Sheehy P F, Fried J, Dowling M D, Clarkson B D
Cancer. 1975 Jul;36(1):203-10. doi: 10.1002/1097-0142(197507)36:1<203::aid-cncr2820360121>3.0.co;2-u.
The kinetics of cell proliferation were studied in a patient with lymphosarcoma in a leukemic phase both before treatment when the disease was very advanced and again at the earliest sign of bone marrow relapse following a drug-induced remission. During advanced disease, the pulse 3H-TdR labeling index (LI) was 11%, the mitotic index (MI) was 0.4% the growth fraction (GF) was 0.6, and the generation time (TG), as measured by the median grain count halving time, was estimated to be 160 hours. The patient went into remission for 25 days after a short course of therapy with prednisolone and arabinosylcytosine (Ara-C). During early relapsing disease, the LI was 17%; MI, 1.1%; GF, 1.0; and TG, 85 hours. The results of this study suggest that the rate of cell proliferation slows in leukemia as the tumor mass increases in volume, and that the slower growth is due to an increase in cell generation time, a decrease in the growth fraction, and an increased rate of spontaneous cell loss.
在一名处于白血病期的淋巴肉瘤患者中,研究了细胞增殖动力学。一次是在疾病非常严重的治疗前阶段,另一次是在药物诱导缓解后骨髓复发的最早迹象出现时。在疾病晚期,脉冲3H - 胸腺嘧啶核苷标记指数(LI)为11%,有丝分裂指数(MI)为0.4%,生长分数(GF)为0.6,通过中位颗粒计数减半时间测得的生成时间(TG)估计为160小时。该患者在接受泼尼松龙和阿糖胞苷(Ara - C)短疗程治疗后缓解了25天。在早期复发疾病期间,LI为17%;MI为1.1%;GF为1.0;TG为85小时。这项研究的结果表明,随着肿瘤体积在白血病中增大,细胞增殖速率减慢,且生长减慢是由于细胞生成时间增加、生长分数降低以及自发细胞丢失率增加所致。