La Quaglia M P, Heller G, Ghavimi F, Casper E S, Vlamis V, Hajdu S, Brennan M F
Department of Surgery, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.
Cancer. 1994 Jan 1;73(1):109-17. doi: 10.1002/1097-0142(19940101)73:1<109::aid-cncr2820730120>3.0.co;2-s.
Survival for rhabdomyosarcoma appears to be more favorable in children and adolescents compared with adults. To determine the significance of age at diagnosis as a prognostic indicator in rhabdomyosarcoma, we performed a retrospective analysis of a combined pediatric and adult rhabdomyosarcoma data base.
Pertinent prognostic variables, including age, TNM stage, histopathologic subtype, anatomic site, resectability, radiation to the primary site, and dose intensity of chemotherapy, were compared in a Cox proportional hazards model with mortality as the outcome variable.
Age at diagnosis (P = 0.0001) and local tumor invasiveness (P < 0.0001), distant parenchymal metastases (P < 0.0001), regional lymph node involvement (P = 0.0027), and histopathologic subtype (P = 0.0446) contributed information to the proportional hazards model.
Age at diagnosis is an independent predictor of outcome in patients with rhabdomyosarcoma along with tumor invasiveness, metastases, regional lymph node involvement, and histopathologic subtype.
与成人相比,横纹肌肉瘤患儿和青少年的生存率似乎更乐观。为了确定诊断时年龄作为横纹肌肉瘤预后指标的意义,我们对儿童和成人横纹肌肉瘤联合数据库进行了回顾性分析。
在以死亡率为结果变量的Cox比例风险模型中,比较包括年龄、TNM分期、组织病理学亚型、解剖部位、可切除性、原发部位放疗以及化疗剂量强度等相关预后变量。
诊断时年龄(P = 0.0001)、局部肿瘤侵袭性(P < 0.0001)、远处实质转移(P < 0.0001)、区域淋巴结受累(P = 0.0027)和组织病理学亚型(P = 0.0446)为比例风险模型提供了信息。
诊断时年龄是横纹肌肉瘤患者预后的独立预测因素,同时还有肿瘤侵袭性、转移、区域淋巴结受累和组织病理学亚型。