Clinical trial · Observational
Stereotactic Body Radiotherapy for the Treatment of Distant Metastases in Thyroid Cancer: A Phase II Prospective Clinical Study
NCT07755423CI-TRIAL-00121205enrolling by invitationClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The goal of this observational study is to evaluate the efficacy and safety of Stereotactic Body Radiotherapy in the treatment of distant metastatic thyroid cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Thyroid Cancer Stage IV | Malignant Thyroid Gland Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| SBRT | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- treatment group
- description
- radiotherapy
- interventionNames
- Radiation: SBRT
Primary outcomes (1)
- measure
- Disease Control Rate,DCR
- timeFrame
- 3 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: 1. Participants with primary lesion pathologically confirmed as thyroid cancer, and distant metastatic lesions confirmed either by pathology or by two types of imaging modalities. Based on the investigator's judgment, the participant's distant metastatic lesions are expected to be tolerable to Stereotactic Body Radiotherapy (SBRT). The distant metastases should be oligometastatic (total number of metastatic lesions ≤ 5). 2. Participants who have failed prior systemic therapy. Systemic therapy includes radioactive iodine therapy, immunotherapy, targeted therapy, clinical trial therapy, etc. 3. Age: 18 - 70 years old. 4. KPS ≥ 70. 5. Expected survival period ≥ 3 months. 6. Before treatment, neutrophils ≥ 1.6 × 109/L, hemoglobin ≥ 80g/L, platelets ≥ 80×109/L; creatinine clearance rate ≥ 60 ml/min; non-hepatic metastasis patients (total bilirubin ≤ 1.5 times the upper limit of normal, ALT ≤ 1.5 times the upper limit of normal, AST ≤ 1.5 times the upper limit of normal), hepatic metastasis patients (total bilirubin ≤ 3 times the upper limit of normal, ALT ≤ 3 times the upper limit of normal, AST ≤ 3 times the upper limit of normal, normal coagulation function, Child-Pugh grade A or B, normal liver tissue volume \> 700 mL) 7. Signed informed consent form and willing to complete the study according to the protocol. Exclusion Criteria: 1. Patients who achieved complete remission after comprehensive treatment. 2. Pathologically confirmed as a second primary tumor. 3. Received radiotherapy to the corresponding area and the radiotherapy site overlapped with this one. 4. Uncontrollable malignant pleural or peritoneal effusion. 5. Severe internal medical complications and contraindications to radiotherapy. 6. Pregnant women of childbearing age with positive pregnancy test or lactating women. 7. Active mental disorders or other psychological disorders that affected the patient's signing of informed consent and understanding ability. 8. Uncontrollable infections or active infections, such as immunodeficiency or AIDS patients.
References
Publications (0)
Data not yet available
No reference posted for this study.