Lau Harold, Brar Sony, Hao Desiree, MacKinnon Jack, Yee Don, Gluck Stefan
Department of Radiation Oncology, Tom Baker Cancer Centre, 1331 29 St NW, Calgary, AB, Canada.
Head Neck. 2006 Mar;28(3):189-96. doi: 10.1002/hed.20324.
Our center sought to implement a simple chemoradiotherapy schedule for patients with locally advanced squamous cell carcinoma of the head and neck (SCCHN) with minimal toxicity to achieve rates of overall survival comparable to other schedules.
The chemoradiotherapy schedule consisted of daily radiation to 70 Gy over 7 weeks with concurrent cisplatin 20 mg/m(2) during days 1 to 4 of weeks 1 and 5. Acute and late toxicities were recorded according to the Radiation Therapy Oncology Group (RTOG) and common toxicity criteria (CTC) grading. The overall, disease-specific, and locoregional recurrence-free survival were calculated using the STATA statistics package. Possible factors influencing these endpoints were analyzed.
Fifty-seven patients were treated, and 56 patients were evaluable for follow-up. Median follow-up of alive patients was 16.1 months. There was an 82% complete response rate to chemoradiotherapy. The 2-year Kaplan-Meier overall, disease-specific, and locoregional recurrence-free survival rates were 62%, 67%, and 63%. Acute grade 3 and 4 radiation toxicity was noted in 61% and 2%, respectively. Grade 3 or 4 hematologic toxicity was noted in 7% of patients. Factors influencing overall survival included: Karnofsky performance status, receiving more than 50% of planned chemotherapy, age, and initial hemoglobin level.
This regimen is tolerable and achieves overall survival and locoregional control rates comparable to other chemoradiotherapy schedules.
我们中心试图为局部晚期头颈部鳞状细胞癌(SCCHN)患者实施一种简单的放化疗方案,使其毒性最小,以达到与其他方案相当的总生存率。
放化疗方案包括在7周内每日放疗至70 Gy,同时在第1周和第5周的第1至4天给予顺铂20 mg/m²。根据放射肿瘤学组(RTOG)和常见毒性标准(CTC)分级记录急性和晚期毒性。使用STATA统计软件包计算总生存率、疾病特异性生存率和局部区域无复发生存率。分析影响这些终点的可能因素。
57例患者接受了治疗,56例患者可进行随访评估。存活患者的中位随访时间为16.1个月。放化疗的完全缓解率为82%。2年的Kaplan-Meier总生存率、疾病特异性生存率和局部区域无复发生存率分别为62%、67%和63%。急性3级和4级放射毒性分别见于61%和2%的患者。7%的患者出现3级或4级血液学毒性。影响总生存的因素包括:卡氏功能状态、接受计划化疗超过50%、年龄和初始血红蛋白水平。
该方案耐受性良好,总生存率和局部区域控制率与其他放化疗方案相当。