跳至主要内容
临床试验/CTRI/2025/07/090058
CTRI/2025/07/090058招募中不适用

Molecular Characterization of Chemoresistance markers in Ovarian Cancer and its impact on Clinical Outcomes

Nitte University1 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2025年7月14日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
42
试验地点
1
主要终点
Clinical Outcomes such as Overall Survival, Progression Free Survival, Chemoresistance and Treatment Response

研究概览

简要总结

Ovarian cancer remains a major contributor to gynecologic cancer-related mortality, primarily due to late-stage diagnosis and the development of chemoresistance. A significant proportion of cases are detected at advanced stages (Stage III – 41.9%, Stage IV – 29%), resulting in poor prognoses despite standard platinum-based chemotherapy regimens. Approximately 70% of patients eventually develop resistance, contributing to suboptimal responses and a five-year overall survival rate of 50.6%. This study aims to investigate the expression patterns of chemoresistance-associated molecular markers in ovarian cancer patients and to evaluate their correlation with clinical outcomes. Particular focus will be placed on the role of Yes-associated protein 1 (YAP1) and Actin-like protein 6A (ACTL6A), both of which are implicated in tumor progression and resistance mechanisms via pathways such as HIPPO-YAP. Expression levels of chemoresistance markers will be correlated with clinical outcomes such as overall survival, progression free survival, chemoresistance and treatment response.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 80.00 Year(s)(—)
性别
Female

入选标准

  • Newly diagnosed ovarian cancer patients above the age of 18 years
  • Ovarian cancer patients who will receive at least 3 cycles of platinum-based chemotherapy.

排除标准

  • Patients with metastatic tumors originating from other primary sites
  • Patients with treatment history of platinum-based chemotherapy
  • Pregnant ovarian cancer patients 4.

结局指标

主要结局

Clinical Outcomes such as Overall Survival, Progression Free Survival, Chemoresistance and Treatment Response

时间窗: Baseline, 9 Weeks (after 3rd Chemotherapy Cycle), 6 months

次要结局

未报告次要终点

研究者

申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Soumya Patil

NGSM Institute of Pharmaceutical Sciences

研究点 (1)

Loading locations...

相似试验