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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03108677
Other study ID # RJ2017NO13
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date May 1, 2017
Est. completion date December 30, 2023

Study information

Verified date October 2023
Source Ruijin Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The purpose of this study is to learn whether the profile of RNA from circulating exosomes can be used as a biomarker for lung metastases of primary high-grade osteosarcoma. Circulating exosomes plays roles in metastases in many kinds of cancer including osteosarcoma. By RNA profiling researchers may find lung metastases earlier than conventional work-up and predict the oncological outcomes.


Description:

Investigators have performed a 4 patients pilot study under the oversight of hospital's ethics committee, and investigator found that the levels and mutations of circulating exosome RNA from patients with or without lung metastasis have significant differences. Then investigators wish to register this study to do a further research, in order to reveal the roles of circulating exosome RNA in metastases of osteosarcoma.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 90
Est. completion date December 30, 2023
Est. primary completion date September 19, 2023
Accepts healthy volunteers No
Gender All
Age group 12 Years to 60 Years
Eligibility Inclusion Criteria: - Diagnosis by biopsy: primary high-grade osteosarcoma, including conventional osteosarcoma, telangiectatic osteosarcoma, small cell osteosarcoma, high-grade surface osteosarcoma. - Tumor located in the extremities or pelvis. - Age 12-60 years. - No prior history of cancer and no prior treatment elsewhere. - No prior history of chronic diseases including autoimmune disease, chronic infection, etc. which may interfere the level of circulating exosomes. Exclusion Criteria: - Initial misdiagnosis confirmed by specimen of definitive surgery. - Applying target drugs in the period of treatment which may reduce tumor derived exosomes - withdraw from the study for any reason

Study Design


Intervention

Other:
Blood samples
15 ml peripheral blood

Locations

Country Name City State
China Ruijin Hospital Shanghai Jiao Tong University School of medicine Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Ruijin Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Differences in the levels and mutations of circulating exosome RNA from patients with or without lung metastasis. Next generation sequencing will be performed to the whole RNA sequencing. Before the neo-adjuvant chemotherapy, before the definitive surgery procedure, every 6 months after surgery. up to 3 years.
Secondary Differences in the classic cell signal pathway mutations of circulating exosome RNA from patients with or without lung metastasis. Next generation sequencing will be performed to the whole RNA sequencing. Before the neo-adjuvant chemotherapy, before the definitive surgery procedure, every 6 months after surgery. up to 3 years.
Secondary Differences in the therapeutic targets mutations of circulating exosome RNA from patients with or without lung metastasis. Next generation sequencing will be performed to the whole RNA sequencing. Before the neo-adjuvant chemotherapy, before the definitive surgery procedure, every 6 months after surgery. up to 3 years.
Secondary The correlation between circulating exosome RNA mutation levels and 3-year disease-free survival (DFS), progression-free survival (PFS), lung metastases. Next generation sequencing will be performed to the whole RNA sequencing. Before the neo-adjuvant chemotherapy, before the definitive surgery procedure, every 6 months after surgery. up to 3 years.
Secondary The correlation between specific circulating exosome RNA mutations and 3-year disease-free survival (DFS), progression-free survival (PFS), lung metastases. Next generation sequencing will be performed to the whole RNA sequencing. Before the neo-adjuvant chemotherapy, before the definitive surgery procedure, every 6 months after surgery. up to 3 years.
Secondary The roles of circulating exosome micro-RNA mutations on regulation of circulating exosome RNA. Next generation sequencing will be performed to the whole RNA sequencing. Before the neo-adjuvant chemotherapy, before the definitive surgery procedure, every 6 months after surgery. up to 3 years.
Secondary The mutations of circulating exosome RNA from patients without metastasis. Next generation sequencing will be performed to the whole RNA sequencing. Before the neo-adjuvant chemotherapy, before the definitive surgery procedure, every 6 months after surgery. up to 3 years.
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