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皮下注射阿仑单抗用于晚期复发慢性淋巴细胞白血病患者且不进行剂量递增的II期研究。

Phase II study of subcutaneous alemtuzumab without dose escalation in patients with advanced-stage, relapsed chronic lymphocytic leukaemia.

作者信息

Karlsson Claes, Lundin Jeanette, Kimby Eva, Kennedy Ben, Moreton Paul, Hillmen Peter, Osterborg Anders

机构信息

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Br J Haematol. 2009 Jan;144(1):78-85. doi: 10.1111/j.1365-2141.2008.07451.x. Epub 2008 Oct 30.

Abstract

This phase II study (n = 20) aimed to evaluate type, severity and duration of side-effects and efficacy following subcutaneous (SC) alemtuzumab, without dose-escalation, in advanced-stage relapsed chronic lymphocytic leukaemia (CLL) patients. Alemtuzumab 30 and 3 mg was administered SC simultaneously day 1, followed by 30 mg three times per week. Injection-site-reactions were recorded every 6-24 h until resolved using National Cancer Institute criteria and a new skin toxicity subscale. The first doses of 30 mg and 3 mg produced injection-site-reactions (all but one were grade 1/2) in 13/20 and 9/20 patients, respectively. The second dose (on day 3) resulted in skin-reactions in 10/20 patients and the third, fourth, fifth and sixth injections produced reactions in 6/20, 1/20, 2/20 and 0/20 patients, respectively. Mild "flu-like" symptoms occurred during week 1 in 10/20 patients. All side-effects had subsided by the sixth dose. 15/20 patients (75%) responded (12 partial responses, three complete responses) with a median time-to-treatment-failure of 20 months. Symptomatic cytomegalovirus-reactivation occurred in 6/20 patients. Two deaths occurred: one bacterial pneumonia and one adenovirus-infection. The present study showed how to assess cutaneous-toxicity in detail and that 30 mg alemtuzumab SC administered upfront was well tolerated. Optimized alemtuzumab therapy in properly selected patients may result in high efficacy even in advanced CLL. Our results need to be confirmed in extended studies.

摘要

这项II期研究(n = 20)旨在评估晚期复发慢性淋巴细胞白血病(CLL)患者皮下注射(SC)阿仑单抗后,在不进行剂量递增的情况下副作用的类型、严重程度和持续时间以及疗效。第1天同时皮下注射30 mg和3 mg阿仑单抗,随后每周3次注射30 mg。使用美国国立癌症研究所标准和新的皮肤毒性子量表,每6 - 24小时记录一次注射部位反应,直至症状消退。30 mg和3 mg的首剂分别在13/20和9/20的患者中产生了注射部位反应(除1例为1/2级外,其余均为1/2级)。第2剂(第3天)使10/20的患者出现皮肤反应,第3、4、5和6次注射分别使6/20、1/20、2/20和0/20的患者出现反应。10/20的患者在第1周出现轻度“流感样”症状。所有副作用在第6剂时均已消退。15/20的患者(75%)有反应(12例部分缓解,3例完全缓解),治疗失败的中位时间为20个月。6/20的患者出现有症状的巨细胞病毒再激活。发生了2例死亡:1例细菌性肺炎和1例腺病毒感染。本研究展示了如何详细评估皮肤毒性,并且预先皮下注射30 mg阿仑单抗耐受性良好。在适当选择的患者中优化阿仑单抗治疗即使在晚期CLL中也可能产生高效。我们的结果需要在扩展研究中得到证实。

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