Malignancy With Immunosuppression After Renal Transplantation: A Competing Risk Analysis.


Journal

Transplantation proceedings
ISSN: 1873-2623
Titre abrégé: Transplant Proc
Pays: United States
ID NLM: 0243532

Informations de publication

Date de publication:
Historique:
received: 20 11 2019
revised: 20 01 2020
accepted: 09 02 2020
pubmed: 18 4 2020
medline: 1 12 2020
entrez: 18 4 2020
Statut: ppublish

Résumé

This study analyzed clinical characteristics of renal transplant recipients who developed malignancy with immunosuppression after transplantation by applying a competing risk analysis to reduce the effects of competing events. All patients who underwent renal transplantation at our institution from 1973 to 2017 were included in this analysis. All data were collected from patient medical records and retrospectively analyzed. The cumulative incidence of malignancy before allograft loss and its risk factors were calculated by a competing risk analysis, the Gray test, and the Fine-Gray proportional hazard model. Of the 596 recipients, 78 developed malignancies. The mean age at transplantation was 38.5 ± 13.1 years. The median time from transplantation to the initial malignancy was 147.0 (5.2-407.3) months. The most common initial malignancy was skin cancer (21.8%), followed by posttransplant lymphoproliferative disease (14.1%). The cumulative incidence of malignancy at 20 years was 16.2% according to a competing risk analysis, whereas the conventional Kaplan-Meier method estimated the cumulative incidence at 20 years to be 25.6%. Increasing age at transplantation was significantly associated with the incidence of malignancy (P = .0091). Overall 10-year survival rates of recipients with and without malignancy were 81.7% and 88.5%, respectively (P < .001). Results of time-to-event analysis must be interpreted with caution in situations with competing events when estimating the cumulative incidence of malignancy with immunosuppression after renal transplantation. Renal transplant recipients with increasing age should be more carefully monitored as a high-risk population for developing malignancies.

Identifiants

pubmed: 32299709
pii: S0041-1345(19)31335-1
doi: 10.1016/j.transproceed.2020.02.124
pii:
doi:

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1775-1777

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Takahiro Yoshida (T)

Department of Urology, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Japan. Electronic address: yakinikugohan@gmail.com.

Soichi Matsumura (S)

Department of Urology, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Japan.

Takahiro Imanaka (T)

Department of Urology, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Japan.

Ayumu Taniguchi (A)

Department of Urology, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Japan.

Kazuaki Yamanaka (K)

Department of Urology, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Japan.

Hidefumi Kishikawa (H)

Department of Urology, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Japan.

Kenji Nishimura (K)

Department of Urology, Hyogo Prefectural Nishinomiya Hospital, Nishinomiya, Japan.

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Classifications MeSH