New York University Cancer Institute, NYU Langone Medical Center, New York, NY, USA. O'
Semin Hematol. 2010 Apr;47 Suppl 1:S11-4. doi: 10.1053/j.seminhematol.2010.01.014.
Though peripheral T-cell lymphoma (PTCL) is an area of significant unmet therapeutic need, a number of new treatment options are available for patients, especially those with relapsed or refractory disease. A plethora of drugs are now in development for PTCL, but drugs that truly target novel disease biology are noticeably absent. Combinations of T-cell centric agents could produce novel platforms of therapy to replace the relatively ineffective CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone)-based regimens. Among agents with T-cell activity are the folate analog pralatrexate, histone deacetylase inhibitors (HDACi) like romidepsin, the proteasome inhibitor bortezomib, the immunomodulatory agent lenalidomide, the purine nucleoside phosphorylase (PNP) inhibitor forodesine, the nucleoside analog gemcitabine, and BH3-only mimetics like ABT-263 and ABT-737.
虽然外周 T 细胞淋巴瘤(PTCL)是一个存在重大未满足治疗需求的领域,但目前有许多新的治疗选择可供患者,尤其是那些复发或难治性疾病的患者。现在有大量的药物正在开发用于治疗 PTCL,但真正针对新型疾病生物学的药物却明显缺乏。以 T 细胞为中心的药物联合使用可能会产生新的治疗平台,以取代相对无效的基于 CHOP(环磷酰胺、多柔比星、长春新碱和泼尼松)的方案。具有 T 细胞活性的药物包括叶酸类似物普拉曲沙、组蛋白去乙酰化酶抑制剂(HDACi)如罗米地辛、蛋白酶体抑制剂硼替佐米、免疫调节剂来那度胺、嘌呤核苷磷酸化酶(PNP)抑制剂氟达拉滨、核苷类似物吉西他滨以及 BH3 仅模拟物如 ABT-263 和 ABT-737。