Division of Gynecologic Surgery, Mayo Clinic, Rochester, MN, United States of America.
Department of Radiology, Mayo Clinic, Rochester, MN, United States of America.
Gynecol Oncol. 2019 Jul;154(1):72-76. doi: 10.1016/j.ygyno.2019.04.011. Epub 2019 Apr 16.
Treatment planning requires accurate estimation of surgical complexity (SC) and residual disease (RD) at primary debulking surgery (PDS) for advanced ovarian cancer (OC). We sought to independently validate two published computed tomography (CT) prediction models.
We included stage IIIC/IV OC patients who underwent PDS from 2003 to 2011. Two prediction models which included imaging and clinical variables to predict RD > 1 and any gross RD, respectively, were applied to our cohort. Two radiologists scored CTs. Discrimination was estimated using the c-index and calibration were assessed by comparing the observed and predicted estimates.
The validation cohort consisted of 276 patients; median age of the cohort was 64 years old and majority had serous histology. The validation and model development cohorts were similar in terms of baseline characteristics, however the RD rates differed between cohorts (9.4% vs 25.4% had RD >1 cm; 50.7% vs. 66.6% had gross RD). Model 1, the model to predict RD >1 cm, did not validate well. The c-index of 0.653 for the validation cohort was lower than reported in the development cohort (0.758) and the model over-predicted the proportion with RD >1 cm. The second model to predict gross RD had excellent discrimination with a c-index of 0.762.
We are able to validate a CT model to predict presence of gross RD in an independent center; the separate model to predict RD >1 cm did not validate. Application of the model to predict gross RD can help with clinical decision making in advanced ovarian cancer.
在高级卵巢癌(OC)的初次减瘤手术(PDS)中,治疗计划需要准确估计手术复杂性(SC)和残留疾病(RD)。我们试图独立验证两个已发表的 CT 预测模型。
我们纳入了 2003 年至 2011 年期间接受 PDS 的 IIIC/IV 期 OC 患者。两个预测模型分别纳入了影像学和临床变量,以分别预测 RD>1 和任何大体 RD。两位放射科医生对 CT 进行评分。通过比较观察到的和预测的估计值来评估判别能力和校准情况。
验证队列包括 276 例患者;队列的中位年龄为 64 岁,大多数为浆液性组织学。验证和模型开发队列在基线特征方面相似,但 RD 发生率不同(9.4%与 25.4%的患者 RD>1cm;50.7%与 66.6%的患者存在大体 RD)。用于预测 RD>1cm 的模型 1 验证效果不佳。验证队列的 C 指数为 0.653,低于开发队列(0.758),且模型过度预测了 RD>1cm 的比例。预测大体 RD 的第二个模型具有出色的判别能力,C 指数为 0.762。
我们能够在一个独立中心验证预测大体 RD 存在的 CT 模型;预测 RD>1cm 的单独模型未得到验证。应用该模型预测大体 RD 有助于在高级卵巢癌中做出临床决策。