Takahashi Toshiaki, Yamamoto Nobuyuki, Tamura Tomohide, Kunitoh Hideo, Nishiwaki Yutaka, Negoro Shunichi
Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777.
Oncol Lett. 2011 Nov;2(6):1033-1040. doi: 10.3892/ol.2011.398. Epub 2011 Aug 29.
Continuous erythropoietin receptor activator (C.E.R.A.) is an innovative erythropoiesis-stimulating agent with unique erythropoietin receptor activity and a prolonged half-life. C.E.R.A. is currently in development for the correction of anemia and stable hemoglobin (Hb) control at extended administration intervals in patients with cancer who are receiving chemotherapy. The purpose of this pharmacological study was to evaluate the pharmacokinetic (PK), pharmacodynamic (PD) and safety profiles of C.E.R.A. administered subcutaneously once every 3 weeks (Q3W) in lung cancer patients with anemia induced by chemotherapy. This open-label, multicenter study recruited 46 patients. Entry Hb levels were not more than 11.0 g/dl. Five dose levels of C.E.R.A. (2.1, 4.2, 6.3, 9 and 12 μg/kg) were tested in sequential cohorts of 8-11 patients for 12 weeks. The mean values for C.E.R.A half-life ranged from 143 to 247 h. The maximum serum concentration (C(max)) following the first administration of C.E.R.A. increased in proportion to the dose. The increase of Hb levels occurred in a dose-dependent manner. No serious adverse events reported as being related to C.E.R.A. were observed during the study period. Thrombovascular events were not observed in any patient. Anti-C.E.R.A antibodies were not detected in any patient. Thus, this pharmacological study confirmed the long half-life of C.E.R.A., thereby supporting subcutaneous administration of C.E.R.A. at the Q3W interval. PK and PD parameters demonstrated dose-proportionality over the range of doses tested in this study. Additionally, C.E.R.A. was generally well tolerated.
连续促红细胞生成素受体激活剂(C.E.R.A.)是一种具有独特促红细胞生成素受体活性和较长半衰期的新型促红细胞生成刺激剂。C.E.R.A.目前正处于研发阶段,用于纠正接受化疗的癌症患者的贫血并在延长给药间隔期稳定血红蛋白(Hb)水平。本药理学研究的目的是评估每3周皮下注射一次(Q3W)C.E.R.A.在化疗所致贫血的肺癌患者中的药代动力学(PK)、药效学(PD)和安全性。这项开放标签、多中心研究招募了46名患者。入选时Hb水平不超过11.0 g/dl。在8至11名患者的连续队列中对5个剂量水平的C.E.R.A.(2.1, 4.2, 6.3, 9和12 μg/kg)进行了为期12周的测试。C.E.R.A.的半衰期平均值在143至247小时之间。首次注射C.E.R.A.后的最大血清浓度(C(max))与剂量成比例增加。Hb水平的升高呈剂量依赖性。在研究期间未观察到与C.E.R.A.相关的严重不良事件。在任何患者中均未观察到血栓血管事件。在任何患者中均未检测到抗C.E.R.A.抗体。因此,本药理学研究证实了C.E.R.A.的长半衰期,从而支持每3周一次的C.E.R.A.皮下给药。在本研究测试的剂量范围内,PK和PD参数显示出剂量比例关系。此外,C.E.R.A.总体耐受性良好。