Evidence map›Paper›PMID 36826816›Full record

ArticleJAMA network open2023

Association of Frequent Aspirin Use With Ovarian Cancer Risk According to Genetic Susceptibility.

Lauren M Hurwitz, Penelope M Webb, Susan J Jordan, Jennifer A Doherty, Holly R Harris, Marc T Goodman, Yurii B Shvetsov, Francesmary Modugno, Kirsten B Moysich, Joellen M Schildkraut and 11 more

Open access · goldAbstract read
In one paragraph

Article in JAMA network open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Global epidemiology of epithelial ovarian cancer.Nature reviews. Clinical oncology · 2024
    Review
  4. 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

21 authors at 18 institutions in 3 countries.

Lauren M HurwitzDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
Penelope M WebbPopulation Health Program, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
Susan J JordanSchool of Public Health, University of Queensland, Brisbane, Queensland, Australia.
Jennifer A DohertyDepartment of Population Health Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City.
Holly R HarrisProgram in Epidemiology, Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Marc T GoodmanSamuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California.
Yurii B ShvetsovCancer Epidemiology Program, University of Hawaii Cancer Center, Honolulu.
Francesmary ModugnoDivision of Gynecologic Oncology, Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Kirsten B MoysichDepartment of Cancer Prevention and Control, Roswell Park Comprehensive Cancer Center, Buffalo, New York.
Joellen M SchildkrautDepartment of Epidemiology, Emory University Rollins School of Public Health, Atlanta, Georgia.
Andrew BerchuckDivision of Gynecologic Oncology, Duke University Medical Center, Durham, North Carolina.
Hoda Anton-CulverDepartment of Epidemiology, University of California, Irvine.
Argyrios ZiogasDepartment of Epidemiology, University of California, Irvine.
Usha MenonMRC Clinical Trials Unit, Institute of Clinical Trials and Methodology, University College London, London, United Kingdom.
Susan J RamusSchool of Clinical Medicine, Faculty of Medicine and Health, University of New South Wales, Sydney, Australia.
Anna H WuKeck School of Medicine, Department of Population and Public Health Sciences, University of Southern California, Los Angeles.
Celeste Leigh PearceDepartment of Epidemiology, University of Michigan School of Public Health, Ann Arbor.
Nicolas WentzensenDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
Shelley S TworogerDepartment of Cancer Epidemiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
Paul D P PharoahDepartment of Public Health and Primary Care, Centre for Cancer Genetic Epidemiology, University of Cambridge, Cambridge, United Kingdom.
Britton TrabertDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland.
National Cancer Institute · USUniversity of California, Irvine · USCancer Research UK Cambridge Center · GBCedars-Sinai Medical Center · USDuke Medical Center · USEmory University · USMoffitt Cancer Center · USMRC Clinical Trials Unit at UCL · GBQIMR Berghofer Medical Research Institute · AURoswell Park Comprehensive Cancer Center · USThe University of Queensland · AUUniversity of Hawaii Cancer CenterUniversity of Michigan · USUniversity of Southern California · USUniversity of Utah · USUniversity of Washington · USUNSW Sydney · AUUPMC Hillman Cancer Center · US

Funding

University of Hawaii Cancer Center CCSGP30CA071789 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI GERTRAUD MASKARINEC · 1996 to 2026
$56.2M
Steroid Hormone Genes and Ovarian Cancer RiskR01CA112523 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ROSSING, MARY ANNE · 2006 to 2010
$3.3M
The Progesterone Receptor Gene and Ovarian Cancer RiskR03CA113148 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI PEARCE, CELESTE LEIGH · 2004 to 2005
$163k
Ovarian Cancer and Gonadotropin SignalingR03CA115195 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI PEARCE, CELESTE LEIGH · 2006 to 2007
$161k
Cancer Research UKMedical Research Council MC_UU_00004/01NCI NIH HHS R01 CA112523NCI NIH HHS R03 CA113148NCI NIH HHS R03 CA115195
6 · The paper itself

Abstract

Importance: Frequent aspirin use is associated with reduced ovarian cancer risk, but it is unknown whether genetic factors modify this association. Understanding effect modifiers is important given that any use of aspirin for ovarian cancer chemoprevention will likely need to focus on specific higher-risk subgroups. Objective: To evaluate whether the association between frequent aspirin use and ovarian cancer is modified by a polygenic score (PGS) for nonmucinous ovarian cancer. Design, Setting, and Participants: We pooled individual-level data from 8 population-based case-control studies from the Ovarian Cancer Association Consortium conducted in the US, UK, and Australia between 1995 and 2009. We included case patients and control participants with both genetic data and data on frequent aspirin use. Case patients with mucinous ovarian cancer were excluded. Data were analyzed between November 1, 2021, and July 31, 2022. Exposures: Frequent aspirin use, defined as daily or almost daily use for 6 months or longer. Main Outcomes and Measures: The main outcome was nonmucinous epithelial ovarian cancer. We used logistic regression to estimate odds ratios (ORs) and 95% CIs and likelihood ratio tests to investigate effect modification by the PGS. Results: There were 4476 case patients with nonmucinous ovarian cancer and 6659 control participants included in this analysis. At study enrollment, the median (IQR) age was 58 (50-66) years for case patients and 57 (49-65) years for control participants. Case patients and control participants self-reported that they were Black (122 [3%] vs 218 [3%]), White (3995 [89%] vs 5851 [88%]), or of other race and ethnicity (348 [8%] vs 580 [9%]; race and ethnicity were unknown for 11 [0%] vs 10 [0%]). There were 575 case patients (13%) and 1030 control participants (15%) who reported frequent aspirin use. The 13% reduction in ovarian cancer risk associated with frequent aspirin use (OR, 0.87 [95% CI, 0.76-0.99]) was not modified by the PGS. Consistent ORs were observed among individuals with a PGS less than (0.85 [0.70-1.02]) and greater than (0.86 [0.74-1.01]) the median. Results were similar by histotype. Conclusions and Relevance: The findings of this study suggest that genetic susceptibility to ovarian cancer based on currently identified common genetic variants does not appear to modify the protective association between frequent aspirin use and ovarian cancer risk. Future work should continue to explore the role of aspirin use for ovarian cancer prevention among individuals who are at higher risk for ovarian cancer.

Indexed as

AspirinOvarian NeoplasmsAgedCarcinoma, Ovarian EpithelialFemaleGenetic Predisposition to DiseaseHumansLogistic ModelsMiddle AgedAspirin

Identifiers

PMID36826816
PMCPMC9958519
OpenAlexW4321748698

What Socratic holds

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LicenceCC BY
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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.