Volume 38, Issue 2 p. 214-219
Original Communication

Restoration of Mannose-Binding Lectin Complement Activity Is Associated With Improved Outcome in Patients With Advanced Pancreatic Cancer Treated With Gemcitabine and Intravenous ω-3 Fish Oil

Ali Arshad MA, MRCS

Corresponding Author

Ali Arshad MA, MRCS

Department of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK

Ali Arshad, MA, MRCS, Department of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Gwendolen Rd, Leicester, LE5 4PW, UK. Email: [email protected]Search for more papers by this author
Wen Chung PhD

Wen Chung PhD

Department of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK

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John Isherwood MRCS

John Isherwood MRCS

Department of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK

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William Steward PhD, FRCP

William Steward PhD, FRCP

Department of Medical Oncology, University Hospitals of Leicester, Leicester, UK

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Matthew Metcalfe MD, FRCS

Matthew Metcalfe MD, FRCS

Department of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK

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Ashley Dennison MD, FRCS

Ashley Dennison MD, FRCS

Department of Hepatobiliary and Pancreatic Surgery, Leicester General Hospital, Leicester, UK

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First published: 19 February 2013
Citations: 13

Abstract

Background: Pancreatic cancer has an extremely poor clinical outcome. Surrogate biomarkers for outcome are scarce. There is mixed evidence for the association of high mannose-binding lectin (MBL) complement activity with cancer outcomes, including reduced survival and increased infectious complications. ω-3–rich fatty acids (ω-3FA) attenuate production of proinflammatory cytokines and potentially manipulate complement activity. Materials and Methods: As part of a single-arm phase II trial in a university hospital, patients with advanced pancreatic adenocarcinoma were treated with weekly ω-3FA–rich intravenous infusion (Lipidem [B. Braun Melsungen AG, Melsungen, Germany]: up to 100 g/wk) plus gemcitabine chemotherapy until withdrawal or tumor progression. Primary outcome measure was objective response rate. Changes in complement activity, which were a secondary outcome measure, were analyzed and relation to clinical outcome determined. Results: Twenty-three patients were assessable for time to progression (TTP), overall survival (OS), and complement activity. No hypoactivity in alternative and classical pathways was demonstrated. Baseline MBL was low in 10 of 23 patients (43.5%). There was no difference in OS or TTP between low- and high-baseline MBL patients. Of these 10 patients, 5 were classified as MBL responders. MBL responders had a tendency toward improved OS over nonresponders (8.9 vs 4.4 months, P = .07). MBL responders had significantly improved TTP over nonresponders (10.6 vs 5.3 months, P = .03). Conclusion: MBL restoration had an association with improved outcome in the cohort of patients with low MBL activity at baseline. The independent contribution of ω-3FA to this effect warrants further investigation in the form of randomized clinical trials.