Rituximab is a chimeric anti CD-20 monoclonal antibody containing human IgG
1 kappa constant regions, with murine variable regions. The anti-lymphoma e
ffects of Rituximab are probably due to complement and antibody-dependent c
ell-mediated cytotoxicity, and induction of apoptosis. Phase II trials have
demonstrated a strong activity of rituximab alone in indolent B non-Hodgki
n lymphoma, especially in patients with follicular lymphoma. The most utili
zed dose-schedule is 375 mg/m(2) weekly x 4. The association with chemother
apy or with interferon-alpha increases Rituximab efficacy. More recently, R
ituximab have showed activity also in diffuse large cell lymphoma, mantle c
ell lymphoma and in other B-malignancies. Good results have also been obtai
ned utilizing Rituximab for in vivo purging. However, we are still far from
having found a definite position for Rituximab in the treatment of lymphop
roliferative disorders. The aim of future studies should be to develop new
strategies that will hopefully produce the most effective Rituximab-based r
egimens in order to find the Rituximab key position in the treatment of B-m
alignancies (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.