Department of Clinical Oncology, University College Hospital, London, UK.
Lancet Oncol. 2010 Jan;11(1):66-74. doi: 10.1016/S1470-2045(09)70306-7. Epub 2009 Oct 29.
Between 1990 and 2000, we examined the effect of timing of non-platinum chemotherapy when combined with radiotherapy. We aimed to determine whether giving chemotherapy concurrently with radiotherapy or as maintenance therapy, or both, affected clinical outcome. Here we report survival and recurrence after 10 years of follow-up.
Between Jan 15, 1990, and June 20, 2000, 966 patients were recruited from 34 centres in the UK and two centres from Malta and Turkey. Patients with locally advanced head and neck cancer, and who had not previously undergone surgery, were randomly assigned to one of four groups in a 3:2:2:2 ratio, stratified by centre and chemotherapy regimen: radical radiotherapy alone (n=233); radiotherapy with two courses of chemotherapy given simultaneously on days 1 and 14 of radiotherapy (SIM alone; n=166); or 14 and 28 days after completing radiotherapy (SUB alone, n=160); or both (SIM+SUB; n=154). Chemotherapy was either methotrexate alone, or vincristine, bleomycin, methotrexate, and fluorouracil. Patients who had previously undergone radical surgery to remove their tumour were only randomised to radiotherapy alone (n=135) or SIM alone (n=118), in a 3:2 ratio. The primary endpoints were overall survival (from randomisation), and event-free survival (EFS; recurrence, new tumour, or death; whichever occurred first) among patients who were disease-free 6 months after randomisation. Analyses were by intention to treat. This trial is registered at www.Clinicaltrials.gov, number NCT00002476.
All 966 patients were included in the analyses. Among patients who did not undergo surgery, the median overall survival was 2.6 years (99% CI 1.9-4.2) in the radiotherapy alone group, 4.7 (2.6-7.8) years in the SIM alone group, 2.3 (1.6-3.5) years in the SUB alone group, and 2.7 (1.6-4.7) years in the SIM+SUB group (p=0.10). The corresponding median EFS were 1.0 (0.7-1.4), 2.2 (1.1-6.0), 1.0 (0.6-1.5), and 1.0 (0.6-2.0) years (p=0.005), respectively. For every 100 patients given SIM alone, there are 11 fewer EFS events (99% CI 1-21), compared with 100 given radiotherapy, 10 years after treatment. Among the patients who had previously undergone surgery, median overall survival was 5.0 (99% CI 1.8-8.0) and 4.6 (2.2-7.6) years in the radiotherapy alone and SIM alone groups (p=0.70), respectively, with corresponding median EFS of 3.7 (99% CI 1.1-5.9) and 3.0 (1.2-5.6) years (p=0.85), respectively. The percentage of patients who had a significant toxicity during treatment were: 11% (radiotherapy alone, n=25), 28% (SIM alone, n=47), 12% (SUB alone, n=19), and 36% (SIM+SUB, n=55) among patients without previous surgery; and 9% (radiotherapy alone, n=12) and 20% (SIM alone, n=24) among those who had undergone previous surgery. The most common toxicity during treatment was mucositis. The percentage of patients who had a significant toxicity at least 6 months after randomisation were: 6% (radiotherapy alone, n=13), 6% (SIM alone, n=10), 4% (SUB alone, n=7), and 6% (SIM+SUB, n=9) among patients who had no previous surgery; and 7% (radiotherapy alone, n=10) and 11% (SIM alone, n=13) among those who had undergone previous surgery. The most common toxicity 6 months after treatment was xerostomia, but this occurred in 3% or less of patients in each group.
Concurrent non-platinum chemoradiotherapy reduces recurrences, new tumours, and deaths in patients who have not undergone previous surgery, even 10 years after starting treatment. Chemotherapy given after radiotherapy (with or without concurrent chemotherapy) is ineffective. Patients who have undergone previous surgery for head and neck cancer do not benefit from non-platinum chemotherapy.
Cancer Research UK, with support from University College London and University College London Hospital Comprehensive Biomedical Research Centre.
在 1990 年至 2000 年间,我们研究了非铂类化疗在联合放疗时的时机选择对疗效的影响。我们旨在确定在放疗时同时给予化疗、放疗后给予维持化疗、或两者并用,是否会影响临床转归。在此我们报告了随访 10 年后的生存和复发情况。
1990 年 1 月 15 日至 2000 年 6 月 20 日,来自英国 34 个中心和马耳他、土耳其的 2 个中心的 966 名患者入组,这些患者均为局部晚期头颈部癌且未接受过手术,按中心和化疗方案以 3:2:2:2 的比例随机分配至以下 4 组之一:单纯根治性放疗(n=233);放疗时于第 1 天和第 14 天同时给予两疗程化疗(SIM 组,n=166);放疗结束后第 14 天和第 28 天给予化疗(SUB 组,n=160);或同时给予化疗(SIM+SUB 组,n=154)。化疗药物为甲氨蝶呤或长春新碱、博来霉素、甲氨蝶呤和氟尿嘧啶。曾行根治性手术切除肿瘤的患者仅随机分至单纯放疗(n=135)或 SIM 组(n=118),比例为 3:2。主要终点是无病生存(从随机分组至随机分组后 6 个月时疾病无进展)和无事件生存(复发、新肿瘤或死亡,以最先出现者为准)。分析为意向治疗。本试验在 ClinicalTrials.gov 注册,编号为 NCT00002476。
所有 966 名患者均纳入分析。未手术患者中,单纯放疗组的中位总生存时间为 2.6 年(99%CI 1.9-4.2),SIM 组为 4.7 年(2.6-7.8),SUB 组为 2.3 年(1.6-3.5),SIM+SUB 组为 2.7 年(1.6-4.7)(p=0.10)。中位无事件生存时间分别为 1.0 年(0.7-1.4)、2.2 年(1.1-6.0)、1.0 年(0.6-1.5)和 1.0 年(0.6-2.0)(p=0.005)。与单纯放疗相比,每 100 例接受 SIM 治疗的患者,10 年后无事件生存时间延长 11 例(99%CI 1-21)。曾行手术的患者中,单纯放疗组和 SIM 组的中位总生存时间分别为 5.0 年(99%CI 1.8-8.0)和 4.6 年(2.2-7.6)(p=0.70),中位无事件生存时间分别为 3.7 年(99%CI 1.1-5.9)和 3.0 年(1.2-5.6)(p=0.85)。治疗期间发生严重毒性的患者比例分别为:无手术史患者中,单纯放疗组为 11%(n=25),SIM 组为 28%(n=47),SUB 组为 12%(n=19),SIM+SUB 组为 36%(n=55);有手术史患者中,单纯放疗组为 9%(n=12),SIM 组为 20%(n=24)。治疗期间最常见的毒性为黏膜炎。随机分组后至少 6 个月时发生严重毒性的患者比例分别为:无手术史患者中,单纯放疗组为 6%(n=13),SIM 组为 6%(n=10),SUB 组为 4%(n=7),SIM+SUB 组为 6%(n=9);有手术史患者中,单纯放疗组为 7%(n=10),SIM 组为 11%(n=13)。治疗后 6 个月时最常见的毒性为口干,但各组中该毒性的发生率均为 3%或更低。
未手术患者接受非铂类同步放化疗可降低复发、新肿瘤和死亡风险,甚至在开始治疗 10 年后仍有获益。放疗后给予化疗(同步或序贯)无效。曾行头颈部癌根治性手术的患者不能从非铂类化疗中获益。
英国癌症研究中心,得到伦敦大学学院和伦敦大学学院医院综合生物医学研究中心的支持。