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First published online October 17, 2007, 10.2967/jnumed.107.043489
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Comparison of 90Y-Ibritumomab Tiuxetan and 131I-Tositumomab in Clinical Practice

Heather A. Jacene*, Ross Filice*, Wayne Kasecamp and Richard L. Wahl

Russell H. Morgan Department of Radiology and Radiological Science, Division of Nuclear Medicine, Johns Hopkins University, Baltimore, Maryland


Figure 1
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FIGURE 1.  Platelet counts (A) and ANCs (B) vs. days from radioimmunotherapy are shown for each patient. Mean maximum percentage decline in platelet count was greater in 90Y-ibritumomab tiuxetan group than in 131I-tositumomab group (79% ± 17% vs. 63% ± 28%, P = 0.04). Mean maximum percentage decline in ANC from baseline to nadir was also higher in 90Y-ibritumomab tiuxetan group than in 131I-tositumomab group, but this difference was not statistically significant (75% ± 16% vs. 63% ± 29%, P = 0.09). Time from treatment to ANC nadir was shorter for 90Y-ibritumomab tiuxetan group than for 131I-tositumomab group (36 ± 9 vs. 46 ± 14 d, P = 0.01). Frequency of hematologic support after radioimmunotherapy was similar between 90Y-ibritumomab tiuxetan and 131I-tositumomab groups (P = 1.00, Fisher exact test). Seven patients in 90Y-ibritumomab tiuxetan group and 8 patients in 131I-tositumomab group required blood, platelets, or granulocyte-colony stimulating factor therapy, contributing to sharp upslopes in some curves.

 

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FIGURE 2.  Fourteen of 30 patients (47%) had response at 12 wk after radioimmunotherapy. Four had CR (13%) and 10 had PR (33%). Cumulative overall survival was significantly longer for patients who responded to radioimmunotherapy at 12 wk than for those who did not (P ≤ 0.05).

 

Figure 3
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FIGURE 3.  Overall survival did not significantly differ between patients who received 90Y-ibritumomab tiuxetan and those who received 131I-tositumomab.

 





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