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Sex differences in cancer outcomes across the range of eGFR.
Shemilt, Richard; Sullivan, Michael K; Hanlon, Peter; Jani, Bhautesh; De La Mata, Nicole; Rosales, Brenda; Elyan, Benjamin M P; Hedley, James A; Cutting, Rachel B; Wyld, Melanie; McAllister, David A; Webster, Angela C; Mark, Patrick B; Lees, Jennifer S.
Affiliation
  • Shemilt R; NHS Greater Glasgow and Clyde, UK.
  • Sullivan MK; School of Medicine, Dentistry and Nursing, University of Glasgow, UK.
  • Hanlon P; NHS Greater Glasgow and Clyde, UK.
  • Jani B; School of Cardiovascular and Metabolic Health, University of Glasgow, UK.
  • De La Mata N; School of Health and Wellbeing, University of Glasgow, UK.
  • Rosales B; School of Health and Wellbeing, University of Glasgow, UK.
  • Elyan BMP; Sydney School of Public Health, University of Sydney, Australia.
  • Hedley JA; Sydney School of Public Health, University of Sydney, Australia.
  • Cutting RB; NHS Greater Glasgow and Clyde, UK.
  • Wyld M; School of Cardiovascular and Metabolic Health, University of Glasgow, UK.
  • McAllister DA; Sydney School of Public Health, University of Sydney, Australia.
  • Webster AC; Sydney School of Public Health, University of Sydney, Australia.
  • Mark PB; Sydney School of Public Health, University of Sydney, Australia.
  • Lees JS; School of Health and Wellbeing, University of Glasgow, UK.
Article in En | MEDLINE | ID: mdl-38460949
ABSTRACT
BACKGROUND AND

HYPOTHESIS:

People with chronic kidney disease (CKD) have increased incidence and mortality from most cancer types. We hypothesised that odds of presenting with advanced cancer may vary according to differences in 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 (2011-2017) and two kidney function tests within two years prior to diagnosis to determine baseline eGFR (mL/min/1.73m2). Logistic regression models determined 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 to 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 HR 1.71, 95%CI 1.56-1.88; male versus female comparison HR 0.88, 95%CI 0.78-0.90).

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 assocation with all-cause mortality in females compared to males with eGFR < 30 is concerning and warrants further scrutiny.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Nephrol Dial Transplant Journal subject: NEFROLOGIA / TRANSPLANTE Year: 2024 Type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Nephrol Dial Transplant Journal subject: NEFROLOGIA / TRANSPLANTE Year: 2024 Type: Article Affiliation country: United kingdom