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血管紧张素II(AII)诱导的不可切除胃癌高血压化疗(IHC):参考降期后的切除情况

Angiotensin II (AII) induced hypertension chemotherapy (IHC) for unresectable gastric cancer: with reference to resection after down staging.

作者信息

Sato H, Sugiyama K, Hoshi M, Urushiyama M, Ishizuka K

机构信息

Institute of Development, Aging, and Cancer, Tohoku University, Sendai, Japan.

出版信息

World J Surg. 1995 Nov-Dec;19(6):836-42. doi: 10.1007/BF00299780.

Abstract

Angiotensin II induced hypertension chemotherapy (IHC) is a drug delivery system for augmentation of anti-cancer effects on the experimental basis of the functional difference of microcirculation between tumor and normal tissue. Blood flow in tumor tissue increased selectively when the blood pressure was elevated by the infusion of angiotensin II. Two randomized controlled trials (RCT) for advanced gastric cancer using AFM regimen; a combination of adriamycin (ADM), 5-fluorouracil (5-FU), and mitomycin (MMC), showed increased response rate by IHC (response rate: IHC/non-IHC; 42.9% vs 10.5% in RCT-1, and 31.3% vs 6.7% in RCT-2, respectively). Toxicities were not different statistically between groups. In phase II for stage IVB gastric cancer patients (the criteria according to the General Rules of the Gastric Cancer Study of Japanese Research Society for Gastric Cancer), 5 complete response (CR) and 10 partial response (PR) (58%) were observed out of 26 unresectable cases without prior chemotherapy. Moreover, 5 of 15 responders could received curative gastrectomy and obtained conclusive down staging (19%). Here we discuss the role of enhancement of drug delivery for cancer chemotherapy on the basis of a series of clinical and experimental evidences.

摘要

血管紧张素II诱导高血压化疗(IHC)是一种基于肿瘤与正常组织微循环功能差异的增强抗癌效果的药物递送系统。通过输注血管紧张素II升高血压时,肿瘤组织中的血流会选择性增加。两项针对晚期胃癌使用AFM方案(阿霉素(ADM)、5-氟尿嘧啶(5-FU)和丝裂霉素(MMC)的联合方案)的随机对照试验(RCT)显示,IHC可提高缓解率(缓解率:RCT-1中IHC/非IHC分别为42.9%对10.5%,RCT-2中为31.3%对6.7%)。两组之间的毒性在统计学上无差异。在IVB期胃癌患者的II期试验中(根据日本胃癌研究学会胃癌研究总则的标准),在26例未经预先化疗的不可切除病例中,观察到5例完全缓解(CR)和10例部分缓解(PR)(58%)。此外,15例缓解者中有5例能够接受根治性胃切除术并实现确定性降期(19%)。在此,我们基于一系列临床和实验证据讨论增强药物递送在癌症化疗中的作用。

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