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台湾肾母细胞瘤的流行病学、临床特征及治疗结果:来自台湾小儿肿瘤学组的报告

Epidemiology, clinical features and treatment outcome of Wilms' tumor in Taiwan: a report from Taiwan Pediatric Oncology Group.

作者信息

Hung Iou-Jih, Chang Wan-Hui, Yang Chao-Ping, Jaing Tang-Her, Liang Der-Cherng, Lin Kai-Hsin, Lin Dong-Tsamn, Hsiao Chih-Cheng, Hsieh Yuh-Lin, Chen Jiann-Shiuh, Chang Tai-Tsung, Peng Ching-Tien, Shu San-Ging, Lin Ming-Tsan, Chen Bow-Wen, Lin Kuo-Sin

机构信息

Division of Hematology/Oncology, Chang Gung Children's Hospital, Linkou, Taiwan.

出版信息

J Formos Med Assoc. 2004 Feb;103(2):104-11.

Abstract

BACKGROUND AND PURPOSE

Taiwan Pediatric Oncology Group (TPOG)-W-91 is the first multi-institutional Wilms' tumor study for children in Taiwan. This clinical trial used a multidisciplinary approach, based on and similar to the National Wilms' Tumor Study 4. The study was conducted to evaluate the epidemiological characteristics and analyze the outcome of Wilms' tumor patients treated with this protocol.

METHODS

Ninety eight children with Wilms' tumor (WT) were analyzed for distributions of age, gender, associated congenital anomalies, tumor sites, histology, tumor weights, and clinical stages. Patients received individualized multimodality treatment based upon the histology of the tumor and clinicopathologic stage. The treatment included surgery, radiotherapy and 2-, 3-, and 4-agent active chemotherapeutic agents. Seventy patients were eligible for analysis of treatment outcome. The endpoints were progression-free and overall survival (PFS, OS). Patients were divided into various subgroups according to the chemotherapy regimen used, tumor stage, age at diagnosis, gender, and tumor weight. The prognostic factors were evaluated and the survival rates of various clinical subgroups were compared using log-rank test.

RESULTS

The average annual incidence rate of WT was 2.9 per million children under 15 years of age. The M/F ratio was 1.04. The mean age at diagnosis was 3.7 years. All bilateral tumors occurred in females. Congenital anomalies were present in 17.3% of patients. Anaplastic histology was found in 6 of 98 cases (6.1%). The stage distribution was: I, 43.2%; II, 19.3%; III, 23.9%; IV, 6.8%; and V, 6.8%. The median follow-up time was 89.1 months (range, 1.8 to 128.1 months). The 5-year PFS rate was 0.7841 (SE, 0.0494; 53 of 70 patients) and the 5-year OS rate was 0.886 (SE, 0.038; 63 of 70 patients). Gender was found to be the only significant prognostic variable.

CONCLUSIONS

This study evaluated the epidemiological characteristics, clinical features, multimodality therapy regimens, and treatment outcome of WT in Taiwan. Data obtained from this study may lead to further improvement in the prognosis of pediatric malignant solid tumor.

摘要

背景与目的

台湾小儿肿瘤研究组(TPOG)-W-91是台湾首个针对儿童肾母细胞瘤的多机构研究。该临床试验采用多学科方法,基于并类似于美国国立肾母细胞瘤研究4。本研究旨在评估肾母细胞瘤患者的流行病学特征,并分析采用该方案治疗的肾母细胞瘤患者的治疗结果。

方法

分析98例肾母细胞瘤(WT)患儿的年龄、性别、相关先天性异常、肿瘤部位、组织学、肿瘤重量和临床分期分布。患者根据肿瘤组织学和临床病理分期接受个体化多模式治疗。治疗包括手术、放疗以及使用2种、3种和4种药物的积极化疗药物。70例患者符合治疗结果分析条件。终点指标为无进展生存期和总生存期(PFS、OS)。根据所用化疗方案、肿瘤分期、诊断时年龄、性别和肿瘤重量将患者分为不同亚组。评估预后因素,并使用对数秩检验比较各临床亚组的生存率。

结果

WT的年平均发病率为每百万15岁以下儿童2.9例。男女比例为1.04。诊断时的平均年龄为3.7岁。所有双侧肿瘤均发生在女性患者中。17.3%的患者存在先天性异常。98例中有6例(6.1%)为间变组织学类型。分期分布为:I期,43.2%;II期,19.3%;III期,23.9%;IV期,6.8%;V期,6.8%。中位随访时间为89.1个月(范围1.8至128.1个月)。5年PFS率为0.7841(SE,0.0494;70例患者中的53例),5年OS率为0.886(SE,0.038;70例患者中的63例)。性别是唯一显著的预后变量。

结论

本研究评估了台湾肾母细胞瘤的流行病学特征、临床特征、多模式治疗方案和治疗结果。本研究获得的数据可能会进一步改善小儿恶性实体瘤的预后。

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