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Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: An analysis from the CAPP2 randomised controlled trial

  • John C. Mathers*
  • , Mohammad Movahedi
  • , Finlay Macrae
  • , Jukka Pekka Mecklin
  • , Gabriela Moeslein
  • , Sylviane Olschwang
  • , Diana Eccles
  • , Gareth Evans
  • , Eamonn R. Maher
  • , Lucio Bertario
  • , Marie Luise Bisgaard
  • , Malcolm Dunlop
  • , Judy W. C. Ho
  • , Shirley Hodgson
  • , Annika Lindblom
  • , Jan Lubinski
  • , Patrick J. Morrison
  • , Victoria Murday
  • , Raj Ramesar
  • , Lucy Side
  • Rodney J. Scott, Huw J.W. Thomas, Hans Vasen, Anne Marie Gerdes, Gail Barker, Gillian Crawford, Faye Elliott, Kirsi Pylvanainen, Juul Wijnen, Riccardo Fodde, Henry Lynch, D. Timothy Bishop, John Burn
*Corresponding author for this work
  • Newcastle University
  • University of Leeds, School of Medicine
  • Beheshti University of Medical Sciences
  • Royal Melbourne Hospital
  • Jyväskylä Central Hospital
  • HELIOS St Josefs Hospital
  • Institut Paoli Calmettes
  • University of Southampton, Faculty of Medicine
  • St Mary's Hospital, Stannington
  • Fondazione IRCCS Istituto Nazionale Dei Tumori
  • Københavns Universitet
  • Western General Hospital
  • Queen Mary Hospital Hong Kong
  • St George's Hospital, London
  • Karolinska Institutet
  • International Hereditary Cancer Centre
  • Queens University Belfast
  • Medical Genetics
  • University of Cape Town
  • Churchill Hospital
  • Hunter Area Pathology Service
  • Imperial College
  • Leiden University Medical Centre
  • Clinical Genetics, Rigshospital
  • Erasmus University Medical Center
  • Creighton University Medical Center

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Observational studies report that higher intake of dietary fibre (a heterogeneous mix including non-starch polysaccharides and resistant starches) is associated with reduced risk of colorectal cancer, but no randomised trials with prevention of colorectal cancer as a primary endpoint have been done. We assessed the effect of resistant starch on the incidence of colorectal cancer. Methods: In the CAPP2 study, individuals with Lynch syndrome were randomly assigned in a two-by-two factorial design to receive 600 mg aspirin or aspirin placebo or 30 g resistant starch or starch placebo, for up to 4 years. Randomisation was done with a block size of 16. Post-intervention, patients entered into double-blind follow-up; participants and investigators were masked to treatment allocation. The primary endpoint for this analysis was development of colorectal cancer in participants randomly assigned to resistant starch or resistant-starch placebo with both intention-to-treat and per-protocol analyses. This study is registered, ISRCTN 59521990. Findings: 463 patients were randomly assigned to receive resistant starch and 455 to receive resistant-starch placebo. At a median follow-up 52·7 months (IQR 28·9-78·4), 53 participants developed 61 primary colorectal cancers (27 of 463 participants randomly assigned to resistant starch, 26 of 455 participants assigned to resistant-starch placebo). Intention-to-treat analysis of time to first colorectal cancer showed a hazard ratio (HR) of 1·40 (95% CI 0·78-2·56; p=0·26) and Poisson regression accounting for multiple primary events gave an incidence rate ratio (IRR) of 1·15 (95% CI 0·66-2·00; p=0·61). For those completing 2 years of intervention, per-protocol analysis yielded a HR of 1·09 (0·55-2·19, p=0·80) and an IRR of 0·98 (0·51-1·88, p=0·95). No information on adverse events was gathered during post-intervention follow-up. Interpretation: Resistant starch had no detectable effect on cancer development in carriers of hereditary colorectal cancer. Dietary supplementation with resistant starch does not emulate the apparently protective effect of diets rich in dietary fibre against colorectal cancer. Funding: European Union, Cancer Research UK, Bayer Corporation, National Starch and Chemical Co, UK Medical Research Council, Newcastle Hospitals Trustees, Cancer Council of Victoria Australia, THRIPP South Africa, The Finnish Cancer Foundation, SIAK Switzerland, and Bayer Pharma.

Original languageEnglish
Pages (from-to)1242-1249
Number of pages8
JournalThe Lancet Oncology
Volume13
Issue number12
Early online date6 Nov 2012
DOIs
Publication statusPublished - Dec 2012

Funding

The CAPP2 study is an academic collaboration. Funding was provided initially by a European Union award supplemented by programme funding in Newcastle and Leeds from Cancer Research UK (C588/A10589). Following completion of design and choice of interventions, Bayer Corporation and National Starch and Chemical Co were approached for support. Both organisations provided free intervention (active agent and matched placebo) including the cost of packaging and made donations to Newcastle University to help cover the cost of administration and distribution of intervention agents.

FundersFunder number
Medical Research CouncilMC_PC_U127527198, G0100496, MC_U127527198
Cancer Research UKC588/A10589
European Commission

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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