Hepatosplenic T-cell lymphoma: treatment challenges.

Details

Serval ID
serval:BIB_E3DB5CF282FC
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
Hepatosplenic T-cell lymphoma: treatment challenges.
Journal
Current opinion in oncology
Author(s)
Bron D., De Leval L., Michiels S., Wittnebel S.
Working group(s)
EuroBloodNet for rare diseases
ISSN
1531-703X (Electronic)
ISSN-L
1040-8746
Publication state
Published
Issued date
01/09/2021
Peer-reviewed
Oui
Volume
33
Number
5
Pages
406-411
Language
english
Notes
Publication types: Journal Article
Publication Status: ppublish
Abstract
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
Create date
30/08/2021 6:50
Last modification date
07/09/2021 5:37
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