Evidence map›Paper›PMID 30252883›Full record

SynthesisPloS one2018

Systematic review update of observational studies further supports aspirin role in cancer treatment: Time to share evidence and decision-making with patients?

Peter C Elwood, Janet E Pickering, Gareth Morgan, Julieta Galante, Alison L Weightman, Delyth Morris, Marcus Longley, Malcolm Mason, Richard Adams, Sunil Dolwani and 2 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
–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

19 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Using aspirin to prevent and treat cancer.Inflammopharmacology · 2024
    Review
  6. Article
  7. Acetylsalicylic Acid-Primus Inter Pares in Pharmacology.Molecules (Basel, Switzerland) · 2022
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Aspirin as a Potential Geroprotector: Experimental Data and Clinical Evidence.Advances in experimental medicine and biology · 2021
    Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Review
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

12 authors.

Peter C ElwoodCochrane Institute of Primary Care and Public Health, Cardiff University, Cardiff, United Kingdom.ORCID 0000-0003-4352-1570
Janet E PickeringCochrane Institute of Primary Care and Public Health, Cardiff University, Cardiff, United Kingdom.
Gareth MorganHywel Dda University Health Board, Llanelli, United Kingdom.
Julieta GalanteDepartment of Psychiatry, University of Cambridge, Cambridge, United Kingdom.
Alison L WeightmanSpecialist Unit for Review Evidence, Cardiff University, Cardiff, United Kingdom.
Delyth MorrisSpecialist Unit for Review Evidence, Cardiff University, Cardiff, United Kingdom.
Marcus LongleyHealth Policy, University of South Wales, Pontypridd, United Kingdom.
Malcolm MasonDivision of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, United Kingdom.
Richard AdamsInstitute of Cancer & Genetics Cardiff University, Cardiff, United Kingdom.
Sunil DolwaniDivision of Population Medicine, School of Medicine, Cardiff University, Cardiff, United Kingdom.
John Chia W KDivision of Medical Oncology, National Cancer Centre, Singapore, Singapore.
Angel LanasUniversity of Zaragoza, IIS Aragón, CIBERehd, Zaragoza, Spain.

Funding

Cancer Research UK 25350
6 · The paper itself

Abstract

backgroundEvidence is growing that low-dose aspirin used as an adjuvant treatment of cancer is associated with an increased survival and a reduction in metastatic spread. We therefore extended up to August 2017 an earlier systematic search and meta-analyses of published studies of low-dose aspirin taken by patients with a diagnosis of cancer.

methodsSearches were completed in Medline and Embase to August 2017 using a pre-defined search strategy to identify reports of relevant studies. References in all the selected papers were scanned. Two reviewers independently applied pre-determined eligibility criteria and extracted data on cause-specific cancer deaths, overall mortality and the occurrence of metastatic spread. Meta-analyses were then conducted for different cancers and heterogeneity and publication bias assessed. Sensitivity analyses and attempts to reduce heterogeneity were conducted.

resultsAnalyses of 29 studies reported since an earlier review up to April 2015 are presented in this report, and these are then pooled with the 42 studies in our earlier publication. Overall meta-analyses of the 71 studies are presented, based on a total of over 120 thousand patients taking aspirin. Ten of the studies also give evidence on the incidence of metastatic cancer spread. There are now twenty-nine observational studies describing colorectal cancer (CRC) and post-diagnostic aspirin. Pooling the estimates of reduction by aspirin which are reported as hazard ratios (HR), gives an overall HR for aspirin and CRC mortality 0.72 (95% CI 0.64-0.80). Fourteen observational studies have reported on aspirin and breast cancer mortality and pooling those that report the association with aspirin as a hazard ratio gives HR 0.69 (0.53-0.90). Sixteen studies report on aspirin and prostate cancer mortality and a pooled estimate yields an HR of 0.87 (95% CI 0.73-1.05). Data from 12 reports relating to other cancers are also listed. Ten studies give evidence of a reduction in metastatic spread; four give a pooled HR 0.31 (95% CI 0.18, 0.54) and five studies which reported odds ratio of metastatic spread give OR 0.79 (0.66 to 0.95).

conclusionBeing almost entirely from observational studies, the evidence of benefit from aspirin is limited. There is heterogeneity between studies and the results are subject to important biases, only some of which can be identified. Nevertheless, the evidence would seem to merit wide discussion regarding whether or not it is adequate to justify the recommendation of low-dose therapeutic aspirin, and if it is, for which cancers?

Indexed as

Adjuvants, PharmaceuticAntineoplastic AgentsAspirinDecision MakingEvidence-Based MedicineHumansNeoplasmsObservational Studies as TopicTreatment OutcomeAdjuvants, PharmaceuticAntineoplastic AgentsAspirin

Identifiers

PMID30252883
PMCPMC6155524

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.