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A phase 2 study of rituximab, bendamustine, bortezomib and dexamethasone for first-line treatment of older patients with mantle cell lymphoma

Authors :
Rémy Gressin
Nicolas Daguindau
Adrian Tempescul
Anne Moreau
Sylvain Carras
Emmanuelle Tchernonog
Anna Schmitt
Roch Houot
Caroline Dartigeas
Jean Michel Pignon
Selim Corm
Anne Banos
Christiane Mounier
Jehan Dupuis
Margaret Macro
Joel Fleury
Fabrice Jardin
Clementine Sarkozy
Ghandi Damaj
Pierre Feugier
Luc Matthieu Fornecker
Cecile Chabrot
Veronique Dorvaux
Krimo Bouadallah
Sandy Amorin
Reda Garidi
Laurent Voillat
Bertrand Joly
Philippe Solal Celigny
Nadine Morineau
Marie Pierre Moles
Hacene Zerazhi
Jean Fontan
Yazid Arkam
Magda Alexis
Vincent Delwail
Jean Pierre Vilque
Loic Ysebaert
Steven Le Gouill
Mary B. Callanan
for the Lymphoma Study Association
Source :
Haematologica, Vol 104, Iss 1 (2019)
Publication Year :
2019
Publisher :
Ferrata Storti Foundation, 2019.

Abstract

We present results of a prospective, multicenter, phase II study evaluating rituximab, bendamustine, bortezomib and dexamethasone as first-line treatment for patients with mantle cell lymphoma aged 65 years or older. A total of 74 patients were enrolled (median age, 73 years). Patients received a maximum of six cycles of treatment at 28-day intervals. The primary objective was to achieve an 18-month progression-free survival rate of 65% or higher. Secondary objectives were to evaluate toxicity and the prognostic impact of mantle cell lymphoma prognostic index, Ki67 expression, [18F]fluorodeoxyglucose-positron emission tomography and molecular minimal residual disease, in peripheral blood or bone marrow. With a median follow-up of 52 months, the 24-month progression-free survival rate was 70%, hence the primary objective was reached. After six cycles of treatment, 91% (54/59) of responding patients were analyzed for peripheral blood residual disease and 87% of these (47/54) were negative. Four-year overall survival rates of the patients who did not have or had detectable molecular residual disease in the blood at completion of treatment were 86.6% and 28.6%, respectively (P

Details

Language :
English
ISSN :
03906078 and 15928721
Volume :
104
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Haematologica
Publication Type :
Academic Journal
Accession number :
edsdoj.79f2a1ceb2cb45838a53d023cfec6ba8
Document Type :
article
Full Text :
https://doi.org/10.3324/haematol.2018.191429