Dobrowsky Werner, Huigol Nagraj G, Jayatilake Ranapala S, Kizilbash Noor-I-Alam, Okkan Sait, Kagiya V Tsutomu, Tatsuzaki Hideo
Northern Centre for Cancer Treatment, Newcastle General Hospital, Newcastle upon Tyne, UK.
Radiother Oncol. 2007 Jan;82(1):24-9. doi: 10.1016/j.radonc.2006.11.007. Epub 2006 Dec 11.
AK-2123, a nitrotriazole hypoxic cell sensitizer, has reportedly improved results in head and neck cancers, uterine cervical cancers and other solid tumours when added to radical radiotherapy. A prospectively randomised trial was initiated by the International Atomic Energy Agency (IAEA) evaluating AK-2123 and radiotherapy in treatment of uterine cervical cancer stage III and IV.
A total of 462 patients were randomised from 8 centres. Patients from four centres were excluded due to lack of accrual, closing of the centre and insufficient documentation and reporting. The final study population consisted of 333 patients who were randomised between May 1995 and December 1998. Patients were randomised to either standard radical treatment (radiation therapy alone, RT) or standard radical radiotherapy and additional administration of AK-2123 (RT+AK-2123). The total dose of 45-50.8 Gy was delivered by 20-28 fractions in an overall time of 4-5 1/2 weeks, with further dose escalation by brachytherapy or external beam. In the study arm, patients received 0.6 g/sqm AK-2123 by intravenous administration before external beam radiotherapy, treating with AK-2123 on alternate days (e.g. Monday-Wednesday-Friday) during the entire course of external beam therapy. Following exclusion of 7 patients who did not undergo treatment, a total of 326 patients remained for evaluation.
The rate of local tumour control was significantly higher in the group after radiotherapy and additional administration of AK-2123. Local tumour control was 61% (95/155) after AK-2123 and 46% (79/171) after radiotherapy alone (p=0.006). The actuarial survival at 60 months was 57% after RT+AK-2123, compared to 41% after RT (Log Rank p=0.01). AK-2123 did neither increase gastro-intestinal toxicity nor was it attributed to any haematological toxicity. A mild peripheral toxicity (Grade 1: 13% and Grade 2: 2%) usually completely reversible was infrequently seen after AK-2123 administration.
We conclude that the addition of AK-2123 to radical radiotherapy significantly increases local tumour control and survival in advanced squamous cell cancer of the uterine cervix without the addition of any major toxicity.
据报道,硝基三唑类乏氧细胞增敏剂AK - 2123与根治性放疗联合应用时,在头颈部癌、子宫颈癌及其他实体瘤的治疗中取得了更好的疗效。国际原子能机构(IAEA)启动了一项前瞻性随机试验,评估AK - 2123与放疗联合治疗III期和IV期子宫颈癌的效果。
共有462例患者从8个中心随机入组。4个中心的患者因入组不足、中心关闭以及记录和报告不充分而被排除。最终研究人群包括1995年5月至1998年12月期间随机分组的333例患者。患者被随机分为标准根治性治疗组(单纯放射治疗,RT)或标准根治性放疗联合额外给予AK - 2123组(RT + AK - 2123)。总剂量45 - 50.8 Gy分20 - 28次给予,总疗程为4 - 5.5周,可通过近距离放疗或外照射进一步增加剂量。在研究组中,患者在体外照射放疗前静脉注射0.6 g/m²的AK - 2123,并在整个体外照射疗程中隔天使用AK - 2123(如周一 - 周三 - 周五)。排除7例未接受治疗的患者后,共有326例患者留作评估。
放疗联合额外给予AK - 2123组的局部肿瘤控制率显著更高。AK - 2123治疗后局部肿瘤控制率为61%(95/155),单纯放疗后为46%(79/171)(p = 0.006)。RT + AK - 2123组60个月的精算生存率为57%,而RT组为41%(对数秩检验p = 0.01)。AK - 2123既未增加胃肠道毒性,也未导致任何血液学毒性。AK - 2123给药后偶尔可见轻度外周毒性(1级:13%,2级:2%),通常完全可逆。
我们得出结论,在根治性放疗中添加AK - 2123可显著提高晚期子宫颈鳞状细胞癌的局部肿瘤控制率和生存率,且未增加任何主要毒性。