Division of Gynecologic Oncology, Hopital Maisonneuve Rosemont, University of Montreal, Montreal, Quebec, Canada.
Department of Pathology, St. James's Hospital, Dublin 8, Ireland.
Gynecol Oncol. 2024 Aug;187:92-97. doi: 10.1016/j.ygyno.2024.04.009. Epub 2024 May 11.
The objective of this study is to assess the correlation between the pre-operative CA125 Elimination rate constant K(KELIM) score and the intraoperative chemo-response score (CRS) in patients with advanced high grade serous ovarian cancer(HGSC) treated with neoadjuvant chemotherapy(NACT).
This is a retrospective cohort study of patients with Stage III-IV HGSC treated with NACT from March 2010 to December 2019 at Princess Margaret Cancer Center, Toronto, Canada. KELIM scores were calculated based on the tool devised by You et al. available online. CRS was assessed using an established 3-tier scoring system. An association analysis was performed to determine if the KELIM score assessed during NACT can predict CRS score at the time of interval cytoreductive surgery(ICS).
172 patients were included in this analysis. Patients with CRS 1-2 had a lower median Platinum Free Interval(PFI) (9.24 vs 13.64 months, p = 0.005), lower median progression free survival(PFS) (14.99 vs 20.29 months, p = 0.003) and lower 5-year overall survival(OS) (63.8% vs 69.7%, p = 0.54) compared to patients with CRS3. Among patients with CRS 1-2(n = 115), 68.7% had KELIM <1, while 56.2% of patients with CRS3 had KELIM ≥1(56.2%), p = 0.0017, suggesting a correlation between the KELIM and CRS scores. Furthermore, patients with KELIM ≥1 and CRS3 had significantly higher PFS compared to other groups(median PFS 28.27 months vs 17.66 months for KELIM ≥1/CRS 1/2; 17.13 months for KELIM <1/CRS 3; and 14.53 months for KELIM <1/CRS 1-2, p = 0.003).
The biochemical KELIM score correlated with the surgical pathologic CRS score and may predict pathological response to chemotherapy. This information can be utilized to tailor and personalize treatment in patients with advanced ovarian malignancy.
本研究旨在评估新辅助化疗(NACT)治疗晚期高级别浆液性卵巢癌(HGSC)患者的术前 CA125 消除率常数 K(KELIM)评分与术中化疗反应评分(CRS)之间的相关性。
这是一项回顾性队列研究,纳入 2010 年 3 月至 2019 年 12 月在加拿大多伦多玛格丽特公主癌症中心接受 NACT 治疗的 III-IV 期 HGSC 患者。KELIM 评分基于 You 等人在线提供的工具计算。CRS 采用已建立的 3 级评分系统进行评估。进行关联分析以确定 NACT 期间评估的 KELIM 评分是否可以预测间隔减瘤手术(ICS)时的 CRS 评分。
本分析共纳入 172 例患者。CRS 为 1-2 的患者中位无铂间隔时间(PFI)较短(9.24 个月 vs 13.64 个月,p=0.005),无进展生存期(PFS)较短(14.99 个月 vs 20.29 个月,p=0.003),5 年总生存期(OS)较低(63.8% vs 69.7%,p=0.54),与 CRS 为 3 的患者相比。在 CRS 为 1-2 的患者中(n=115),68.7%的患者 KELIM<1,而 CRS 为 3 的患者中有 56.2%的患者 KELIM≥1(56.2%),p=0.0017,提示 KELIM 与 CRS 评分之间存在相关性。此外,KELIM≥1 且 CRS3 的患者的 PFS 显著长于其他组(KELIM≥1/CRS1/2 的中位 PFS 为 28.27 个月 vs 17.66 个月;KELIM<1/CRS3 的中位 PFS 为 17.13 个月;KELIM<1/CRS1-2 的中位 PFS 为 14.53 个月,p=0.003)。
生化 KELIM 评分与手术病理 CRS 评分相关,可能预测化疗的病理反应。该信息可用于定制和个性化治疗晚期卵巢恶性肿瘤患者。