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神经母细胞瘤治疗中的放射疗法:杜克大学医学中心1967 - 1984年的经验

Radiation therapy in the management of neuroblastoma: the Duke University Medical Center experience 1967-1984.

作者信息

Halperin E C, Cox E B

出版信息

Int J Radiat Oncol Biol Phys. 1986 Oct;12(10):1829-37. doi: 10.1016/0360-3016(86)90326-3.

Abstract

We have evaluated the role of radiotherapy in providing local control of primary tumors and to palliate metastases from neuroblastoma (NB). Fifty-five children with histologically verified NB were evaluated and treated from 1967 to 1984. In univariate analysis, the actuarial survival of eight children with thoracic primaries (85%) was significantly better than the survival of 39 children with intra-abdominal primaries (35%, p = 0.0287). The survival of 28 children less than or equal to 18 months of age at diagnoses was 73%, whereas 27 children older than 18 months had a survival probability of 10% (p = 0.0001). The survival by Evans stage was: I 100% (2 patients), II 85% (7), III 60% (13), IV 4% (27) and IV-S 100% (6). According to the Pediatric Oncology Group (POG) staging system, the survival was: A 100% (3), B 66% (9), C 66% (9), D 23% (34). A multivariable analysis indicated that the Evans staging system was a more powerful indicator of prognosis than the POG system. The analysis also indicated that Evans stage and patient age were independent determinants of survival. The primary tumor site did not add significant prognostic information beyond these two factors. Children with Stage I disease were treated with surgery alone. Most children with Stages II and III disease were treated with surgery, irradiation, and Cyclophosphamide or Cyclophosphamide plus Vincristine. All seven patients with Stage II disease received post-operative irradiation to the primary tumor and were locally controlled with doses of 4.8 to 26.5 Gy. Eleven of the 13 patients with Stage III disease were irradiated post-operatively. Seven of these 11 patients were locally controlled with doses of 12 to 48.4 Gy. The four Stage III patients with in-field recurrences were older children with large radiotherapy fields and/or low doses administered. The Radiation Therapy Oncology Group pain score system was used to evaluate response of painful bony metastases to irradiation. A response was observed in 65% of the sites irradiated. A response was observed at 67% of the soft tissue metastases irradiated. Hepatomegaly causing respiratory embarrassment or inferior vena cava obstruction was treated with irradiation in seven patients. All patients responded with doses ranging from 5 to 24.4 Gy. Five of the 17 children who survived for more than 5 years following treatment had significant scoliosis or kyphosis secondary to vertebral body abnormalities in irradiated bones. All five children were irradiated at a young age with megavoltage equipment.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

我们评估了放射治疗在实现神经母细胞瘤(NB)原发性肿瘤局部控制及缓解转移灶方面的作用。1967年至1984年期间,对55例经组织学证实的NB患儿进行了评估和治疗。单因素分析显示,8例胸段原发性肿瘤患儿的精算生存率(85%)显著高于39例腹内原发性肿瘤患儿的生存率(35%,p = 0.0287)。诊断时年龄小于或等于18个月的28例患儿生存率为73%,而27例年龄大于18个月的患儿生存概率为10%(p = 0.0001)。按埃文斯分期的生存率为:I期100%(2例),II期85%(7例),III期60%(13例),IV期4%(27例),IV-S期100%(6例)。根据儿童肿瘤学组(POG)分期系统,生存率为:A期100%(3例),B期66%(9例),C期66%(9例),D期23%(34例)。多变量分析表明,埃文斯分期系统比POG系统更能有力地预测预后。分析还表明,埃文斯分期和患儿年龄是生存的独立决定因素。原发性肿瘤部位在这两个因素之外并未增加显著的预后信息。I期疾病患儿仅接受手术治疗。大多数II期和III期疾病患儿接受了手术、放疗以及环磷酰胺或环磷酰胺加长春新碱治疗。所有7例II期疾病患儿均接受了原发性肿瘤术后放疗,局部控制剂量为4.8至26.5 Gy。13例III期疾病患儿中有11例接受了术后放疗。这11例患儿中有7例通过12至48.4 Gy的剂量实现了局部控制。4例III期野内复发患儿为年龄较大的儿童,放疗野大且/或给予的剂量低。采用放射治疗肿瘤学组疼痛评分系统评估疼痛性骨转移对放疗的反应。65%的照射部位观察到反应。67%的软组织转移照射部位观察到反应。7例因肝肿大导致呼吸窘迫或下腔静脉梗阻的患儿接受了放疗。所有患儿均有反应,剂量范围为5至24.4 Gy。17例治疗后存活超过5年的患儿中有5例因照射骨骼椎体异常继发严重脊柱侧弯或后凸。所有5例患儿均在幼年时使用兆伏级设备进行了照射。(摘要截取自400字)

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