跳至主要内容
临床试验/CTRI/2026/04/109472
CTRI/2026/04/109472尚未招募不适用

Study of correlation of PD-L1 expression with prognosis in Urothelial Carcinoma of Urinary Bladder: A Hospital Based Cross-Sectional Study.

Najeeb Ahmed Memon1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2026年5月15日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
44
试验地点
1

研究概览

简要总结

Programmed cell death ligand 1 (PD-L1) is an immune checkpoint inhibitor that is a transmembrane glycoprotein belonging to the B7/CD28 co-stimulatory family. By binding to the programmed death-1 (PD-1) receptor on T lymphocytes, PD-L1 downregulates immune responses by inducing T-cell apoptosis and functional exhaustion, thereby allowing tumour cells to evade immune surveillance. The PD-1/PD-L1 signalling axis plays a critical role in tumour immune escape, and therapeutic blockade of this pathway has been shown to restore antitumor immunity, leading to significant clinical benefit in several malignancies, including urothelial carcinoma.

PD-L1 expression has been associated with more aggressive clinical features, increased recurrence rate and reduced overall survival in patients with urothelial carcinoma. However, other studies have concluded that there is a positive relation between PD-L1 expression and favourable outcome of the disease.

Given the conflicting evidence regarding the prognostic role of PD-L1 in urothelial carcinoma of the urinary bladder which remains controversial, it is important to further define its prognostic relevance.

Hence, this study is being undertaken to evaluate the correlation of PD-L1 expression with prognosis in patients with urothelial carcinoma of the urinary bladder and further support the need for development of newer immune checkpoint inhibitors.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 85.00 Year(s)(—)
性别
All

入选标准

  • All the histopathologically diagnosed cases of UC of the Urinary Bladder that include:
  • Small, intermediate & large biopsies.
  • Resected specimens (Cystectomy) of Urothelial Carcinoma of the Urinary Bladder.

排除标准

  • Benign lesions of the Urinary Bladder.
  • Metastatic lesions.
  • Improperly preserved samples.
  • Inadequate samples/specimens.

研究者

发起方
Najeeb Ahmed Memon
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Najeeb Ahmed Memon

KAHERs JNMC, Belagavi

研究点 (1)

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