Establishment and Clinical Transformation of ADC Drug Efficacy Evaluation System for Breast Cancer Based on Molecular Imaging

ConditionBreast Cancer
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorPeking University Cancer Hospital & Institute

About this trial

The objective of the study is to construct a noninvasive approach 68Ga-TTP PET/CT to detect the TROP2 expression of tumor lesions in patients with breast tumors and evaluate the efficacy of ADC drug therapy.

Eligibility criteria

Qualifiers

Age 18-75 years old, male or female, ECOG score 0 or 1 points (see the table in Annex 2 for the score table);

Blood routine and liver and kidney function meet the following criteria: Blood routine: WBC ≥ 4.0×109 L or neutrophil ≥1.5×109 /L, PLT ≥ 100×109/L, Hb≥ 90 g/L; PT or APTT ≤ 1.5 ULN; Liver and kidney function: T-Bil ≤ 1.5×ULT(upper limit of normal), ALT and AST≤ 2.5 ULN or ≤ 5×ULT(subjects with liver metastasis), ALP ≤ 2.5 ULN(ALP ≤ 4.5 ULN if there is bone metastasis or liver metastasis); BUN ≤ 1.5×ULT, SCr ≤ 1.5×ULT;

Patients with confirmed or suspected breast cancer;

Expected survival ≥12 weeks;

Disqualifiers

Severe abnormal liver and kidney function;

Pregnant, pregnant and lactating women;

Can not lie flat for half an hour;

Unable to obtain informed consent;

Trial design

Treatments tested in this trial

  • 18F-FDG
  • [68Ga]Ga-TTP

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators