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临床试验/NCT07151807
NCT07151807进行中(未招募)不适用

Evaluation of Serum IGF-1 and IGF-1Ec (E-peptide/MGF) Levels and Their Association With Tumor Burden in Patients With Solid Tumors

Çanakkale Onsekiz Mart University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
100
试验地点
1
主要终点
IGF-1 and IGF-1Ec levels

研究概览

简要总结

This cross-sectional study investigates the relationship between serum IGF-1 and IGF-1Ec (E-peptide/MGF) levels and tumor burden in patients with solid tumors. By analyzing serum samples using ELISA and correlating them with clinical data such as tumor stage, size, metastasis, and lymph node involvement, the study aims to explore whether these biomarkers-particularly IGF-1Ec and the IGF-1Ec/IGF-1 ratio-can reflect tumor progression and serve as potential prognostic indicators.

详细描述

Background: Insulin-like Growth Factor-1 (IGF-1) and its splice variant IGF-1Ec (also known as Mechano Growth Factor, MGF) play critical roles in cell proliferation, survival, and tumor progression. Recent evidence suggests that IGF-1Ec may act independently of the classical IGF-1 receptor pathway and contribute to aggressive tumor behavior. However, data on serum IGF-1Ec levels and their correlation with clinical tumor burden remain limited.

Objective

This cross-sectional analytical study aims to quantify serum IGF-1 and IGF-1Ec levels in patients with solid tumors and investigate their association with tumor burden parameters such as clinical stage, tumor size, lymph node involvement, and metastasis. The IGF-1Ec/IGF-1 ratio will also be evaluated as a potential prognostic biomarker.

Methods: Serum samples will be collected from approximately 60 patients diagnosed with solid tumors. IGF-1 and IGF-1Ec levels will be measured using validated ELISA kits. Clinical tumor burden will be assessed from medical records (TNM staging, metastasis, tumor diameter). Statistical analysis will include group comparisons and correlation tests.

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age ≥ 18 years
  • •Histologically confirmed diagnosis of a solid tumor
  • •Clinically stable condition, prior to chemotherapy or during standard follow-up
  • •Ability to provide informed consent

排除标准

  • •Hematological malignancies (e.g., leukemia, lymphoma)
  • •Acute or chronic liver or kidney failure
  • •Current use (within 1 month) of corticosteroids, growth hormone, or medications affecting IGF-1 levels
  • •Pregnancy or lactation
  • •Coagulopathy or severe anemia preventing safe venipuncture

结局指标

主要结局

IGF-1 and IGF-1Ec levels

时间窗: From enrollment to 6 month

Blood values

次要结局

未报告次要终点

研究者

发起方
Çanakkale Onsekiz Mart University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Cemre Aydeğer

Research asistant, PhD

Çanakkale Onsekiz Mart University

研究点 (1)

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