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口腔区域鳞状细胞癌的细胞动力学分析以及5-氟尿嘧啶与放疗联合治疗的效果。对肿瘤细胞同步化讨论的一项贡献。

Cell-kinetical analyses of squamous cell carcinomas of the oral region and the effect of a combined therapy of 5 fluorouracil and irradiation. A contribution to the discussion about tumorcell-synchronization.

作者信息

Helpap B, Herberhold C, Thelen M, Stiens R, Koch U

出版信息

Strahlentherapie. 1977 Nov;153(11):774-80.

PMID:73240
Abstract

Out of 180 incubations of human biopsies 33 were from patients with malignant tumors of the oral region. In 9 cases it was possible to analyse the cell cycle of the tumor cells with the double labeling in vitro method (3H and 14C-thymidine). Histologically the tumors were keratinizing squamous cell carcinomas with high labeling indices. The generation time of the tumor cells ranged from 20 to 130 hours. The length of the DNA synthesis phase varied between 7.3 and 17.9 hours. With the knowledge of the cell-kinetic data the patients received an infusion of 5 Fluorouracil throughout the length or parts of the calculated G 1 phase. At the end of the 5 FU infusion there was a constant two-hour pause and after the duration of the calculated DNA synthesis phase the tumors were irradiated with 150 rd per session. The treatment was repeated until a total dose of 6000 rd was achieved. Under the combined therapy of 5 FU and irradiation the inoperable keratinizing highly differentiated squamous cell carcinomas regressed extraordinarily fast. The patients were free of pain after a very short time. No vital tumor tissue was visible in control biopsies. Some patients remained without any tumor recurrence now more than 2 years after onset of therapy. In the discussion it is stressed that the reason for the successful treatment of highly differentiated squamous cell carcinomas with 5 Fluorouracil and subsequent irradiation is not easily explained, because recent experimental findings and impulsecytophotometrical studies on human biopsy material suggest that both the synergistic action of thecytostatic drug and the irradiation as well as an altered recruitment of the tumor cells are responsible for the clinical success rather than a synchronisation effect.

摘要

在对180份人体活检组织进行的培养中,有33份来自口腔区域恶性肿瘤患者。其中9例能够采用体外双标记法(3H和14C - 胸腺嘧啶核苷)分析肿瘤细胞的细胞周期。组织学检查显示,这些肿瘤为高标记指数的角化鳞状细胞癌。肿瘤细胞的增殖周期时间为20至130小时。DNA合成期的时长在7.3至17.9小时之间变化。根据细胞动力学数据,患者在计算出的G1期全程或部分时段接受5 - 氟尿嘧啶输注。在5 - 氟尿嘧啶输注结束时,有一个持续两小时的间歇期,在计算出的DNA合成期时长结束后,每次对肿瘤进行150拉德的照射。该治疗重复进行,直至达到6000拉德的总剂量。在5 - 氟尿嘧啶与放疗的联合治疗下,无法手术切除的高分化角化鳞状细胞癌消退异常迅速。患者在很短时间后就不再疼痛。对照活检中未见有活性的肿瘤组织。一些患者在治疗开始后已超过两年仍未出现任何肿瘤复发。在讨论中强调,用5 - 氟尿嘧啶及后续放疗成功治疗高分化鳞状细胞癌的原因并不容易解释,因为近期对人体活检材料的实验研究结果和脉冲细胞光度测定研究表明,细胞抑制药物与放疗的协同作用以及肿瘤细胞募集的改变是临床成功的原因,而非同步化效应。

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