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临床试验/NCT07468422
NCT07468422进行中(未招募)不适用

Repurposing Drugs Guided by Tissue Slice Screening in Cancer Patients Without Standard Treatment

China Medical University Hospital1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2025年10月27日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
200
试验地点
1
主要终点
response rate

研究概览

简要总结

The goal of this clinical trial is to learn whether a new laboratory method called OPTin can help doctors select the most effective, personalized cancer therapies for patients with advanced or treatment-resistant tumors. The study will also learn about the safety and feasibility of using OPTin to guide treatment decisions across different cancer types.

The main questions it aims to answer are:

Does OPTin accurately identify which drugs or drug combinations work best for each patient's tumor?

Does OPTin-guided therapy improve tumor response or remission rates when the patients don't have any standard treatment selection?

Study Design:

Researchers will collect treatment outcomes in patients whose therapy is chosen based on OPTin results or not in cancer patients without standard treatment.

Participants will:

Provide a small tumor tissue sample for OPTin testing.

Receive either a drug or drug combination identified by OPTin, or a physician's decision treatment.

Visit the clinic regularly for imaging, blood tests, and side-effect monitoring.

Be followed for several months to evaluate treatment response and overall health.

Example Case:

In a previous proof-of-concept study, OPTin screening in a patient with advanced hypopharyngeal carcinoma identified venetoclax as effective for the primary tumor and lenvatinib as a sensitizing agent for metastasis. Combination therapy led to near-complete remission and a significant drop in serum AFP levels.

These results support evaluating OPTin in a prospective clinical trial involving diverse cancer types to confirm its usefulness in guiding precision oncology.

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 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults aged 18 years or older.
  • Willing to sign the informed consent form prior to any study-related procedures.
  • Histologically confirmed participants with metastatic or advanced solid tumor that is not curable with local therapies.
  • Able to provide a tissue specimen larger than [(0.5 cm)³] via surgery during the screening period.
  • Willing to allow the use of their previous test data and leftover tissue samples for analysis.

排除标准

  • Patients who are unable to provide sufficient tissue samples via surgery.
  • The investigator determines that the patient is not eligible for enrollment.

结局指标

主要结局

response rate

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

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ching Yun Hsieh

Attending physician

China Medical University Hospital

研究点 (1)

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