Safran M R, Kody M H, Namba R S, Larson K R, Kabo J M, Dorey F J, Eilber F R, Eckardt J J
Department of Orthopaedic Surgery, UCLA School of Medicine, Los Angeles, California.
Contemp Orthop. 1994 Jul;29(1):15-25.
As part of the UCLA limb salvage program, 151 patients received 151 endoprostheses for primary tumors involving bone. Follow-up of all patients was to death (56), revision (21), or a minimum two years for the 74 additional survivors (range: 24-114 months; mean: 52 months). Endoprosthetic replacements were of the distal femur (81), proximal femur (19), proximal humerus (13), proximal tibia (11), scapula (11), total femur (8), total humerus (4), intercalary prostheses (2), and one each of the distal humerus and the pelvis. There were three soft tissue sarcomas, five benign bone lesions, and 143 primary malignant tumors of bone. MSTS function was good-excellent in 78%. There were 64 local complications in 55 patients (36%). Mechanical failure occurred in 24 patients (15.9%), local recurrence occurred in ten (6.6%), minor wound healing problems in nine (5.9%), and infection in eight (5.3%). Few systemic complications were reported. Function appeared to be location dependent. All of the 29 patients with benign or low grade malignant tumors (parosteal, IA, IB) have survived. Of the 116 patients with stage IIA and IIB disease, 59% survived three years, and a Kaplan-Meier analysis projects that 56% are expected to survive at five years. Only 17 (11%) of these 151 endoprostheses have been revised; an additional four (3%) eventually came to amputation. The Kaplan-Meier analysis revealed that 91% of the prostheses survived three years and 83% survived five years. The Cox Proportional Hazards model revealed that for patients with stage IIA and IIB disease, the risk of death is four times the risk of the need for revision at five years. Although endoprosthetic reconstructions have their own unique complications, they have proven durable in this series of patients. Local problems usually can be managed without amputation, and patient satisfaction is high.
作为加州大学洛杉矶分校肢体挽救计划的一部分,151例患者接受了151个用于治疗累及骨骼的原发性肿瘤的内置假体。所有患者随访至死亡(56例)、翻修(21例),或其余74例幸存者至少随访两年(范围:24 - 114个月;平均:52个月)。内置假体置换部位包括股骨远端(81例)、股骨近端(19例)、肱骨近端(13例)、胫骨近端(11例)、肩胛骨(11例)、全股骨(8例)、全肱骨(4例)、节段性假体(2例),以及肱骨远端和骨盆各1例。其中有3例软组织肉瘤、5例良性骨病变和143例原发性骨恶性肿瘤。肌肉骨骼肿瘤协会(MSTS)功能评估为良好至优秀的占78%。55例患者(36%)出现64例局部并发症。24例患者(15.9%)发生机械故障,10例(6.6%)出现局部复发,9例(5.9%)有轻微伤口愈合问题,8例(5.3%)发生感染。报告的全身并发症较少。功能似乎与部位有关。29例良性或低级别恶性肿瘤(骨旁型、IA期、IB期)患者全部存活。116例IIA期和IIB期疾病患者中,59%存活3年,卡普兰 - 迈耶分析预测5年生存率为56%。这151个内置假体中仅17个(11%)进行了翻修;另外4个(3%)最终接受了截肢。卡普兰 - 迈耶分析显示,91%的假体存活3年,83%存活5年。Cox比例风险模型显示,对于IIA期和IIB期疾病患者,5年时死亡风险是翻修需求风险的4倍。虽然内置假体重建有其独特的并发症,但在这组患者中已证明具有耐久性。局部问题通常无需截肢即可处理,患者满意度较高。