Alastair G.W. Moses
Edinburgh Royal Infirmary
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Featured researches published by Alastair G.W. Moses.
Journal of Clinical Oncology | 2006
Kenneth Fearon; Matthew D. Barber; Alastair G.W. Moses; Sam H. Ahmedzai; Gillian S. Taylor; Michael J. Tisdale; Gordon Murray
PURPOSE Eicosapentaenoic acid (EPA) has been proposed to have specific anticachectic effects. This trial compared EPA diethyl ester with placebo in cachectic cancer patients for effects on weight and lean body mass. PATIENTS AND METHODS Five hundred eighteen weight-losing patients with advanced gastrointestinal or lung cancer were studied in a multicenter, double-blind, placebo controlled trial. Patients were randomly assigned to receive a novel preparation of pure EPA at a dose of 2 g or 4 g daily or placebo (2g EPA, n = 175; 4 g EPA, n = 172; placebo, n = 171). Patients were assessed at 4 weeks and 8 weeks. RESULTS The groups were well balanced at baseline. Mean weight loss at baseline was 18% (n = 518). Over the 8-week treatment period, both intention-to-treat analysis and per protocol analysis revealed no statistically significant improvements in survival, weight, or other nutritional variables. There was, however, a trend in favor of EPA with analysis of the primary end point, weight, at 8 weeks showing a borderline, nonsignificant treatment effect (P = .066). Relative to placebo, mean weight increased by 1.2 kg with 2 g EPA (95% CI, 0 kg to 2.3 kg) and by 0.3 kg with 4 g EPA (-0.9 kg to 1.5 kg). CONCLUSION The results indicate no statistically significant benefit from single agent EPA in the treatment of cancer cachexia. Future studies should concentrate on other agents or combination regimens.
Current Opinion in Clinical Nutrition and Metabolic Care | 1999
James A. Ross; Alastair G.W. Moses; Kenneth Fearon
The reversal of catabolic processes remains a significant challenge, partly related to the complexity of such processes and our incomplete understanding of the mechanisms involved. The n-3 fatty acids may be able to attenuate catabolism. This review examines the potential sites of action for these fatty acids and the evidence that supports their anti-catabolic properties.
Supportive Care in Cancer | 2011
Richard J.E. Skipworth; Alastair G.W. Moses; Kathryn Sangster; Catharine M. Sturgeon; Anne Coble Voss; Marie Fallon; Richard A. Anderson; James A. Ross; Kenneth Fearon
PurposeHypogonadism has been linked with systemic inflammation and opioid use in males with advanced cancer. We aimed to investigate the interaction of gonadal status with systemic inflammation and opioids in determining nutritional status and prognosis in advanced pancreatic cancer.MethodsOne hundred and seventy-five patients (92 males, 83 postmenopausal females) with unresectable pancreatic cancer were studied. Serum sex steroids (total testosterone [TT], calculated free testosterone [cFT], oestradiol, sex hormone binding globulin), gonadotropins (follicle-stimulating hormone and luteinising hormone) and pro-inflammatory mediators (C-reactive protein [CRP], interleukin-6 [IL-6], soluble tumour necrosis factor receptor 75 [sTNFR75]) were measured, and nutritional assessment and opioid use recorded.ResultsSeventy-three percent of males were hypogonadal (by cFT definition). cFT correlated positively with BMI (r2 = 0.349; p < 0.001) and grip strength (r2 = 0.229; p = 0.034) and inversely with weight loss (r2 = −0.287; p = 0.007), CRP (r2 = −0.426; p < 0.001) and IL-6 (r2 = −0.303; p = 0.004). CRP (p = 0.007), opioid dosage (p = 0.009) and BMI (p = 0.005) were independent determinants of cFT on ANOVA. Hypogonadal males demonstrated worsened survival compared with eugonadal patients (TT: OR of death = 2.87; p < 0.001; cFT: OR = 2.26; p = 0.011). Furthermore, male opioid use was associated with decreased TT (p < 0.001) and cFT (p < 0.001) and worsened survival (OR = 1.96; p = 0.012). In contrast, 18% of postmenopausal females exhibited premenopausal (“hyperoestrogenic”) oestradiol levels. Oestradiol correlated positively with sTNFR75 (r2 = 0.299; p = 0.008). CRP (p < 0.001) was an independent determinant of oestradiol. Hyperoestrogenic females demonstrated worsened survival compared with eugonadal patients (OR = 2.43; p = 0.013).ConclusionsIn males with pancreatic cancer, systemic inflammation and opioid use are associated with hypogonadism. Male hypogonadism and female hyperoestrogenism are associated with shortened survival in advanced pancreatic cancer.
Journal of Cachexia, Sarcopenia and Muscle | 2015
David P.J. van Dijk; Marcel C. G. van de Poll; Alastair G.W. Moses; Tom Preston; Steven W.M. Olde Damink; Sander S. Rensen; Nicolaas E. P. Deutz; P.B. Soeters; James A. Ross; Kenneth Fearon; C.H.C. Dejong
Pancreatic cancer is often accompanied by cachexia, a syndrome of severe weight loss and muscle wasting. A suboptimal response to nutritional support may further aggravate cachexia, yet the influence of nutrition on protein kinetics in cachectic patients is poorly understood.
Oncology Reports | 2009
Alastair G.W. Moses; Jean P. Maingay; Kathryn Sangster; Kenneth Fearon; James A. Ross
Oncology Reports | 2005
Cornelis H.C. Dejong; Sylvia Busquets; Alastair G.W. Moses; Patrick Schrauwen; Jim A. Ross; Josep M. Argilés; Kenneth Fearon
Surgical Oncology Clinics of North America | 2001
Kenneth Fearon; Matthew D. Barber; Alastair G.W. Moses
British Journal of Surgery | 2009
Alastair G.W. Moses; Christine Slater; Matthew D. Barber; Tom Preston; K. C. H. Fearon
British Journal of Surgery | 2009
Alastair G.W. Moses; Christine Slater; Matthew D. Barber; Tom Preston; Kenneth Fearon
Archive | 2006
Michael J. Tisdale; A. Giacosa; A. Van Gossum; Jürgen M. Bauer; Matthew D. Barber; Neil K. Aaronson; M.F. von Meyenfeldt; Alastair G.W. Moses; R. van Geenen; A Roy