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I期睾丸精原细胞瘤的主动脉旁照射:675例患者的前瞻性研究结果。德国睾丸癌研究组(GTCSG)的一项试验。

Para-aortic irradiation for stage I testicular seminoma: results of a prospective study in 675 patients. A trial of the German testicular cancer study group (GTCSG).

作者信息

Classen J, Schmidberger H, Meisner C, Winkler C, Dunst J, Souchon R, Weissbach L, Budach V, Alberti W, Bamberg M

机构信息

Department of Radiation Oncology, Universitätsklinikum, Hoppe-Seyler-Strasse 3, D-72076 Tübingen, Germany.

出版信息

Br J Cancer. 2004 Jun 14;90(12):2305-11. doi: 10.1038/sj.bjc.6601867.

Abstract

A prospective nonrandomised trial was performed in order to evaluate tumour control and toxicity of low-dose adjuvant radiotherapy in stage I seminoma with treatment portals confined to the para-aortic lymph nodes. Between April 1991 and March 1994, 721 patients were enrolled for the trial by 48 centres in Germany. Patients with pure seminoma and no evidence of lymph node involvement or distant metastases received 26 Gy prophylactic limited para-aortic radiotherapy. Disease-free survival at 5 years was the primary end point. With a median follow-up of 61 months, 675 patients with follow-up investigations were evaluable for this analysis. Kaplan-Meier estimates of disease-free and disease-specific survival were 95.8% (95% CI: 94.2-97.4) and 99.6% (95% CI: 99.2-100%) at 5 years and 94.9% (95% CI: 92.5-97.4%) and 99.6% (95% CI: 99.2-100%) at 8 years, respectively. A total of 26 patients relapsed. All except two were salvaged from relapse. In all, 21 recurrences were located in infradiaphragmatic lymph nodes without any 'in-field' relapse. Nausea and diarrhoea grade 3 were observed in 4.0 and 1.0% of the patients, respectively. Grade 3 late effects have not been observed so far. The results of our trial lend further support to the concept of limited para-aortic irradiation as the recently defined new standard of radiotherapy in stage I seminoma. There is no obvious compromise in disease-specific or disease-free survival compared to more extensive hockey-stick portals, which were used as standard portals at the time this study was initiated.

摘要

为了评估低剂量辅助放疗对局限于主动脉旁淋巴结的Ⅰ期精原细胞瘤的肿瘤控制情况及毒性,开展了一项前瞻性非随机试验。1991年4月至1994年3月期间,德国48个中心的721例患者纳入该试验。纯精原细胞瘤且无淋巴结受累或远处转移证据的患者接受26 Gy预防性局限主动脉旁放疗。5年无病生存率是主要终点。中位随访61个月,675例有随访调查的患者可纳入本分析。5年时无病生存率和疾病特异性生存率的Kaplan-Meier估计值分别为95.8%(95%CI:94.2 - 97.4)和99.6%(95%CI:99.2 - 100%),8年时分别为94.9%(95%CI:92.5 - 97.4%)和99.6%(95%CI:99.2 - 100%)。共有26例患者复发。除2例之外均从复发中挽救过来。总共21例复发位于膈肌以下淋巴结,无任何“野内”复发。分别有4.0%和 1.0%的患者出现3级恶心和腹泻。目前尚未观察到3级晚期效应。我们试验的结果进一步支持了局限主动脉旁照射的概念,即作为Ⅰ期精原细胞瘤最近定义的放疗新标准。与本研究开展时作为标准野的更广泛的曲棍球棒野相比,疾病特异性或无病生存率没有明显降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9681/2409532/676cffc61bf7/90-6601867f1.jpg

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