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The benefits of cancer screening in kidney transplant recipients: a single‐center experience

The frequency of malignancy is increasing in kidney transplant recipients. Posttransplant malignancy (PTM) is a major cause of long‐term graft survival inhibition. In this study, we evaluated the frequency and prognosis of PTM at our center and examined the efficacy of cancer screening. Between 1972...

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Autores principales: Kato, Taigo, Kakuta, Yoichi, Abe, Toyofumi, Yamanaka, Kazuaki, Imamura, Ryoichi, Okumi, Masayoshi, Ichimaru, Naotsugu, Takahara, Shiro, Nonomura, Norio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735786/
https://www.ncbi.nlm.nih.gov/pubmed/26686199
http://dx.doi.org/10.1002/cam4.568
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author Kato, Taigo
Kakuta, Yoichi
Abe, Toyofumi
Yamanaka, Kazuaki
Imamura, Ryoichi
Okumi, Masayoshi
Ichimaru, Naotsugu
Takahara, Shiro
Nonomura, Norio
author_facet Kato, Taigo
Kakuta, Yoichi
Abe, Toyofumi
Yamanaka, Kazuaki
Imamura, Ryoichi
Okumi, Masayoshi
Ichimaru, Naotsugu
Takahara, Shiro
Nonomura, Norio
author_sort Kato, Taigo
collection PubMed
description The frequency of malignancy is increasing in kidney transplant recipients. Posttransplant malignancy (PTM) is a major cause of long‐term graft survival inhibition. In this study, we evaluated the frequency and prognosis of PTM at our center and examined the efficacy of cancer screening. Between 1972 and 2013, 750 patients were followed‐up at our center. Annual physical examinations and screenings were performed to detect PTM. We investigated the detail of two distinctive cancer groups: screening‐detected cancers and symptom‐detected cancers. Seventy‐seven PTM were identified during the follow‐up period. The mean age at the initial PTM detection was 43.6 ± 12.8 years. The mean interval from transplantation to cancer diagnosis was 134.5 ± 11.3 months. Among the 77 patients, posttransplant lymphoproliferative disease (PTLD) was the most common cancer (19.5%, 15/77), followed by renal cell carcinoma (15.6%, 12/77). Of the cancer cases, 46.8% (36/77) were detected via screening. The most frequently screening‐detected cancer was renal cell carcinoma of the native kidney and breast cancer (22.2%, 8/36). However, it was difficult to detect PTLD, urothelial carcinoma, and colorectal cancer via screening. Interestingly, Cox proportional regression analyses revealed nonscreened recipients to be a significant prognostic factor for PTM (P < 0.001). This study is the first to report that appropriate screening tests play a key role in early PTM diagnosis and lead to reduce the mortality rate in kidney transplant recipients. These findings support the provision of long‐term appropriate screening for kidney transplant recipients.
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spelling pubmed-47357862016-02-09 The benefits of cancer screening in kidney transplant recipients: a single‐center experience Kato, Taigo Kakuta, Yoichi Abe, Toyofumi Yamanaka, Kazuaki Imamura, Ryoichi Okumi, Masayoshi Ichimaru, Naotsugu Takahara, Shiro Nonomura, Norio Cancer Med Clinical Cancer Research The frequency of malignancy is increasing in kidney transplant recipients. Posttransplant malignancy (PTM) is a major cause of long‐term graft survival inhibition. In this study, we evaluated the frequency and prognosis of PTM at our center and examined the efficacy of cancer screening. Between 1972 and 2013, 750 patients were followed‐up at our center. Annual physical examinations and screenings were performed to detect PTM. We investigated the detail of two distinctive cancer groups: screening‐detected cancers and symptom‐detected cancers. Seventy‐seven PTM were identified during the follow‐up period. The mean age at the initial PTM detection was 43.6 ± 12.8 years. The mean interval from transplantation to cancer diagnosis was 134.5 ± 11.3 months. Among the 77 patients, posttransplant lymphoproliferative disease (PTLD) was the most common cancer (19.5%, 15/77), followed by renal cell carcinoma (15.6%, 12/77). Of the cancer cases, 46.8% (36/77) were detected via screening. The most frequently screening‐detected cancer was renal cell carcinoma of the native kidney and breast cancer (22.2%, 8/36). However, it was difficult to detect PTLD, urothelial carcinoma, and colorectal cancer via screening. Interestingly, Cox proportional regression analyses revealed nonscreened recipients to be a significant prognostic factor for PTM (P < 0.001). This study is the first to report that appropriate screening tests play a key role in early PTM diagnosis and lead to reduce the mortality rate in kidney transplant recipients. These findings support the provision of long‐term appropriate screening for kidney transplant recipients. John Wiley and Sons Inc. 2015-12-21 /pmc/articles/PMC4735786/ /pubmed/26686199 http://dx.doi.org/10.1002/cam4.568 Text en © 2015 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Kato, Taigo
Kakuta, Yoichi
Abe, Toyofumi
Yamanaka, Kazuaki
Imamura, Ryoichi
Okumi, Masayoshi
Ichimaru, Naotsugu
Takahara, Shiro
Nonomura, Norio
The benefits of cancer screening in kidney transplant recipients: a single‐center experience
title The benefits of cancer screening in kidney transplant recipients: a single‐center experience
title_full The benefits of cancer screening in kidney transplant recipients: a single‐center experience
title_fullStr The benefits of cancer screening in kidney transplant recipients: a single‐center experience
title_full_unstemmed The benefits of cancer screening in kidney transplant recipients: a single‐center experience
title_short The benefits of cancer screening in kidney transplant recipients: a single‐center experience
title_sort benefits of cancer screening in kidney transplant recipients: a single‐center experience
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735786/
https://www.ncbi.nlm.nih.gov/pubmed/26686199
http://dx.doi.org/10.1002/cam4.568
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