Effects of neoadjuvant hyperthermic intraperitoneal chemotherapy on chemotherapy response score and recurrence in high-grade serous ovarian cancer patients with advanced disease: A multicentre retrospective cohort study

被引:8
作者
Wu, Miao-fang [1 ]
Liang, Jin-xiao [1 ]
Li, Hui [1 ]
Ye, Yan-fang [2 ]
Liang, Wei-feng [3 ]
Wang, Li-juan [1 ]
Zhang, Bing-zhong [1 ]
Chen, Qing [1 ]
Lin, Zhong-qiu [1 ]
Li, Jing [1 ,4 ]
机构
[1] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Gynaecol Oncol, Guangzhou, Peoples R China
[2] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Clin Res Design Div, Guangzhou, Peoples R China
[3] Shandong Univ, Qilu Hosp Qingdao, Cheeloo Coll Med, Dept Gynaecol & Obstet, Qingdao, Peoples R China
[4] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Dept Gynaecol Oncol, 33 Yingfeng Rd, Guangzhou 510000, Peoples R China
关键词
chemotherapy response score; high-grade serous ovarian cancer; hyperthermic intraperitoneal chemotherapy; neoadjuvant chemotherapy; prognosis; CYTOREDUCTIVE SURGERY; GYNECOLOGIC ONCOLOGY; RECOMMENDATIONS; RATIONALE; CARCINOMA; CONSENSUS; SOCIETY; HIPEC; TRIAL;
D O I
10.1111/1471-0528.17323
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
ObjectiveTo investigate whether the combination of neoadjuvant hyperthermic intraperitoneal chemotherapy (NHIPEC) plus intravenous neoadjuvant chemotherapy (IV NACT) has superior efficacy to IV NACT alone. DesignRetrospective cohort study. SettingTwo tertiary referral university hospitals. PopulationPatients with ovarian cancer who received NACT-interval debulking surgery (IDS) between 2012 and 2020. MethodsThe tumour response to NACT was evaluated with the chemotherapy response score (CRS) system. Survival outcomes were compared. Main outcome measuresCRS 3, progression-free survival (PFS), and overall survival (OS). ResultsIn total, 127 patients were included, and 46 received NHIPEC plus IV NACT. The addition of NHIPEC was independently associated with an increased likelihood of CRS 3 (p = 0.033). Patients who received NHIPEC + IV NACT had significantly improved PFS compared with those who received IV NACT alone (median PFS: 22 versus 16 months, p < 0.001). The use of NHIPEC was identified as an independent predictor of PFS (p < 0.0001). OS did not differ significantly between treatment groups (p = 0.062), although a trend favouring NHIPEC was noted. Incidence of grade 3-4 adverse events and the surgical complexity score of IDS were similar between the two groups. ConclusionsCompared with IV NACT alone, the combination of NHIPEC and IV NACT resulted in improved tumour response and longer PFS. The addition of NHIPEC did not increase the risk of adverse effects or affect the complexity of IDS.
引用
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页码:5 / 13
页数:9
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