Brentuximab vedotin in real life, a seven year experience in patients with refractory/relapsed CD30+ T cell lymphoma.


Journal

Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners
ISSN: 1477-092X
Titre abrégé: J Oncol Pharm Pract
Pays: England
ID NLM: 9511372

Informations de publication

Date de publication:
Oct 2021
Historique:
pubmed: 27 10 2020
medline: 25 11 2021
entrez: 26 10 2020
Statut: ppublish

Résumé

Brentuximab vedotin (Bv) has been approved for the treatment of Refractory/Relapsed (R/R) Anaplastic Large Cell Lymphomas (ALCL) and cutaneous T-Cell Lymphomas, but is also effective in other CD30+ malignancies. We report here the outcomes of patients with various R/R Peripheral T Cell Lymphoma (PTCL) treated with Bv in real life practice. This was a retrospective, single-center study based on medical records of patients with R/R PTCL treated either with Bv alone or in combination with chemotherapy. Among 27 patients treated with Bv, neutropenia was the main serious adverse event observed in particular when Bv was used as combination treatment. The complete Response Rates (CRR) was 40.7%; it was significantly improved when Bv was used as combination treatment. The majority of eligible patients (7/10) underwent Stem Cell Transplantation. Median Progression Free Survival (PFS) and Overall Survival (OS) were 5.2 months and 12.5 months respectively. Our current study shows that Bv used in combination with chemotherapy provides a high CRR and thereby allows SCT in R/R PTCL. The use of Bv treatments in this setting warrants further investigation.

Identifiants

pubmed: 33100177
doi: 10.1177/1078155220968615
doi:

Substances chimiques

Immunoconjugates 0
Ki-1 Antigen 0
Brentuximab Vedotin 7XL5ISS668

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1730-1735

Auteurs

Lucie Oberic (L)

Department of Haematology, IUCT-Oncopole, CHU Toulouse, Toulouse, France.

Faustine Delzor (F)

Pharmacy Department IUCT (Institut Universitaire du Cancer) Oncopole, University Hospital Toulouse, Toulouse, France.

Caroline Protin (C)

Department of Haematology, IUCT-Oncopole, CHU Toulouse, Toulouse, France.

Sophie Perriat (S)

Pharmacy Department IUCT (Institut Universitaire du Cancer) Oncopole, University Hospital Toulouse, Toulouse, France.

Camille Laurent (C)

Department of Pathology, IUCT-Oncopole, CHU Toulouse, Toulouse, France.
Centre de Recherches en Cancérologie de Toulouse (CRCT), Team 9, INSERM UMR1037, Université de Toulouse, Toulouse, France.

Anaïs Grand (A)

Pharmacy Department IUCT (Institut Universitaire du Cancer) Oncopole, University Hospital Toulouse, Toulouse, France.

Jean Marie Canonge (JM)

Pharmacy Department IUCT (Institut Universitaire du Cancer) Oncopole, University Hospital Toulouse, Toulouse, France.

Cécile Borel (C)

Department of Haematology, IUCT-Oncopole, CHU Toulouse, Toulouse, France.

Martin Gauthier (M)

Department of Haematology, IUCT-Oncopole, CHU Toulouse, Toulouse, France.

Loïc Ysebaert (L)

Department of Haematology, IUCT-Oncopole, CHU Toulouse, Toulouse, France.
Centre de Recherches en Cancérologie de Toulouse (CRCT), Team 9, INSERM UMR1037, Université de Toulouse, Toulouse, France.

Florent Puisset (F)

Pharmacy Department IUCT (Institut Universitaire du Cancer) Oncopole, Institut Claudius Regaud, Toulouse, France.
Centre de Recherches en Cancérologie de Toulouse (CRCT), Team 14, INSERM UMR1037, Université de Toulouse, Toulouse, France.

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Classifications MeSH