Tahara M, Sasaki Y
Division of GI Oncology/Digestive Endoscopy, National Cancer Center Hospital East, Kashiwa, Japan.
Gan To Kagaku Ryoho. 2000 Oct;27(11):1759-63.
During the last decade, advances in cell biology and molecular biology have produced molecular targets for cancer treatment, and many molecular targeted drugs, or "cytostatic agents," have been clinically evaluated. Dose limiting toxicities are not always observed with these drugs and there is little relationship between drug dose and biological effect. Therefore, the traditional strategy used in the clinical development of cytotoxic drugs may not be appropriate for evaluation of these cytostatic agents. In order to determine the optimum dose for these agents, new clinical strategies must be developed on the basis of the following considerations: 1. the relationship between the effective plasma concentration in preclinical data and mean trough plasma levels in clinical trials, 2. changes in plasma concentration in the tumor or expression of molecular targets according to dose escalation, and 3. application of surrogate markers for biological activity.
在过去十年中,细胞生物学和分子生物学的进展产生了癌症治疗的分子靶点,并且许多分子靶向药物或“细胞生长抑制剂”已进行了临床评估。使用这些药物时并不总是观察到剂量限制性毒性,并且药物剂量与生物学效应之间几乎没有关联。因此,细胞毒性药物临床开发中使用的传统策略可能不适用于评估这些细胞生长抑制剂。为了确定这些药物的最佳剂量,必须基于以下考虑因素制定新的临床策略:1. 临床前数据中的有效血浆浓度与临床试验中的平均谷值血浆水平之间的关系;2. 根据剂量递增,肿瘤中的血浆浓度变化或分子靶点的表达;3. 生物学活性替代标志物的应用。