Sociedad Argentina de Hematología

Revista Hematología

 

 

 

 

 

Revista Argentina de Hematología

Abstract

Volumen:    20    # Number : 2

Publication Date :    Mayo - Agosto    Year:    2016

   ARTÍCULO ORIGINAL

Brentuximab vedotin, a new therapeutic alternative in patients with relapsed or refractory Hodgkin lymphoma: the argentine experience

Authors: Negri Aranguren F, Prates MV, Burgos R, Shanley, C, Kusmisnky, G, Fernández I, Otero V, Schutz N, Cranco S, Pavlovsky MA, Cerutti I, Huber M, Riveros D, Jarchum G, Remaggi G, García JJ, Mariano R, Miodosky M, Zárate T, Tamashiro M, Tosin MF, Zerga M, Szelagowski M, Intile D, Pavlovsky A

Abstract: Brentuximab vedotin (BV) is an antibody-drug conjugate that selectively delivers monomethyl auristatin E, an antimicrotubele agent, into CD30 expressing cells. It proved to be effective in the treatment of patients with relapsed or refractory Hodgkin lymphoma (R/R HL) with a suitable toxicity profile(1). Patients and methods: Forty nine patients with relapsed refractory HL and treated with BV, from 17 centers in Argentina were evaluated retrospectively. The dose of BV was 1.8 mg/kg intravenously once every 3 weeks, the median number of cycles was 7 (range 2-18). Results: The OR was 61% (30 patients), 24% (12 patients) achieved CR. The subgroups of patients which had relapsed after one year had an OR of 90% compared with 49% in primary refractory patients or in those who relapsed within the first year (p = 0.0015). The median PFS and median OS for the whole group were 20 and 29 months respectively. In patients who achieved CR the median PFS was 55 months. The most common adverse events (AE) were nausea (35%), infections (32%) and peripheral sensory neuropathy (32%). Nine patients (18%) experienced AE grade 3-4. conclusion: In our experience BV was associated with manageable toxicity and induced objective responses in 61% of patients with R/R HL: the subgroup of patients with relapses after their first year had better outcome.

Key words: Hodgkin lymphoma Brentuximab vedotin Antineoplastic agents

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