First salvage treatment with bendamustine and brentuximab vedotin in Hodgkin lymphoma: a phase 2 study of the Fondazione Italiana Linfomi.


Journal

Blood cancer journal
ISSN: 2044-5385
Titre abrégé: Blood Cancer J
Pays: United States
ID NLM: 101568469

Informations de publication

Date de publication:
11 12 2019
Historique:
received: 24 07 2019
accepted: 20 11 2019
revised: 12 11 2019
entrez: 13 12 2019
pubmed: 13 12 2019
medline: 16 5 2020
Statut: epublish

Résumé

Effective salvage options inducing high complete metabolic response (CMR) rates without significant toxicity are needed for Hodgkin lymphoma (HL) patients failing induction treatment and who are candidate to autologous stem cell transplantation (ASCT). Brentuximab vedotin (BV) and bendamustine are active monotherapies in the relapsed/refractory setting and their combination (the BBV regimen) possibly enhances their activity. This single-arm multicenter phase 2 study investigated the efficacy and safety of BBV as first salvage therapy in 40 patients with relapsed/refractory HL. Thirty-eight patients were evaluable for efficacy: 30 (78.9%) had a CMR and 2 (5.3%) a partial response, leading to an overall response rate (ORR) of 84.2%. The ORR in the primary refractory subset was 75.0%, among relapsed patients it was 94.4%. Thirty-five patients could mobilize peripheral blood stem cells and 33 underwent ASCT. At a median follow-up of 23 months, the estimated 3-year overall survival and progression-free survival are 88.1% and 67.3%. During therapy, only 3 grade IV cases of neutropenia occurred and resolved within a week. No grade 4 extrahematologic toxicities were reported; skin reactions were however rather frequent (65%). These results suggest that the BBV regimen exhibits promising efficacy and a manageable toxicity in a challenging subpopulation of HL patients.

Identifiants

pubmed: 31827067
doi: 10.1038/s41408-019-0265-x
pii: 10.1038/s41408-019-0265-x
pmc: PMC6906387
doi:

Substances chimiques

Brentuximab Vedotin 7XL5ISS668
Bendamustine Hydrochloride 981Y8SX18M

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

100

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Auteurs

A Broccoli (A)

Institute of Hematology "L. e A. Seràgnoli", University of Bologna, Bologna, Italy.

L Argnani (L)

Institute of Hematology "L. e A. Seràgnoli", University of Bologna, Bologna, Italy.

B Botto (B)

Hematology, Department of Oncology, University Hospital Città della Salute e della Scienza, Torino, Italy.

P Corradini (P)

IRCCS Istituto Nazionale dei Tumori, University of Milano, Milano, Italy.

A Pinto (A)

Hematology-Oncology and Stem Cell Transplantation Unit, National Cancer Institute, Fondazione Pascale, Napoli, Italy.

A Re (A)

Hematology, Azienda socio-sanitaria territoriale, Spedali Civili di Brescia, Brescia, Italy.

U Vitolo (U)

Hematology, Department of Oncology, University Hospital Città della Salute e della Scienza, Torino, Italy.

S Fanti (S)

Nuclear Medicine, Sant'Orsola-Malpighi University Hospital, University of Bologna, Bologna, Italy.

V Stefoni (V)

Institute of Hematology "L. e A. Seràgnoli", University of Bologna, Bologna, Italy.

P L Zinzani (PL)

Institute of Hematology "L. e A. Seràgnoli", University of Bologna, Bologna, Italy. pierluigi.zinzani@unibo.it.

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Classifications MeSH