| |
|
Headlines:
|
 |
Back
to index
Yttrium-90-labeled ibritumomab regimen
Abstract: Randomized controlled trial of yttrium-90-labeled ibritumomab
tiuxetan radioimmunotherapy versus rituximab immunotherapy for patients
with relapsed or refractory low-grade, follicular, or transformed B-cell
non-Hodgkin's lymphoma.
PURPOSE: Radioimmunotherapy combines biologic and radiolytic mechanisms
to target and destroy tumor cells, thus offering a needed therapeutic alternative
for refractory non-Hodgkin's lymphoma (NHL) patients. This phase III randomized
study compares the novel radioimmunotherapy yttrium-90 ((90)Y) ibritumomab
tiuxetan with a control immunotherapy, rituximab, in 143 patients with relapsed
or refractory low-grade, follicular, or transformed CD20(+) transformed
NHL. PATIENTS AND METHODS: Patients received either a single intravenous
(IV) dose of (90)Y ibritumomab tiuxetan 0.4 mCi/kg (n = 73) or rituximab
375 mg/m(2) IV weekly for four doses (n = 70). The radioimmunotherapy group
was pretreated with two rituximab doses (250 mg/m(2)) to improve biodistribution
and one dose of indium-111 ibritumomab tiuxetan for imaging and dosimetry.
The primary end point, overall response rate (ORR), was assessed by an independent,
blinded, lymphoma expert panel. RESULTS: ORR was 80% for the (90)Y ibritumomab
tiuxetan group versus 56% for the rituximab group (P =.002). Complete response
(CR) rates were 30% and 16% in the (90)Y ibritumomab tiuxetan and rituximab
groups, respectively (P =.04). An additional 4% achieved an unconfirmed
CR in each group. Kaplan-Meier estimated median duration of response was
14.2 months in the (90)Y ibritumomab tiuxetan group versus 12.1 months in
the control group (P =.6), and time to progression was 11.2 versus 10.1
months (P =.173) in all patients. Durable responses of > or = 6 months were
64% versus 47% (P =.030). Reversible myelosuppression was the primary toxicity
noted with (90)Y ibritumomab tiuxetan. CONCLUSION: Radioimmunotherapy with
(90)Y ibritumomab tiuxetan is well tolerated and produces statistically
and clinically significant higher ORR and CR compared with rituximab alone.
References
Witzig TE, Gordon LI, Cabanillas F, Czuczman MS, Emmanouilides C, Joyce
R, Pohlman BL, Bartlett NL, Wiseman GA, Padre N, Grillo-Lopez AJ, Multani
P, White CA. Randomized controlled trial of yttrium-90-labeled ibritumomab
tiuxetan radioimmunotherapy versus rituximab immunotherapy for patients
with relapsed or refractory low-grade, follicular, or transformed B-cell
non-Hodgkin's lymphoma. J Clin Oncol. 2002 May 15;20(10):2453-63.

|
|
|
|
Are you a doctor or a nurse?
Do you want to join the Doctors Lounge online medical community?
Participate in editorial activities (publish, peer review, edit) and
give a helping hand to the largest online community of patients.
Click on the link below to see the requirements:
Doctors Lounge Membership
Application |
|
| Regimen |
|
| A single intravenous (IV) dose
of (90)Y ibritumomab tiuxetan 0.4 mCi/kg. |
|
|
| |
|
|
| |
Summary |
|
| |
Overall Response
Rate |
|
| |
Progression
Free Survival |
|
| |
Overall Survival |
|
| |
Toxicity |
|
| |
|
|
|
|