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Ibrutinib-Associated Skin Toxicity: A Case of Maculopapular Rash in a 79-Year Old Caucasian Male Patient with Relapsed Waldenstrom’s Macroglobulinemia and Review of the Literature

Waldenstrom's macroglobulinamia (WM) is a rare malignant lymphoproliferative disorder, characterized by monoclonal IgM paraproteinemia and neoplastic proliferation of malignant lymphoplasmacytoid cells in the bone marrow. Traditionally, WM has been treated with modalities similar to those used...

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Autores principales: Jensen, Anders Bisgaard, Stausbøl-Grøn, Birgitte, Riber-Hansen, Rikke, d’Amore, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402616/
https://www.ncbi.nlm.nih.gov/pubmed/28469834
http://dx.doi.org/10.4081/dr.2017.6976
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author Jensen, Anders Bisgaard
Stausbøl-Grøn, Birgitte
Riber-Hansen, Rikke
d’Amore, Francesco
author_facet Jensen, Anders Bisgaard
Stausbøl-Grøn, Birgitte
Riber-Hansen, Rikke
d’Amore, Francesco
author_sort Jensen, Anders Bisgaard
collection PubMed
description Waldenstrom's macroglobulinamia (WM) is a rare malignant lymphoproliferative disorder, characterized by monoclonal IgM paraproteinemia and neoplastic proliferation of malignant lymphoplasmacytoid cells in the bone marrow. Traditionally, WM has been treated with modalities similar to those used in the management of other indolent lymphomas. Just recently, based on impressive clinical trial results in heavily pretreated WM patients, a new Bruton Tyrosine Kinase-inhibitor, Ibrutinib, has been approved for the treatment of this disorder. As the use of Ibrutinib in WM outside clinical trials is still limited, only few clinical reports illustrating treatment side effects are currently available. Here we review the current literature specific on Ibrutinib-associated rash in hematologic patients, and report on an elderly patient with WM, who developed a red maculopapular non-pruritic rash 12 weeks after starting Ibrutinib therapy. Without modifications of the ongoing Ibrutinib schedule, the rash regressed within two weeks of treatment with topical steroid-containing dermatological compounds.
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spelling pubmed-54026162017-05-03 Ibrutinib-Associated Skin Toxicity: A Case of Maculopapular Rash in a 79-Year Old Caucasian Male Patient with Relapsed Waldenstrom’s Macroglobulinemia and Review of the Literature Jensen, Anders Bisgaard Stausbøl-Grøn, Birgitte Riber-Hansen, Rikke d’Amore, Francesco Dermatol Reports Case Report Waldenstrom's macroglobulinamia (WM) is a rare malignant lymphoproliferative disorder, characterized by monoclonal IgM paraproteinemia and neoplastic proliferation of malignant lymphoplasmacytoid cells in the bone marrow. Traditionally, WM has been treated with modalities similar to those used in the management of other indolent lymphomas. Just recently, based on impressive clinical trial results in heavily pretreated WM patients, a new Bruton Tyrosine Kinase-inhibitor, Ibrutinib, has been approved for the treatment of this disorder. As the use of Ibrutinib in WM outside clinical trials is still limited, only few clinical reports illustrating treatment side effects are currently available. Here we review the current literature specific on Ibrutinib-associated rash in hematologic patients, and report on an elderly patient with WM, who developed a red maculopapular non-pruritic rash 12 weeks after starting Ibrutinib therapy. Without modifications of the ongoing Ibrutinib schedule, the rash regressed within two weeks of treatment with topical steroid-containing dermatological compounds. PAGEPress Publications, Pavia, Italy 2017-04-20 /pmc/articles/PMC5402616/ /pubmed/28469834 http://dx.doi.org/10.4081/dr.2017.6976 Text en ©Copyright A.B. Jensen et al., 2017 http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Jensen, Anders Bisgaard
Stausbøl-Grøn, Birgitte
Riber-Hansen, Rikke
d’Amore, Francesco
Ibrutinib-Associated Skin Toxicity: A Case of Maculopapular Rash in a 79-Year Old Caucasian Male Patient with Relapsed Waldenstrom’s Macroglobulinemia and Review of the Literature
title Ibrutinib-Associated Skin Toxicity: A Case of Maculopapular Rash in a 79-Year Old Caucasian Male Patient with Relapsed Waldenstrom’s Macroglobulinemia and Review of the Literature
title_full Ibrutinib-Associated Skin Toxicity: A Case of Maculopapular Rash in a 79-Year Old Caucasian Male Patient with Relapsed Waldenstrom’s Macroglobulinemia and Review of the Literature
title_fullStr Ibrutinib-Associated Skin Toxicity: A Case of Maculopapular Rash in a 79-Year Old Caucasian Male Patient with Relapsed Waldenstrom’s Macroglobulinemia and Review of the Literature
title_full_unstemmed Ibrutinib-Associated Skin Toxicity: A Case of Maculopapular Rash in a 79-Year Old Caucasian Male Patient with Relapsed Waldenstrom’s Macroglobulinemia and Review of the Literature
title_short Ibrutinib-Associated Skin Toxicity: A Case of Maculopapular Rash in a 79-Year Old Caucasian Male Patient with Relapsed Waldenstrom’s Macroglobulinemia and Review of the Literature
title_sort ibrutinib-associated skin toxicity: a case of maculopapular rash in a 79-year old caucasian male patient with relapsed waldenstrom’s macroglobulinemia and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402616/
https://www.ncbi.nlm.nih.gov/pubmed/28469834
http://dx.doi.org/10.4081/dr.2017.6976
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