标准盆腔与中央小盆腔野辅助放疗治疗IB期淋巴结阴性宫颈癌的回顾性研究

IF 0.1 Q4 OBSTETRICS & GYNECOLOGY
T. Ralefala, L. Van Wijk, R. Saidu
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引用次数: 2

摘要

目的:比较南非开普敦Groote Schuur医院治疗早期结阴性癌症的两种术后放射治疗(PORT)。材料和方法:对1984年至2010年间接受根治性手术治疗的癌症IB期患者进行回顾性观察研究。被认为有盆腔复发风险的淋巴结阴性患者接受了PORT,同时或不同时接受顺铂或额外的阴道近距离放射治疗。PORT采用全骨盆野(WPF)或中央小骨盆野(SPF)。从临床记录中提取有关辅助治疗适应症、治疗结果和3-4级治疗相关毒性(包括腿部淋巴水肿)的数据。结果:31例患者接受WPF,56例SPF。总的5年生存率为85%。WPF组和SPF组的生存率没有显著差异(log秩p=0.67)。尽管WPF组中有两名患者(6%)死于治疗相关并发症,但复发模式和粗略的3-4级治疗发病率没有差异。结论:仅针对宫颈肿瘤床和宫颈旁组织的SPF PORT的预期益处是降低小肠发病率和淋巴水肿。从这次审计中无法确定SPF技术是否减少了并发症,或者是否增加了骨盆外复发。似乎不太可能进行随机对照试验,因为需要大量的样本。将汇集的SPF数据与历史WPF对照进行比较似乎是确定该方法安全性的最佳选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A retrospective study of stage IB node-negative cervical cancer treated with adjuvant radiation with standard pelvic versus central small pelvic fields
Objective: To compare two types of postoperative radiation therapy (PORT) in early-stage, node-negative cervical cancer treated at Groote Schuur Hospital, Cape Town, South Africa. Materials and methods: A retrospective observational study of patients with stage IB cervical cancer treated with radical surgery between 1984 and 2010. Node-negative patients regarded as at risk of pelvic recurrence received PORT, with or without concurrent cisplatin or additional vaginal brachytherapy. The PORT was given with either whole pelvis fields (WPF), or with central small pelvic fields (SPF). Data concerning indications for adjuvant therapy, treatment outcomes and grade 3–4 treatment-related toxicities, including leg lymphoedema, were extracted from clinical records. Results: Thirty-one patients received WPF, and 56 SPF. The overall 5-year survival rate was 85%. No significant differences in survival rates were found between the WPF and SPF groups (log rank p = 0.67). Relapse patterns and the crude grade 3–4 treatment morbidity rates did not differ, although two patients in the WPF group (6%) died of treatment-related complications. Conclusions: The expected benefit of PORT with SPF, which targets the cervical tumour bed and para-cervical tissues only, is a reduction in small bowel morbidity and lymphoedema. It is not possible to ascertain from this audit whether the SPF technique reduces complications, or that it increases out-of-field pelvic relapses. It seems unlikely that a randomised controlled trial will ever be performed, as a large sample size would be required. Comparisons of pooled SPF data with historical WPF controls seem the best option to establish the safety of this approach.
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