcm seems to be a poor prognostic factor. It could be more frequently associated with a poor ecog ps and a nlr greater than 5 in this group of patients. In patients with mpdac and pcm, either synchronous or metachronous, folfirinox remains an efficient regimen.

Highlights

  • Pancreatic ductal adenocarcinoma is the 4th leading cause of cancer deaths worldwide, and incidence rates are predicted to increase 3% per year[1]

  • All patients presented with pcm either synchronously or metachronously. Those groups differed significantly by baseline ecog ps and neutrophil-tolymphocyte ratio, with ecog ps being poorer and nlr being higher in group 1

  • Some of those factors have been used in developing various prognostic scores: the Glasgow Prognostic Score and the modified gps[10,11]; the neutrophil-to-lymphocyte ratio[12,13,14,15] and the platelet-to-lymphocyte ratio; the prognostic index; and the prognostic nutritional index

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Summary

Introduction

Pancreatic ductal adenocarcinoma (pdac) is the 4th leading cause of cancer deaths worldwide, and incidence rates are predicted to increase 3% per year[1]. Some of those factors have been used in developing various prognostic scores: the Glasgow Prognostic Score (gps) and the modified gps (mgps)[10,11]; the neutrophil-to-lymphocyte ratio (nlr)[12,13,14,15] and the platelet-to-lymphocyte ratio; the prognostic index; and the prognostic nutritional index. None of those scores have been implemented in clinical practice or prospectively investigated in clinical trials. The objective of the present study was to describe the management and outcome of patients diagnosed with pcm

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