Association of Prediagnosis Obesity and Postdiagnosis Aspirin With Survival From Stage IV Colorectal Cancer.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
03 10 2022
Historique:
entrez: 14 10 2022
pubmed: 15 10 2022
medline: 19 10 2022
Statut: epublish

Résumé

The potential relationship between obesity and colorectal cancer (CRC) outcome is poorly understood in patients with late-stage disease. Increased body mass index may negate aspirin use for cancer prevention, but its role as a factor on the effectiveness of postdiagnosis aspirin use is unclear. To evaluate how prediagnosis obesity and postdiagnosis aspirin use may be associated with overall survival in patients with late-stage colorectal cancer. This cross-sectional study used self-reported data from patients with metastatic or treatment-refractory disease who consented to a clinical protocol at MD Anderson Cancer Center, a large US cancer treatment center. Patients were enrolled between 2010 and 2018 and followed up for mortality through July 2020. Analyses were conducted through March 2022. Body mass index in the decade prior to initial diagnosis and regular aspirin use at survey completion. Overall survival was measured from stage IV diagnosis until death or last follow-up. Cox proportional hazards models were constructed to estimate associations of prediagnosis obesity and postdiagnosis aspirin use with overall survival. Of 656 patients included in this analysis, 280 (42.7%) were women, 135 (20.6%) were diagnosed with CRC before age 45 years, 414 (63.1%) were diagnosed between ages 45 and 65 years, and 107 (16.3%) were diagnosed at 65 years or older; 105 patients (16.0%) were Black or Hispanic, and 501 (76.4%) were non-Hispanic White. Controlling for age, sex, race, stage at initial diagnosis, and weight change between prediagnosis and survey date, patients with obesity in the decade prior to CRC diagnosis had significantly higher likelihood of death (hazard ratio, 1.45; 95% CI, 1.11-1.91) compared with those with normal prediagnosis body mass index. Furthermore, only patients with normal prediagnosis body mass index experienced significant survival benefit with postdiagnosis aspirin use (hazard ratio, 0.59; 95% CI, 0.39-0.90). In this cross-sectional study, our findings suggest potentially differential tumor development in the long-term physiologic host environment of obesity. Confirmation and further evaluation are needed to determine whether prediagnosis body mass index may be used to estimate the benefit from postdiagnosis aspirin use.

Identifiants

pubmed: 36239938
pii: 2797320
doi: 10.1001/jamanetworkopen.2022.36357
pmc: PMC9568800
doi:

Substances chimiques

Aspirin R16CO5Y76E

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2236357

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States

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Auteurs

Jennifer S Davis (JS)

Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston.
Now with Department of Cancer Biology, University of Kansas Medical Center, Kansas City.

Janelle C Chavez (JC)

Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston.
Department of Cancer Prevention Research Training Program, The University of Texas MD Anderson Cancer Center, Houston.
Now with Stanford University School of Medicine, Stanford, California.

Melissa Kok (M)

Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston.
Department of Cancer Prevention Research Training Program, The University of Texas MD Anderson Cancer Center, Houston.
Now with Baylor College of Medicine, Houston, Texas.

Yazmin San Miguel (Y)

Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston.
Department of Cancer Prevention Research Training Program, The University of Texas MD Anderson Cancer Center, Houston.
Now with Abbott Laboratories, Chicago, Illinois.

Hwa Young Lee (HY)

Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston.
Department of Cancer Prevention Research Training Program, The University of Texas MD Anderson Cancer Center, Houston.

Henry Henderson (H)

Department of Cancer Prevention Research Training Program, The University of Texas MD Anderson Cancer Center, Houston.
Department of Cancer Systems Imaging, The University of Texas MD Anderson Cancer Center, Houston.
Now with Foundation Medicine, Atlanta, Georgia.

Michael J Overman (MJ)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Van Morris (V)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Bryan Kee (B)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

David Fogelman (D)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.
Now with Merck & Co, Philadelphia, Pennsylvania.

Shailesh M Advani (SM)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.
Now with Terasaki Institute of Biomedical Innovation, Los Angeles, California.

Benny Johnson (B)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Christine Parseghian (C)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

John Paul Shen (JP)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Arvind Dasari (A)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Kenna R Shaw (KR)

Department of Sheikh Khalifa Nahyan Ben Zayed Institute for Personalized Cancer Therapy, The University of Texas MD Anderson Cancer Center, Houston.

Eduardo Vilar (E)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.
Department of Clinical Cancer Prevention, The University of Texas MD Anderson Cancer Center, Houston.

Kanwal P Raghav (KP)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Imad Shureiqi (I)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.
Now with Department of Cancer Biology, University of Michigan Medical School, Ann Arbor.

Robert A Wolff (RA)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Funda Meric-Bernstam (F)

Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston.

Dipen Maru (D)

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston.

David G Menter (DG)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Scott Kopetz (S)

Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Shine Chang (S)

Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston.
Department of Cancer Prevention Research Training Program, The University of Texas MD Anderson Cancer Center, Houston.

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