University of Connecticut, Department of Internal Medicine, 263 Farmington Avenue, Farmington, CT 06030, USA.
Expert Opin Pharmacother. 2013 Mar;14(4):515-23. doi: 10.1517/14656566.2013.770474. Epub 2013 Feb 14.
Pralatrexate is a novel antifolate agent that belongs to the class of 10-deazaaminopterins. Its clinical efficacy as a single agent in relapsed or refractory peripheral T-cell lymphoma (PTCL) has been established in randomized trials. Treatment with this agent is generally safe.
This paper discusses the pharmacokinetics and efficacy of pralatrexate in T-cell lymphoma in clinical trials. In addition, the authors highlight pralatrexate-associated adverse effects and safety concerns.
Although established as a second-line therapy, pralatrexate offers a clinical benefit to less than one-third of patients with PTCL. In addition, toxicity of this agent can be significant, especially mucositis, immunosuppression and thrombocytopenia. Currently, the potential synergy between pralatrexate and other agents in T-cell lymphoma is being explored in a number of studies. These results will hopefully prove the validity of this approach, leading to improved quantity of life in these patients, with an acceptable comfort index.
普拉曲沙是一种新型叶酸拮抗剂,属于 10-去氮叶酸类药物。在随机试验中已确立其作为单一药物治疗复发或难治性外周 T 细胞淋巴瘤(PTCL)的临床疗效。该药物的治疗通常是安全的。
本文讨论了普拉曲沙在临床试验中治疗 T 细胞淋巴瘤的药代动力学和疗效。此外,作者还强调了普拉曲沙相关的不良反应和安全问题。
虽然已被确立为二线治疗药物,但普拉曲沙对不到三分之一的 PTCL 患者具有临床获益。此外,该药物的毒性可能非常显著,尤其是粘膜炎、免疫抑制和血小板减少症。目前,许多研究正在探索普拉曲沙与 T 细胞淋巴瘤其他药物之间的协同作用。这些结果有望证实这种方法的有效性,从而提高这些患者的生活质量,并具有可接受的舒适度指数。