New hematologic populations at risk of invasive aspergillosis: focus on new targeted, biological, and cellular therapies [version 1; peer review: 3 approved]

The introduction of new targeted, biological, and cellular therapies in patients with hematologic malignancies has improved the outcomes of patients but in parallel has changed the frequency and epidemiology of infections, including invasive aspergillosis (IA). In this article, recent literature on...

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Main Author: Corrado Girmenia
Format: Article
Language:English
Published: F1000 Research Ltd 2019-07-01
Series:F1000Research
Online Access:https://f1000research.com/articles/8-1202/v1
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spelling doaj-76dd424978794062ad4116f647b35d172020-11-25T03:32:08ZengF1000 Research LtdF1000Research2046-14022019-07-01810.12688/f1000research.17836.119501New hematologic populations at risk of invasive aspergillosis: focus on new targeted, biological, and cellular therapies [version 1; peer review: 3 approved]Corrado Girmenia0Dipartimento di Ematologia, Oncologia, e Dermatologia, Azienda Policlinico Umberto I, Sapienza University of Rome, Rome, ItalyThe introduction of new targeted, biological, and cellular therapies in patients with hematologic malignancies has improved the outcomes of patients but in parallel has changed the frequency and epidemiology of infections, including invasive aspergillosis (IA). In this article, recent literature on the epidemiology and clinical findings of IA in patients who have lymphoproliferative and myeloproliferative diseases and are undergoing novel targeted treatment with kinase inhibitors, agents targeting cell surface antigens, chimeric antigen receptor-modified T cells, and antibodies to immune checkpoint molecules is reviewed and the clinical impact of IA on the overall management of the underlying disease is discussed. Overall, IA represents a variable and uncommon complication in these populations, but given the increasing eligibility criteria of these novel treatments (particularly in patients with relapsed or refractory hematologic malignancies) and the prolonged periods of therapy, a considerable number of unusual cases of Aspergillus infections can be expected in clinical practice.https://f1000research.com/articles/8-1202/v1
collection DOAJ
language English
format Article
sources DOAJ
author Corrado Girmenia
spellingShingle Corrado Girmenia
New hematologic populations at risk of invasive aspergillosis: focus on new targeted, biological, and cellular therapies [version 1; peer review: 3 approved]
F1000Research
author_facet Corrado Girmenia
author_sort Corrado Girmenia
title New hematologic populations at risk of invasive aspergillosis: focus on new targeted, biological, and cellular therapies [version 1; peer review: 3 approved]
title_short New hematologic populations at risk of invasive aspergillosis: focus on new targeted, biological, and cellular therapies [version 1; peer review: 3 approved]
title_full New hematologic populations at risk of invasive aspergillosis: focus on new targeted, biological, and cellular therapies [version 1; peer review: 3 approved]
title_fullStr New hematologic populations at risk of invasive aspergillosis: focus on new targeted, biological, and cellular therapies [version 1; peer review: 3 approved]
title_full_unstemmed New hematologic populations at risk of invasive aspergillosis: focus on new targeted, biological, and cellular therapies [version 1; peer review: 3 approved]
title_sort new hematologic populations at risk of invasive aspergillosis: focus on new targeted, biological, and cellular therapies [version 1; peer review: 3 approved]
publisher F1000 Research Ltd
series F1000Research
issn 2046-1402
publishDate 2019-07-01
description The introduction of new targeted, biological, and cellular therapies in patients with hematologic malignancies has improved the outcomes of patients but in parallel has changed the frequency and epidemiology of infections, including invasive aspergillosis (IA). In this article, recent literature on the epidemiology and clinical findings of IA in patients who have lymphoproliferative and myeloproliferative diseases and are undergoing novel targeted treatment with kinase inhibitors, agents targeting cell surface antigens, chimeric antigen receptor-modified T cells, and antibodies to immune checkpoint molecules is reviewed and the clinical impact of IA on the overall management of the underlying disease is discussed. Overall, IA represents a variable and uncommon complication in these populations, but given the increasing eligibility criteria of these novel treatments (particularly in patients with relapsed or refractory hematologic malignancies) and the prolonged periods of therapy, a considerable number of unusual cases of Aspergillus infections can be expected in clinical practice.
url https://f1000research.com/articles/8-1202/v1
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