Rios Velazquez Emmanuel, Hoebers Frank, Aerts Hugo J W L, Rietbergen Michelle M, Brakenhoff Ruud H, Leemans René C, Speel Ernst-Jan, Straetmans Jos, Kremer Bernd, Lambin Philippe
Department of Radiation Oncology (MAASTRO), Research Institute GROW, Maastricht University, Maastricht, The Netherlands; Department of Radiation Oncology, Dana-Farber Cancer Institute, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Department of Radiation Oncology (MAASTRO), Research Institute GROW, Maastricht University, Maastricht, The Netherlands.
Radiother Oncol. 2014 Dec;113(3):324-30. doi: 10.1016/j.radonc.2014.09.005. Epub 2014 Oct 24.
Due to the established role of the human papillomavirus (HPV), the optimal treatment for oropharyngeal carcinoma is currently under debate. We evaluated the most important determinants of treatment outcome to develop a multifactorial predictive model that could provide individualized predictions of treatment outcome in oropharyngeal carcinoma patients.
We analyzed the association between clinico-pathological factors and overall and progression-free survival in 168 OPSCC patients treated with curative radiotherapy or concurrent chemo-radiation. A multivariate model was validated in an external dataset of 189 patients and compared to the TNM staging system. This nomogram will be made publicly available at www.predictcancer.org.
Predictors of unfavorable outcomes were negative HPV-status, moderate to severe comorbidity, T3-T4 classification, N2b-N3 stage, male gender, lower hemoglobin levels and smoking history of more than 30 pack years. Prediction of overall survival using the multi-parameter model yielded a C-index of 0.82 (95% CI, 0.76-0.88). Validation in an independent dataset yielded a C-index of 0.73 (95% CI, 0.66-0.79. For progression-free survival, the model's C-index was 0.80 (95% CI, 0.76-0.88), with a validation C-index of 0.67, (95% CI, 0.59-0.74). Stratification of model estimated probabilities showed statistically different prognosis groups in both datasets (p<0.001).
This nomogram was superior to TNM classification or HPV status alone in an independent validation dataset for prediction of overall and progression-free survival in OPSCC patients, assigning patients to distinct prognosis groups. These individualized predictions could be used to stratify patients for treatment de-escalation trials.
鉴于人乳头瘤病毒(HPV)已明确的作用,目前口咽癌的最佳治疗方法仍存在争议。我们评估了治疗结果的最重要决定因素,以建立一个多因素预测模型,该模型可为口咽癌患者的治疗结果提供个性化预测。
我们分析了168例接受根治性放疗或同步放化疗的口咽鳞状细胞癌(OPSCC)患者的临床病理因素与总生存期和无进展生存期之间的关联。在一个包含189例患者的外部数据集中对多变量模型进行了验证,并与TNM分期系统进行了比较。该列线图将在www.predictcancer.org上公开提供。
不良预后的预测因素包括HPV状态阴性、中度至重度合并症、T3-T4分级、N2b-N3期、男性、血红蛋白水平较低以及吸烟史超过30包年。使用多参数模型预测总生存期的C指数为0.82(95%CI,0.76-0.88)。在独立数据集中进行验证,C指数为0.73(95%CI,0.66-0.79)。对于无进展生存期,该模型的C指数为0.80(95%CI,0.76-0.88),验证C指数为0.67(95%CI,0.59-0.74)。模型估计概率的分层在两个数据集中均显示出统计学上不同的预后组(p<0.001)。
在独立验证数据集中,该列线图在预测OPSCC患者的总生存期和无进展生存期方面优于单独的TNM分类或HPV状态,可将患者分为不同的预后组。这些个性化预测可用于对患者进行分层,以开展治疗降阶梯试验。