Hepatosplenic T-cell lymphoma: treatment challenges.

Détails

ID Serval
serval:BIB_E3DB5CF282FC
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Institution
Titre
Hepatosplenic T-cell lymphoma: treatment challenges.
Périodique
Current opinion in oncology
Auteur⸱e⸱s
Bron D., De Leval L., Michiels S., Wittnebel S.
Collaborateur⸱rice⸱s
EuroBloodNet for rare diseases
ISSN
1531-703X (Electronic)
ISSN-L
1040-8746
Statut éditorial
Publié
Date de publication
01/09/2021
Peer-reviewed
Oui
Volume
33
Numéro
5
Pages
406-411
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Résumé
Hepatosplenic lymphoma (HSTCL) is a rare T-cell malignancy occurring in young males, associated with immune deficiency in 20% of the cases which, despite aggressive treatments, has a poor survival. Specific recommendations for first-line treatment remain debatable.
Published data covering case reports or series of HSTCL concur that allogeneic stem cell transplant should be proposed as a consolidation after response to chemotherapy in all patients eligible for transplant. In the light of two recent clinical examples, we also confirm that specific chemotherapy and a first-line consolidation with allogeneic transplantation when a donor is available to represent a treatment of choice these rare and distinctive lymphomas. Recent molecular studies are summarized in this review and suggest potential targets for new therapeutic strategies.
Major progresses have been achieved in improving the outcome of HSTCL l patients using intensive chemotherapy and allogeneic transplantation.
Pubmed
Web of science
Création de la notice
30/08/2021 7:50
Dernière modification de la notice
07/09/2021 6:37
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