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临床试验/NCT05750511
NCT05750511招募中不适用

Prospective Multicenter Translational Study to Validate Molecular Biomarkers (TMB, PD-L1) on Pre-treatment Tumor Tissue as Predictors of Therapy Outcome in Metastatic Melanoma Patients

Dermatologic Cooperative Oncology Group10 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2014年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
1,000
试验地点
10
主要终点
BOR

研究概览

简要总结

The prospective multicenter translational study Tissue Registry in Melanoma (ADOREG/TRIM; CA209-578) aimed to validate the Tumor Mutational Burden (TMB) and the PD-L1 expression (PD-L1) from a pre-therapeutically obtained tumor tissue sample as a predictor of a subsequent systemic therapy in a large real-world cohort of metastatic melanoma patients.

详细描述

The aim of the present study is to identify and validate molecular and clinical biomarkers of therapy outcome in metastatic melanoma. Clinical and molecular parameters of melanoma patients and their tumors will be collected in an online-based registry (ADOREG), and thereafter correlated with the outcome of subsequent systemic therapies in terms of progression-free survival, overall survival, and treatment response. Systemic therapies will include all types of currently used regimens (kinase inhibitors, immune checkpoint inhibitors, chemotherapy). FFPE tissue samples will comprise different time points (primary tumors versus metastases) as well as tumor sites (lymph node versus organ metastases) to identify potential differences in the predictive value of these materials. The anticipated results from these analyses are of essential importance for future patient selection for individualized therapy strategies.

研究设计

研究类型
Observational
观察模型
Cohort
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

入选标准

  • Patients with histologically confirmed melanoma stage III or IV.
  • Clinically eligible for systemic cancer therapy (immune checkpoint inhibitors, targeted agents).
  • Tumor tissue biopsy already existing (metastasis tissue as recent as possible, but older tissue material or primary tumor tissue also possible).
  • Patient has given written informed consent for the current study as well as for his data to be entered into the ADOREG online database system.
  • Patient is ≥18 years old.

排除标准

  • 未提供

结局指标

主要结局

BOR

时间窗: through study completion, an average of 1 year

best overall response (BOR)

OS

时间窗: through study completion, an average of 1 year

overall survival (OS)

PFS

时间窗: through study completion, an average of 1 year

progression-free survival (PFS)

次要结局

未报告次要终点

研究者

发起方
Dermatologic Cooperative Oncology Group
申办方类型
Other
责任方
Sponsor

研究点 (10)

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