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Changes in 18F-NaF PET/CT and 18F-FDG PET/CT after 223Ra Dichloride Treatment in Patients With Locally Recurrent of Metastatic Osteosarcoma

Changes in 18F-NaF PET/CT and 18F-FDG PET/CT after 223Ra Dichloride Treatment in Patients With Locally Recurrent of Metastatic Osteosarcoma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002905
Enrollment
20
Registered
2018-06-01
Start date
2018-05-01
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Sponsors

Korea Cancer Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patient with osteosarcoma with local recurrence or metastasis - At least one recurrence or metastatic lesion confirmed with 18F-NaF PET/CT - Patients with pulmonary metastases who are unable to treat with surgical resection. - Patients with bone metastasis or local recurrence confirmed progressive disease after radiotherapy or chemotherapy 2. Able to provide informed consent and have signed an approved consent form that conforms to institutional guidelines to ensure compliance 3. Patients from 19 to 80 years of age 4. The Eastern Cooperative Oncology Group (ECOG) _ Performance scale =2 5. Those who satisfy the following conditions in blood test - absolute neutrophil count (ANC)=1,500/µL - Platelet count (PLT)=100,000/µL - hemoglobin=10g/dL (100g/L; 6.2 mmol/L)

Exclusion criteria

Exclusion criteria: 1. A person who is judged to be difficult to perform a clinical trial due to a serious medical condition 2. A person who is determined to have a mental disorder that is difficult to perform PET scan 3. Pre-menopausal women who are pregnant or breastfeeding during screening, or who plan to become pregnant during the test 4. Those participating in other clinical trials at screening and participating in clinical trials should be able to influence the acquisition of 18F-FDG or 18F-NaF PET images (For example, if you are participating in another cohort-based trial that is simply focused on monitoring that you do not receive medicines during screening, you can participate in the current clinical trials.) 5. Those who participated in other clinical trials that may affect the acquisition of 18F-FDG or 18F-NaF PET images from the time of registration until the end of the study, or that may affect the safety assessment following intravenous injection of 223Ra dichloride 6. Those who are likely to influence the acquisition of 18F-FDG PET imaging due to unadjusted diabetes 7. Any condition which, in the investigator's opinion, makes the subject unsuitable for trial participation. 8. Vulnerable subjects (researchers or students who participated in research, family members, researchers or students of researchers participating in research)

Design outcomes

Primary

MeasureTime frame
standardized uptake value (SUV) of 18F-NaF PET;standardized uptake value (SUV) of 18F-FDG PET

Secondary

MeasureTime frame
ALP (alkaline phosphatase);osteocalcin

Countries

Korea, Republic of

Contacts

Public ContactInki Lee

Korea Cancer Center Hospital

inkilee2080@gmail.com+82-2-970-2241

Outcome results

None listed

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