Current Treatment of Peripheral T-cell Lymphoma.
Journal
Oncology (Williston Park, N.Y.)
ISSN: 0890-9091
Titre abrégé: Oncology (Williston Park)
Pays: United States
ID NLM: 8712059
Informations de publication
Date de publication:
09 05 2022
09 05 2022
Historique:
entrez:
16
5
2022
pubmed:
17
5
2022
medline:
20
5
2022
Statut:
ppublish
Résumé
The peripheral T-cell lymphomas (PTCLs) are a notoriously diverse family of non-Hodgkin lymphomas with generally aggressive biology. Clinical management is challenging given a largely inadequate literature base comprised of few randomized trials and heterogeneous observational reports. Herein, we provide an account of our practice in the treatment of the 3 most common nodal PTCLs: PTCL, not otherwise specified, angioimmunoblastic T-cell lymphoma, and anaplastic large cell lymphoma (ALCL). In the up-front setting, we employ anthracycline-based induction, with the incorporation of brentuximab vedotin for all those with ALCL and consideration in those with other CD30-expressing PTCLs based on improved progression-free and overall survival in the absence of additional toxicity in the ECHELON-2 trial. We strongly consider high-dose therapy with autologous stem cell rescue in first complete remission. In the relapsed or refractory (R/R) setting, we often look to clinical trials or choose from 4 FDA-approved single agents-belinostat, brentuximab vedotin, romidepsin, and pralatrexate-based on tumor phenotype and side-effect profiles. Our goal in the R/R setting is achievement of complete remission followed by allogeneic transplant with curative intent in appropriate candidates or long-term disease control in others. Numerous investigational agents are advancing through trials and have potential to alter standards of care in the near future.
Identifiants
pubmed: 35576176
pii: 25920960
doi: 10.46883/2022.25920960
doi:
Substances chimiques
Brentuximab Vedotin
7XL5ISS668
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
293-305Commentaires et corrections
Type : CommentIn