Abstract
The aim of this study was to determine the maximum tolerated dose (MTD) and to explore the clinical response to 177Lu-DOTA-rituximab in the treatment of patients with relapsed follicular, mantle cell, or other indolent lymphomas such as marginal zone lymphoma. Methods: To evaluate the MTD, we adjusted the dosage of the radiopharmaceutical according to body surface area (BSA). Results: The MTD using 177Lu-DOTA-rituximab was 1,665 MBq/m2 of BSA. Thrombocytopenia and leukopenia were the dose-limiting toxicities. Significant anemia occurred only at dose level 7 (1,850 MBq/m 2 of BSA). We observed the nadir of platelets after a median of 36 d from treatment and the nadir of granulocytes after a median of 50 d. Median time to recovery to the next lower grade of toxicity was 7 d. Nonhematologic toxicity was negligible. We observed clinical responses at all dose levels and for all lymphoma entities. Some of the responses were durable; the longest follow-up is currently over 8 y. At present, 11 patients are alive and 8 patients are disease-free. Conclusion: Our results demonstrate the safety and feasibility of 177Lu-DOTA-rituximab treatment for the lymphoma entities tested in this study. © 2013 by the Society of Nuclear Medicine.
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Forrer, F., Oechslin-Oberholzer, C., Campana, B., Herrmann, R., Maecke, H. R., Mueller-Brand, J., & Lohri, A. (2013). Radioimmunotherapy with 177Lu-DOTA-Rituximab: Final results of a phase i/ii study in 31 patients with relapsing follicular, mantle cell, and other indolent B-Cell lymphomas. Journal of Nuclear Medicine, 54(7), 1045–1052. https://doi.org/10.2967/jnumed.112.115170
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