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Original Article: Clinical

Phase 1 study of radiosensitization using bortezomib in patients with relapsed non-Hodgkin lymphoma receiving radioimmunotherapy with 131I-tositumomab

, , , , , , , , , , , , , , , & show all
Pages 342-346 | Received 05 Feb 2014, Accepted 13 Feb 2014, Published online: 17 Jun 2014
 

Abstract

Radioimmunotherapy (RIT) is effective treatment for indolent non-Hodgkin lymphomas (NHLs), but response durations are usually limited, especially in aggressive NHL. We hypothesized that administration of bortezomib as a radiosensitizer with RIT would be tolerable and improve efficacy in NHL. This phase 1 dose-escalation study evaluated escalating doses of bortezomib combined with 131I-tositumomab in patients with relapsed/refractory NHL. Twenty-five patients were treated. Treatment was well tolerated, with primarily hematologic toxicity. The maximum tolerated dose (MTD) was determined to be 0.9 mg/m2 bortezomib, in combination with a standard dose of 75 cGy 131I-tositumomab. Sixteen patients responded (64%), including 44% complete responses (CRs), with 82% CR in patients with follicular lymphoma (FL). At a median follow-up of 7 months, median progression-free survival was 7 months, and seven of 11 patients with FL remained in remission at a median of 22 months. In conclusion, bortezomib can be safely administered in combination with 131I-tositumomab with promising response rates.

Acknowledgements

R.L.E. was supported in part by the Charles, Lillian and Betty Neuwirth Clinical Scholar Award. P.J.C. and M.M. were partially supported by the following grant: Clinical Translational Science Center (CTSC) (UL1-TR000457-06). J.O. was partially supported by a grant from the Center to Reduce Cancer Health Disparity (R21 CA153177-03).

Potential conflict of interest

Disclosure forms provided by the authors are available with the full text of this article at www.informahealthcare.com/lal.

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