Division of Gynecologic Oncology, Segal Cancer Center, Jewish General Hospital, McGill University, Montreal, QC, Canada.
Department of Oncology, McGill University, Montreal, QC, Canada.
Acta Obstet Gynecol Scand. 2020 Jul;99(7):933-940. doi: 10.1111/aogs.13814. Epub 2020 Feb 5.
The objective was to assess whether an early response to neoadjuvant chemotherapy in women with advanced ovarian cancer may predict short- and long-term clinical outcome.
This is a retrospective study of all women with stage III-IV tubo-ovarian cancer treated with neoadjuvant chemotherapy at a single center in Montreal between 2003 and 2014. Logistic regression models were used to evaluate the association between cancer antigen 125 (CA-125) levels during neoadjuvant chemotherapy and debulking success. Cox proportional hazard models were used to estimate hazard ratios and their respective 95% CI for death and recurrence. Harrell's concordance indices were calculated to evaluate which variables best predicted the chemotherapy-free interval and overall survival in our population.
In all, 105 women were included. Following the first, second, and third cycles of neoadjuvant chemotherapy, CA-125 levels had a median reduction of 43.2%, 85.4%, and 92.9%, respectively, compared with CA-125 levels at diagnosis. As early as the second cycle, CA-125 was associated with overall survival (hazard ratio 1.03, 95% CI 1.01-1.05, per 50 U/mL increment). By the third cycle, CA-125 did not only predict overall survival (hazard ratio 1.04, 95% CI 1.01-1.08), but it predicted overall survival better than the success of debulking surgery (Harrell's concordance index 0.646 vs 0.616). Both absolute CA-125 levels and relative reduction in CA-125 levels after 2 and 3 cycles predicted the chance to achieve complete debulking (P < .05).
Reduction of CA-125 levels during neoadjuvant chemotherapy provides an early predictive tool that strongly correlates with successful cytoreductive surgery and long-term clinical outcome in women with advanced high-grade serous and endometrioid ovarian cancer.
本研究旨在评估晚期卵巢癌患者新辅助化疗的早期应答是否可以预测短期和长期临床结局。
这是一项回顾性研究,纳入了 2003 年至 2014 年在蒙特利尔的一家中心接受新辅助化疗的所有 III-IV 期卵巢癌患者。使用逻辑回归模型评估新辅助化疗期间癌抗原 125(CA-125)水平与肿瘤细胞减灭术成功之间的关联。使用 Cox 比例风险模型估计死亡和复发的风险比及其各自的 95%置信区间。计算 Harrell 一致性指数以评估哪些变量最能预测本人群的化疗无间期和总生存期。
共纳入 105 例患者。与诊断时的 CA-125 水平相比,新辅助化疗的第 1、2 和 3 个周期后,CA-125 水平分别中位数降低了 43.2%、85.4%和 92.9%。早在第 2 个周期,CA-125 与总生存期相关(风险比 1.03,95%CI 1.01-1.05,每增加 50 U/mL)。到第 3 个周期,CA-125 不仅预测总生存期(风险比 1.04,95%CI 1.01-1.08),而且预测总生存期的能力优于肿瘤细胞减灭术的成功(Harrell 一致性指数 0.646 比 0.616)。第 2 和第 3 周期的 CA-125 绝对值和相对降低水平均预测完全肿瘤细胞减灭术的机会(P<0.05)。
新辅助化疗期间 CA-125 水平的降低提供了一个早期预测工具,该工具与晚期高级别浆液性和子宫内膜样卵巢癌患者成功的肿瘤细胞减灭术和长期临床结局具有强烈相关性。