Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Haematologica. 2013 Jun;98(6):964-70. doi: 10.3324/haematol.2013.086207. Epub 2013 May 3.
This study assessed the safety and preliminary efficacy of escalated dose subcutaneous alemtuzumab in combination with rituximab in chronic lymphocytic leukemia. Twenty-eight patients with relapsed refractory chronic lymphocytic leukemia were treated on four dosing cohorts of weekly rituximab at 375 mg/m(2) and alemtuzumab doses that started at 30 mg three times per week and escalated to weekly dosing over four weeks, culminating with 90 mg weekly. One dose limiting toxicity of a rituximab infusion reaction was seen in cohort 2, but the regimen was otherwise well tolerated without evidence of differential toxicity by cohort. The overall response rate by National Cancer Institute-Working Group criteria was 61%, and the rate of complete bone marrow response was 43%, most of whom were negative for minimal residual disease. The addition of CT scan evaluation per International Workshop on Chronic Lymphocytic Leukemia 2008 criteria reduced the overall response rate to 14%. Median overall survival was 35 months, with 12 patients able to proceed to stem cell transplantation. Pharmacokinetic studies showed that chronic lymphocytic leukemia involving more than 80% of the bone marrow at study start was associated with lower trough concentrations of alemtuzumab and rituximab, and that higher trough serum concentrations of alemtuzumab were associated with complete bone marrow clearance. We conclude that escalated subcutaneous doses of alemtuzumab given weekly are well tolerated and result in excellent bone marrow clearance of chronic lymphocytic leukemia, helping patients to proceed to stem cell transplantation. This study is registered at ClinicalTrials.gov (Identifier:00330252).
本研究评估了递增剂量皮下注射阿仑单抗联合利妥昔单抗治疗慢性淋巴细胞白血病的安全性和初步疗效。28 例复发难治性慢性淋巴细胞白血病患者接受了四个剂量队列的治疗,每周给予 375mg/m2 的利妥昔单抗和起始剂量为 30mg、每周三次的阿仑单抗,四周后增至每周剂量,最终剂量为 90mg 每周。在队列 2 中观察到一种利妥昔单抗输注反应的剂量限制毒性,但该方案耐受性良好,各队列间无差异毒性证据。根据国家癌症研究所工作组标准,总体缓解率为 61%,完全骨髓缓解率为 43%,其中大多数患者微小残留病为阴性。按照慢性淋巴细胞白血病国际研讨会 2008 标准进行 CT 扫描评估后,总体缓解率降至 14%。中位总生存期为 35 个月,有 12 例患者能够进行干细胞移植。药代动力学研究表明,研究开始时骨髓受累超过 80%的慢性淋巴细胞白血病患者阿仑单抗和利妥昔单抗的谷浓度较低,而阿仑单抗的血清谷浓度较高与完全骨髓清除有关。我们得出结论,每周给予递增剂量的皮下阿仑单抗耐受性良好,可显著清除慢性淋巴细胞白血病,有助于患者进行干细胞移植。本研究在 ClinicalTrials.gov 注册(标识符:00330252)。