Takizawa K, Harada M, Fujimaru J, Matsushiro N, Shima Y, Andoh I, Satoh M, Yokoo I, Iguchi T, Hirabayashi K
Department of Obstetrics and Gynecology, Tokyo Women's Medical College.
Nihon Sanka Fujinka Gakkai Zasshi. 1992 May;44(5):595-602.
Thirty-six courses of chemotherapy with cisplatin (CDDP) and sodium thiosulfate (STS) were performed in 31 patients with gynecologic cancer 2 weeks after operation under the hypertensive condition induced by angiotensin II (AT-II). One hundred-fifty mg of CDDP/body was intraperitoneally administered while the usual systolic blood pressure was increased to 130-140% by AT-II. The hypertension was maintained for 15 minutes after finishing CDDP infusion, then 8g of STS was intravenously infused immediately after the cessation of AT-II. The urinary Pt level measured 15 minutes after finishing CDDP infusion was extremely low at 1.37 +/- 0.47 micrograms/ml, in spite of the significantly high levels of plasma total Pt (7.83 +/- 0.85 micrograms/ml) and filtrable Pt (4.02 +/- 0.55 micrograms/ml). This suggests that, during renal vasoconstriction induced by AT-II, the renal blood flow as well as renal uptake of CDDP was decreased. Plasma filtrable Pt levels were measured at 15, 30, 60 and 120 minutes after intraperitoneal administration of CDDP. At 15 and 30 minutes a significantly higher blood concentration was found than in the control group (p less than 0.05). However, CDDP-induced toxicities of the bone marrow, liver, kidney and alimentary tract were not increased. The extreme vasoconstriction in the kidneys and other organs induced by AT-II might have protected these organs from the toxicities of CDDP despite the fact that STS infusion was delayed by 15 minutes after CDDP infusion. STS infused immediately after the cessation of AT-II could neutralize the CDDP preventing the occurrence of toxicities.(ABSTRACT TRUNCATED AT 250 WORDS)
在31例妇科癌症患者术后2周,于血管紧张素II(AT-II)诱导的高血压状态下,进行了36疗程顺铂(CDDP)和硫代硫酸钠(STS)化疗。在通过AT-II将通常的收缩压提高至130 - 140%时,腹腔内给予150mg/体的CDDP。在完成CDDP输注后,高血压维持15分钟,然后在AT-II停止后立即静脉输注8g的STS。尽管血浆总铂(7.83±0.85μg/ml)和可滤过铂(4.02±0.55μg/ml)水平显著升高,但在完成CDDP输注15分钟后测得的尿铂水平极低,为1.37±0.47μg/ml。这表明,在AT-II诱导的肾血管收缩期间,肾血流量以及CDDP的肾摄取量均降低。在腹腔内给予CDDP后的15、30、60和120分钟测量血浆可滤过铂水平。在15和30分钟时,发现血药浓度显著高于对照组(p<0.05)。然而,CDDP诱导的骨髓、肝脏、肾脏和消化道毒性并未增加。尽管在CDDP输注后STS输注延迟了15分钟,但AT-II诱导的肾脏和其他器官的极度血管收缩可能保护了这些器官免受CDDP的毒性。在AT-II停止后立即输注的STS可以中和CDDP,防止毒性的发生。(摘要截短于250字)