Liu Yu, Cao Lili, Chen Wei, Wang Jingjing, Wang Wenting, Liang Zhiqing
Department of Obstetrics and Gynecology of the First Affiliated Hospital of Third Military Medical University (Army Medical University), Chongqing, China.
Medicine (Baltimore). 2020 Sep 4;99(36):e22100. doi: 10.1097/MD.0000000000022100.
Intraperitoneal (IP) chemotherapy is believed to prolong the survival of patients with advanced ovarian cancer after primary debulking surgery. However, there is little knowledge about IP chemotherapy in the setting of neoadjuvant chemotherapy, and there are contradictory conclusions about adjuvant IP chemotherapy. Here, we evaluated the feasibility of neoadjuvant and adjuvant IP chemotherapy in patients with advanced epithelial ovarian cancer (AEOC).We retrospectively reviewed the data of 114 patients with AEOC who received neoadjuvant chemotherapy followed by laparoscopic conservative interval debulking surgery (NACT + LIDS) in our institution from January 1, 2009 to December 31, 2017.The median overall survival (OS) was 56 months and the median disease-free interval (DFI) was 14 months for the entire study population. Neoadjuvant IP chemotherapy cycles were crucial for the treatment of no gross residual (R0) disease (hazard ratio [HR] = 0.446, 95% confidence interval [CI] = 0.245-0.811), which was independently associated with OS of the entire study population (HR = 9.589, 95% CI = 3.911-23.507). In addition, residual disease and body mass index (BMI) were the prognostic factors for DFI (HR = 6.022, 95% CI = 3.632-9.986; HR = 1.085, 95% CI = 1.012-1.163). However, adjuvant IP cycles along with BMI were the determining factors for DFI in the R0 group (HR = 0.703, 95% CI = 0.525-0.941; HR = 1.130, 95% CI = 1.025-1.247), and were associated with OS in the R0 group (HR = 0.488, 95% CI = 0.289-0.824). The OS and DFI Kaplan-Meier curves stratified by adjuvant IP chemothearpy cycles within the R0 group were statistically significant (P = .024 and P = .033, respectively).Our results showed improvement in patients with AEOC in terms of survival, thus suggesting the feasibility of neoadjuvant and adjuvant IP chemotherapy.
腹腔内(IP)化疗被认为可延长晚期卵巢癌患者在初次肿瘤细胞减灭术后的生存期。然而,对于新辅助化疗背景下的IP化疗了解甚少,且关于辅助性IP化疗存在相互矛盾的结论。在此,我们评估了新辅助和辅助性IP化疗在晚期上皮性卵巢癌(AEOC)患者中的可行性。
我们回顾性分析了2009年1月1日至2017年12月31日在我院接受新辅助化疗后行腹腔镜保守性中间型肿瘤细胞减灭术(NACT + LIDS)的114例AEOC患者的数据。
整个研究人群的中位总生存期(OS)为56个月,中位无病间期(DFI)为14个月。新辅助IP化疗周期对于无肉眼残留(R0)疾病的治疗至关重要(风险比[HR] = 0.446,95%置信区间[CI] = 0.245 - 0.811),这与整个研究人群的OS独立相关(HR = 9.589,95% CI = 3.911 - 23.507)。此外,残留疾病和体重指数(BMI)是DFI的预后因素(HR = 6.022,95% CI = 3.632 - 9.986;HR = 1.085,95% CI = 1.012 - 1.163)。然而,在R0组中,辅助性IP化疗周期与BMI是DFI的决定因素(HR = 0.703,95% CI = 0.525 - 0.941;HR = 1.130,95% CI = 1.025 - 1.247),并且与R0组的OS相关(HR = 0.488,95% CI = 0.289 - 0.824)。R0组内按辅助性IP化疗周期分层的OS和DFI的Kaplan - Meier曲线具有统计学意义(分别为P = 0.024和P = 0.033)。
我们的结果显示AEOC患者的生存期有所改善,从而表明新辅助和辅助性IP化疗的可行性。