Division of Gynecologic Oncology, Obstetrics, Gynecology and Women's Health Institute, Cleveland Clinic, Desk A81, 9500 Euclid Avenue, Cleveland, OH 44195, United States of America.
Division of Gynecologic Oncology, Obstetrics, Gynecology and Women's Health Institute, Cleveland Clinic, Desk A81, 9500 Euclid Avenue, Cleveland, OH 44195, United States of America.
Gynecol Oncol. 2020 Dec;159(3):699-705. doi: 10.1016/j.ygyno.2020.09.010. Epub 2020 Sep 17.
OBJECTIVE(S): To determine whether antibiotic treatment (ABX) during platinum chemotherapy (PC) for epithelial ovarian cancer (EOC) impacts progression-free survival (PFS) and overall survival (OS).
Retrospective single institution cohort study in women with newly diagnosed stage III/IV EOC (n = 424) who underwent cytoreductive surgery (CRS) and PC from 2009 to 2015. ABX for >48 h, including ABX against gram-positive (anti-G + ABX) bacteria were recorded. The impact of ABX on PFS and OS was assessed using univariate and multivariable Cox regression models.
Of 424 eligible women, 34.7% (n = 147) received ABX, with 11.3% (n = 48) treated with anti-G + ABX. ABX decreased PFS (17.4 vs. 23.1 months, HR 1.50, 95% CI 1.20-1.88, p < 0.001) and OS (45.6 vs. 62.4 months, HR 1.63, 95% CI 1.27-2.08, p < 0.001) compared to no ABX. Similarly, anti-G + ABX worsened PFS (16.5 vs. 23.1 months; HR 1.85, 95% CI 1.33-2.55) and OS (35.0 vs. 62.4 months; HR 2.12, 95% CI 1.50-3.0, p < 0.001). On multivariable analysis, all ABX and anti-G + ABX significantly worsened PFS (HR 1.31, 95% CI 1.04-1.65, p = 0.02), (HR 1.50, 95% CI 1.07-2.10, p = 0.02) and OS (HR 1.52, 95% CI 1.18-1.96, p = 0.001), (HR 1.83, 95% CI 1.27-2.62, p = 0.001) respectively. Increased Clavien Dindo score was associated with worsened PFS (1-2 - HR 1.52, 95% CI 1.14-2.03, p = 0.004; 3-4 - HR 1.86, 95% CI 1.27-2.72, p = 0.001) but not OS (1/2 - HR 1.35, 95% CI 0.97-1.88, p = 0.08; 3/4 - HR 1.53, 95% CI 1.00-2.34, p = 0.05); residual disease (p < 0.05) and neoadjuvant chemotherapy (p < 0.001) were associated with worse PFS and OS.
CONCLUSION(S): In this retrospective cohort study of women with advanced EOC undergoing PC, ABX treatment was associated with decreased PFS and OS. Mechanistic studies are needed to investigate the negative impact of ABX upon PC response in EOC.
确定上皮性卵巢癌(EOC)铂类化疗期间使用抗生素(ABX)是否会影响无进展生存期(PFS)和总生存期(OS)。
对 2009 年至 2015 年间接受细胞减灭术(CRS)和铂类化疗的新诊断为 III/IV 期 EOC 的女性(n=424)进行回顾性单机构队列研究。记录 ABX 超过 48 小时的情况,包括针对革兰阳性(抗 G+ABX)细菌的 ABX。使用单变量和多变量 Cox 回归模型评估 ABX 对 PFS 和 OS 的影响。
在 424 名符合条件的女性中,34.7%(n=147)接受了 ABX,其中 11.3%(n=48)接受了抗 G+ABX 治疗。与未使用 ABX 相比,使用 ABX 降低了 PFS(17.4 与 23.1 个月,HR 1.50,95%CI 1.20-1.88,p<0.001)和 OS(45.6 与 62.4 个月,HR 1.63,95%CI 1.27-2.08,p<0.001)。同样,抗 G+ABX 也恶化了 PFS(16.5 与 23.1 个月;HR 1.85,95%CI 1.33-2.55)和 OS(35.0 与 62.4 个月;HR 2.12,95%CI 1.50-3.0,p<0.001)。多变量分析显示,所有 ABX 和抗 G+ABX 显著降低了 PFS(HR 1.31,95%CI 1.04-1.65,p=0.02)和 OS(HR 1.50,95%CI 1.07-2.10,p=0.02),HR 1.52,95%CI 1.18-1.96,p=0.001)和 OS(HR 1.83,95%CI 1.27-2.62,p=0.001)。Clavien-Dindo 评分增加与 PFS 恶化相关(1-2 分,HR 1.52,95%CI 1.14-2.03,p=0.004;3-4 分,HR 1.86,95%CI 1.27-2.72,p=0.001),但与 OS 无关(1/2 分,HR 1.35,95%CI 0.97-1.88,p=0.08;3/4 分,HR 1.53,95%CI 1.00-2.34,p=0.05);残留疾病(p<0.05)和新辅助化疗(p<0.001)与 PFS 和 OS 恶化相关。
在这项对接受铂类化疗的晚期 EOC 女性进行的回顾性队列研究中,ABX 治疗与 PFS 和 OS 降低有关。需要进行机制研究以调查 ABX 对 EOC 铂类化疗反应的负面影响。