ACTRN12616001000493已完成未知
A national multicentre clinical trial to assess the feasibility of performing genomic testing of rare cancers to match the cancer to treatment.
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Diagnosis
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •* Patients aged over 18 years, with signed informed consent and ability to comply with protocol requirements
- •* Patients with Eastern Cooperative Oncology Group (ECOG) performance status 0-1
- •* Patients with a life expectance of >12 weeks
- •* Access to tumour tissue is available from core biopsy or surgical resection from a disease site
- •* Histologically confirmed rare histopathology diagnosis according to the RARECARE group definition
- •* Malignancy where little evidence-based care or standard of care therapies exist
- •* Tumour type associated with a poor outcome
排除标准
- •* Patients who are unable, or unwilling to consent to the study.
- •* Patients who have a concurrent active malignancy other than adequately treated non-melanomatous skin cancer, early prostatic adenocarcinoma treated with curative intent or non-invasive carcinoma / in-situ neoplasm of the cervix or breast. Patients with a previous history of malignancy will be eligible provided they have been disease-free for >5 years.
研究者
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