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Successful kidney transplantation in a patient with pre‐existing chronic myeloid leukemia treated with imatinib

Active malignancy is an absolute contraindication to kidney transplantation. As for chronic myeloid leukemia (CML), a Philadelphia chromosome‐positive myeloproliferative neoplasm, the introduction of tyrosine kinase inhibitors has transformed CML from a lethal into a manageable chronic disease with...

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Autores principales: Thiem, Ursula, Buxhofer‐Ausch, Veronika, Kranewitter, Wolfgang, Webersinke, Gerald, Enkner, Wolfgang, Cejka, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818412/
https://www.ncbi.nlm.nih.gov/pubmed/32654389
http://dx.doi.org/10.1111/ajt.16194
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author Thiem, Ursula
Buxhofer‐Ausch, Veronika
Kranewitter, Wolfgang
Webersinke, Gerald
Enkner, Wolfgang
Cejka, Daniel
author_facet Thiem, Ursula
Buxhofer‐Ausch, Veronika
Kranewitter, Wolfgang
Webersinke, Gerald
Enkner, Wolfgang
Cejka, Daniel
author_sort Thiem, Ursula
collection PubMed
description Active malignancy is an absolute contraindication to kidney transplantation. As for chronic myeloid leukemia (CML), a Philadelphia chromosome‐positive myeloproliferative neoplasm, the introduction of tyrosine kinase inhibitors has transformed CML from a lethal into a manageable chronic disease with a close‐to‐normal life expectancy. To date it is unknown whether kidney transplantation can be safely performed in patients with pre‐existing CML. We describe the clinical course of a 57‐year‐old male patient with chronic kidney disease caused by reflux nephropathy. This patient had undergone first kidney transplantation 20 years earlier and had again been on chronic hemodialysis for 6 years when CML was diagnosed. First‐line therapy with 400 mg imatinib daily was well tolerated and induced an optimal cytogenetic and molecular response 3 months after initiation. One and a half years after CML diagnosis, a second kidney transplantation from a deceased donor was performed. Immunosuppression included basiliximab, tacrolimus, mycophenolate mofetil, and corticosteroids. Currently, 2 years posttransplant, renal allograft function is stable (serum creatinine 1.09 mg/dL, estimated glomerular filtration rate 75 mL/min per 1.73 m(2)), and CML remains in deep molecular remission with imatinib. Imatinib‐treated CML in deep molecular remission could be regarded as inactive malignancy and may therefore not be viewed as an absolute contraindication to kidney transplantation.
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spelling pubmed-78184122021-01-29 Successful kidney transplantation in a patient with pre‐existing chronic myeloid leukemia treated with imatinib Thiem, Ursula Buxhofer‐Ausch, Veronika Kranewitter, Wolfgang Webersinke, Gerald Enkner, Wolfgang Cejka, Daniel Am J Transplant Case Reports Active malignancy is an absolute contraindication to kidney transplantation. As for chronic myeloid leukemia (CML), a Philadelphia chromosome‐positive myeloproliferative neoplasm, the introduction of tyrosine kinase inhibitors has transformed CML from a lethal into a manageable chronic disease with a close‐to‐normal life expectancy. To date it is unknown whether kidney transplantation can be safely performed in patients with pre‐existing CML. We describe the clinical course of a 57‐year‐old male patient with chronic kidney disease caused by reflux nephropathy. This patient had undergone first kidney transplantation 20 years earlier and had again been on chronic hemodialysis for 6 years when CML was diagnosed. First‐line therapy with 400 mg imatinib daily was well tolerated and induced an optimal cytogenetic and molecular response 3 months after initiation. One and a half years after CML diagnosis, a second kidney transplantation from a deceased donor was performed. Immunosuppression included basiliximab, tacrolimus, mycophenolate mofetil, and corticosteroids. Currently, 2 years posttransplant, renal allograft function is stable (serum creatinine 1.09 mg/dL, estimated glomerular filtration rate 75 mL/min per 1.73 m(2)), and CML remains in deep molecular remission with imatinib. Imatinib‐treated CML in deep molecular remission could be regarded as inactive malignancy and may therefore not be viewed as an absolute contraindication to kidney transplantation. John Wiley and Sons Inc. 2020-08-04 2021-01 /pmc/articles/PMC7818412/ /pubmed/32654389 http://dx.doi.org/10.1111/ajt.16194 Text en © 2020 The Authors. American Journal of Transplantation published by Wiley Periodicals LLC on behalf of The American Society of Transplantation and the American Society of Transplant Surgeons This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
Thiem, Ursula
Buxhofer‐Ausch, Veronika
Kranewitter, Wolfgang
Webersinke, Gerald
Enkner, Wolfgang
Cejka, Daniel
Successful kidney transplantation in a patient with pre‐existing chronic myeloid leukemia treated with imatinib
title Successful kidney transplantation in a patient with pre‐existing chronic myeloid leukemia treated with imatinib
title_full Successful kidney transplantation in a patient with pre‐existing chronic myeloid leukemia treated with imatinib
title_fullStr Successful kidney transplantation in a patient with pre‐existing chronic myeloid leukemia treated with imatinib
title_full_unstemmed Successful kidney transplantation in a patient with pre‐existing chronic myeloid leukemia treated with imatinib
title_short Successful kidney transplantation in a patient with pre‐existing chronic myeloid leukemia treated with imatinib
title_sort successful kidney transplantation in a patient with pre‐existing chronic myeloid leukemia treated with imatinib
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7818412/
https://www.ncbi.nlm.nih.gov/pubmed/32654389
http://dx.doi.org/10.1111/ajt.16194
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