Rossi J-F, Moreaux J, Hose D, Requirand G, Rose M, Rouillé V, Nestorov I, Mordenti G, Goldschmidt H, Ythier A, Klein B
CIC-Biothérapie BT 509, CHU Montpellier, Montpellier, France.
Br J Cancer. 2009 Oct 6;101(7):1051-8. doi: 10.1038/sj.bjc.6605241.
Advanced multiple myeloma (MM) and Waldenström'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.
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)).
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.
Atacicept is well tolerated in patients with MM and WM, and shows clinical and biological activity consistent with its mechanism of action.
晚期多发性骨髓瘤(MM)和华氏巨球蛋白血症(WM)是无法治愈的B细胞恶性肿瘤。这是关于阿他西普(一种融合蛋白,可结合并中和B细胞存活因子、B淋巴细胞刺激因子(BLyS)和增殖诱导配体(APRIL))在MM和WM中的首份完整临床报告。
在这项开放标签的I期研究中,16例晚期疾病患者(12例MM,4例WM)接受了一个周期的阿他西普皮下注射,每周一次,共五次(剂量为2、4、7或10 mg·kg⁻¹)。第1周期后病情稳定的患者进入扩展研究(另外两个周期(2、4和7 mg·kg⁻¹队列)或连续15周每周注射阿他西普10 mg·kg⁻¹)。
阿他西普在全身和局部耐受性良好;未确定最大耐受剂量。11例完成初始治疗的MM患者中,5例在第1周期后无进展,4例在扩展治疗后无进展。4例WM患者中,3例在第1周期后无进展。与阿他西普的作用机制一致,多克隆免疫球蛋白亚型和总B细胞减少。骨髓密度、骨髓瘤细胞数量和可溶性CD138的血浆浓度也降低。
阿他西普在MM和WM患者中耐受性良好,并显示出与其作用机制一致的临床和生物学活性。