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Organotypic Platform for Therapeutic Investigation (OPTin) for Guiding Cancer Patients Treatment

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

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07468422
Acronym
OPTin
Enrollment
200
Registered
2026-03-12
Start date
2025-10-27
Completion date
2028-12-31
Last updated
2026-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer (Advanced Stage), Cancer Patients With Solid Tumors

Brief summary

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.

Interventions

OTHEROPTin: Organotypic Platform for Therapeutic Investigation

a screening system that integrates organotypic tissue slice cultures, optical clearing, and high-resolution fluorescence imaging.

Sponsors

China Medical University Hospital
Lead SponsorOTHER
China Medical University, Taiwan
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

1. Adults aged 18 years or older. 2. Willing to sign the informed consent form prior to any study-related procedures. 3. Histologically confirmed participants with metastatic or advanced solid tumor that is not curable with local therapies. 4. Able to provide a tissue specimen larger than \[(0.5 cm)³\] via surgery during the screening period. 5. Willing to allow the use of their previous test data and leftover tissue samples for analysis.

Exclusion criteria

1. Patients who are unable to provide sufficient tissue samples via surgery. 2. The investigator determines that the patient is not eligible for enrollment.

Design outcomes

Primary

MeasureTime frame
response ratethrough study completion, an average of 1 year"

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026