Defining the molecular pathology of pancreatic body and tail adenocarcinoma

S. B. Dreyer, N. B. Jamieson, R. Upstill-Goddard, P. J. Bailey, C. J. McKay, Australian Pancreatic Cancer Genome Initiative, Vincent Lam, A. V. Biankin, D. K. Chang

Research output: Contribution to journalArticlepeer-review

42 Citations (Scopus)
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Abstract

Background: Pancreatic ductal adenocarcinoma (PDAC) remains a dismal disease, with very little improvement in survival over the past 50 years. Recent large‐scale genomic studies have improved understanding of the genomic and transcriptomic landscape of the disease, yet very little is known about molecular heterogeneity according to tumour location in the pancreas; body and tail PDACs especially tend to have a significantly worse prognosis. The aim was to investigate the molecular differences between PDAC of the head and those of the body and tail of the pancreas.

Methods: Detailed correlative analysis of clinicopathological variables, including tumour location, genomic and transcriptomic data, was performed using the Australian Pancreatic Cancer Genome Initiative (APGI) cohort, part of the International Cancer Genome Consortium study.

Results: Clinicopathological data were available for 518 patients recruited to the APGI, of whom 421 underwent genomic analyses; 179 of these patients underwent whole‐genome and 96 RNA sequencing. Patients with tumours of the body and tail had significantly worse survival than those with pancreatic head tumours (12·1 versus 22·0 months; P = 0·001). Location in the body and tail was associated with the squamous subtype of PDAC. Body and tail PDACs enriched for gene programmes involved in tumour invasion and epithelial‐to‐mesenchymal transition, as well as features of poor antitumour immune response. Whether this is due to a molecular predisposition from the outset, or reflects a later time point on the tumour molecular clock, requires further investigation using well designed prospective studies in pancreatic cancer.

Conclusion: PDACs of the body and tail demonstrate aggressive tumour biology that may explain worse clinical outcomes.
Original languageEnglish
Pages (from-to)e183—e191
Number of pages9
JournalBritish Journal of Surgery
Volume105
Issue number2
DOIs
Publication statusPublished - 1 Jan 2018

Bibliographical note

Copyright the Author(s) 2018. Version archived for private and non-commercial use with the permission of the author/s and according to publisher conditions. For further rights please contact the publisher.

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