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Soluble B7-H3 as a Biomarker for Osteosarcoma

P

Peking University

Status

Enrolling

Conditions

Osteosarcoma
Surveillance
Biomarker
Progression

Treatments

Diagnostic Test: ELISA: enzyme-linked immunosorbent assay

Study type

Observational

Funder types

Other

Identifiers

NCT05942456
PKUPH-sarcoma 16

Details and patient eligibility

About

Increasing data has indicated an association between increased soluble B7-H3 (sB7-H3) levels and unfavorable prognosis in patients with malignancies. However, the level of sB7-H3 and its clinical significance in osteosarcoma are not well known. In this present study, we investigated whether sB7-H3 levels in serum could be as a biomarker for osteosarcoma treatment.

Enrollment

200 estimated patients

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • High Grade osteosarcoma verified with pathologic diagnosis.
  • systemic treatment-naive before the first time Blood drawing.
  • ECOG 0 or 1 and all the other imagings indicate that patients could tolerate standard PKUPH-OS-02 protocol neoadjuvant chemotherapy.
  • All radiographs are complete for clinical evaluation.

Exclusion criteria

  • Patients who Can't tolerate blood drawing.
  • Patients without complete medical records in PKUPH system.
  • Patients who can't tolerate PKUPH-OS-02 neoadjuvant chemotherapy.
  • other conditions that investigators think are not suitable for this study.

Trial design

200 participants in 2 patient groups

sB7-H3 of treatment-naive osteosarcoma patients
Description:
Before delivering neoadjuvant chemotherapy, using ELISA to test the protein expression of sB7-H3 of Peripheral Blood
Treatment:
Diagnostic Test: ELISA: enzyme-linked immunosorbent assay
sB7-H3 after neoadjuvant chemotherapy for osteosarcoma patients
Description:
After neoadjuvant chemotherapy and before definitive surgery, using ELISA to test the protein expression of sB7-H3 of Peripheral Blood
Treatment:
Diagnostic Test: ELISA: enzyme-linked immunosorbent assay

Trial contacts and locations

1

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Central trial contact

Lu Xie, M.D.

Data sourced from clinicaltrials.gov

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