Bleehen N M, Newman H V, Rampling R P, Ramsay J R, Roberts J T, Bedford P, Nethersell A B
University Department, Addenbrooke's Hospital, Cambridge, UK.
Br J Cancer. 1995 Sep;72(3):766-8. doi: 10.1038/bjc.1995.407.
Piritrexim is a lipid-soluble drug which is as effective an inhibitor of dihydrofolate reductase as methotrexate. Phase I and II studies have indicated activity in some tumour types. Because of its lipophilicity we have conducted a phase II study in recurrent high-grade malignant glioma (grades III and IV). Twenty-seven patients were treated with 25 mg p.o. three times daily for five consecutive days, repeated weekly, with provision for dose escalation or reduction according to toxicity. Five patients received less than 4 weeks' treatment because of disease progression or death. Twenty-two patients were evaluable for response. One complete and one partial response was seen (duration 262+ and 241+ weeks) and 13 patients had static disease for a median duration of 13 weeks (range 7-35). The major toxicity was myelosuppression. This response rate of 9% of evaluable patients is much lower than that seen for some conventionally used drugs and we conclude that piritrexim is unlikely to be of value in the management of high-grade gliomas.
吡曲克辛是一种脂溶性药物,它作为二氢叶酸还原酶抑制剂的效果与甲氨蝶呤相当。I期和II期研究表明其在某些肿瘤类型中具有活性。由于其亲脂性,我们对复发性高级别恶性胶质瘤(III级和IV级)进行了一项II期研究。27例患者口服25毫克,每日三次,连续五天,每周重复一次,并根据毒性情况调整剂量增减。5例患者因疾病进展或死亡接受治疗时间不足4周。22例患者可评估疗效。观察到1例完全缓解和1例部分缓解(持续时间分别为262+周和241+周),13例患者病情稳定,中位持续时间为13周(范围7 - 35周)。主要毒性为骨髓抑制。可评估患者的这一缓解率为9%,远低于一些传统使用药物的缓解率,我们得出结论,吡曲克辛在高级别胶质瘤的治疗中不太可能有价值。