Rituximab plus gemcitabine and oxaliplatin in patients with refractory/relapsed diffuse large B-cell lymphoma who are not candidates for high-dose therapy. A phase II Lymphoma Study Association trial
Nicolas Mounier,
Taoufik El Gnaoui,
Hervé Tilly,
Danièle Canioni,
Catherine Sebban,
René-Olivier Casasnovas,
Richard Delarue,
Anne Sonet,
Pauline Beaussart,
Tony Petrella,
Sylvie Castaigne,
Serge Bologna,
Gilles Salles,
Alain Rahmouni,
Philippe Gaulard,
Corinne Haioun
Affiliations
Nicolas Mounier
Onco-Hematology Dept., Hospital l’Archet, Nice, France
Taoufik El Gnaoui
Lymphoid Malignancies Unit, Hospital Henri Mondor, Créteil, France
Hervé Tilly
Hematology Dept., Hospital Béquerel, Rouen, France
Danièle Canioni
Pathology Dept., Hospital Necker, Paris, France
Catherine Sebban
Hematology Dept., Hospital Leon Berard, Lyon, France
René-Olivier Casasnovas
Hematology Dept., Hospital Le Bocage, Dijon, France
Richard Delarue
Hematology Dept., Hospital Necker, Paris, France
Anne Sonet
Hematology Dept., Hospital Mont Godinne, Yvoir, Belgium
Pauline Beaussart
Medical Imaging Dept., Hospital Henri Mondor, Créteil, France
Tony Petrella
Pathology Dept., Hospital Le Bocage, Dijon, France
Sylvie Castaigne
Hematology Dept., Hospital Mignot, Versailles, France
Serge Bologna
Hematology Dept., Hospital Brabois, Nancy, France
Gilles Salles
Hematology Dept., Hospital Lyon-Sud, Pierre Bénite, France
Alain Rahmouni
Medical Imaging Dept., Hospital Henri Mondor, Créteil, France
Philippe Gaulard
Pathology Dept., Hospital Henri Mondor, Créteil, France
Corinne Haioun
Lymphoid Malignancies Unit, Hospital Henri Mondor, Créteil, France
A previous pilot study with rituximab, gemcitabine and oxaliplatin showed promising activity in patients with refractory/relapsed B-cell lymphoma. We, therefore, conducted a phase II study to determine whether these results could be reproduced in a multi-institutional setting. This phase II study included 49 patients with refractory (n=6) or relapsing (n=43) diffuse large B-cell lymphoma. The median age of the patients was 69 years. Prior treatment included rituximab in 31 (63%) and autologous transplantation in 17 (35%) patients. International Prognostic Index at enrollment was >2 in 34 patients (71%). The primary endpoint was overall response rate after four cycles of treatment. Patients were planned to receive eight cycles if they reached at least partial remission after four cycles. After four cycles 21 patients (44%) were in complete remission and 8 (17%) in partial remission, resulting in an overall response rate of 61%. Factors significantly affecting overall response rate were early (