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Conversion to mammalian target of rapamycin inhibitors in kidney transplant recipients with de novo cancers
OBJECTIVE: To investigate the impact of mammalian target of rapamycin (mTOR) inhibitor conversion together with minimization of calcineurin inhibitor on allograft outcome and patient survival in kidney transplant recipients with post-transplant cancers. METHODS: A retrospective study of all kidney t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546523/ https://www.ncbi.nlm.nih.gov/pubmed/28160552 http://dx.doi.org/10.18632/oncotarget.14908 |
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author | Cheung, Chi Yuen Ma, Maggie Kam Man Chak, Wai Leung Chau, Ka Foon Tang, Sydney Chi Wai |
author_facet | Cheung, Chi Yuen Ma, Maggie Kam Man Chak, Wai Leung Chau, Ka Foon Tang, Sydney Chi Wai |
author_sort | Cheung, Chi Yuen |
collection | PubMed |
description | OBJECTIVE: To investigate the impact of mammalian target of rapamycin (mTOR) inhibitor conversion together with minimization of calcineurin inhibitor on allograft outcome and patient survival in kidney transplant recipients with post-transplant cancers. METHODS: A retrospective study of all kidney transplant recipients diagnosed to have post-transplant cancers between the period 1/1/1994 and 30/6/2015. Patients were divided into 2 groups: mTOR inhibitor group and non-conversion group. Outcome included allograft function, patient survival, graft survival, acute rejection and cancer recurrence. RESULTS: 115 patients (56 in mTOR inhibitor group and 59 in non-conversion group) were analyzed. Median follow up was 28 months (range: 1 month – 20 years). The allograft function at 1-year remained similar between both groups. There was no significant difference in the patient survival, graft survival and rejection free survival between both groups. More patients in the non-conversion group developed recurrence of cancers than mTOR inhibitor group but statistically not significant. CONCLUSIONS: Use of mTOR inhibitors together with calcineurin inhibitor minimization offer a reasonable option in kidney transplant recipients who developed post-transplant cancers in view of stable renal function, low rejection rate and low cancer recurrence rate. |
format | Online Article Text |
id | pubmed-5546523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55465232017-08-23 Conversion to mammalian target of rapamycin inhibitors in kidney transplant recipients with de novo cancers Cheung, Chi Yuen Ma, Maggie Kam Man Chak, Wai Leung Chau, Ka Foon Tang, Sydney Chi Wai Oncotarget Clinical Research Paper OBJECTIVE: To investigate the impact of mammalian target of rapamycin (mTOR) inhibitor conversion together with minimization of calcineurin inhibitor on allograft outcome and patient survival in kidney transplant recipients with post-transplant cancers. METHODS: A retrospective study of all kidney transplant recipients diagnosed to have post-transplant cancers between the period 1/1/1994 and 30/6/2015. Patients were divided into 2 groups: mTOR inhibitor group and non-conversion group. Outcome included allograft function, patient survival, graft survival, acute rejection and cancer recurrence. RESULTS: 115 patients (56 in mTOR inhibitor group and 59 in non-conversion group) were analyzed. Median follow up was 28 months (range: 1 month – 20 years). The allograft function at 1-year remained similar between both groups. There was no significant difference in the patient survival, graft survival and rejection free survival between both groups. More patients in the non-conversion group developed recurrence of cancers than mTOR inhibitor group but statistically not significant. CONCLUSIONS: Use of mTOR inhibitors together with calcineurin inhibitor minimization offer a reasonable option in kidney transplant recipients who developed post-transplant cancers in view of stable renal function, low rejection rate and low cancer recurrence rate. Impact Journals LLC 2017-01-30 /pmc/articles/PMC5546523/ /pubmed/28160552 http://dx.doi.org/10.18632/oncotarget.14908 Text en Copyright: © 2017 Cheung et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Clinical Research Paper Cheung, Chi Yuen Ma, Maggie Kam Man Chak, Wai Leung Chau, Ka Foon Tang, Sydney Chi Wai Conversion to mammalian target of rapamycin inhibitors in kidney transplant recipients with de novo cancers |
title | Conversion to mammalian target of rapamycin inhibitors in kidney transplant recipients with de novo cancers |
title_full | Conversion to mammalian target of rapamycin inhibitors in kidney transplant recipients with de novo cancers |
title_fullStr | Conversion to mammalian target of rapamycin inhibitors in kidney transplant recipients with de novo cancers |
title_full_unstemmed | Conversion to mammalian target of rapamycin inhibitors in kidney transplant recipients with de novo cancers |
title_short | Conversion to mammalian target of rapamycin inhibitors in kidney transplant recipients with de novo cancers |
title_sort | conversion to mammalian target of rapamycin inhibitors in kidney transplant recipients with de novo cancers |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546523/ https://www.ncbi.nlm.nih.gov/pubmed/28160552 http://dx.doi.org/10.18632/oncotarget.14908 |
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