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Clinical study for individualized neoantigen-based dendritic cell therapy for anaplastic thyroid cancer

clinical study for individualized neoantigen-based dendritic cell therapy for anaplastic thyroid cancer

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021174
Enrollment
Unknown
Registered
2019-01-31
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-02-04

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

Conditions

anaplastic thyroid cancer

Interventions

Case series:DC immunocyte therapy

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. aged 18-75 years; 2. postoperative pathology confirmed ATC diagnosis; 3. postoperative ATC patients, or patients undergoing adjuvant therapy (assisted radiotherapy, chemotherapy); 4. ECOG PS score 0-1 points; 5. qualified bone marrow function, liver and kidney function; 6. major organs function normally; 7. patients during childbearing age are required to contracept; 8. patient consensus. Written informed consent was provided prior to enrolling in the study and the patient was informed that they have rights to withdraw at any time during the study without any loss.

Exclusion criteria

Exclusion criteria: 1. combined with other malignant tumors; Chemotherapy contraindication; received radiotherapy at the target lesion and preoperative chemotherapy and immunotherapy; 2. anemia, Hb <90g / L; 3. poor vascular conditions, that can not meet the requirements of peripheral blood collection; 4. aberrant blood coagulation, or receiving thrombolytic or anticoagulant therapy; 5. has a blood-borne infectious disease, such as active hepatitis; 6. has a mental disorder; 7. severe concomitant disease, the estimated survival time is less than 1 years; 8. accompanied with other immune diseases or long-term use of immunosuppressants or hormones; 9. poor compliance and are difficult to follow up for a long time; 10. doctors think it is an unsuitable situation for patient.

Design outcomes

Primary

MeasureTime frame
Immunotoxicity;Immunogenicity;Treatment tolerance;

Secondary

MeasureTime frame
Overall Survival;Median survival;Disease Free Survival;metastasis;

Countries

China

Contacts

Public ContactJingqiang Zhu

West China hospital

zjq-wkys@163.com+86 18980601477

Outcome results

None listed

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