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同步持续静脉输注化疗和放疗。

Concomitant continuous infusion chemotherapy and radiation.

作者信息

Rotman M, Aziz H

机构信息

Department of Radiation Oncology, State University of New York, Brooklyn 11203-2098.

出版信息

Cancer. 1990 Feb 1;65(3 Suppl):823-35. doi: 10.1002/1097-0142(19900201)65:3+<823::aid-cncr2820651330>3.0.co;2-9.

Abstract

Attempts to duplicate the cytotoxic effect of oxygen on radioresistant tissues spurred a search by radiation oncologists for other radiosensitizing techniques. This led to large-scale investigations using neutrons and other heavy particle radiations, hyperthermia, altered fractionation schedules, and the systemic use of the halogenated pyrimidines and the electron-affinic compounds. Unfortunately, the promise that the nitroimidazole compounds would selectively sensitize the radioresistant tumor cells and prove to be an effective systemic agent has not been borne out in clinical trials thus far. Existing pharmokinetic and cytokinetic studies have suggested that continuous infusion chemotherapy given concomitantly (CCIC) with irradiation (RT) acts synergistically, resulting in a significant increase in tumor cell killing. These observations have been supported by clinical research studies treating certain epithelial cancers that have resulted in considerably higher locoregional control rates and improved survival. Although initially used in treatment of only advanced or inoperable epithelial carcinomas, CCIC and RT are now being employed in the treatment of lower staged cancers as an organ-sparing procedure. Carcinoma of the anus treated by anteroposterior (AP) resection alone have reported 5-year survival rates of 30% to 60%. CCIC and RT using 5-fluorouracil (5-FU) and mitomycin C have achieved a local control rate of 90% to 100% and a 5-year survival rate of 80% to 86% with sphincter preservation in 90% of these cases. The 5-year survival rate in advanced urinary bladder carcinoma is 25% to 30% for either radiation or surgery and 42% when combined in a preoperative radiation schedule. Using 5-FU CCIC and RT, the local control rate of transitional cell carcinoma of the bladder has been 71% to 86% with a 5-year survival of 62%. 5-FU CCIC and cisplatin and RT used in the treatment of Stages III and IV carcinoma of the cervix yields a locoregional control of 74% compared with the radiation alone local control of 63% for Stage III and 30% for Stage IV disease. Advanced head and neck and paranasal sinus carcinomas treated by cisplatin CCIC and RT show improved tumor clearance even in the presence of bone destruction. A complete response rate of 87% has been reported with the use of cisplatin CCIC and hyperfractionated radiation. Hyperfractionated radiation also appears to improve the local control of advanced head and neck cancers over patients treated with single fractions of radiation with 66% surviving at 22 months.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

试图复制氧气对放射抗拒组织的细胞毒性作用,促使放射肿瘤学家寻找其他放射增敏技术。这引发了对中子和其他重粒子辐射、热疗、改变分割方案以及全身使用卤代嘧啶和电子亲和化合物的大规模研究。不幸的是,迄今为止,硝基咪唑化合物能选择性地使放射抗拒的肿瘤细胞增敏并被证明是一种有效的全身用药的前景,在临床试验中尚未得到证实。现有的药代动力学和细胞动力学研究表明,与放疗(RT)同时进行的持续输注化疗(CCIC)具有协同作用,可显著增加肿瘤细胞杀伤。这些观察结果得到了治疗某些上皮癌的临床研究的支持,这些研究导致局部区域控制率显著提高,生存率得到改善。尽管CCIC和RT最初仅用于治疗晚期或无法手术的上皮癌,但现在它们正被用于治疗较低分期的癌症,作为一种保留器官的方法。仅通过前后位(AP)切除治疗的肛门癌,其5年生存率报告为30%至60%。使用5-氟尿嘧啶(5-FU)和丝裂霉素C的CCIC和RT,在90%的病例中实现了90%至100%的局部控制率和80%至86%的5年生存率,且保留了括约肌。晚期膀胱癌单纯放疗或手术的5年生存率为25%至30%,术前放疗联合手术时为42%。使用5-FU CCIC和RT,膀胱移行细胞癌的局部控制率为71%至86%,5年生存率为62%。用于治疗III期和IV期宫颈癌的5-FU CCIC和顺铂及RT,局部区域控制率为74%,而单独放疗时III期疾病的局部控制率为63%,IV期疾病为30%。通过顺铂CCIC和RT治疗的晚期头颈癌和鼻窦癌,即使存在骨质破坏,肿瘤清除情况也有所改善。使用顺铂CCIC和超分割放疗报告的完全缓解率为87%。与单次分割放疗的患者相比,超分割放疗似乎也改善了晚期头颈癌的局部控制,22个月时生存率为66%。(摘要截选至400字)

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