Clinical Trial · NCT06411678

Application of 68GA-labeled CD73 Targeting Probe PET/CT Imaging in the Diagnosis of Breast Cancer

Overview

The investigators plan to conduct a 68Ga-DOTA-dPNE PET/CT imaging study in breast cancer patients to observe the binding of the tracer to tumor lesions and evaluate CD73 expression. As part of the study design, a subset of patients will initially undergo dynamic PET/CT imaging to evaluate the safety profile and pharmacokinetic distribution of the radiotracer in vivo. Subsequently, static PET/CT imaging will be performed on additional patients to assess the diagnostic effectiveness of 68Ga-DOTA-dPNE. Imaging results will be correlated with relevant clinical indicators to evaluate the potential of this tracer in diagnosing breast cancer, guiding therapeutic decisions, and predicting responses to targeted therapies.

Phase

Early Phase 1

Contacts

Xianzhong ZHANG (CONTACT)

zhangxzh@pumch.cn

18950190564

Xianzhong ZHANG (PRINCIPAL_INVESTIGATOR)

Chenhao JIA (CONTACT)

jiachenhao24@163.com

18548703382

ClinicalTrials.gov

NCT06411678

Drug / Compound

dPNE

Isotope(s):
Target(s):
  • CD73
Ligand Class: Peptides
Chelator: DOTA

Eligibility

Inclusion

Inclusion criteria not yet provided.

Exclusion

  • Severe hepatic or renal dysfunction Pregnant, breastfeeding, planning to become pregnant, or planning to have children during the study period; women of childbearing potential must use effective contraception during the study Unable to lie flat for 30 minutes History of claustrophobia or other psychiatric disorders Any other condition deemed unsuitable for participation by the investigator Refusal to participate in the clinical study