A multicentre, phase II trial of ofatumumab monotherapy in relapsed/progressive diffuse large B-cell lymphoma

被引:40
作者
Coiffier, Bertrand [1 ]
Radford, John [2 ,3 ]
Bosly, Andre [4 ]
Martinelli, Giovanni [5 ]
Barca, Gabriela [6 ]
Davies, Andrew [7 ]
Decaudin, Didier [8 ,9 ]
Gallop-Evans, Eve [10 ]
Padmanabhan-Iyer, Swaminathan [11 ]
Van Eygen, Koen [12 ]
Wu, Ka Lung [13 ]
Gupta, Ira V. [14 ]
Lin, Thomas S. [14 ]
Goldstein, Nancy [15 ]
Jewell, Roxanne C. [15 ]
Winter, Paul [16 ]
Lisby, Steen [17 ]
机构
[1] Hosp Civils Lyon, Serv Hematol, Lyon, France
[2] Christie NHS Fdn Trust, Manchester, Lancs, England
[3] Univ Manchester, Manchester, Lancs, England
[4] Clin Univ UCL Mt Godinne, Serv Hematol, Yvoir, Belgium
[5] Ist Europeo Oncol, Div Ematoncol, Milan, Italy
[6] Coltea Clin Hosp, Dept Hematol, Bucharest, Romania
[7] Univ Southampton, Canc Res UK Ctr, Southampton, Hants, England
[8] Inst Curie, Dept Med Oncol, Paris, France
[9] Inst Curie, Dept Translat Res, Paris, France
[10] Velindre Canc Ctr, Dept Clin Oncol, Cardiff, S Glam, Wales
[11] Univ Texas Hlth Sci Ctr San Antonio, Inst Drug Dev, San Antonio, TX 78229 USA
[12] AZ Groeninge, Oncol Ctr, Kortrijk, Belgium
[13] Ziekenhuis Stuivenberg, Dept Hematol, Antwerp, Belgium
[14] GlaxoSmithKline, Collegeville, PA USA
[15] GlaxoSmithKline, Res Triangle Pk, NC USA
[16] GlaxoSmithKline, London, England
[17] Genmab, Copenhagen, Denmark
关键词
haematological malignancies; immunotherapy; lymphoid malignancies; non-Hodgkin lymphoma; diffuse large B-cell lymphoma; REFRACTORY FOLLICULAR LYMPHOMA; ANTI-CD20; MONOCLONAL-ANTIBODY; ELDERLY-PATIENTS; RITUXIMAB; CHOP; CD20;
D O I
10.1111/bjh.12537
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This international, multicentre phase II study was conducted to assess ofatumumab, a human anti-CD20 monoclonal antibody, in patients with relapsed/progressive diffuse large B-cell lymphoma (DLBCL) who were ineligible for autologous stem cell transplantation (TI) or who had relapse/progression after transplantation (PT). Eighty-one patients received ofatumumab 300mg intravenously (IV) on Day 1, followed by seven weekly IV infusions of 1000mg. Patients in the TI and PT groups had received a median of 3 (range, 1-7) and 5 (range, 2-7) prior therapies, respectively. One-third of patients did not respond to the last prior therapy, and 53% had failed two or more rituximab-containing therapies. Overall response rate was 13% for the TI group (seven partial responses) and 8% for the PT group (two complete responses). Median progression-free survival was 2 center dot 6 months, and median duration of response was 9 center dot 5 months. The most common Grade 3-4 adverse events were neutropenia (11%), leucopenia (6%), lymphopenia (6%) and thrombocytopenia (6%). Sixteen deaths have been reported, with disease progression as the most common cause of death. In conclusion, ofatumumab monotherapy was well tolerated and provided clinical benefit to some DLBCL patients in this study. This trial was registered at www.clinicaltrials.gov (NCT00622388).
引用
收藏
页码:334 / 342
页数:9
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