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Tacrolimus Levels Are Not Associated with Risk of Malignancy in Lung Transplant Recipients

BACKGROUND: Lung transplant (LTx) recipients suffer from high rates of malignancy. Exposure to immunosuppressive medication such as tacrolimus has been proposed as a risk factor for tumorigenesis. We hypothesized that chronically high levels of tacrolimus would be associated with risk of malignancy....

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Autores principales: Fox, Benjamin Daniel, Ashquar, Fadi, Raviv, Yael, Rozengarten, Dror, Straichman, Osnat, Izhakian, Shimon, Kramer, Mordechai Reuven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6248030/
https://www.ncbi.nlm.nih.gov/pubmed/29133776
http://dx.doi.org/10.12659/AOT.904417
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author Fox, Benjamin Daniel
Ashquar, Fadi
Raviv, Yael
Rozengarten, Dror
Straichman, Osnat
Izhakian, Shimon
Kramer, Mordechai Reuven
author_facet Fox, Benjamin Daniel
Ashquar, Fadi
Raviv, Yael
Rozengarten, Dror
Straichman, Osnat
Izhakian, Shimon
Kramer, Mordechai Reuven
author_sort Fox, Benjamin Daniel
collection PubMed
description BACKGROUND: Lung transplant (LTx) recipients suffer from high rates of malignancy. Exposure to immunosuppressive medication such as tacrolimus has been proposed as a risk factor for tumorigenesis. We hypothesized that chronically high levels of tacrolimus would be associated with risk of malignancy. MATERIAL/METHODS: The study was performed in a transplant center in Israel, with a nested case-control design. Cases were LTx recipients who were diagnosed with any solid or hematological malignancy except non-melanoma skin cancer. Controls were tumor-free during their entire follow-up after LTx and had at least the same follow-up time as their matched case. Controls were matched to cases by age and type of transplant received (single/double). Tacrolimus levels were extracted and analyzed for median drug level and also integrated over time (area under the curve – AUC-tacrolimus). RESULTS: We reviewed 412 LTx recipients in our registry. Thirty-nine cases of malignancy were diagnosed and 160 controls were matched, giving a crude tumor incidence rate of 26/100 000/year. Lung cancers were the commonest diagnosis. Cases and controls were well matched by age, smoking status, and LTx type. Median tacrolimus levels were 11.0 ng/ml and 11.3 ng/ml in cases and controls, respectively (p=0.88). The median log (AUC-tacrolimus) was 9.4 in the cases and 9.5 in the controls (p=0.59). CONCLUSIONS: In this nested case-control study, exposure to tacrolimus was similar in tumor cases and non-tumor controls. These data, based on a cohort with modest size, suggest either that tumorigenesis in LTx recipients is unrelated to tacrolimus exposure or that levels in these patients are above an unknown threshold at which the dose-response effect is saturated.
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spelling pubmed-62480302018-11-28 Tacrolimus Levels Are Not Associated with Risk of Malignancy in Lung Transplant Recipients Fox, Benjamin Daniel Ashquar, Fadi Raviv, Yael Rozengarten, Dror Straichman, Osnat Izhakian, Shimon Kramer, Mordechai Reuven Ann Transplant Original Paper BACKGROUND: Lung transplant (LTx) recipients suffer from high rates of malignancy. Exposure to immunosuppressive medication such as tacrolimus has been proposed as a risk factor for tumorigenesis. We hypothesized that chronically high levels of tacrolimus would be associated with risk of malignancy. MATERIAL/METHODS: The study was performed in a transplant center in Israel, with a nested case-control design. Cases were LTx recipients who were diagnosed with any solid or hematological malignancy except non-melanoma skin cancer. Controls were tumor-free during their entire follow-up after LTx and had at least the same follow-up time as their matched case. Controls were matched to cases by age and type of transplant received (single/double). Tacrolimus levels were extracted and analyzed for median drug level and also integrated over time (area under the curve – AUC-tacrolimus). RESULTS: We reviewed 412 LTx recipients in our registry. Thirty-nine cases of malignancy were diagnosed and 160 controls were matched, giving a crude tumor incidence rate of 26/100 000/year. Lung cancers were the commonest diagnosis. Cases and controls were well matched by age, smoking status, and LTx type. Median tacrolimus levels were 11.0 ng/ml and 11.3 ng/ml in cases and controls, respectively (p=0.88). The median log (AUC-tacrolimus) was 9.4 in the cases and 9.5 in the controls (p=0.59). CONCLUSIONS: In this nested case-control study, exposure to tacrolimus was similar in tumor cases and non-tumor controls. These data, based on a cohort with modest size, suggest either that tumorigenesis in LTx recipients is unrelated to tacrolimus exposure or that levels in these patients are above an unknown threshold at which the dose-response effect is saturated. International Scientific Literature, Inc. 2017-11-14 /pmc/articles/PMC6248030/ /pubmed/29133776 http://dx.doi.org/10.12659/AOT.904417 Text en © Ann Transplant, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Original Paper
Fox, Benjamin Daniel
Ashquar, Fadi
Raviv, Yael
Rozengarten, Dror
Straichman, Osnat
Izhakian, Shimon
Kramer, Mordechai Reuven
Tacrolimus Levels Are Not Associated with Risk of Malignancy in Lung Transplant Recipients
title Tacrolimus Levels Are Not Associated with Risk of Malignancy in Lung Transplant Recipients
title_full Tacrolimus Levels Are Not Associated with Risk of Malignancy in Lung Transplant Recipients
title_fullStr Tacrolimus Levels Are Not Associated with Risk of Malignancy in Lung Transplant Recipients
title_full_unstemmed Tacrolimus Levels Are Not Associated with Risk of Malignancy in Lung Transplant Recipients
title_short Tacrolimus Levels Are Not Associated with Risk of Malignancy in Lung Transplant Recipients
title_sort tacrolimus levels are not associated with risk of malignancy in lung transplant recipients
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6248030/
https://www.ncbi.nlm.nih.gov/pubmed/29133776
http://dx.doi.org/10.12659/AOT.904417
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