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Patients with relapsed/refractory hairy‐cell leukemia

BACKGROUND: Hairy cell leukemia (HCL) is a rare chronic B‐cell neoplasm with good long‐term prognosis. First and second‐line therapies include purine nucleoside analogues (PNAs) and rituximab, but until recently, limited alternative options were available for patients with two or more relapses. AIM:...

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Autores principales: Paillassa, Jérôme, Troussard, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8955050/
https://www.ncbi.nlm.nih.gov/pubmed/34250762
http://dx.doi.org/10.1002/cnr2.1495
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author Paillassa, Jérôme
Troussard, Xavier
author_facet Paillassa, Jérôme
Troussard, Xavier
author_sort Paillassa, Jérôme
collection PubMed
description BACKGROUND: Hairy cell leukemia (HCL) is a rare chronic B‐cell neoplasm with good long‐term prognosis. First and second‐line therapies include purine nucleoside analogues (PNAs) and rituximab, but until recently, limited alternative options were available for patients with two or more relapses. AIM: The aim of this study is to describe our real‐life experience with HCL patients in third and fourth‐line therapies. METHODS AND RESULTS: Data from 49 HCL patients with two or more relapses, including 16 patients with three or more relapses, were collected from the French retrospective HCL cohort covering the period from 1980 until 2011. They were analyzed to assess hematological response, relapse free survival (RFS) and overall survival (OS) after third (L3) and fourth line (L4). The median age at diagnosis was 53 years. PNAs were the most frequently used treatments. As L3 therapy, 29 patients received PNAs (66%) and 15 (34%) other treatments (rituximab [11%] or interferon [7%] alone or in combination [16%]). The distribution of L4 treatments was similar. The overall hematological response rate (OHRR) after L3 was 97% (complete hematological response 86%) with a 40% five‐year cumulative incidence of relapse (CIR), a median RFS of 104 months, and a median OS of 235 months. After L4, the OHRR was 94% with a two‐year CIR of fourth relapse of 27%. Eleven secondary cancers (5‐year cumulative incidence of 12%) were diagnosed in 10 patients. Patients with ≥2 relapses experience frequent further relapses, with increasingly shorter time to next treatment as the number of treatment lines increases. Furthermore, treatment strategies are associated with substantial toxicities. CONCLUSION: All these points lead to the need for novel treatments.
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spelling pubmed-89550502022-03-29 Patients with relapsed/refractory hairy‐cell leukemia Paillassa, Jérôme Troussard, Xavier Cancer Rep (Hoboken) Clinical Research Articles BACKGROUND: Hairy cell leukemia (HCL) is a rare chronic B‐cell neoplasm with good long‐term prognosis. First and second‐line therapies include purine nucleoside analogues (PNAs) and rituximab, but until recently, limited alternative options were available for patients with two or more relapses. AIM: The aim of this study is to describe our real‐life experience with HCL patients in third and fourth‐line therapies. METHODS AND RESULTS: Data from 49 HCL patients with two or more relapses, including 16 patients with three or more relapses, were collected from the French retrospective HCL cohort covering the period from 1980 until 2011. They were analyzed to assess hematological response, relapse free survival (RFS) and overall survival (OS) after third (L3) and fourth line (L4). The median age at diagnosis was 53 years. PNAs were the most frequently used treatments. As L3 therapy, 29 patients received PNAs (66%) and 15 (34%) other treatments (rituximab [11%] or interferon [7%] alone or in combination [16%]). The distribution of L4 treatments was similar. The overall hematological response rate (OHRR) after L3 was 97% (complete hematological response 86%) with a 40% five‐year cumulative incidence of relapse (CIR), a median RFS of 104 months, and a median OS of 235 months. After L4, the OHRR was 94% with a two‐year CIR of fourth relapse of 27%. Eleven secondary cancers (5‐year cumulative incidence of 12%) were diagnosed in 10 patients. Patients with ≥2 relapses experience frequent further relapses, with increasingly shorter time to next treatment as the number of treatment lines increases. Furthermore, treatment strategies are associated with substantial toxicities. CONCLUSION: All these points lead to the need for novel treatments. John Wiley and Sons Inc. 2021-07-12 /pmc/articles/PMC8955050/ /pubmed/34250762 http://dx.doi.org/10.1002/cnr2.1495 Text en © 2021 The Authors. Cancer Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research Articles
Paillassa, Jérôme
Troussard, Xavier
Patients with relapsed/refractory hairy‐cell leukemia
title Patients with relapsed/refractory hairy‐cell leukemia
title_full Patients with relapsed/refractory hairy‐cell leukemia
title_fullStr Patients with relapsed/refractory hairy‐cell leukemia
title_full_unstemmed Patients with relapsed/refractory hairy‐cell leukemia
title_short Patients with relapsed/refractory hairy‐cell leukemia
title_sort patients with relapsed/refractory hairy‐cell leukemia
topic Clinical Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8955050/
https://www.ncbi.nlm.nih.gov/pubmed/34250762
http://dx.doi.org/10.1002/cnr2.1495
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