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Cancer Risk Following HLA-Incompatible Living Donor Kidney Transplantation.
Motter, Jennifer D; Massie, Allan B; Garonzik-Wang, Jacqueline M; Pfeiffer, Ruth M; Yu, Kelly J; Segev, Dorry L; Engels, Eric A.
Affiliation
  • Motter JD; Department of Surgery, New York University Grossman School of Medicine, New York, NY.
  • Massie AB; Department of Surgery, New York University Grossman School of Medicine, New York, NY.
  • Garonzik-Wang JM; Department of Population Health, New York University Grossman School of Medicine, New York, NY.
  • Pfeiffer RM; Department of Surgery, University of Wisconsin-Madison, Madison, WI.
  • Yu KJ; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD.
  • Segev DL; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD.
  • Engels EA; Department of Surgery, New York University Grossman School of Medicine, New York, NY.
Transplant Direct ; 9(8): e1505, 2023 Aug.
Article in En | MEDLINE | ID: mdl-37492080
ABSTRACT
Incompatible living donor kidney transplant recipients (ILDKTr) require desensitization to facilitate transplantation, and this substantial upfront immunosuppression may result in serious complications, including cancer.

Methods:

To characterize cancer risk in ILDKTr, we evaluated 858 ILDKTr and 12 239 compatible living donor kidney transplant recipients (CLDKTr) from a multicenter cohort with linkage to the US transplant registry and 33 cancer registries (1997-2016). Cancer incidence was compared using weighted Cox regression.

Results:

Among ILDKTr, the median follow-up time was 6.7 y (maximum 16.1 y) for invasive cancers (ascertained via cancer registry linkage) and 5.0 y (maximum 16.1 y) for basal and squamous cell carcinomas (ascertained via the transplant registry and censored for transplant center loss to follow-up). Invasive cancers occurred in 53 ILDKTr (6.2%) and 811 CLDKTr (6.6%; weighted hazard ratio [wHR] 1.01; 95% confidence interval [CI], 0.76-1.35). Basal and squamous cell carcinomas occurred in 41 ILDKTr (4.8%) and 737 CLDKTr (6.0%) (wHR 0.99; 95% CI, 0.69-1.40). Cancer risk did not vary according to donor-specific antibody strength, and in an exploratory analysis, was similar between CLDKTr and ILDKTr for most cancer types and according to cancer stage, except ILDKTr had a suggestively increased risk of colorectal cancer (wHR 3.27; 95% CI, 1.23-8.71); however, this elevation was not significant after correction for multiple comparisons.

Conclusions:

These findings indicate that the risk of cancer is not increased for ILDKTr compared with CLDKTr. The possible elevation in colorectal cancer risk is unexplained and might suggest a need for tailored screening or prevention.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Risk_factors_studies Language: En Journal: Transplant Direct Year: 2023 Document type: Article Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Risk_factors_studies Language: En Journal: Transplant Direct Year: 2023 Document type: Article Publication country: EEUU / ESTADOS UNIDOS / ESTADOS UNIDOS DA AMERICA / EUA / UNITED STATES / UNITED STATES OF AMERICA / US / USA