We evaluated clinical activity of 90Yttrium-ibritumomab (90Y-ibritumomab) tiuxetan in extranodal marginal-zone lymphoma. From May 2004 to April 2011, 30 patients affected by relapsed/refractory marginal-zone lymphoma\u2014arisen at any extranodal site\u2014received 90Y-ibritumomab tiuxetan at the activity of 0.4mCi/kg. Median age was 57 years. At time of treatment, 13 out of 30 patients had disseminated disease (stage III/IV). All patients had received a previous treatment with a maximum of 7. Overall response rate was 90%: 23 patients achieved a complete response (77%); partial response occurred in 4 patients (13%), stable disease in 2 patients (7%) and 1 progression (3%). With a median follow-up of 5.3 years, median time to relapse was no...
To assess the efficacy of radioimmunotherapy (RIT) with 90yttrium-ibrutinib-tiuxetan (90Y-IT) in man...
Background. Based on historical data we reviewed our hospital clinical database to analyse our updat...
Purpose We conducted an international, randomized, phase III trial to evaluate the efficacy and safe...
We evaluated clinical activity of 90Yttrium-ibritumomab (90Y-ibritumomab) tiuxetan in extranodal mar...
(90) Yttrium ((90) Y)-Ibritumomab-Tiuxetan combines the targeting advantage of a monoclonal antibody...
A prospective, multicenter, nonrandomized phase 2 trial was conducted to evaluate the efficacy and s...
90-Yttrium-ibritumomab-tiuxetan is approved for treatment of rituximab-relapsed/refractory CD20+ fol...
Matthew S McKinney, Anne W Beaven Division of Hematologic Malignancies, Department of Medicine, Duke...
Updated results are presented after a median follow-up of 7.3 years from the phase III First-Line In...
We previously demonstrated that yt-trium-90 (Y-90) ibritumomab tiuxetan (Zevalin) radioimmunotherapy...
90-yttrium-ibritumomab-tiuxetan is approved for treatment of rituximab-relapsed/refractory CD201 fol...
none16siPolish Lymphoma Research Group performed a phase-II trial to test whether (90)Y ibritumomab ...
We retrospectively evaluated our single-center clinical experi-ence with 90Y-ibritumomab tiuxetan an...
Targeted radioimmunotherapy with 90Y-labeled ibritumomab tiuxetan is a novel therapeutic approach f...
Radioimmunotherapy, targeting the CD20 antigen, in B-cell lymphoma has clearly demonstrated efficacy...
To assess the efficacy of radioimmunotherapy (RIT) with 90yttrium-ibrutinib-tiuxetan (90Y-IT) in man...
Background. Based on historical data we reviewed our hospital clinical database to analyse our updat...
Purpose We conducted an international, randomized, phase III trial to evaluate the efficacy and safe...
We evaluated clinical activity of 90Yttrium-ibritumomab (90Y-ibritumomab) tiuxetan in extranodal mar...
(90) Yttrium ((90) Y)-Ibritumomab-Tiuxetan combines the targeting advantage of a monoclonal antibody...
A prospective, multicenter, nonrandomized phase 2 trial was conducted to evaluate the efficacy and s...
90-Yttrium-ibritumomab-tiuxetan is approved for treatment of rituximab-relapsed/refractory CD20+ fol...
Matthew S McKinney, Anne W Beaven Division of Hematologic Malignancies, Department of Medicine, Duke...
Updated results are presented after a median follow-up of 7.3 years from the phase III First-Line In...
We previously demonstrated that yt-trium-90 (Y-90) ibritumomab tiuxetan (Zevalin) radioimmunotherapy...
90-yttrium-ibritumomab-tiuxetan is approved for treatment of rituximab-relapsed/refractory CD201 fol...
none16siPolish Lymphoma Research Group performed a phase-II trial to test whether (90)Y ibritumomab ...
We retrospectively evaluated our single-center clinical experi-ence with 90Y-ibritumomab tiuxetan an...
Targeted radioimmunotherapy with 90Y-labeled ibritumomab tiuxetan is a novel therapeutic approach f...
Radioimmunotherapy, targeting the CD20 antigen, in B-cell lymphoma has clearly demonstrated efficacy...
To assess the efficacy of radioimmunotherapy (RIT) with 90yttrium-ibrutinib-tiuxetan (90Y-IT) in man...
Background. Based on historical data we reviewed our hospital clinical database to analyse our updat...
Purpose We conducted an international, randomized, phase III trial to evaluate the efficacy and safe...