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[通过人肿瘤干细胞分析(HTSCA)确定的妇科恶性肿瘤的化疗敏感性]

[Chemotherapy sensitivity of gynecologic malignancies determined by the human tumor stem cell assay (HTSCA)].

作者信息

Obi S

出版信息

Nihon Sanka Fujinka Gakkai Zasshi. 1987 May;39(5):792-8.

PMID:3598274
Abstract

HTSCA was used to study the chemotherapy sensitivity of gynecological malignant tumors. 34 specimens were obtained from 32 patients. 11 of the 34 specimens (32%) yielded a sufficient number of colonies for testing. On these, 51 separate drug assays were done, each at the 1/10 peak plasma level. 20 drugs were identified as active among 51 drugs tested. Clinical correlations of sensitivity (S) and resistance (R) were studied in 6 patients treated with combination therapies, including drugs selected on the basis of in vitro sensitivity. (formula; see text) We conclude that HTSCA can aid in identifying active drugs for use in designing treatment protocols. However, because of difficulty in preparing a single cell suspension, and the small proportion of tumors suitable for testing, HTSCA will not be used in routine drug sensitivity testing until these drawbacks are eliminated.

摘要

采用人肿瘤单细胞克隆药敏分析法(HTSCA)研究妇科恶性肿瘤的化疗敏感性。从32例患者身上获取了34个标本。34个标本中有11个(32%)产生了足够数量的集落用于检测。在这些标本上,进行了51次单独的药物检测,每次检测药物浓度均为血浆峰值水平的1/10。在所检测的51种药物中,有20种被确定为有活性。对6例接受联合治疗的患者进行了敏感性(S)和耐药性(R)的临床相关性研究,联合治疗药物是根据体外敏感性选择的。(公式;见正文)我们得出结论,HTSCA有助于识别用于设计治疗方案的活性药物。然而,由于制备单细胞悬液存在困难,且适合检测的肿瘤比例较小,在这些缺点消除之前,HTSCA不会用于常规药物敏感性检测。

相似文献

1
[Chemotherapy sensitivity of gynecologic malignancies determined by the human tumor stem cell assay (HTSCA)].[通过人肿瘤干细胞分析(HTSCA)确定的妇科恶性肿瘤的化疗敏感性]
Nihon Sanka Fujinka Gakkai Zasshi. 1987 May;39(5):792-8.
2
Use of the human tumor stem cell assay to study chemotherapy sensitivity in cancer of the cervix.
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Potentials and drawbacks of the human tumor stem cell assay.人类肿瘤干细胞检测的潜力与缺陷
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In vitro chemotherapy testing of gynecologic tumors: basis for planning therapy?妇科肿瘤的体外化疗测试:治疗规划的依据?
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Limitations of drug sensitivity testing in soft agar for clinical management of patients with ovarian carcinoma.用于卵巢癌患者临床管理的软琼脂药敏试验的局限性。
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