Synchronizing the use of allogeneic hematopoietic cell transplantation in checkpoint blockade therapy for Hodgkin lymphoma.


Journal

Expert review of hematology
ISSN: 1747-4094
Titre abrégé: Expert Rev Hematol
Pays: England
ID NLM: 101485942

Informations de publication

Date de publication:
09 2021
Historique:
pubmed: 10 8 2021
medline: 3 3 2022
entrez: 9 8 2021
Statut: ppublish

Résumé

The use of checkpoint blockade therapy (CBT) has shown impressive results for the treatment of relapsed/refractory Hodgkin lymphoma (cHL). The impact of CBT depends on the reversal of an exhausted T-cell immune phenotype and a consequential increase in the immunological, anti-tumor effect derived from a patient's adaptive immunity. As most patients with classical Hodgkin lymphoma will relapse during or after this treatment, clinicians often provide consolidation with allogeneic hematopoietic cell transplantation (alloHCT) in fit patients. However, the mechanisms responsible for CBT efficacy can also be those that increase the risk of immunological complications after alloHCT. We carried out in-depth research on the current medical literature to report and discuss the mechanism of action of CBT within a cHL setting; clinical results of CBT in cHL setting pre-alloHCT and post-alloHCT; interactions between CBT and alloHCT; and further clinical considerations. Checkpoint blockade therapy is an effective strategy for relapsed/refractory cHL. Its use is associated with higher immunological toxicities when administered before or after alloHCT. Whenever alloHCT is planned, clinicians should follow international recommendations such as using post-transplant cyclophosphamide GVHD prophylaxis.

Identifiants

pubmed: 34369849
doi: 10.1080/17474086.2021.1965874
doi:

Substances chimiques

Cyclophosphamide 8N3DW7272P

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

809-818

Auteurs

Alberto Mussetti (A)

Clinical Hematology Department, Institut Català d'Oncologia-Hospitalet, Barcelona, Spain.
Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), Barcelona, Spain.

Anna Bosch Vilaseca (A)

Clinical Hematology Department, Institut Català d'Oncologia-Hospitalet, Barcelona, Spain.
Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), Barcelona, Spain.

Rocío Parody (R)

Clinical Hematology Department, Institut Català d'Oncologia-Hospitalet, Barcelona, Spain.
Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), Barcelona, Spain.

Annalisa Paviglianiti (A)

Clinical Hematology Department, Institut Català d'Oncologia-Hospitalet, Barcelona, Spain.
Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), Barcelona, Spain.

Eva Domingo-Domenech (E)

Clinical Hematology Department, Institut Català d'Oncologia-Hospitalet, Barcelona, Spain.
Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), Barcelona, Spain.

Ana Maria Sureda (AM)

Clinical Hematology Department, Institut Català d'Oncologia-Hospitalet, Barcelona, Spain.
Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), Barcelona, Spain.

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Classifications MeSH