NCT03023202招募中不适用
UWCCC Precision Medicine Molecular Tumor Board Registry
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 10,000
- 试验地点
- 1
- 主要终点
- Benefit from PMMTB recommended treatment
研究概览
简要总结
This study seeks to evaluate the clinical utility of the Precision Medicine Molecular Tumor Board, and to track patient outcomes.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 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
- •Clinically suspected or histologically confirmed solid or hematological malignancy
- •Undergoing genetic testing of tumor
- •Ability to understand written informed consent document
- •Willingness to sign written informed consent document
排除标准
- •Pediatric patients (age<18 years) will be excluded due to a lack of expertise on the molecular tumor committee
研究组 & 干预措施
PMMTB
This study of the PMMTB will include all patients >= 18 with clinically suspected or histologically confirmed solid or hematological malignancy who will undergo genetic testing of their tumor.
All standard of care functions will be performed by standard procedures.
干预措施: PMMTB (Precision Medicine Molecular Tumor Board) (Other)
结局指标
主要结局
Benefit from PMMTB recommended treatment
时间窗: Up to 5 years
Whether patients benefit from PMMTB recommended treatment
Frequency of acceptance of molecular tumor board recommendations
时间窗: Up to 5 years
How often the molecular tumor board's recommendations are accepted
次要结局
- Correlation of mutations with protein overexpression(Up to 5 years)
- Correlations of mutations with spheroid culture investigations(Up to 5 years)
- Correlations of mutations with circulating tumor DNA(Up to 5 years)
研究者
研究点 (1)
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