Evidence map›Paper›PMID 40515653›Full record

Trial reportJournal of the National Cancer Institute2025

Association of non-steroidal anti-inflammatory medications and aspirin with colorectal cancer incidence in older adults.

Farzana Y Zaman, Suzanne G Orchard, Galina Polekhina, Peter Gibbs, Wendy B Bernstein, Finlay Macrae, Jeanne Tie, Jeremy Millar, Lucy Gately, Luz María Rodríguez and 10 more

Abstract readObservational StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of the National Cancer Institute, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Farzana Y ZamanDepartment of Medical Oncology, Alfred Health, Melbourne, VIC, Australia.ORCID 0000-0002-2095-0850
Suzanne G OrchardSchool of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.ORCID 0000-0003-0211-3183
Galina PolekhinaSchool of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.ORCID 0000-0001-9535-9291
Peter GibbsPersonalised Oncology Division, Walter and Eliza Hall Institute for Medical Research, Melbourne, VIC, Australia.ORCID 0000-0003-1423-4484
Wendy B BernsteinDepartment of Medical Oncology, Walter Reed National Military Medical Center, Bethesda, MD, United States.
Finlay MacraeDepartment of Colorectal Medicine and Genetics, The Royal Melbourne Hospital, Melbourne, VIC, Australia.ORCID 0000-0003-4035-9678
Jeanne TiePersonalised Oncology Division, Walter and Eliza Hall Institute for Medical Research, Melbourne, VIC, Australia.ORCID 0000-0001-9244-2057
Jeremy MillarSchool of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.ORCID 0000-0001-8202-8602
Lucy GatelyDepartment of Medical Oncology, Alfred Health, Melbourne, VIC, Australia.
Luz María RodríguezDivision of Cancer Prevention, National Cancer Institute, Bethesda, MD, United States.
Gijsberta J van LondenDivision of Cancer Prevention, National Cancer Institute, Bethesda, MD, United States.ORCID 0000-0001-6047-6172
Victoria MarSchool of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.ORCID 0000-0001-9423-3435
Emma HiscuttSchool of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.ORCID 0000-0002-3914-1084
Nikki AdlerSchool of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.
Aaron KentDepartment of Radiation Oncology, Alfred Health, Melbourne, VIC, Australia.ORCID 0009-0003-5732-281X
Wee Loon OngSchool of Public Health and Preventive Medicine, Monash University, Melbourne, VIC, Australia.ORCID 0000-0001-6657-7193
Andrew HaydonDepartment of Medical Oncology, Alfred Health, Melbourne, VIC, Australia.ORCID 0000-0002-4631-5855
Erica WarnerClinical and Translational Epidemiology Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.ORCID 0000-0002-2671-0313
Andrew T ChanClinical and Translational Epidemiology Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.ORCID 0000-0001-7284-6767
John ZalcbergDepartment of Medical Oncology, Alfred Health, Melbourne, VIC, Australia.ORCID 0000-0002-6624-0782

Funding

ASPirin in Reducing Events in the ElderlyU01AG029824 · NIA · HENNEPIN HEALTHCARE RESEARCH INSTITUTE · PI MCNEIL, JOHN JAMES, MURRAY, ANNE M · 2009 to 2018
$64.6M
Main Administrative CoreU19AG062682 · NIA · HENNEPIN HEALTHCARE RESEARCH INSTITUTE · PI CHAN, ANDREW T, MCNEIL, JOHN JAMES · 2019 to 2023
$42.9M
American Cancer Society Research Professor R35 CA253135National Health and Medical Research Council of Australia, and by Monash University and the Victorian Cancer AgencyNCI NIH HHSNIA NIH HHS U01 AG029824NIA NIH HHS U01AG029824NIA NIH HHS U19 AG062682NIA NIH HHS U19AG062682NIH HHS 1127060NIH HHS 334047
6 · The paper itself

Abstract

backgroundThe relationship between aspirin, and/or other non-steroidal anti-inflammatory drugs (NSAIDs), and colorectal cancer (CRC) risk in older adults is uncertain. This study investigated the association between non-aspirin NSAIDs (NA-NSAIDs) use, alone or combined with aspirin, on CRC incidence in older adults.

methodsThis is a post hoc analysis of ASPirin in Reducing Events in the Elderly (ASPREE) randomized controlled trial data and its observational continuation, ASPREE-XT (median follow-up, 8.4 years [IQR: 7.2-9.6]). NA-NSAID exposure was ascertained by self-report and medical record review at baseline, for all ASPREE participants, and for Australian participants, via linkage to the Pharmaceutical Benefits Scheme (PBS). CRC was an adjudicated secondary endpoint of ASPREE. We investigated the association between NA-NSAID use alone, and in combination with randomized aspirin use, on the incidence of CRC in time-to-event analyses.

resultsOf 19 114 ASPREE participants, 2713 (14%) reported NA-NSAID use at baseline. NA-NSAID use was associated with a reduced incidence of CRC (HRNA-NSAID use: Yes vs No = 0.74; 95% CI = 0.56 to 0.98). This association between NA-NSAIDs and CRC was not modified by aspirin (P-value for interaction term of 0.81). When assessing NA-NSAID use over 2 years post-randomization in Australian participants who consented to the use of PBS data (n = 13 725), a similar reduction in CRC risk was observed (HRHigh NA-NSAID use vs None = 0.52, 95% CI = 0.32 to 0.83).

conclusionsNA-NSAID use in Australian and American adults over the age of 70 years was associated with a reduced CRC incidence, which increased with increasing exposure. Aspirin did not modify the effect of NA-NSAIDs on CRC incidence.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalAspirinColorectal NeoplasmsAgedAged, 80 and overAustraliaFemaleHumansIncidenceLongitudinal StudiesMaleRisk FactorsAnti-Inflammatory Agents, Non-SteroidalAspirin

Identifiers

PMID40515653
PMCPMC12415954

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.