Sigal Darren S, Saven Alan
Division of Hematology/Oncology, Scripps Clinic, 10666 N. Torrey Pines Road, M/S 217 La Jolla, CA 92037, USA.
Expert Rev Anticancer Ther. 2008 Apr;8(4):535-45. doi: 10.1586/14737140.8.4.535.
Before the advent of rationally designed targeted antineoplastic therapies, cladribine was identified as a lymphocyte-specific cytotoxic agent. Cladribine is a purine nucleoside analogue that is resistant to cellular catabolism. Through diverse mechanisms, cladribine is equally toxic to dividing and nondividing cells, making it highly active in indolent lymphoproliferative diseases. In clinical practice, cladribine is mostly used in the treatment of hairy cell leukemia and Waldenström's macroglobulinemia. However, its remarkable activity in follicular lymphoma and other indolent non-Hodgkin's lymphoma subtypes has not been more widely appreciated. Cladribine compares favorably to other standard treatments for these conditions. Future Phase III clinical studies should incorporate cladribine into multiagent chemotherapy programs to more fully evaluate its potential in indolent non-Hodgkin's lymphoma.
在合理设计的靶向抗肿瘤疗法出现之前,克拉屈滨被确定为一种淋巴细胞特异性细胞毒性药物。克拉屈滨是一种对细胞分解代谢具有抗性的嘌呤核苷类似物。通过多种机制,克拉屈滨对分裂和非分裂细胞均具有同等毒性,使其在惰性淋巴细胞增殖性疾病中具有高度活性。在临床实践中,克拉屈滨主要用于治疗毛细胞白血病和华氏巨球蛋白血症。然而,其在滤泡性淋巴瘤和其他惰性非霍奇金淋巴瘤亚型中的显著活性尚未得到更广泛的认可。与这些病症的其他标准治疗方法相比,克拉屈滨具有优势。未来的III期临床研究应将克拉屈滨纳入多药化疗方案中,以更全面地评估其在惰性非霍奇金淋巴瘤中的潜力。