van der Velden Joanne M, Peters Max, Verlaan Jorrit-Jan, Versteeg Anne L, Zhang Liying, Tsao May, Danjoux Cyril, Barnes Elizabeth, van Vulpen Marco, Chow Edward, Verkooijen Helena M
Department of Radiotherapy, University Medical Center Utrecht, Utrecht, The Netherlands; Sunnybrook Odette Cancer Centre, University of Toronto, Toronto, Ontario, Canada.
Department of Radiotherapy, University Medical Center Utrecht, Utrecht, The Netherlands.
Int J Radiat Oncol Biol Phys. 2017 Nov 15;99(4):859-866. doi: 10.1016/j.ijrobp.2017.07.029. Epub 2017 Jul 31.
To investigate the relationship between patient and tumor characteristics and pain response in patients with metastatic bone disease, and construct and internally validate a clinical prediction model for pain response to guide individualized treatment decision making.
A total of 965 patients with painful bone metastases undergoing palliative radiation therapy at a tertiary referral center between 1999 and 2007 were identified. Pain scores were measured at 1, 2, and 3 months after radiation therapy. Pain response was defined as at least a 2-point decrease on a pain score scale of 0-10, without increase in analgesics, or an analgesic decrease of at least 25% without an increase in pain score. Thirteen candidate predictors were identified from the literature and expert experience. After multiple imputation, final predictors were selected using stepwise regression and collapsed into a prediction model. Model performance was evaluated by calibration and discrimination and corrected for optimism.
Overall 462 patients (47.9%) showed a response. Primary tumor site, performance status, and baseline pain score were predictive for pain response, with a corrected c-statistic of 0.63. The predicted response rates after radiation therapy increased from 37.5% for patients with the highest risk score to 79.8% for patients with the lowest risk score and were in good agreement with the observed response rates.
A prediction score for pain response after palliative radiation therapy was developed. The model performance was moderate, showing that prediction of pain response is difficult. New biomarkers and predictors may lead to improved identification of the large group of patients who are unlikely to respond and who may benefit from other or innovative treatment options.
探讨转移性骨病患者的患者及肿瘤特征与疼痛反应之间的关系,并构建并进行内部验证一个临床预测模型,以指导疼痛反应的个体化治疗决策。
确定了1999年至2007年期间在一家三级转诊中心接受姑息性放射治疗的965例骨转移疼痛患者。在放射治疗后1、2和3个月测量疼痛评分。疼痛反应定义为在0-10分的疼痛评分量表上至少降低2分,且镇痛药用量未增加,或镇痛药用量至少减少25%且疼痛评分未增加。从文献和专家经验中确定了13个候选预测因素。经过多重填补后,使用逐步回归选择最终预测因素,并将其纳入一个预测模型。通过校准和区分对模型性能进行评估,并对乐观性进行校正。
总体上462例患者(47.9%)显示有反应。原发肿瘤部位、体能状态和基线疼痛评分可预测疼痛反应,校正后的c统计量为0.63。放射治疗后的预测反应率从风险评分最高的患者的37.5%增加到风险评分最低的患者的79.8%,与观察到的反应率高度一致。
建立了姑息性放射治疗后疼痛反应的预测评分。模型性能中等,表明疼痛反应的预测具有难度。新的生物标志物和预测因素可能有助于更好地识别一大群不太可能有反应且可能从其他或创新治疗方案中获益的患者。