Nandra Rajpal, Parry Michael, Forsberg Jonathan, Grimer Robert
The Royal Orthopaedic Hospital, The Woodlands, Bristol Road South, Birmingham, B31 2AP, UK.
Section of Orthopaedics and Sports Medicine, Karolinska University Hospital, Stockholm, Sweden.
Clin Orthop Relat Res. 2017 Jun;475(6):1681-1689. doi: 10.1007/s11999-017-5346-1. Epub 2017 Apr 10.
Extremity sarcoma has a preponderance to present late with advanced stage at diagnosis. It is important to know why these patients die early from sarcoma and to predict those at high risk. Currently we have mid- to long-term outcome data on which to counsel patients and support treatment decisions, but in contrast to other cancer groups, very little on short-term mortality. Bayesian belief network modeling has been used to develop decision-support tools in various oncologic diagnoses, but to our knowledge, this approach has not been applied to patients with extremity sarcoma.
QUESTIONS/PURPOSES: We sought to (1) determine whether a Bayesian belief network could be used to estimate the likelihood of 1-year mortality using receiver operator characteristic analysis; (2) describe the hierarchal relationships between prognostic and outcome variables; and (3) determine whether the model was suitable for clinical use using decision curve analysis.
We considered all patients treated for primary bone sarcoma between 1970 and 2012, and excluded secondary metastasis, presentation with local recurrence, and benign tumors. The institution's database yielded 3499 patients, of which six (0.2%) were excluded. Data extracted for analysis focused on patient demographics (age, sex), tumor characteristics at diagnosis (size, metastasis, pathologic fracture), survival, and cause of death. A Bayesian belief network generated conditional probabilities of variables and survival outcome at 1 year. A lift analysis determined the hierarchal relationship of variables. Internal validation of 699 test patients (20% dataset) determined model accuracy. Decision curve analysis was performed comparing net benefit (capped at 85.5%) for all threshold probabilities (survival output from model).
We successfully generated a Bayesian belief network with five first-degree associates and describe their conditional relationship with survival after the diagnosis of primary bone sarcoma. On internal validation, the resultant model showed good predictive accuracy (area under the curve [AUC] = 0.767; 95% CI, 0.72-0.83). The factors that predict the outcome of interest, 1-year mortality, in order of relative importance are synchronous metastasis (6.4), patient's age (3), tumor size (2.1), histologic grade (1.8), and presentation with a pathologic fracture (1). Patient's sex, tumor location, and inadvertent excision were second-degree associates and not directly related to the outcome of interest. Decision curve analysis shows that clinicians can accurately base treatment decisions on the 1-year model rather than assuming all patients, or no patients, will survive greater than 1 year. For threshold probabilities less than approximately 0.5, the model is no better or no worse than assuming all patients will survive.
We showed that a Bayesian belief network can be used to predict 1-year mortality in patients presenting with a primary malignancy of bone and quantified the primary factors responsible for an increased risk of death. Synchronous metastasis, patient's age, and the size of the tumor had the largest prognostic effect. We believe models such as these can be useful as clinical decision-support tools and, when properly externally validated, provide clinicians and patients with information germane to the treatment of bone sarcomas.
Bone sarcomas are difficult to treat requiring multidisciplinary input to strategize management. An evidence-based survival prediction can be a powerful adjunctive to clinicians in this scenario. We believe the short-term predictions can be used to evaluate services, with 1-year mortality already being a quality indicator. Mortality predictors also can be incorporated in clinical trials, for example, to identify patients who are least likely to experience the side effects of experimental toxic chemotherapeutic agents.
肢体肉瘤在诊断时多表现为晚期。了解这些患者为何早期死于肉瘤以及预测高危患者很重要。目前我们有中长期结局数据用于为患者提供咨询并支持治疗决策,但与其他癌症群体相比,关于短期死亡率的数据很少。贝叶斯信念网络建模已被用于开发各种肿瘤诊断中的决策支持工具,但据我们所知,这种方法尚未应用于肢体肉瘤患者。
问题/目的:我们试图(1)使用受试者工作特征分析确定贝叶斯信念网络是否可用于估计1年死亡率的可能性;(2)描述预后和结局变量之间的层次关系;(3)使用决策曲线分析确定该模型是否适合临床使用。
我们纳入了1970年至2012年间接受原发性骨肉瘤治疗的所有患者,并排除了继发性转移、局部复发表现和良性肿瘤。该机构的数据库中有3499例患者,其中6例(0.2%)被排除。提取用于分析的数据集中在患者人口统计学特征(年龄、性别)、诊断时的肿瘤特征(大小、转移、病理性骨折)、生存情况和死亡原因。贝叶斯信念网络生成变量和1年生存结局的条件概率。提升分析确定变量的层次关系。对699例测试患者(20%的数据集)进行内部验证以确定模型准确性。进行决策曲线分析,比较所有阈值概率(模型的生存输出)下的净收益(上限为85.5%)。
我们成功生成了一个具有五个一级关联因素的贝叶斯信念网络,并描述了它们与原发性骨肉瘤诊断后生存的条件关系。在内部验证中,所得模型显示出良好的预测准确性(曲线下面积[AUC]=0.767;95%CI,0.72 - 0.83)。按相对重要性顺序预测感兴趣结局(1年死亡率)的因素为同时性转移(6.4)、患者年龄(3)、肿瘤大小(2.1)、组织学分级(1.8)和病理性骨折表现(1)。患者性别、肿瘤位置和意外切除为二级关联因素,与感兴趣的结局无直接关系。决策曲线分析表明,临床医生可以准确地基于1年模型做出治疗决策,而不是假设所有患者或没有患者能存活超过1年。对于阈值概率小于约0.5的情况,该模型与假设所有患者都能存活相比,效果相当。
我们表明贝叶斯信念网络可用于预测原发性骨恶性肿瘤患者的1年死亡率,并量化了导致死亡风险增加的主要因素。同时性转移、患者年龄和肿瘤大小具有最大的预后影响。我们认为这样的模型可作为临床决策支持工具,并且在经过适当的外部验证后,能为临床医生和患者提供与骨肉瘤治疗相关的信息。
骨肉瘤难以治疗,需要多学科投入来制定管理策略。在这种情况下,基于证据的生存预测对临床医生可能是一个强大的辅助工具。我们认为短期预测可用于评估服务,1年死亡率已经是一个质量指标。死亡率预测因素也可纳入临床试验,例如,以识别最不可能经历实验性毒性化疗药物副作用的患者。