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Combination of bendamustine and rituximab as frontline therapy for patients with chronic lymphocytic leukaemia: multicenter, retrospective clinical practice experience with 279 cases outside of controlled clinical trials

Authors :
Maurizio Musso
Donato Mannina
Nicola Di Renzo
Francesca Romana Mauro
Maria Rosaria De Paolis
Fortunato Morabito
Ilaria Scortechini
Stefania Ciolli
Lucia Mastrullo
Katja Zirlik
Pier Luigi Zinzani
Iolanda Vincelli
Gerardo Musuraca
Giuseppe Tarantini
Annamaria Giordano
Attilio Guarini
Francesco Angrilli
Tamar Tadmor
Angela Giannotta
Maria Rosaria Villa
Aaron Polliack
Annalisa Chiarenza
Annalisa Arcari
Massimo Gentile
Yair Herishanu
Lev Shvidel
Felicetto Ferrara
Giuseppe Caparrotti
Roberta Murru
Fiorella Ilariucci
Lorella Orsucci
Luciano Levato
Giuseppe Mineo
Angela Rago
Francesco Di Raimondo
Stefano Molica
Carmine Selleri
Giovanni Tripepi
Marta Coscia
Gentile, Massimo
Zirlik, Katja
Ciolli, Stefania
Mauro, Francesca R.
Di Renzo, Nicola
Mastrullo, Lucia
Angrilli, Francesco
Molica, Stefano
Tripepi, Giovanni
Giordano, Annamaria
Di Raimondo, Francesco
Selleri, Carmine
Coscia, Marta
Musso, Maurizio
Orsucci, Lorella
Mannina, Donato
Rago, Angela
Giannotta, Angela
Ferrara, Felicetto
Herishanu, Yair
Shvidel, Lev
Tadmor, Tamar
Scortechini, Ilaria
Ilariucci, Fiorella
Murru, Roberta
Guarini, Attilio
Musuraca, Gerardo
Mineo, Giuseppe
Vincelli, Iolanda
Arcari, Annalisa
Tarantini, Giuseppe
Caparrotti, Giuseppe
Chiarenza, Annalisa
Levato, Luciano
Villa, Maria Rosaria
De Paolis, Maria Rosaria
Zinzani, Pier Luigi
Polliack, Aaron
Morabito, Fortunato
Publication Year :
2016

Abstract

Recently, encouraging results in terms of safety and efficacy have been obtained using bendamustine–rituximab (BR) in untreated chronic lymphocytic leukaemia (CLL) patients enrolled in a phase II study. Here, we report a retrospective international multicenter study of CLL patients treated with BR as front-line therapy. The cohort included 279 patients with progressive CLL from 33 centers (29 Italian, 3 Israeli and 1 German) who received at least 1 cycle of BR as first-line treatment during the 2008–2014 period. The primary objective of this study was to evaluate the efficacy and safety of BR administered as front-line therapy, outside of controlled clinical trials. Median age was 70 years (range, 43–86 years); 62.4% were males and 35.8% had Binet stage C. Forty-two patients (15.2%) were unfit (cumulative illness rating scale [CIRS] score ≥7), and 140 (50.2%) had creatinine clearance ≤70 ml/min. Fluorescent in situ hybridisation analysis, available for 192 cases, showed that 21 (10.9%) had del11q and 18 (9.4%) del17p. The overall response rate (ORR) was 86.4%, with a complete remission rate of 28%. Patients with del17p had an ORR of 66.7%. After median follow-up of 24 months, the 2-year progression-free survival (PFS) was 69.9%; CIRS ≥7, immunoglobulin heavy-chain variable-region (IGHV) unmutated status, del17p and BR dose intensity

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....114baa853d29fe5a5d9d6edcc0a3f001