Rose P G, Koolemans-Beynen A, Boutselis J G, Minton J P, Milo G E
Am J Obstet Gynecol. 1987 Mar;156(3):730-4. doi: 10.1016/0002-9378(87)90088-3.
To evaluate the effect of improved growth rates of ovarian cancers in the human tumor stem cell assay and its value in predicting clinical chemotherapy response, we studied 59 assays in 54 patients. A total of 81.6% of solid specimens and 85.7% of ascites specimens were successfully cultured and yielded an overall growth rate of 82.9%. Simultaneous primary and metastatic cultures were concordant for chemosensitivity in 80% (n = 16). The patients were evaluated for previous chemotherapy, residual volume of tumor, histologic type, and grade, and these were not statistically different between clinical responders and nonresponders. In vivo-in vitro correlations were made in 27 patients and yielded a predictive response of 13% and predictive resistance of 86% at 70% colony inhibition and 31% and 71% at 50% colony inhibition. Improved growth rates therefore did not result in better predictive correlations. The reported experience in ovarian cancer is summarized and the current status of the human tumor stem cell assay is reviewed.
为评估在人肿瘤干细胞试验中提高卵巢癌生长率的效果及其在预测临床化疗反应中的价值,我们研究了54例患者的59次试验。81.6%的实体标本和85.7%的腹水标本成功培养,总体生长率为82.9%。同时进行的原发灶和转移灶培养在化疗敏感性方面的一致性为80%(n = 16)。对患者既往化疗情况、肿瘤残留体积、组织学类型和分级进行评估,临床反应者和无反应者之间这些指标无统计学差异。对27例患者进行了体内-体外相关性分析,在集落抑制率为70%时,预测反应率为13%,预测耐药率为86%;在集落抑制率为50%时,预测反应率为31%,预测耐药率为71%。因此,提高生长率并未带来更好的预测相关性。本文总结了卵巢癌的相关报道经验,并综述了人肿瘤干细胞试验的现状。