Atacicept in relapsed/refractory multiple myeloma or active Waldenstrom's macroglobulinemia: a phase I study

被引:61
作者
Rossi, J-F [1 ,3 ,4 ,5 ]
Moreaux, J. [1 ,3 ]
Hose, D. [2 ]
Requirand, G. [1 ]
Rose, M. [5 ]
Rouille, V. [5 ]
Nestorov, I. [6 ]
Mordenti, G. [7 ]
Goldschmidt, H. [2 ]
Ythier, A. [7 ]
Klein, B. [1 ,3 ,4 ]
机构
[1] INSERM, U847, Montpellier, France
[2] Univ Klinikum Heidelberg, Med Klin & Poliklin 5, Heidelberg, Germany
[3] CHU Montpellier, CIC Biotherapie BT 509, Montpellier, France
[4] Univ Montpellier 1, F-34006 Montpellier, France
[5] CHU Montpellier, Dept Haematol & Clin Oncol, Montpellier, France
[6] ZymoGenetics Inc, Clin Dev, Seattle, WA USA
[7] Merck KGaA, Clin Dev, Merck Serono SA, Darmstadt, Germany
关键词
atacicept; multiple myeloma; Waldenstrom's macroglobulinemia; BLyS; APRIL; MEMORY B-CELLS; INTERNATIONAL WORKSHOP; AUTOIMMUNE-DISEASE; PLASMA-CELLS; BAFF-R; TACI; APRIL; GROWTH; EXPRESSION; SURVIVAL;
D O I
10.1038/sj.bjc.6605241
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Advanced multiple myeloma ( MM) and Waldenstrom's macroglobulinemia (WM) are incurable B-cell malignancies. This is the first full clinical report of atacicept, a fusion protein that binds to and neutralises the B-cell survival factors, B-lymphocyte stimulator ( BLyS) and A proliferation-inducing ligand (APRIL), in MM and WM. METHODS: In this open-label phase-I study, 16 patients with advanced disease ( 12 MM, 4 WM) received one cycle of five once-weekly subcutaneous injections of atacicept (2, 4, 7 or 10 mg kg(-1)). Patients with stable disease after cycle 1 entered an extension study ( either two additional cycles ( 2, 4 and 7 mg kg(-1) cohorts) or 15 consecutive weekly injections of atacicept 10 mg kg(-1)). RESULTS: Atacicept was well tolerated, systemically and locally; the maximum tolerated dose was not identified. Of 11 patients with MM who completed initial treatment, five patients were progression-free after cycle 1 and four patients were progression-free after extended therapy. Of four patients with WM, three patients were progression-free after cycle 1. Consistent with atacicept's mechanism of action, polyclonal immunoglobulin isotypes and total B cells were reduced. Bone-marrow density, myeloma cell numbers and plasma concentrations of soluble CD138 also decreased. CONCLUSION: Atacicept is well tolerated in patients with MM and WM, and shows clinical and biological activity consistent with its mechanism of action. British Journal of Cancer (2009) 101, 1051-1058. doi:10.1038/sj.bjc.6605241 www.bjcancer.com (C) 2009 Cancer Research UK
引用
收藏
页码:1051 / 1058
页数:8
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