Morsy Ahmed M, Ahmed Badawy M, Rezk Khalid M, Ramadan Islam K-A, Aboelgheit Amir M, Eltyb Hanan A, Abd Elbadee Osama M, El-Naggar Maha S
Departments of Pediatric Oncology.
Surgical Oncology.
J Pediatr Hematol Oncol. 2020 Mar;42(2):e66-e78. doi: 10.1097/MPH.0000000000001506.
The aims of this study were to assess survival outcome of pediatric patients with localized osteosarcoma of the extremities in Upper Egypt, identify factors of prognostic significance for survival, and to determine factors predictive of surgical methods used in these patients, as well as developing a clinical model for risk prediction.
A retrospective analysis of data assembled from medical records of 30 pediatric patients with a histologically verified nonmetastatic osteosarcoma of the extremities treated at South Egypt Cancer Institute with a unified chemotherapy protocol between January 2001 and December 2015 was carried out. Prognostic factors were determined using univariable and multivariable methods. A model for surgical outcomes in these patients based on the baseline clinical factors, and the parameters predictive of their tumor response to chemotherapy, was developed.
With a median follow-up of 63 months for the study population, the estimates for event-free survival and overall survival (OS) at 3 and 5 years were 69.5% and 79% and 65.2% and 65.3%, respectively. Age 16 years or above was independently associated with both worse metastasis-free survival (hazard ratio [HR]=6.05, 95% confidence interval [CI]: 1.43-25.6, P=0.015) and OS (HR=7.9, 95% CI: 1.71-36.2, P=0.008). In the multivariable analysis, a proximal location within the limb gained a statistical significance to be independently associated with worse OS (HR=2.4, 95% CI: 1.13-22.1, P=0.003). Poor response to chemotherapy was marginally associated with worse metastasis-free survival (HR=4.9, 95% CI: 1.02-23.8, P=0.047) only in the univariable analysis. The patients found to be more likely to undergo an amputation surgery (odds ratio=14.1, 95% CI: 1.34-149.4, P=0.028) were those in whom a tumor was poorly responding to chemotherapy.
In Upper Egypt, despite the reasonable survival outcomes in nonmetastatic osteosarcoma, a relatively high limb amputation rate has been encountered. The development of a clinical prediction model for future planning of possible outcome improvement in these patients, however, is still feasible.
本研究旨在评估上埃及地区儿童肢体局限性骨肉瘤患者的生存结局,确定具有预后意义的生存因素,确定这些患者手术方法的预测因素,并建立一个风险预测的临床模型。
对2001年1月至2015年12月在南埃及癌症研究所接受统一化疗方案治疗的30例经组织学证实为肢体非转移性骨肉瘤的儿童患者的病历数据进行回顾性分析。采用单变量和多变量方法确定预后因素。基于基线临床因素以及预测其肿瘤对化疗反应的参数,建立了这些患者手术结局的模型。
研究人群的中位随访时间为63个月,3年和5年的无事件生存率和总生存率(OS)估计分别为69.5%和79%以及65.2%和65.3%。16岁及以上年龄与较差的无转移生存率(风险比[HR]=6.05,95%置信区间[CI]:1.43 - 25.6,P = 0.015)和OS(HR = 7.9,95% CI:1.71 - 36.2,P = 0.008)均独立相关。在多变量分析中,肢体近端位置具有统计学意义,与较差的OS独立相关(HR = 2.4,95% CI:1.13 - 22.1,P = 0.003)。仅在单变量分析中,化疗反应差与较差的无转移生存率略有相关(HR = 4.9,95% CI:1.02 - 23.8,P = 0.047)。发现化疗反应差的患者更有可能接受截肢手术(优势比 = 14.1,95% CI:1.34 - 149.4,P = 0.028)。
在上埃及,尽管非转移性骨肉瘤患者的生存结局尚可,但截肢率相对较高。然而,为这些患者未来改善可能结局的规划建立临床预测模型仍然是可行的。