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Establishment and Application of Personliazed Therapeutic Effect Prediction and Drug Efficacy Evaluation System For Head and Neck Cancer

Establishment and Application of Personliazed Therapeutic Effect Prediction and Drug Efficacy Evaluation System For Head and Neck Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800019347
Enrollment
Unknown
Registered
2018-11-07
Start date
2018-12-01
Completion date
Unknown
Last updated
2018-11-19

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

Conditions

Head and Neck Cancer

Interventions

Case series:MINIPDX

Sponsors

First Affiliated Hospital, College of medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Pathological histological diagnosis of head and neck cancer(required neoadjuvant therapy); 2. The patient should live without any other cancers according to the clinical examination; 3. The patients could provide biopsy,fresh tumor tissue or pleuroperitoneal fluids samples; 4. Objective tumors that meet RECIST 1.1 criteria and can be evaluated by CT/MRI; 5. KPS score = 60, expected survival time = 3 months; Comprehensive assessment of patients who can tolerate chemotherapy and targeted therapy; 6. The patient voluntarily signed the informed consent form, with good compliance, willing active treatment and follow-up.

Exclusion criteria

Exclusion criteria: 1. Unplanned reoperation after surgery; 2. The patient was confirmed to living with other cancers which may cause interferences to this resaerch; 3. KPS score = 60 points or blood biochemical tests suggest that patients are not suitable for continuing chemotherapy or chemotherapy has been delayed; 4. Cannot or refuse to collect tumor samples; 5. Refused to receive treatment plans or follow-up plans.

Design outcomes

Primary

MeasureTime frame
Objective response rate;Five-year survival rate;

Secondary

MeasureTime frame
Progression-Free-Surviva;Overall survival;

Countries

China

Contacts

Public ContactYulong Zheng

First Affiliated Hospital, College of Medicine, Zhejiang University

drzhengyu@126.com+86 13588166206

Outcome results

None listed

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