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未选择的神经母细胞瘤患者预后因素的首次经验。奥地利神经母细胞瘤87研究。

First experience with prognostic factors in unselected neuroblastoma patients. The Austrian Neuroblastoma 87 Study.

作者信息

Ladenstein R, Urban C, Gadner H, Fink F M, Zoubek A, Emminger W, Grienberger H, Schmitt K, Ambros P F, Ambros I M

机构信息

St Anna Children's Hospital, Vienna, Austria.

出版信息

Eur J Cancer. 1995;31A(4):637-41. doi: 10.1016/0959-8049(95)00069-u.

Abstract

Between January 1987 and December 1993, 117 patients were registered in the Austrian A-NB87 study. The male/female ratio was 1.18, with 50 patients below the age of 1 year at diagnosis. Patients were assigned to stage according to the result of primary surgery in localised disease. Age, ferritin and neuron specific enolase were used in addition in stage III disease for risk-adapted treatment. Adrenal or pelvic primary tumour sites were mainly associated (81%) with advanced disease. The median observation time of the study is 3.5 years. The overall survival at 3 years was excellent in low stage disease and IVs patients, i.e. 100% for stage I and IIA (20 patients), 92% in stage IVs (13 patients), 81% in stage IIIA (18 patients) and 69% in stage IIB (8 patients). Stage IV (38 patients) showed a survival rate of 51%, whereas stage IIB (10 patients) had the worst outcome in this study, i.e. 20%, due to treatment-related toxicity. Significant unfavourable prognostic factors were neuron specific enolase (NSE) > 100 ng/ml, ferritin > 300 micrograms/ml and amplified MYCN. This study achieved a better survival rate in stage IV patients and a subgroup of stage III in comparison to our previous study (Pädiatrie und Pädologie 1986, 21, 269) and gives the basis to further reduce treatment intensity in low-risk disease based on biological factors. However, prognosis for high-risk cases was still poor in spite of a very aggressive treatment concept.

摘要

1987年1月至1993年12月期间,奥地利A-NB87研究登记了117例患者。男女比例为1.18,诊断时50例患者年龄在1岁以下。对于局限性疾病,根据初次手术结果对患者进行分期。对于III期疾病,还使用年龄、铁蛋白和神经元特异性烯醇化酶进行风险适应性治疗。肾上腺或盆腔原发性肿瘤部位主要与晚期疾病相关(81%)。该研究的中位观察时间为3.5年。低分期疾病和IVs期患者的3年总生存率良好,即I期和IIA期(20例患者)为100%,IVs期(13例患者)为92%,IIIA期(18例患者)为81%,IIB期(8例患者)为69%。IV期(38例患者)的生存率为51%,而IIB期(10例患者)在本研究中预后最差,为20%,原因是治疗相关毒性。显著的不良预后因素为神经元特异性烯醇化酶(NSE)>100 ng/ml、铁蛋白>300μg/ml和MYCN扩增。与我们之前的研究(《儿科与儿科学》1986年,21卷,269页)相比,本研究在IV期患者和III期亚组中实现了更高的生存率,并为基于生物学因素进一步降低低风险疾病的治疗强度提供了依据。然而,尽管采用了非常积极的治疗方案,高危病例的预后仍然很差。

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