Alektiar Kaled M, McKee Andrea, Venkatraman Ennapadam, McKee Brady, Zelefsky Micheal J, Mychalczak Boris R, Hoskins William J, Barakat Richard R
Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
Int J Radiat Oncol Biol Phys. 2002 Jul 1;53(3):707-13. doi: 10.1016/s0360-3016(02)02792-x.
To evaluate the outcome of patients with Stage IB Grades 1 and 2 endometrial cancer treated with adjuvant high-dose-rate intravaginal brachytherapy.
Between November 1987 and October 1999, 233 patients with Stage IB FIGO Grades 1 and 2 were treated with postoperative adjuvant high-dose-rate intravaginal brachytherapy. The median dose was 21 Gy in 7 Gy/fraction given at 2-week intervals. The mean age was 60 years. All patients underwent simple hysterectomy. Comprehensive surgical staging, defined as pelvic washing and pelvic and paraaortic lymph nodes sampling, was done in 9% of patients. Patients with FIGO Grade 3, papillary serous cancer, or clear-cell cancer were excluded from this analysis. Complications were assessed in terms of late Radiation Therapy Oncology Group toxicity (Grade > or =3) of the gastrointestinal tract, genitourinary tract, and vagina.
With a median follow-up of 57 months, the 5-year vaginal/pelvic control, disease-free survival, and overall survival rate was 96% (95% confidence interval [CI] 94-99%), 94% (95% CI 91-98%), and 94% (95% CI 91-98%), respectively. The influence on outcome of age, grade (1 vs. 2), depth of invasion (one-third or less or greater than one-third), capillary space-like invasion, lower uterine segment involvement, and comprehensive surgical staging was evaluated. None of these factors significantly affected the rate of vaginal/pelvic control. Only age > or =60 years influenced the outcome for disease-free and overall survival. The 5-year rate for both disease-free and overall survival was 90% (95% CI 84-97%) for patients > or =60 years old compared with 99% (95% CI 96-100%) for those <60 years (p = 0.03 and 0.005, respectively). Of 233 patients, 3 (1%) developed Grade 3 or greater complications, with a 5-year actuarial rate of 2% (95% CI 0-5%). Two patients developed Grade 3 genitourinary toxicity, and 1 Grade 4 vaginal toxicity.
On the basis of this retrospective study, adjuvant postoperative high-dose-rate intravaginal brachytherapy provides excellent outcomes and acceptable morbidity. These results compare very favorably with those reported in the literature using surgery alone or with pelvic radiation.
评估采用辅助高剂量率阴道近距离放疗治疗的ⅠB期1级和2级子宫内膜癌患者的治疗结果。
1987年11月至1999年10月期间,233例国际妇产科联盟(FIGO)ⅠB期1级和2级患者接受了术后辅助高剂量率阴道近距离放疗。中位剂量为21Gy,分7次给予,每次7Gy,间隔2周。平均年龄为60岁。所有患者均接受了单纯子宫切除术。9%的患者进行了包括盆腔冲洗及盆腔和腹主动脉旁淋巴结取样的全面手术分期。FIGO 3级、乳头状浆液性癌或透明细胞癌患者被排除在本分析之外。根据放射肿瘤学组对胃肠道、泌尿生殖道和阴道的晚期毒性(≥3级)评估并发症。
中位随访57个月,5年阴道/盆腔控制率、无病生存率和总生存率分别为96%(95%置信区间[CI]94 - 99%)、94%(95%CI 91 - 98%)和94%(95%CI 91 - 98%)。评估了年龄、分级(1级与2级)、浸润深度(三分之一或以下或大于三分之一)、脉管间隙样浸润、子宫下段受累及全面手术分期对治疗结果的影响。这些因素均未显著影响阴道/盆腔控制率。只有年龄≥60岁影响无病生存率和总生存率。≥60岁患者的5年无病生存率和总生存率均为90%(95%CI 84 - 97%),而<60岁患者为99%(95%CI 96 - 100%)(p分别为0.03和0.005)。233例患者中,3例(1%)发生3级或更高级别的并发症,5年精算发生率为2%(95%CI 0 - 5%)。2例患者发生3级泌尿生殖系统毒性,1例发生4级阴道毒性。
基于这项回顾性研究,辅助术后高剂量率阴道近距离放疗可提供优异的治疗结果和可接受的发病率。这些结果与文献中报道的单纯手术或盆腔放疗的结果相比非常有利。