Tubiana M
Int J Radiat Oncol Biol Phys. 1982 Sep;8(9):1471-89. doi: 10.1016/0360-3016(82)90607-1.
Development of the study of human tumor cell kinetics during the past decades has deepened our understanding of the natural history of human cancers. Mathematical models based on the data which have been accumulated may help to evaluate, for the various types of human tumors, the time during their growth that the dissemination process occurred and to calculate the size distribution of the subclinical metastases at the time of treatment of the primary tumor. The perturbations caused by radiotherapy and chemotherapy are complex and include reassortment of surviving cells and repopulation. Currently it appears difficult in clinical practice to take advantage of cell reassortment while the differences in the rate and in the duration of repopulation between normal and neoplastic tissues are exploited in most therapeutic regimens. A better knowledge of cell and tissue kinetics following treatment may help to optimize the treatment scheduling in particular during combined administration of radiotherapy and chemotherapy. The study of the kinetics of proliferation in normal tissue has shown the existence of several types of inhibitory and stimulatory humoral factors. These, when purified, can be used to manipulate the proliferation of critical normal tissues in order to protect them during the administration of cell cycle specific drug or to accelerate their regeneration after treatment.
在过去几十年里,人类肿瘤细胞动力学研究的发展加深了我们对人类癌症自然史的理解。基于已积累数据的数学模型可能有助于评估各类人类肿瘤在生长过程中发生播散的时间,并计算在原发性肿瘤治疗时亚临床转移灶的大小分布。放疗和化疗所引起的扰动很复杂,包括存活细胞的重新分布和再增殖。目前在临床实践中似乎难以利用细胞重新分布,而大多数治疗方案利用的是正常组织和肿瘤组织在再增殖速率和持续时间上的差异。更好地了解治疗后细胞和组织的动力学,可能有助于优化治疗方案安排,尤其是在放疗和化疗联合应用期间。对正常组织增殖动力学的研究表明存在几种抑制性和刺激性体液因子。这些因子纯化后,可用于调控关键正常组织的增殖,以便在给予细胞周期特异性药物时保护它们,或在治疗后加速其再生。