国际肿瘤学杂志 ›› 2026, Vol. 53 ›› Issue (10): 600-607.doi: 10.3760/cma.j.cn371439-20251217-00095

• 论著 • 上一篇    下一篇

基于KELIM评分构建卵巢高级别浆液性腺癌患者NACT+IDS治疗后无进展生存期预测模型

李平1, 陈真云2, 牛洪朋2()   

  1. 1 山东省临沂市妇幼保健院妇女保健科, 临沂 276000
    2 山东省临沂市肿瘤医院妇科, 临沂 276000
  • 收稿日期:2025-12-17 出版日期:2026-10-08 发布日期:2026-10-10
  • 通讯作者: 牛洪朋,Email:1042258089@qq.com
  • 作者简介:

    李平:数据收集、整理,统计学分析及论文撰写;陈真云:数据整理、统计学分析、论文修改;牛洪朋:研究指导、数据收集、论文修改

A progression-free survival prediction model based on KELIM score for patients with high-grade serous ovarian carcinoma after NACT+IDS treatment

Li Ping1, Chen Zhenyun2, Niu Hongpeng2()   

  1. 1 Department of Women's Health, Women & Children's Health Care Hospital of Linyi,Shandong Province, Linyi 276000, China
    2 Department of Gynecology, Linyi Cancer Hospital,Shandong Province, Linyi 276000, China
  • Received:2025-12-17 Online:2026-10-08 Published:2026-10-10
  • Contact: Niu Hongpeng,Email:1042258089@qq.com

摘要:

目的 基于模拟糖类抗原125(CA125)消除速率常数K(KELIM)评分构建卵巢高级别浆液性腺癌(HGSOC)患者新辅助化疗(NACT)+间歇性肿瘤细胞减灭术(IDS)治疗后无进展生存期(PFS)的预测模型。方法 回顾性收集2022年5月至2024年1月山东省临沂市肿瘤医院接受NACT+IDS治疗的180例HGSOC患者的临床资料,按7∶3比例分为训练集(126例)和验证集(54例),计算NACT期间KELIM评分,用Kaplan-Meier法和log-rank检验比较不同KELIM评分组患者的生存差异,采用多因素Cox比例风险回归模型分析PFS的影响因素。基于KELIM评分构建HGSOC患者NACT+IDS治疗后PFS的预测模型,通过受试者操作特征(ROC)曲线、校准曲线评估基于KELIM评分的PFS预测模型的预测效能。结果 训练集HGSOC患者KELIM评分≥1分59例,KELIM评分<1分67例;治疗后1年内,因疾病进展或全因死亡45例(35.71%)。KELIM评分≥1分组PFS的受限平均生存时间(RMST)(11.3个月比9.1个月)、OS的RMST(11.7个月比10.9个月)均长于KELIM评分<1分组(χ2=14.07,P<0.001;χ2=4.74,P=0.030)。疾病进展或全因死亡患者年龄≥60岁(χ2=6.37,P=0.012)、国际妇产科联盟(FIGO)分期Ⅳ期(χ2=7.62,P=0.006)、术后肿瘤残留非R0(χ2=6.61,P=0.010)、KELIM评分<1分(χ2=11.43,P<0.001)占比均高于无进展存活患者。多因素分析结果显示,年龄≥60岁(HR=2.82,95%CI为1.50~5.29,P=0.001)、FIGO分期Ⅳ期(HR=2.23,95%CI为1.24~4.04,P=0.008)、术后肿瘤残留非R0(HR=2.01,95%CI为1.10~3.65,P=0.022)、KELIM评分<1分(HR=3.30,95%CI为1.70~6.42,P<0.001)均是HGSOC患者NACT+IDS治疗后PFS的独立危险因素。基于上述因素构建列线图模型,校准曲线显示,训练集和验证集列线图模型的预测概率接近实际概率,校准度好。ROC曲线分析显示,训练集和验证集列线图模型预测PFS的曲线下面积分别为0.81(95%CI为0.73~0.89)、0.88(95%CI为0.77~0.99)。结论 KELIM评分与HGSOC患者NACT+IDS治疗后PFS有关,KELIM评分<1分的患者PFS及OS均较短,基于KELIM评分构建的列线图模型能够较好地预测HGSOC患者NACT+IDS治疗后的PFS。

关键词: 卵巢肿瘤, 囊腺瘤, 浆液, CA-125抗原, 动力学, 肿瘤细胞减灭术, 无进展生存期

Abstract:

Objective To construct a progression-free survival prediction model based on the modeled carbohydrate antigen 125 (CA125) elimination rate constant K (KELIM) for patients with high-grade serous ovarian carcinoma (HGSOC) after neoadjuvant chemotherapy (NACT) and interval debulking surgery (IDS). Methods The clinical data of 180 HGSOC patients who received NACT+IDS treatment at Linyi Cancer Hospital,Shandong Province from May 2022 to January 2024 were retrospectively collected. Patients were divided into a training set (126 cases) and a validation set (54 cases) in a 7∶3 ratio. The KELIM score during NACT was calculated. Kaplan-Meier method and log-rank test were used to compare the survival differences of patients with different KELIM scores,and multivariate Cox proportional hazard regression model was used to analyze the influencing factors of PFS. The prediction model of PFS after NACT+IDS treatment in HGSOC patients was constructed based on the KELIM score. The predictive efficacy of the PFS prediction model based on KELIM score were evaluated by receiver operator characteristic (ROC) curve and calibration curve. Results Among the HGSOC patients in the training set,59 cases had KELIM scores ≥1 point,and 67 cases had KELIM scores <1 point. Forty-five cases (35.71%) died due to disease progression or all-cause within one year after treatment. The restricted mean survival time (RMST) for PFS (11.3 months vs. 9.1 months) and for OS (11.7 months vs. 10.9 months) of the KELIM score ≥1 group were longer than those of the <1 group (χ2=14.07,P<0.001; χ2=4.74,P=0.030). The proportion of patients aged ≥60 years with disease progression or all-cause mortality (χ2=6.37,P=0.012),patients in the International Federation of Gynecology and Obstetrics (FIGO) stage Ⅳ (χ2=7.62,P=0.006),postoperative non-R0 tumor residual (χ2=6.61,P=0.010),and KELIM score <1 (χ2=11.43,P<0.001) were higher than those who survived without progression. Multivariate analysis showed that age ≥60 years (HR=2.82,95%CI:1.50-5.29,P=0.001),FIGO stage Ⅳ (HR=2.23,95%CI:1.24-4.04,P=0.008),postoperative non-R0 tumor residual (HR=2.01,95%CI:1.10-3.65,P=0.022),KELIM score <1 (HR=3.30,95%CI:1.70-6.42,P<0.001) were all the independent risk factors of PFS after NACT+IDS treatment in HGSOC patients. Based on the above factors,a nomogram model was constructed,and the calibration curve showed that the predicted probabilities of the nomogram model in the training set and validation set were close to the actual probabilities,indicating good calibration. ROC curve analysis showed that the areas under the curve of the nomogram model for predicting PFS of the training and validation sets were 0.81 (95%CI:0.73-0.89) and 0.88 (95%CI:0.77-0.99),respectively. Conclusions The KELIM score is related to the PFS of HGSOC patients after NACT+IDS treatment. Patients with KELIM score <1 have shorter PFS and OS. The nomogram model constructed on the basis of the KELIM score demonstrates good performance in predicting PFS of HGSOC patients following NACT+IDS treatment.

Key words: Ovarian neoplasms, Cystadenoma, serous, CA-125 antigen, Kinetics, Cytoreduction surgical procedures, Progression-free survival