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本妥昔单抗维达汀治疗 CD30+淋巴瘤。

Brentuximab vedotin for the treatment of CD30+ lymphomas.

机构信息

Washington University, St Louis School of Medicine, St Louis, MO 63110, USA.

出版信息

Immunotherapy. 2011 Apr;3(4):475-85. doi: 10.2217/imt.11.15.

Abstract

Brentuximab vedotin is a novel antibody-drug conjugate consisting of the anti-CD30 antibody cAC10 chemically conjugated to monomethylauristatin E, a potent antimicrotubule agent. Preliminary response rates of 75% in relapsed/refractory Hodgkin's lymphoma and 87% in relapsed/refractory systemic anaplastic large-cell lymphoma were recently reported in large Phase II trials. Brentuximab vedotin is well tolerated with manageable side effects including peripheral sensory neuropathy. This antibody-drug conjugate is currently under investigation in numerous clinical trials, including in combination with front-line chemotherapy for high-risk Hodgkin's lymphoma and in a placebo-controlled, Phase III trial for patients with Hodgkin's lymphoma at high risk for residual disease following autologous stem cell transplant. The impressive response rates and limited toxicity of brentuximab vedotin are very promising for relapsed/refractory patients with few treatment options. In addition, the possibilities for incorporation into front-line therapies for both Hodgkin's lymphoma and systemic anaplastic large-cell lymphoma are intriguing.

摘要

本妥昔单抗维迪是一种新型抗体药物偶联物,由抗 CD30 抗体 cAC10 与单甲基澳瑞他汀 E 化学偶联而成,后者是一种强效的微管抑制剂。最近的两项大型 II 期临床试验报告,该药在复发/难治性霍奇金淋巴瘤中的初步缓解率为 75%,在复发/难治性系统性间变性大细胞淋巴瘤中的缓解率为 87%。本妥昔单抗维迪具有良好的耐受性,副作用可管理,包括周围感觉神经病。该药目前正在多项临床试验中进行研究,包括与一线化疗联合用于高危霍奇金淋巴瘤,以及与安慰剂对照的 III 期临床试验,用于自体干细胞移植后有残留疾病高风险的霍奇金淋巴瘤患者。对于治疗选择有限的复发/难治性患者,本妥昔单抗维迪的显著缓解率和有限的毒性非常有希望。此外,将其纳入霍奇金淋巴瘤和系统性间变性大细胞淋巴瘤的一线治疗的可能性也很有吸引力。

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