Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-chou, Mizuho-ku, Nagoya, Aichi 467-8601, Japan.
Int J Hematol. 2011 Nov;94(5):443-52. doi: 10.1007/s12185-011-0941-5. Epub 2011 Oct 13.
Adult T-cell leukemia-lymphoma (ATL) has a very poor prognosis. Since there currently are limited treatment options for ATL patients, several novel agents are being developed and tested clinically. Antibody therapy against ATL was initially started with interleukin-2 receptor α-subunit, CD25, as a target molecule in the late 1980s, and is currently ongoing. CC chemokine receptor 4 (CCR4) was postulated as a novel molecular target in ATL antibody therapy, and humanized anti-CCR4 mAb (KW-0761), whose Fc region was defucosylated to enhance antibody-dependent cellular cytotoxicity, was developed. A phase I study of KW-0761 in relapsed ATL and peripheral T-cell lymphoma was started in 2006, and a subsequent phase II study was completed in 2010. KW-0761 showed a clinically meaningful antitumor activity in patients with relapsed ATL, with an acceptable toxicity profile. The prognosis of ATL patients should be improved in the near future with clinical applications of novel treatment strategies, including those involving KW-0761 and other promising antibody therapies targeting CD25 or CD30.
成人 T 细胞白血病/淋巴瘤(ATL)预后极差。由于目前 ATL 患者的治疗选择有限,因此正在开发和临床测试几种新型药物。20 世纪 80 年代末,针对 ATL 患者的抗体治疗最初以白细胞介素-2 受体 α 亚基(CD25)为靶点分子开始,目前仍在进行中。CC 趋化因子受体 4(CCR4)被认为是 ATL 抗体治疗的新型分子靶点,开发了人源化抗 CCR4 mAb(KW-0761),其 Fc 区去岩藻糖基化以增强抗体依赖性细胞毒性。2006 年开始了 KW-0761 在复发 ATL 和外周 T 细胞淋巴瘤中的 I 期研究,并于 2010 年完成了后续的 II 期研究。KW-0761 在复发 ATL 患者中显示出有临床意义的抗肿瘤活性,且毒性可接受。随着包括 KW-0761 在内的新型治疗策略的临床应用,包括针对 CD25 或 CD30 的其他有前途的抗体疗法,ATL 患者的预后将在不久的将来得到改善。