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Intensity-modulated Radiotherapy in Anal Cancer - Where Do We Go from Here?

机译:调强放射疗法在肛门癌中的应用-我们从这里去哪里?

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Although increasing in incidence, squamous cell carcinomas of the anal canal remain relatively rare (less than 1000 cases per annum in the UK). Preliminary results of the UK National Anal Cancer Trial (ACT II) show excellent complete response rates (95%), with 3 year recurrence-free survival rates of 75% in T1/T2 tumours, and 68% for more advanced T3/T4 tumours [1]. The dose and treatment schedule with concurrent 5-fluorouracil and mitomycin used in the ACT II trial is now the current standard of care in the UK for anal cancer. However, treatment planning with large parallel-opposed anterior-posterior/posterior-anterior (AP/PA) fields is inevitably associated with significant acute toxicity, with moist desquamation of the groins, perineum and scrotum. Severe genitourinary and gastrointestinal effects and 20-25% haematological grade 3 toxicity are also observed. This toxicity can result in significant delays in completing prescribed treatment on time without interruptions and frequent in-patient admission. Retrospective series also show poor bowel, urinary and sexual late function and impaired quality of life in this patient group.
机译:尽管发病率增加,但肛管鳞状细胞癌仍然相对罕见(英国每年少于1000例)。英国国家肛门癌试验(ACT II)的初步结果显示,其优异的完全缓解率(95%),T1 / T2肿瘤的3年无复发存活率分别为75%和68%的晚期T3 / T4肿瘤[1]。 ACT II试验中同时使用5-氟尿嘧啶和丝裂霉素的剂量和治疗方案现在是英国目前用于肛门癌的护理标准。然而,大面积平行对置的前后/后(AP / PA)区域的治疗计划不可避免地会导致明显的急性毒性,并导致腹股沟,会阴和阴囊湿润脱皮。还观察到了严重的泌尿生殖道和胃肠道作用以及20-25%的血液学3级毒性。这种毒性可能导致按时完成指定治疗的重大延误,而不会中断和频繁住院。回顾性系列还显示该患者组的肠道,尿液和性功能较晚,生活质量受损。

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