Cargando…

Drug-Related Cutaneous Adverse Events in Philadelphia Chromosome-Negative Myeloproliferative Neoplasms: A Literature Review

Since myeloproliferative neoplasms (MPN) pose a significant risk for vascular and thrombotic complications, cytoreductive therapies, such as hydroxyurea (HU), interferon (IFN) inhibitors, and Janus kinase (JAK) inhibitors are recommended for patients at high risk. However, these agents also place pa...

Descripción completa

Detalles Bibliográficos
Autores principales: Malato, Alessandra, Rossi, Elena, Palumbo, Giuseppe Alberto, Guglielmelli, Paola, Pugliese, Novella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7312244/
https://www.ncbi.nlm.nih.gov/pubmed/32486130
http://dx.doi.org/10.3390/ijms21113900
_version_ 1783549686909501440
author Malato, Alessandra
Rossi, Elena
Palumbo, Giuseppe Alberto
Guglielmelli, Paola
Pugliese, Novella
author_facet Malato, Alessandra
Rossi, Elena
Palumbo, Giuseppe Alberto
Guglielmelli, Paola
Pugliese, Novella
author_sort Malato, Alessandra
collection PubMed
description Since myeloproliferative neoplasms (MPN) pose a significant risk for vascular and thrombotic complications, cytoreductive therapies, such as hydroxyurea (HU), interferon (IFN) inhibitors, and Janus kinase (JAK) inhibitors are recommended for patients at high risk. However, these agents also place patients at increased risk for drug-related cutaneous adverse events. Herein, we review the literature on skin toxicity related to the use of drugs for the treatment of MPN. Overall, the cytoreductive agents used for MPN are generally well tolerated and considered to be safe, except IFN, for which dropout rates as high as 25% have been reported. While IFN is known to give rise to flu syndrome, it rarely leads to hematological alterations. The most common hematological side effects of HU are mild and include granulocytopenia, anemia, and thrombocytopenia. The JAK inhibitor ruxolitinib has been associated with cytopenia and a higher incidence of viral infections, as well as increased risk for basal cell carcinoma (BCC) and squamous cell carcinoma (SCC). Based on the present analysis, it can be concluded that cutaneous toxicity is not a negligible complication of commonly used treatments for MPN. While further research is needed, patients on these agents, and especially those with a history of cutaneous malignancies, should undergo thorough skin examination before and during therapy. In addition, detailed history is critical since many patients who develop non-melanoma skin cancer have multiple preexisting risk factors for cutaneous carcinogenesis.
format Online
Article
Text
id pubmed-7312244
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-73122442020-06-26 Drug-Related Cutaneous Adverse Events in Philadelphia Chromosome-Negative Myeloproliferative Neoplasms: A Literature Review Malato, Alessandra Rossi, Elena Palumbo, Giuseppe Alberto Guglielmelli, Paola Pugliese, Novella Int J Mol Sci Review Since myeloproliferative neoplasms (MPN) pose a significant risk for vascular and thrombotic complications, cytoreductive therapies, such as hydroxyurea (HU), interferon (IFN) inhibitors, and Janus kinase (JAK) inhibitors are recommended for patients at high risk. However, these agents also place patients at increased risk for drug-related cutaneous adverse events. Herein, we review the literature on skin toxicity related to the use of drugs for the treatment of MPN. Overall, the cytoreductive agents used for MPN are generally well tolerated and considered to be safe, except IFN, for which dropout rates as high as 25% have been reported. While IFN is known to give rise to flu syndrome, it rarely leads to hematological alterations. The most common hematological side effects of HU are mild and include granulocytopenia, anemia, and thrombocytopenia. The JAK inhibitor ruxolitinib has been associated with cytopenia and a higher incidence of viral infections, as well as increased risk for basal cell carcinoma (BCC) and squamous cell carcinoma (SCC). Based on the present analysis, it can be concluded that cutaneous toxicity is not a negligible complication of commonly used treatments for MPN. While further research is needed, patients on these agents, and especially those with a history of cutaneous malignancies, should undergo thorough skin examination before and during therapy. In addition, detailed history is critical since many patients who develop non-melanoma skin cancer have multiple preexisting risk factors for cutaneous carcinogenesis. MDPI 2020-05-30 /pmc/articles/PMC7312244/ /pubmed/32486130 http://dx.doi.org/10.3390/ijms21113900 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Malato, Alessandra
Rossi, Elena
Palumbo, Giuseppe Alberto
Guglielmelli, Paola
Pugliese, Novella
Drug-Related Cutaneous Adverse Events in Philadelphia Chromosome-Negative Myeloproliferative Neoplasms: A Literature Review
title Drug-Related Cutaneous Adverse Events in Philadelphia Chromosome-Negative Myeloproliferative Neoplasms: A Literature Review
title_full Drug-Related Cutaneous Adverse Events in Philadelphia Chromosome-Negative Myeloproliferative Neoplasms: A Literature Review
title_fullStr Drug-Related Cutaneous Adverse Events in Philadelphia Chromosome-Negative Myeloproliferative Neoplasms: A Literature Review
title_full_unstemmed Drug-Related Cutaneous Adverse Events in Philadelphia Chromosome-Negative Myeloproliferative Neoplasms: A Literature Review
title_short Drug-Related Cutaneous Adverse Events in Philadelphia Chromosome-Negative Myeloproliferative Neoplasms: A Literature Review
title_sort drug-related cutaneous adverse events in philadelphia chromosome-negative myeloproliferative neoplasms: a literature review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7312244/
https://www.ncbi.nlm.nih.gov/pubmed/32486130
http://dx.doi.org/10.3390/ijms21113900
work_keys_str_mv AT malatoalessandra drugrelatedcutaneousadverseeventsinphiladelphiachromosomenegativemyeloproliferativeneoplasmsaliteraturereview
AT rossielena drugrelatedcutaneousadverseeventsinphiladelphiachromosomenegativemyeloproliferativeneoplasmsaliteraturereview
AT palumbogiuseppealberto drugrelatedcutaneousadverseeventsinphiladelphiachromosomenegativemyeloproliferativeneoplasmsaliteraturereview
AT guglielmellipaola drugrelatedcutaneousadverseeventsinphiladelphiachromosomenegativemyeloproliferativeneoplasmsaliteraturereview
AT pugliesenovella drugrelatedcutaneousadverseeventsinphiladelphiachromosomenegativemyeloproliferativeneoplasmsaliteraturereview