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Consistency of Organoid Drug Sensitivity Test and Clinical Efficacy of Nasopharyngeal Carcinoma

Consistency of Organoid Drug Sensitivity Test and Clinical Efficacy of Nasopharyngeal Carcinoma

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027081
Enrollment
Unknown
Registered
2019-10-31
Start date
2020-03-01
Completion date
Unknown
Last updated
2019-11-04

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

Conditions

Nasopharyngeal Carcinoma

Interventions

Gold Standard:Response Evaluation Criteria in Solid Tumors(RECIST) (1) Complete Response,CR (2)Partial Response,PR (3)Stable Disease,SD (4)Progressive Disease,PD
Test&#32

Sponsors

Nanfang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Locally advanced and/or metastatic nasopharyngeal carcinoma confirmed by histology and/or cytology; 2. Failure of the first-line of comprehensive treatment or tumor progression (if recurrence or metastasis occurs during neoadjuvant chemotherapy followed by radiotherapy or within one year after completion, the first-line comprehensive treatment is considered to be unsuccessful); 3. Aged 18-75 years; 4. Clearly measurable lesions assessed as required by RECIST 1.1; 5. Eastern cooperative oncology group performance scores (ECOG-PS)of 0-1;

Exclusion criteria

Exclusion criteria: 1. Patients undergoing concurrent chemoradiotherapy and having undergone radiotherapy for less than half a year or during the study; 2. Requirement for surgery, intervention, radiofrequency ablation and other tumor treatment or targeted antibody drug therapy during the study; 3. Immunodeficiency or severe myelosuppression; 4. Severe liver and kidney disease, cardiovascular disease, blood disease, etc.; 5. Illegal use of drugs or chronic alcohol abuse or total daily alcohol intake > 50 g/d; 6. Lack of autonomy, inability to walk, or inability to participate in 6 months of follow-up.

Design outcomes

Primary

MeasureTime frame
Half Maximal Inhibitory Concentration;tumor lesion diameter length;Progress Free Survival,PFS;Progress Free Survival,PFS;Disease Control Rate,DCR;Overall survival,OS;Specimen Evaluability Rate;SEN, SPE, ACC, AUC of ROC;Kappa;

Countries

China

Contacts

Public ContactLi Gang

Nanfang Hospital of Southern Medical University

1142238311@qq.com+86 13560378862

Outcome results

None listed

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