Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Oct 30;39(11):1799-1808.
doi: 10.1093/ndt/gfae059.

Sex differences in cancer outcomes across the range of eGFR

Affiliations

Sex differences in cancer outcomes across the range of eGFR

Richard Shemilt et al. Nephrol Dial Transplant. .

Erratum in

  • Correction.
    [No authors listed] [No authors listed] Nephrol Dial Transplant. 2025 May 30;40(6):1261. doi: 10.1093/ndt/gfae219. Nephrol Dial Transplant. 2025. PMID: 39436739 Free PMC article. No abstract available.

Abstract

Background: People with chronic kidney disease (CKD) have increased incidence and mortality of most cancer types. We hypothesized that the odds of presenting with advanced cancer may vary according to differences in estimated glomerular filtration rate (eGFR), that this could contribute to increased all-cause mortality and that sex differences may exist.

Methods: Data were from Secure Anonymised Information Linkage Databank, including people with de novo cancer diagnosis (2011-17) and two kidney function tests within 2 years prior to diagnosis to determine baseline eGFR (mL/min/1.73 m2). Logistic regression models determined the odds of presenting with advanced cancer by baseline eGFR. Cox proportional hazards models tested associations between baseline eGFRCr and all-cause mortality.

Results: eGFR <30 was associated with higher odds of presenting with advanced cancer of prostate, breast and female genital organs, but not other cancer sites. Compared with eGFR >75-90, eGFR <30 was associated with greater hazards of all-cause mortality in both sexes, but the association was stronger in females [female: hazard ratio (HR) 1.71, 95% confidence interval (CI) 1.56-1.88; male versus female comparison: HR 0.88, 95% CI 0.78-0.99].

Conclusions: Lower or higher eGFR was not associated with substantially higher odds of presenting with advanced cancer across most cancer sites, but was associated with reduced survival. A stronger association with all-cause mortality in females compared with males with eGFR <30 is concerning and warrants further scrutiny.

Keywords: cancer; chronic kidney disease; cohort studies; female; male.

PubMed Disclaimer

Conflict of interest statement

Outside the submitted work, J.S.L. has received personal lectureship honoraria from AstraZeneca, Pfizer and Bristol Myers Squibb. P.B.M. reports lecture honoraria from AstraZeneca, Pharmacomsos, Astellas, GSK and Boehringer Ingelheim outside the submitted work.

Figures

Graphical Abstract
Graphical Abstract
Figure 1:
Figure 1:
(A) Plot displaying OR (95% CI) of presentation with advanced cancer, adjusted for age, smoking status, deprivation status, number of comorbidities and cancer site. (B) Plot displaying HR (95% CI) of death after cancer diagnosis, adjusted for age, smoking status, deprivation status, number of comorbidities, cancer site and presenting cancer stage. Results are stratified by sex. Asterisk indicates presence of a significant interaction between sex and eGFR category. Reference eGFR category: 75–<90 mL/min/1.73 m2.
Figure 2:
Figure 2:
Plot displaying OR (95% CI) of presentation with advanced (stage 3 or 4) site-specific cancer. Models are adjusted for age, sex, smoking status, deprivation status and number of comorbidities. Results are stratified by sex and cancer site. Asterisk indicates presence of a significant interaction between sex and eGFR category.
Figure 3:
Figure 3:
Plot displaying HR (95% CI) of death (any cause) after site-specific cancer diagnosis. Models are adjusted for age, sex, smoking status, deprivation status, number of comorbidities and presenting cancer stage. Results are stratified by sex and cancer site. Asterisk indicates presence of a significant interaction between sex and eGFR category.

References

    1. Hill NR, Fatoba ST, Oke JLHet al. Global Prevalence of chronic kidney disease—a systematic review and meta-analysis. PLoS One 2016;11:e0158765. 10.1371/journal.pone.0158765 - DOI - PMC - PubMed
    1. GBD Chronic Kidney Disease Collaboration . Global, regional, and national burden of chronic kidney disease, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet 2020;395:709–33. 10.1016/S0140-6736(20)30045-3 - DOI - PMC - PubMed
    1. Ciorcan M, Chisavu L, Mihaescu Aet al. Chronic kidney disease in cancer patients, the analysis of a large oncology database from Eastern Europe. PLoS One 2022;17:e0265930. 10.1371/journal.pone.0265930 - DOI - PMC - PubMed
    1. Tu H, Wen CP, Tsai SPet al. Cancer risk associated with chronic diseases and disease markers: prospective cohort study. BMJ 2018;360:k134. 10.1136/bmj.k134 - DOI - PMC - PubMed
    1. De La Mata NL, Rosales B, MacLeod Get al. Sex differences in mortality among binational cohort of people with chronic kidney disease: population based data linkage study. BMJ 2021;375:e068247. 10.1136/BMJ-2021-068247 - DOI - PMC - PubMed