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Cancer Prevention with Resistant Starch in Lynch Syndrome Patients in the CAPP2-Randomized Placebo Controlled Trial: Planned 10-Year Follow-up.
Mathers, John C; Elliott, Faye; Macrae, Finlay; Mecklin, Jukka-Pekka; Möslein, Gabriela; McRonald, Fiona E; Bertario, Lucio; Evans, D Gareth; Gerdes, Anne-Marie; Ho, Judy W C; Lindblom, Annika; Morrison, Patrick J; Rashbass, Jem; Ramesar, Raj S; Seppälä, Toni T; Thomas, Huw J W; Sheth, Harsh J; Pylvänäinen, Kirsi; Reed, Lynn; Borthwick, Gillian M; Bishop, D Timothy; Burn, John.
Afiliação
  • Mathers JC; Human Nutrition Research Centre, Population Heath Sciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Elliott F; Division of Haematology and Immunology, Leeds Institute of Medical Research at St James's, University of Leeds, Leeds, United Kingdom.
  • Macrae F; Division Colorectal Medicine and Genetics, Royal Melbourne Hospital, Melbourne, Australia.
  • Mecklin JP; Department of Education & Research, Jyväskylä Central Hospital, Jyväskylä, Finland.
  • Möslein G; Sport & Health Sciences, University of Jyväskylä, Jyväskylä, Finland.
  • McRonald FE; Center for Hereditary Tumors, Ev. BEHESDA Khs. zu Duisburg GmbH, Germany.
  • Bertario L; National Cancer Registration and Analysis Service, Public Health England.
  • Evans DG; Instituto Nazionale per lo Studio e, la Cura dei Tumori, Milan, Italy.
  • Gerdes AM; Division of Evolution and Genomic Medicine, University of Manchester, St Mary's Hospital, Manchester Universities Foundation Trust, Manchester, United Kingdom.
  • Ho JWC; Medical Genetics Clinic, ICMM; Clinical Genetics, Rigshospital, Copenhagen, Denmark.
  • Lindblom A; Hereditary GI Cancer Registry, Department of Surgery, Queen Mary Hospital, Hong Kong, China.
  • Morrison PJ; Department of Molecular Medicine & Surgery, Karolinska Institutet, Stockholm, Sweden.
  • Rashbass J; The Department of Medical Genetics, Queens University Belfast, Belfast City Hospital HSC Trust, Belfast, United Kingdom.
  • Ramesar RS; National Cancer Registration and Analysis Service, Public Health England.
  • Seppälä TT; MRC Genomic and Precision Medicine Research Unit, Division of Human Genetics, Institute for Infectious Diseases and Molecular Medicine, University of Cape Town, Observatory, South Africa.
  • Thomas HJW; Department of Gastrointestinal Surgery, Helsinki University Hospital, Helsinki, Finland.
  • Sheth HJ; St Mark's Hospital, London & Faculty of Medicine, Imperial College London, London, United Kingdom.
  • Pylvänäinen K; Newcastle University Translational and Clinical Research Institute, Newcastle upon Tyne, United Kingdom.
  • Reed L; Department of Education & Research, Jyväskylä Central Hospital, Jyväskylä, Finland.
  • Borthwick GM; Newcastle University Translational and Clinical Research Institute, Newcastle upon Tyne, United Kingdom.
  • Bishop DT; Newcastle University Translational and Clinical Research Institute, Newcastle upon Tyne, United Kingdom.
  • Burn J; Division of Haematology and Immunology, Leeds Institute of Medical Research at St James's, University of Leeds, Leeds, United Kingdom.
Cancer Prev Res (Phila) ; 15(9): 623-634, 2022 09 01.
Article em En | MEDLINE | ID: mdl-35878732
ABSTRACT: The CAPP2 trial investigated the long-term effects of aspirin and resistant starch on cancer incidence in patients with Lynch syndrome (LS). Participants with LS were randomized double-blind to 30 g resistant starch (RS) daily or placebo for up to 4 years. We present long-term cancer outcomes based on the planned 10-year follow-up from recruitment, supplemented by National Cancer Registry data to 20 years in England, Wales, and Finland. Overall, 463 participants received RS and 455 participants received placebo. After up to 20 years follow-up, there was no difference in colorectal cancer incidence (n = 52 diagnosed with colorectal cancer among those randomized to RS against n = 53 on placebo) but fewer participants had non-colorectal LS cancers in those randomized to RS (n = 27) compared with placebo (n = 48); intention-to-treat (ITT) analysis [HR, 0.54; 95% confidence interval (CI), 0.33-0.86; P = 0.010]. In ITT analysis, allowing for multiple primary cancer diagnoses among participants by calculating incidence rate ratios (IRR) confirmed the protective effect of RS against non-colorectal cancer LS cancers (IRR, 0.52; 95% CI, 0.32-0.84; P = 0.0075). These effects are particularly pronounced for cancers of the upper GI tract; 5 diagnoses in those on RS versus 21 diagnoses on placebo. The reduction in non-colorectal cancer LS cancers was detectable in the first 10 years and continued in the next decade. For colorectal cancer, ITT analysis showed no effect of RS on colorectal cancer risk (HR, 0.92; 95% CI, 0.62-1.34; P = 0.63). There was no interaction between aspirin and RS treatments. In conclusion, 30 g daily RS appears to have a substantial protective effect against non-colorectal cancer cancers for patients with LS. PREVENTION RELEVANCE: Regular bowel screening and aspirin reduce colorectal cancer among patients with LS but extracolonic cancers are difficult to detect and manage. This study suggests that RS reduces morbidity associated with extracolonic cancers. See related Spotlight, p. 557.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose Tipo de estudo: Clinical_trials / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose Tipo de estudo: Clinical_trials / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article