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An open, non-interventional study based on the drug sensitivity detection technology of tumor patient-derived organoids

An open, non-interventional study based on the drug sensitivity detection technology of tumor patient-derived organoids

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100051210
Enrollment
Unknown
Registered
2021-09-15
Start date
2021-09-30
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

colorectal cancer

Interventions

case series:Nil

Sponsors

Affiliated Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged from 18 to 70 years, regardless of gender; 2. Patients who are clinically diagnosed as colorectal cancer and need systemic anti-tumor therapy after clinical evaluation, including: chemotherapy, targeted drug therapy, signal transduction inhibitors , Immunotherapy, or other treatments that are not specified in the research protocol but meet the definition of systemic anti-tumor therapy; 3. Fresh tumor tissue samples in vitro that meet the requirements can be obtained. The source of the samples is >=1, and the sources include surgical resection, puncture biopsy, Colonoscopy biopsy; 4. The number of lesions that can be evaluated according to RECIST vl.l is >= 1; 5. Able to understand the relevant content in the informed consent form, willing to cooperate with treatment, follow-up and other examinations, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with primary cancers other than colorectal cancer; 2. Patients who are receiving or have previously received systemic anti-tumor therapy; 3. Patients undergoing radiotherapy; 4. Patients who need to receive radiation therapy in addition to systemic anti-tumor therapy; 5. Female patients who are pregnant or breastfeeding; 6. Patients who are participating in other studies; 7. There are other situations that are not suitable for participating in the research (if such a situation exists, it should be specified in the research medical record and case report form).

Design outcomes

Primary

MeasureTime frame
pdo modeling success rate(%);

Secondary

MeasureTime frame
Drug sensitivity test index after successful PDO modeling;

Countries

China

Contacts

Public ContactZhou Yanbing

Affiliated Hospital of Qingdao University

zhouyanbing999@aliyun.com+86 13708971773

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026