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实验室化学敏感性测试在为个体患者选择癌症化疗方案中的作用。

Role of laboratory chemosensitivity testing in the selection of cancer chemotherapy for individual patients.

作者信息

Selby P J, Raghavan D

出版信息

J Clin Pathol. 1981 May;34(5):455-63. doi: 10.1136/jcp.34.5.455.

Abstract

Recently several assays have been developed which allow the growth of colonies from cell suspensions prepared from human tumour biopsy specimens. It has been suggested that such assays will provide a reliable means of measuring the chemosensitivity of human tumours for predicting the response to treatment in patients. We have briefly reviewed the previous, largely unsuccessful, attempts at chemosensitivity testing and the potential place of the new assays. The measurement of the survival of clonogenic tumour cells after cytotoxic treatment probably reflects to some extent the survival of cells which in vivo are capable of proliferating to repopulate and regrow the tumour. This endpoint therefore has advantages over alternatives that do not directly measure reproductive cell death, and the assays also have the advantage of suppressing the growth of many non-malignant cells found in tumours. However, technical problems such as the preparation of cell suspensions and the artificial nature of the drug exposure phase of the assays have not been completely overcome and the plating efficiencies remain low in most systems. Work with model systems such as human tumour xenografts tends to support the usefulness of the assays but also highlights some difficulties. Clinical studies of chemosensitivity testing are in progress and initial results are encouraging but inconclusive.

摘要

最近已经开发出几种检测方法,这些方法能够使源自人类肿瘤活检标本制备的细胞悬液形成菌落。有人提出,此类检测方法将提供一种可靠的手段来测量人类肿瘤的化学敏感性,从而预测患者对治疗的反应。我们简要回顾了以往在化学敏感性检测方面大多未成功的尝试以及新检测方法的潜在作用。细胞毒性处理后克隆形成性肿瘤细胞存活率的测定在一定程度上可能反映了体内能够增殖以重新填充和使肿瘤再生的细胞的存活率。因此,该终点相对于不直接测量生殖细胞死亡的其他方法具有优势,并且这些检测方法还具有抑制肿瘤中发现的许多非恶性细胞生长的优势。然而,诸如细胞悬液的制备以及检测中药物暴露阶段的人为性质等技术问题尚未完全克服,并且在大多数系统中接种效率仍然较低。对诸如人类肿瘤异种移植等模型系统的研究倾向于支持这些检测方法的实用性,但也突出了一些困难。化学敏感性检测的临床研究正在进行中,初步结果令人鼓舞但尚无定论。

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本文引用的文献

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Cell Biol Int Rep. 1980 May;4(5):479-86. doi: 10.1016/0309-1651(80)90035-1.
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