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

被引:8
作者
Elstrom, Rebecca L. [1 ]
Ruan, Jia [1 ]
Christos, Paul J. [2 ]
Martin, Peter [1 ]
Lebovic, Daniel [4 ]
Osborne, Joseph [3 ]
Goldsmith, Stanley [3 ]
Greenberg, June [1 ]
Furman, Richard R. [1 ]
Avram, Anca [5 ]
Putman, Ryan [4 ]
Chapman, Erica [4 ]
Mazumdar, Madhu [2 ]
Griffith, Kent [6 ]
Coleman, Morton [1 ]
Leonard, John P. [1 ]
Kaminski, Mark S. [4 ]
机构
[1] Weill Cornell Med Coll, Div Hematol Oncol, Dept Med, New York, NY USA
[2] Weill Cornell Med Coll, Dept Publ Hlth, Div Biostat & Epidemiol, New York, NY USA
[3] Weill Cornell Med Coll, Dept Radiol, Div Nucl Med, New York, NY USA
[4] Univ Michigan, Sch Med, Dept Med, Div Hematol Oncol, Ann Arbor, MI 48104 USA
[5] Univ Michigan, Sch Med, Div Nucl Med, Dept Radiol, Ann Arbor, MI USA
[6] Univ Michigan, Sch Med, Dept Biostat, Ann Arbor, MI USA
关键词
Lymphoma; radioimmunotherapy; radiosensitization; proteasome; ANTI-CD20; MONOCLONAL-ANTIBODY; IODINE I-131 TOSITUMOMAB; LATE-ONSET TOXICITIES; LOW-GRADE; IBRITUMOMAB TIUXETAN; MULTIPLE-MYELOMA; MANTLE CELL; THERAPY; EFFICACY; TRIALS;
D O I
10.3109/10428194.2014.914195
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 I-131-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/m(2) bortezomib, in combination with a standard dose of 75 cGy I-131-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 I-131-tositumomab with promising response rates.
引用
收藏
页码:342 / 346
页数:5
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