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临床试验/NCT05734911
NCT05734911已完成不适用

Real-world Data From a Multi-center Study: Insights to the Effectiveness and Safety in Patients With Ovarian Cancer Receiving Niraparib as First-line Maintenance Therapy

Zhongda Hospital1 个研究点 分布在 1 个国家目标入组 199 人开始时间: 2019年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
199
试验地点
1
主要终点
progression-free survival(PFS)

研究概览

简要总结

In order to explore the real situation of niraparib in clinical application more comprehensively and deeply, we conducted the first multicenter, real-world study in China. This large observational study used real-world data to assess the effectiveness and safety of niraparib as maintenance therapy in patients with advanced ovarian cancer (AOC) in China and investigated clinical factors associated with prolonged benefits of niraparib so as to achieve the maximum clinical benefit of patients.

详细描述

This is a retrospective multicentric study including advanced ovarian cancer patients that have used niraparib as first-line maintenance therapy after chemotherapy from fourteen hospitals in China between January 2019 and December 2021. The database lock-time was on December 31, 2022. All data were retrieved from the patients' medical records. Clinical data, including patient demographics, clinicopathological characteristics, residual disease after primary surgery, genetic-testing results and so on, were collected. Missing information was supplemented by telephone follow-up or face-to-face inquiries (only for patients who were alive and accessible). The incidence of AEs, as well as dose reductions, dose interruption, and discontinuation of treatment due to AEs were recorded.All analyses were performed on the safety population. The categorical variables were described as a frequency and percentage, and the continuous variables were described as a median and range. No formal sample size calculation was performed since the study was exploratory. Survival analyses were conducted using the Kaplan-Meier method and log-rank test. 95% confidence intervals (CIs) were calculated using the Clopper-Pearson method. Univariate and multivariate Cox regression models were established to determine factors that could affect the PFS for patients receiving niraparib maintenance treatment. Missing data were assigned as unknown for the univariate and multivariate analysis. The method of cox analysis was stepwise regression, and the screening criterion was Akaike Information Criterion (AIC). A P-value of <0.05 was considered statistically significant. Descriptive statistics (number and percentage) were used to summarize the safety data by treatment. Statistical analyses were performed using the R software version 4.2.2 (R Project for Statistical Computing).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
26 Years 至 78 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • 18 years of age or older
  • diagnosed with histologically confirmed ovarian cancer (International Federation of Gynecology and Obstetrics [FIGO] Stage II-IV)
  • underwent surgery and first-line chemotherapy and were treated with niraparib as maintenance therapy
  • the date to start maintenance therapy with niraparib is from January 2019 to December 2021

排除标准

  • had experienced other malignancies within the previous 5 years
  • enrolled in clinical trials in which investigators were blinded to the treatments
  • with a previous or current diagnosis of myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML)

研究组 & 干预措施

patients with ovarian cancer (OC) received niraparib as first-line (1st-L) maintenance therapy

This multi-center, observational, retrospective study collected real-world medical record data of patients with advanced ovarian cancer treated with niraparib as first-line maintenance therapy from fourteen hospitals in China. In reality, these patients received different oral doses of niraparib until disease progression, severe toxicity occurred, or death. A total of 199 patients were included in a centralized database ultimately with a median age of 57.0 years (range, 51.0-63.5 years).

干预措施: Niraparib (Drug)

结局指标

主要结局

progression-free survival(PFS)

时间窗: up to 29 months

time from the date of initiation of maintenance therapy with niraparib to the date of disease progression in our study

次要结局

  • time to first subsequent therapy (TFST)(up to 13 months)
  • time to treatment discontinuation (TTD)(up to 29months)

研究者

发起方
Zhongda Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Yang Shen

Department of Obstetrics and Gynaecology, Zhongda Hospital, School of Medicine, Southeast University

Zhongda Hospital

研究点 (1)

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