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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

Cancer prevention with resistant starch in lynch syndrome patients in the CAPP2-randomized placebo controlled trial: Planned 10-year follow-up
Cancer prevention with resistant starch in lynch syndrome patients in the CAPP2-randomized placebo controlled trial: Planned 10-year follow-up
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.
1940-6207
623-634
Mathers, John C.
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Elliott, Faye
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Macrae, Finlay
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Mecklin, Jukka-pekka
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Möslein, Gabriela
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Mcronald, Fiona E.
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Bertario, Lucio
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Evans, D. Gareth
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Gerdes, Anne-marie
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Ho, Judy W.c.
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Lindblom, Annika
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Morrison, Patrick J.
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Rashbass, Jem
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Ramesar, Raj S.
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Seppälä, Toni T.
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Thomas, Huw J.w.
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Sheth, Harsh J.
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Pylvänäinen, Kirsi
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Reed, Lynn
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Borthwick, Gillian M.
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Bishop, D. Timothy
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Burn, John
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Eccles, Diana
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Side, Lucy E.
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CAPP2 Investigators
Mathers, John C.
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Elliott, Faye
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Macrae, Finlay
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Mecklin, Jukka-pekka
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Möslein, Gabriela
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Mcronald, Fiona E.
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Bertario, Lucio
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Evans, D. Gareth
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Gerdes, Anne-marie
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Ho, Judy W.c.
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Lindblom, Annika
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Morrison, Patrick J.
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Rashbass, Jem
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Ramesar, Raj S.
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Seppälä, Toni T.
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Thomas, Huw J.w.
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Sheth, Harsh J.
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Pylvänäinen, Kirsi
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Reed, Lynn
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Borthwick, Gillian M.
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Bishop, D. Timothy
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Burn, John
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Eccles, Diana
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Side, Lucy E.
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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 and Burn, John , CAPP2 Investigators (2022) Cancer prevention with resistant starch in lynch syndrome patients in the CAPP2-randomized placebo controlled trial: Planned 10-year follow-up. Cancer Prevention Research, 15 (9), 623-634. (doi:10.1158/1940-6207.CAPR-22-0044).

Record type: Article

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.

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Accepted/In Press date: 1 July 2022
e-pub ahead of print date: 25 July 2022
Published date: 1 September 2022
Additional Information: ©2022 The Authors; Published by the American Association for Cancer Research.

Identifiers

Local EPrints ID: 471647
URI: http://eprints.soton.ac.uk/id/eprint/471647
ISSN: 1940-6207
PURE UUID: 1b71676b-2a3a-4c01-9943-a0b8d4bac94b
ORCID for Diana Eccles: ORCID iD orcid.org/0000-0002-9935-3169

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Date deposited: 15 Nov 2022 17:58
Last modified: 17 Mar 2024 02:36

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Contributors

Author: John C. Mathers
Author: Faye Elliott
Author: Finlay Macrae
Author: Jukka-pekka Mecklin
Author: Gabriela Möslein
Author: Fiona E. Mcronald
Author: Lucio Bertario
Author: D. Gareth Evans
Author: Anne-marie Gerdes
Author: Judy W.c. Ho
Author: Annika Lindblom
Author: Patrick J. Morrison
Author: Jem Rashbass
Author: Raj S. Ramesar
Author: Toni T. Seppälä
Author: Huw J.w. Thomas
Author: Harsh J. Sheth
Author: Kirsi Pylvänäinen
Author: Lynn Reed
Author: Gillian M. Borthwick
Author: D. Timothy Bishop
Author: John Burn
Author: Diana Eccles ORCID iD
Author: Lucy E. Side
Corporate Author: CAPP2 Investigators

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