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Enrolling by Invitation

NCT Number: NCT07755423

Stereotactic Body Radiotherapy for the Treatment of Distant Metastases in Thyroid Cancer: A Phase II Prospective Clinical Study

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.

Enrolling by Invitation

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Fudan University Shanghai Cancer Center

Shanghai, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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).
  • Participants who have failed prior systemic therapy. Systemic therapy includes radioactive iodine therapy, immunotherapy, targeted therapy, clinical trial therapy, etc.
  • Age: 18 - 70 years old.
  • KPS ≥ 70.
  • Expected survival period ≥ 3 months.
  • 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)
  • Signed informed consent form and willing to complete the study according to the protocol.

Exclusion criteria

  • Patients who achieved complete remission after comprehensive treatment.
  • Pathologically confirmed as a second primary tumor.
  • Received radiotherapy to the corresponding area and the radiotherapy site overlapped with this one.
  • Uncontrollable malignant pleural or peritoneal effusion.
  • Severe internal medical complications and contraindications to radiotherapy.
  • Pregnant women of childbearing age with positive pregnancy test or lactating women.
  • Active mental disorders or other psychological disorders that affected the patient's signing of informed consent and understanding ability.
  • Uncontrollable infections or active infections, such as immunodeficiency or AIDS patients.

Treatment and study plan

SBRT

Radiation

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).

Primary outcomes

  1. Disease Control Rate,DCR

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

Fudan University

Other

Registry information

Important dates

Study start
2026
Primary completion
2030
Study completion
2030
First posted
Aug 10, 2026
Registry last updated
Aug 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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