Liu H D, Wu H L, Ma L L, Cui Y, Wang S W, Shen G H
Department of Obstetrics and Gynecology, Beijing Hospital, National Center of Gerontology, Beijing 100005, China.
Department of Obstetrics and Gynecology, Capital Medical University Beijing Friendship Hospital Pinggu Hospital, Beijing 101200, China.
Zhonghua Fu Chan Ke Za Zhi. 2025 Jun 25;60(6):461-468. doi: 10.3760/cma.j.cn112141-20250102-00001.
To investigate the predictive value of the cancer antigen 125 (CA) elimination rate constant K (KELIM) score for no visible residual disease (R0) and prognosis in high-grade serous ovarian carcinoma (HGSOC) patients undergoing neoadjuvant chemotherapy (NACT)+interval debulking surgery (IDS). A retrospective analysis was conducted on 78 HGSOC patients treated with NACT+IDS at Beijing Hospital, from June 2014 to June 2024. The KELIM score was calculated, and its predictive value for R0 resection, chemotherapy response score (CRS), platinum-free interval (PFI), progression-free survival (PFS) time, and overall survival (OS) time was analyzed. (1) The mean age at diagnosis was (61.9±9.9) years. The mean KELIM score was 1.1±0.4, with 44 patients having KELIM score≥1 and 34 having KELIM score <1. (2) Patients with KELIM score ≥1 had significantly higher rates of R0 resection (84% vs 56%; =0.006), CRS3 grading (41% vs 0; <0.001), and PFI ≥6 months (84% vs 53%; =0.04) compared to those with KELIM score <1. Additionally, the median PFS time (18.7 vs 13.2 months; <0.001) and OS time (34.8 vs 29.9 months; =0.007) were significantly longer in the KELIM score ≥1 group. Chemosensitivity: patients with PFI <6 months had a significantly lower median KELIM score than those with PFI ≥6 months (0.8 vs 1.2; =0.005). Surgical outcome: patients achieving R0 resection had a significantly higher median KELIM score than those without R0 (1.2 vs 0.7; <0.001). (3) Univariate analysis identified non-R0 resection, CRS3 grading, lack of poly adenosine diphosphate ribose polymerase (PARP) inhibitor maintenance therapy, and KELIM score <1 as significant risk factors for OS time (all <0.05). Multivariate analysis confirmed non-R0 resection (=3.78,95%: 1.13-12.66; =0.031), no PARP inhibitor maintenance (=7.41,95%:1.82-30.15; =0.005), and KELIM score <1 (=5.14,95%:1.41-18.72; =0.013) as independent risk factors for OS time. The KELIM score may serve as a predictive marker for chemosensitivity, R0 resection, PFS time, and OS time in HGSOC patients undergoing NACT+IDS. KELIM score<1 is an independent risk factor for OS.
为研究癌症抗原125(CA)清除率常数K(KELIM)评分对接受新辅助化疗(NACT)+中间减瘤手术(IDS)的高级别浆液性卵巢癌(HGSOC)患者无可见残留病灶(R0)及预后的预测价值。对2014年6月至2024年6月在北京医院接受NACT+IDS治疗的78例HGSOC患者进行回顾性分析。计算KELIM评分,并分析其对R0切除、化疗反应评分(CRS)、无铂间期(PFI)、无进展生存期(PFS)时间和总生存期(OS)时间的预测价值。(1)诊断时的平均年龄为(61.9±9.9)岁。KELIM评分均值为1.1±0.4,44例患者KELIM评分≥1,34例患者KELIM评分<1。(2)与KELIM评分<1的患者相比,KELIM评分≥1的患者R0切除率(84%对56%;P=0.006)、CRS3分级率(41%对0;P<0.001)和PFI≥6个月的比例(84%对53%;P=0.04)显著更高。此外,KELIM评分≥1组的中位PFS时间(18.7对13.2个月;P<0.001)和OS时间(34.8对29.9个月;P=0.007)显著更长。化疗敏感性:PFI<6个月的患者中位KELIM评分显著低于PFI≥6个月的患者(0.8对1.2;P=0.005)。手术结果:实现R0切除的患者中位KELIM评分显著高于未实现R0切除的患者(1.2对0.7;P<0.001)。(3)单因素分析确定非R0切除、CRS3分级、缺乏聚腺苷二磷酸核糖聚合酶(PARP)抑制剂维持治疗和KELIM评分<1是OS时间的显著危险因素(均P<0.05)。多因素分析证实非R0切除(P=3.78,95%置信区间:1.13-12.66;P=0.031)、无PARP抑制剂维持(P=7.41,95%置信区间:1.82-30.15;P=0.005)和KELIM评分<1(P=5.14,95%置信区间:1.41-18.72;P=0.013)是OS时间的独立危险因素。KELIM评分可作为接受NACT+IDS的HGSOC患者化疗敏感性、R0切除、PFS时间和OS时间的预测标志物。KELIM评分<1是OS的独立危险因素。