drugset / Trial / NCT04348032

Apatinib Combined With PLD vs PLD for Platinum-resistant Recurrent Ovarian Cancer

NCT04348032 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

Epithelial ovarian cancer is the most fatal gynecological malignancy. Despite initial therapeutic response, the majority of advanced-stage patients relapse and eventually succumb to chemoresistant disease. The prognosis of patients with platinum-resistant or refractory ovarian cancer was very poor, with the response rate of 20%\~25% after chemotherapy. The purpose of treatment for recurrent ovarian cancer is mainly to improve the quality of life of patients and prolong survival. Angiogenesis is essential for tumor growth and metastasis.And VEGF/VEGF receptor(VEGFR) signaling pathway is the most promising angiogenic target due to its key roles in angiogenesis and tumor growth.This study sought to assess the efficacy and safety of the combination therapy of apatinib and PLD, clarifying whether combination therapy could improve the outcomes of patients with platinum-resistant recurrent ovarian cancer.

Timeline

Start
2018-03-22
Primary completion
2021-01-28
Completion
2022-06-30

Outcome

Met primary endpoint

paper The median PFS was 5.8 months (95% CI, 3.8-8.8) for treatment with apatinib plus PLD vs 3.3 months (95% CI, 2.1-3.8) for PLD PMID 35771546 ↗

paper hazard ratio, 0.44; 95% CI, 0.28-0.71; P < .001). PMID 35771546 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Doxorubicin Other / unclassified 40 mg/m2 Intravenous
Subject Rivoceranib Small molecule 250 mg Oral

Indications

No indication recorded.