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多西氟尿苷:晚期胃肠道癌的一种活性药物。

Doxifluridine: an active agent in advanced gastrointestinal cancer.

作者信息

Di Bartolomeo M, Bajetta E, Somma L, Buzzoni R

机构信息

Division of Medical Oncology B, Istituto Nazionale per lo Studio e la Cura dei Tumori, Milan, Italy.

出版信息

Tumori. 1995 May-Jun;81(3 Suppl):147-50.

PMID:7571047
Abstract

BACKGROUND

The results of the use of chemotherapy in patients with advanced gastrointestinal malignancies have been disappointing. Complete responses are rare, and even partial responses are generally few with no benefit on survival. Since its introduction in clinical trials more than 30 years ago, fluorouracil has remained the most effective single agent in the treatment of these diseases. Doxifluridine is a new fluoropyrimidine derivative, that is converted into fluorouracil, its active component. Experimental data confirm cytotoxic selectivity for human tumor cells.

METHODS

Three trials have been conducted at the Istituto Nazionale Tumori of Milan, to evaluate the tolerability and efficacy of doxifluridine administered endovenously or orally in patients affected by different gastrointestinal neoplasms. The data will be discussed.

CONCLUSIONS

Our results indicate that doxifluridine may be superior to fluorouracil, the biochemical modulator as folinic acid seems to enhance its activity in colorectal patients. The oral schedule is feasible for home treatment.

摘要

背景

晚期胃肠道恶性肿瘤患者使用化疗的结果一直令人失望。完全缓解很少见,即使是部分缓解通常也很少,且对生存无益处。自30多年前引入临床试验以来,氟尿嘧啶一直是治疗这些疾病最有效的单一药物。去氧氟尿苷是一种新的氟嘧啶衍生物,可转化为其活性成分氟尿嘧啶。实验数据证实了对人类肿瘤细胞的细胞毒性选择性。

方法

在米兰国家肿瘤研究所进行了三项试验,以评估静脉或口服给予去氧氟尿苷对不同胃肠道肿瘤患者的耐受性和疗效。将对数据进行讨论。

结论

我们的结果表明,去氧氟尿苷可能优于氟尿嘧啶,亚叶酸作为生化调节剂似乎可增强其在结直肠癌患者中的活性。口服给药方案便于在家治疗。

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