Awwad H K, Barsoum M, El Merzabani M, Omar S, El Badawy S, Ezzat S, El Baki H A, Zaki A
Am J Clin Oncol. 1983 Feb;6(1):91-7.
Twenty-one patients with Stage III or IV head and neck epidermoid cancer were treated by a three-fractions per day radiotherapy regime plus misonidazole (MIS). An initial course of 45 Gy was used, spread over 12 days and divided into 30 fractions 1.5 Gy each with a 3-hour interval between fractions. A daily MIS dose of 1 g/m2 was given 2 hours prior to the first fraction. A boost dose of 22.5 Gy/5 days was given to 10 patients, 4 weeks after the initial course, using the same fractionation scheme. The local acute and chronic reactions were acceptable. Eight patients suffered mild reversible peripheral neuropathy. The mean MIS blood level corresponded to an enhancement ratio of about 1.45. The 1-year disease-free survival rate was 9/21 and was significantly greater in patients receiving the boost irradiation. The control rate of nodal disease was encouraging. Based on this pilot study, a prospective trial is proposed aiming at testing the usefulness of MIS in MDF regimens in advanced head and neck cancer, either as the sole method of treatment or as a preoperative measure.
21例Ⅲ期或Ⅳ期头颈部表皮样癌患者接受了每天三次分割的放疗方案加米索硝唑(MIS)治疗。采用初始疗程45 Gy,持续12天,分为30次分割,每次1.5 Gy,分割间隔3小时。在第一次分割前2小时给予每日MIS剂量1 g/m²。10例患者在初始疗程4周后,采用相同的分割方案给予22.5 Gy/5天的追加剂量。局部急性和慢性反应均可接受。8例患者出现轻度可逆性周围神经病变。MIS的平均血药浓度对应的增强比约为1.45。1年无病生存率为9/21,接受追加照射的患者该生存率显著更高。淋巴结疾病的控制率令人鼓舞。基于这项初步研究,提出了一项前瞻性试验,旨在测试MIS在晚期头颈部癌的多分次放疗方案中作为唯一治疗方法或术前措施的有效性。