首页   按字顺浏览 期刊浏览 卷期浏览 Antitumor Effects of Internal Iliac Arterial Infusion of Plantinum Compounds in a Rabbi...
Antitumor Effects of Internal Iliac Arterial Infusion of Plantinum Compounds in a Rabbit Cervical Cancer Model

 

作者: HIROAKI ITAMOCHI,   JUNZO KIGAWA,   YUKIHISA MINAGAWA,   XIUSI CHENG,   MAKOTO OKADA,   NAOKI TERAKAWA,  

 

期刊: Obstetrics & Gynecology  (OVID Available online 1997)
卷期: Volume 89, issue 2  

页码: 286-290

 

ISSN:0029-7844

 

年代: 1997

 

出版商: OVID

 

数据来源: OVID

 

摘要:

ObjectiveTo compare three platinum compounds for their antitumor effects on cervical cancer after systemic and intraarterial infusion.MethodsAdult female rabbits with squamous cell carcinoma of the uterine cervix received infusion of 1.7 mg/kg cisplatin, 10 mg/kg carboplatin, or 6 mg/kg cis-diammine (glycolato) platinum (254-S) via the internal iliac artery or ear vein. Platinum concentrations in the tumor and tumor size were measured after internal iliac arterial or intravenous (IV) infusion with these platinum compounds.ResultsThe platinum concentration in the tumor after intra-arterial infusion was significantly higher than that after IV infusion for cisplatin. However, the tumor concentrations of platinum for carboplatin and 254-S did not differ between the infusion methods. The platinum concentration 20 minutes after IV infusion was significantly higher for 254-S than for cisplatin or carboplatin. The platinum concentration 7 days after intra-arterial infusion was significanlty higher with cisplatin than with carboplatin or 254-S. Tumor size 7 days after intra-arterial infusion was significantly smaller than that after IV infusion for cisplatin (1.85 ± 0.54 versus 5.60 ± 2.60 cm2;P< .05). Tumor size was significantly smaller with 254-S than with cisplatin or carboplatin using the IV infusion method (2.40 ± 0.21 cm2for 254-S, 5.60 ± 2.60 cm2for cisplatin, and 5.13 ± 1.59 cm2for carboplatin,P< .05).ConclusionsIntra-arterial infusion seems to be a suitable route of administration for cisplatin, whereas IV infusion appears to have an advantage for 254-S in the treatment of cervical cancer.

 

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