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利用放射性测量系统与克隆系统为患者选择化疗方案。

Selection of chemotherapy for patient treatment utilizing a radiometric versus a cloning system.

作者信息

Von Hoff D D, Forseth B J, Turner J N, Clark G M, Warfel L E

出版信息

Int J Cell Cloning. 1986 Jan;4(1):16-26. doi: 10.1002/stem.5530040103.

Abstract

From the 1950s to the 1970s, a number of in vitro systems that measured inhibition of glucose metabolism were used to predict the responsiveness of patients' tumors to chemotherapy. In vitro-in vivo correlations were excellent, with true positive predictions ranging from 68% to 96% and true negative predictions of 95% to 100%. The radiometric system is a new in vitro technique that measures the conversion of 14C-glucose to 14CO2. The system already has been utilized to screen prospective new antineoplastic agents for cytotoxicity. The present study was undertaken to determine if the radiometric system might be used to predict correctly the responsiveness of an individual patient's tumor to single-agent or combination-agent chemotherapy. Fifty-six tumor specimens were divided and tested for drug sensitivity in the radiometric system and a conventional human tumor clonning system. Overall, there was a significant correlation between in vitro and in vivo results for the conventional cloning system (P = 0.03). However, there was no significant relationship between in vitro and in vivo results for the radiometric system. The radiometric system consistently failed to predict the tumor's clinical sensitivity to single agents. A radiometric system is not useful in predicting the responsiveness of a patient's tumor to single agent chemotherapy and is not a replacement for the more biologically attractive human tumor cloning system.

摘要

从20世纪50年代到70年代,一些用于测量葡萄糖代谢抑制的体外系统被用来预测患者肿瘤对化疗的反应性。体外与体内的相关性非常好,真阳性预测范围为68%至96%,真阴性预测为95%至100%。放射性测量系统是一种新的体外技术,用于测量14C-葡萄糖向14CO2的转化。该系统已被用于筛选有前景的新型抗肿瘤药物的细胞毒性。本研究旨在确定放射性测量系统是否可用于正确预测个体患者肿瘤对单药或联合化疗的反应性。56个肿瘤标本被分开,并在放射性测量系统和传统的人类肿瘤克隆系统中进行药物敏感性测试。总体而言,传统克隆系统的体外和体内结果之间存在显著相关性(P = 0.03)。然而,放射性测量系统的体外和体内结果之间没有显著关系。放射性测量系统始终无法预测肿瘤对单药的临床敏感性。放射性测量系统在预测患者肿瘤对单药化疗的反应性方面没有用处,也不能替代更具生物学吸引力的人类肿瘤克隆系统。

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