TY - JOUR
T1 - Weekly versus twice weekly bortezomib given in conjunction with rituximab, in patients with recurrent follicular lymphoma, mantle cell lymphoma and Waldenström macroglobulinaemia
AU - Agathocleous, Agathoclis
AU - Rohatiner, Ama
AU - Rule, Simon
AU - Hunter, Hannah
AU - Kerr, Jonathan Paul
AU - Neeson, Susan M.
AU - Matthews, Janet
AU - Strauss, Sandra
AU - Montoto, Silvia
AU - Johnson, Peter
AU - Radford, John
AU - Lister, Andrew
PY - 2010/11
Y1 - 2010/11
N2 - The combination of bortezomib and rituximab was evaluated in patients with mantle cell lymphoma (MCL), follicular lymphoma (FL) and Waldenström macroglobulinaemia (WM), in a Phase I and later, a randomized Phase II study. In the randomized study, 42 patients with recurrent/refractory disease received either: bortezomib 1.3 mg/m2 on days 1, 4, 8 and 11 of a 3-week cycle with rituximab 375 mg/m2 on day 1 (21 patients) or: bortezomib 1.6 mg/m2 and rituximab on days 1, 8, 15 and 22 of a 5-week cycle (with rituximab being given only in cycles 1 and 4). Twenty-eight patients were withdrawn (toxicity 16, progression 7, and 'patient choice' 5). The main toxicities were neurological, gastro-intestinal and haematological. The overall response rate was 28/42(67%) and by histology: MCL 11/19, FL 8/15, and WM 9/10. Ten of 28 responding patients remained progression-free at 1-3.5 years. Toxicity and efficacy were equivalent between the two groups. The combination has significant toxicity but is effective, particularly in patients with WM. © 2010 Blackwell Publishing Ltd.
AB - The combination of bortezomib and rituximab was evaluated in patients with mantle cell lymphoma (MCL), follicular lymphoma (FL) and Waldenström macroglobulinaemia (WM), in a Phase I and later, a randomized Phase II study. In the randomized study, 42 patients with recurrent/refractory disease received either: bortezomib 1.3 mg/m2 on days 1, 4, 8 and 11 of a 3-week cycle with rituximab 375 mg/m2 on day 1 (21 patients) or: bortezomib 1.6 mg/m2 and rituximab on days 1, 8, 15 and 22 of a 5-week cycle (with rituximab being given only in cycles 1 and 4). Twenty-eight patients were withdrawn (toxicity 16, progression 7, and 'patient choice' 5). The main toxicities were neurological, gastro-intestinal and haematological. The overall response rate was 28/42(67%) and by histology: MCL 11/19, FL 8/15, and WM 9/10. Ten of 28 responding patients remained progression-free at 1-3.5 years. Toxicity and efficacy were equivalent between the two groups. The combination has significant toxicity but is effective, particularly in patients with WM. © 2010 Blackwell Publishing Ltd.
KW - B-cell malignancies
KW - Bortezomib
KW - Rituximab
U2 - 10.1111/j.1365-2141.2010.08340.x
DO - 10.1111/j.1365-2141.2010.08340.x
M3 - Article
C2 - 20880120
SN - 0007-1048
VL - 151
SP - 346
EP - 353
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 4
ER -