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阿仑单抗治疗齐多夫定/干扰素-α难治性成人T细胞白血病后持久的血液学完全缓解及HTLV-1病毒载量抑制

Durable hematologic complete response and suppression of HTLV-1 viral load following alemtuzumab in zidovudine/IFN-{alpha}-refractory adult T-cell leukemia.

作者信息

Mone Andrew, Puhalla Shannon, Whitman Susan, Baiocchi Robert A, Cruz Julio, Vukosavljevic Tamara, Banks Amy, Eisenbeis Charles F, Byrd John C, Caligiuri Michael A, Porcu Pierluigi

机构信息

Division of Hematology-Oncology, Department of Internal Medicine, The Comprehensive Cancer Center, The Ohio State University, Columbus, 43210, USA.

出版信息

Blood. 2005 Nov 15;106(10):3380-2. doi: 10.1182/blood-2005-01-0335. Epub 2005 Aug 2.

Abstract

Adult T-cell leukemia (ATL) is a highly chemoresistant and usually fatal T-cell malignancy due to the human T-cell lymphotropic virus-1 (HTLV-1). After chemotherapy failure, antiretrovirals and interferon-alpha (IFN-alpha) produce brief responses followed by progression and death. More effective agents and new approaches to detect and treat minimal residual disease are needed. ATL cells express CD52, the target of the antibody alemtuzumab, which is active in a preclinical model of ATL and is cytotoxic for p53-deficient cells. A patient with refractory chronic ATL in transformation achieved longer than a 1-year complete hematologic response following 12 weeks of outpatient subcutaneous alemtuzumab. Persistent suppression of HTLV-1 viral load, even at recovery of T cells, after alemtuzumab and efficient in vitro complement-mediated cytotoxicity of primary ATL cells with mutated TP53 were observed. The unprecedented response and the profound suppression of HTLV-1 viral load observed in this patient suggest that further clinical investigation of alemtuzumab in ATL is warranted.

摘要

成人T细胞白血病(ATL)是一种由人类T细胞嗜淋巴细胞病毒1型(HTLV-1)引起的具有高度化疗耐药性且通常致命的T细胞恶性肿瘤。化疗失败后,抗逆转录病毒药物和α干扰素(IFN-α)只能产生短暂反应,随后病情进展并导致死亡。因此需要更有效的药物以及检测和治疗微小残留病的新方法。ATL细胞表达CD52,这是抗体阿仑单抗的靶点,阿仑单抗在ATL临床前模型中具有活性,对p53缺陷细胞具有细胞毒性。一名难治性慢性转化型ATL患者在接受门诊皮下注射阿仑单抗12周后,获得了超过1年的完全血液学缓解。在阿仑单抗治疗后,即使在T细胞恢复时,也观察到HTLV-1病毒载量持续受到抑制,并且原发性ATL细胞对突变型TP53具有高效的体外补体介导的细胞毒性。该患者出现的前所未有的缓解以及对HTLV-1病毒载量的深度抑制表明,有必要对阿仑单抗在ATL中的应用进行进一步的临床研究。

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