Final Report of a Phase 2 Clinical Trial of Lenalidomide Monotherapy for Patients With T-Cell Lymphoma

被引:84
作者
Toumishey, Ethan [1 ]
Prasad, Angeli [2 ]
Dueck, Greg [3 ]
Chua, Neil [2 ]
Finch, Daygen [3 ]
Johnston, James [4 ]
van der Jagt, Richard [5 ]
Stewart, Doug [6 ]
White, Darrell [7 ]
Belch, Andrew [2 ]
Reiman, Tony [1 ,8 ]
机构
[1] Dalhousie Univ, Dept Med, St John, NB, Canada
[2] Univ Alberta, Dept Oncol, Edmonton, AB, Canada
[3] British Columbia Canc Agcy, Ctr Southern Interior, Med Oncol, Kelowna, BC, Canada
[4] Univ Manitoba, Dept Med, Winnipeg, MB, Canada
[5] Univ Ottawa, Dept Med, Ottawa, ON, Canada
[6] Univ Calgary, Dept Med, Calgary, AB, Canada
[7] Dalhousie Univ, Dept Med, Halifax, NS, Canada
[8] Univ New Brunswick, Canadian Canc Soc Res Chair, Fredericton, NB, Canada
关键词
lenalidomide; T-cell lymphoma; immunomodulation; phase 2 clinical trial; SINGLE-AGENT LENALIDOMIDE; NON-HODGKIN-LYMPHOMA; DIAGNOSED MULTIPLE-MYELOMA; OPEN-LABEL; II TRIAL; IN-VIVO; THERAPY; DEXAMETHASONE; COMBINATION; THALIDOMIDE;
D O I
10.1002/cncr.29103
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUNDPatients with T-cell lymphomas face a poorer prognosis compared with patients with B-cell lymphomas. New therapeutic approaches need to be developed to improve outcomes for these patients. METHODSForty patients with recurrent and refractory T-cell lymphomas other than mycosis fungoides and patients with untreated T-cell lymphoma who were not candidates for combination chemotherapy were prescribed oral lenalidomide at a dose of 25 mg daily on days 1 to 21 of each 28-day cycle, with standardized dose reductions for toxicity. The primary endpoint was overall response rate (ORR), and secondary endpoints were complete and partial response rates, progression-free survival (PFS), overall survival (OS), and safety. The authors also determined duration of response (DoR). RESULTSA total of 40 patients were enrolled in the current study; 1 patient was subsequently deemed ineligible. The ORR was 10 of 39 patients (26%); 3 patients (8%) achieved complete responses and 7 patients achieved partial responses. Three patients had stable disease for 5 cycles. The median OS was 12 months (range <1 month to 69 months), the median PFS was 4 months (range, <1 month to 50 months), and the median DoR was 13 months (range 2 months to 37 months), including 5 responses that lasted >1 year. Toxicity was in keeping with the known safety profile of lenalidomide. Among the patients who had recurrent/refractory peripheral T-cell lymphoma (29 patients), the ORR was 24%, the median OS was 12 months, the median PFS was 4 months, and the median DoR was 5 months (range, 2 months to 37 months). CONCLUSIONSIn the current study, the use of oral lenalidomide monotherapy demonstrated clinically relevant efficacy among patients with systemic T-cell lymphomas. It appears to have excellent potential as an agent in combination therapy for patients with T-cell lymphoma. Cancer 2015;121:716-723. (c) 2014 American Cancer Society. Lenalidomide monotherapy demonstrates clinically relevant activity in patients with T-cell lymphoma and has a good safety profile. Lenalidomide has excellent potential as an agent in combination therapy for patients with T-cell lymphoma.
引用
收藏
页码:716 / 723
页数:8
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