Your browser doesn't support javascript.
loading
First salvage treatment with bendamustine and brentuximab vedotin in Hodgkin lymphoma: a phase 2 study of the Fondazione Italiana Linfomi.
Broccoli, A; Argnani, L; Botto, B; Corradini, P; Pinto, A; Re, A; Vitolo, U; Fanti, S; Stefoni, V; Zinzani, P L.
Afiliação
  • Broccoli A; Institute of Hematology "L. e A. Seràgnoli", University of Bologna, Bologna, Italy.
  • Argnani L; Institute of Hematology "L. e A. Seràgnoli", University of Bologna, Bologna, Italy.
  • Botto B; Hematology, Department of Oncology, University Hospital Città della Salute e della Scienza, Torino, Italy.
  • Corradini P; IRCCS Istituto Nazionale dei Tumori, University of Milano, Milano, Italy.
  • Pinto A; Hematology-Oncology and Stem Cell Transplantation Unit, National Cancer Institute, Fondazione Pascale, Napoli, Italy.
  • Re A; Hematology, Azienda socio-sanitaria territoriale, Spedali Civili di Brescia, Brescia, Italy.
  • Vitolo U; Hematology, Department of Oncology, University Hospital Città della Salute e della Scienza, Torino, Italy.
  • Fanti S; Nuclear Medicine, Sant'Orsola-Malpighi University Hospital, University of Bologna, Bologna, Italy.
  • Stefoni V; Institute of Hematology "L. e A. Seràgnoli", University of Bologna, Bologna, Italy.
  • Zinzani PL; Institute of Hematology "L. e A. Seràgnoli", University of Bologna, Bologna, Italy. pierluigi.zinzani@unibo.it.
Blood Cancer J ; 9(12): 100, 2019 12 11.
Article em En | MEDLINE | ID: mdl-31827067
ABSTRACT
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Hodgkin / Protocolos de Quimioterapia Combinada Antineoplásica Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Cancer J Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Hodgkin / Protocolos de Quimioterapia Combinada Antineoplásica Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Cancer J Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Itália