Patients with follicular lymphoma and a low tumor burden have a median over
all survival of more than 10 years. Toxic conventional chemotherapy regimen
s are inappropriate in these patients as they do not improve overall surviv
al and the patients do not require palliation of symptoms. However, as most
of these patients will ultimately die of their lymphoma, new therapies, wi
th curative intent, are required. Rituximab is a human-mouse chimeric monoc
lonal antibody that has shown efficacy in patients with non-Hodgkin's lymph
oma (NHL). The benign tolerability profile of rituximab makes it a suitable
candidate for first-line treatment of follicular NHL patients with a low t
umor burden. In a trial of 49 patients, 73% achieved a clinical response (2
6% complete response) with rituximab treatment. Molecular studies showed th
at 57% of patients achieved molecular remission (clearance of the bcl-2 mol
ecular translocation from the blood, evaluated by polymerase chain reaction
), 62% of these remaining bcl-2(-) far at least 1 year. There was a good co
rrelation between molecular and clinical responses, with patients failing t
o achieve a molecular response at higher risk of disease progression. Ritux
imab monotherapy is therefore an effective and well-tolerated treatment for
patients with low-grade lymphoma and a low tumor burden. [(C) 2001 Lippinc
ott Williams & Wilkins.].