首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >A phase I-II study of synchronous chemoradiotherapy for poor prognosis locally advanced bladder cancer.
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A phase I-II study of synchronous chemoradiotherapy for poor prognosis locally advanced bladder cancer.

机译:I-II期同步放化疗治疗局部晚期膀胱癌预后不良的研究。

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BACKGROUND: The management of locally advanced bladder cancer remains controversial with poor local control with radiotherapy alone. Synchronous chemotherapy regimens have yielded encouraging results in other primary sites. PATIENTS AND METHODS: Patients with T2-T4a N0/NX M0 bladder cancer were entered into this single centre phase I-II study. Patients received radiotherapy to 55 Gy in 20 fractions over four weeks. Concurrent chemotherapy was given with Mitomycin C 12 mg/m2 day 1 and 5-fluorouracil 500 mg/m2/24 hours weeks one and four of radiotherapy for five or seven days on each occasion. RESULTS: Thirty-one patients entered the trial from March 1998 to December 1999 (22: 5-day; 9: 7-day schedule). Median age was 68 (range 58-79) years, 23 males and 8 females. T2: 9 (29%); T3a: 4 (12%); T3b: 9 (29%); T4: 9 (29%); TCC grade 2: 8 (26%) and grade 3: 23 (74%); 14 of 31 had hydronephrosis. Ten of thirty-one had a GFR < 50 ml/min. Toxicity was mild to moderate with the five-day schedule. More severe toxicity was seen with the seven-day schedule: five of nine patients failed to complete planned therapy. Pathological complete response rate at three months was 74% (5-day regimen) and 50% (7-day regimen). Overall 12-month survival was 65%. CONCLUSION: Chemoradiotherapy with the five-day schedule is feasible with acceptable toxicity in poor prognosis patients. A randomised trial is being launched.
机译:背景:局部进展期膀胱癌的治疗仍存在争议,仅通过放疗就不能很好地控制局部。同步化疗方案在其他主要部位取得了令人鼓舞的结果。患者和方法:将T2-T4a N0 / NX M0膀胱癌患者纳入该单中心I-II期研究。患者在四个星期内分20步接受放疗至55 Gy。在第1周和第4周放疗的同时,分别在第1天和第4周放疗时,用丝裂霉素C 12 mg / m2第1天和5-氟尿嘧啶500 mg / m2 / 24小时进行放化疗,每种情况下进行5或7天。结果:从1998年3月至1999年12月,有31例患者参加了该试验(22天:5天; 9天:7天)。中位年龄为68岁(58-79岁),男23例,女8例。 T2:9(29%); T3a:4(12%); T3b:9(29%); T4:9(29%); TCC等级2:8(26%)和等级3:23(74%); 31人中有14人患有肾积水。 31人中有10人的GFR <50 ml / min。每天五天,毒性从轻到中度。在7天的疗程中观察到了更严重的毒性反应:9名患者中有5名未能完成计划的治疗。三个月的病理完全缓解率分别为74%(5天方案)和50%(7天方案)。总体12个月生存率为65%。结论:放疗五天是可行的,对于预后不良的患者可以接受可接受的毒性。正在开展一项随机试验。

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