First salvage treatment with bendamustine and brentuximab vedotin in Hodgkin lymphoma: a phase 2 study of the Fondazione Italiana Linfomi.
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Bendamustine Hydrochloride
Brentuximab Vedotin
Combined Modality Therapy
Female
Hodgkin Disease
/ diagnosis
Humans
Magnetic Resonance Imaging
Male
Middle Aged
Neoplasm Grading
Salvage Therapy
Tomography, X-Ray Computed
Treatment Outcome
Young Adult
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
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
100Références
Ann Oncol. 2019 Apr 1;30(4):612-620
pubmed: 30657848
J Clin Oncol. 2013 Feb 1;31(4):456-60
pubmed: 23248254
Leuk Lymphoma. 2009 Aug;50(8):1257-60
pubmed: 19544140
Blood. 2018 Mar 15;131(11):1183-1194
pubmed: 29229594
Blood. 2016 Sep 22;128(12):1562-6
pubmed: 27432875
Haematologica. 2019 Apr;104(4):e151-e153
pubmed: 30381303
J Clin Oncol. 2007 Feb 10;25(5):579-86
pubmed: 17242396
J Clin Oncol. 2016 Sep 20;34(27):3293-9
pubmed: 27382096
Blood Adv. 2019 May 14;3(9):1546-1552
pubmed: 31088808
Lancet Oncol. 2018 Feb;19(2):257-266
pubmed: 29276022
Br J Haematol. 2019 Jan;184(1):93-104
pubmed: 30407612
Lancet. 2002 Jun 15;359(9323):2065-71
pubmed: 12086759
J Clin Oncol. 2012 Jun 20;30(18):2183-9
pubmed: 22454421
Br J Haematol. 2014 Jun;165(6):793-800
pubmed: 24628515
Clin Lymphoma Myeloma Leuk. 2015 Jul;15(7):404-8
pubmed: 25840816
Blood. 2018 Jul 5;132(1):40-48
pubmed: 29703778
Haematologica. 2012 Jul;97(7):1073-9
pubmed: 22271893
Lancet. 1993 Apr 24;341(8852):1051-4
pubmed: 8096958
Ann Oncol. 2005 Apr;16(4):625-33
pubmed: 15737986
Br J Haematol. 2010 Mar;148(6):890-7
pubmed: 20085577
Lancet Oncol. 2015 Mar;16(3):284-92
pubmed: 25683846
J Clin Oncol. 2014 Sep 20;32(27):3059-68
pubmed: 25113753
Blood. 2010 Dec 2;116(23):4934-7
pubmed: 20733154
Leuk Lymphoma. 2013 Nov;54(11):2531-3
pubmed: 23617324