PET/CT for Trop2 ADC Response Evaluation NSCLC

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorThe First Affiliated Hospital of Xiamen University

About this trial

To evaluate whether serial 68Ga-MY6349 PET/CT imaging can serve as a noninvasive biomarker to predict the therapeutic efficacy of Trop2-targeted antibody-drug conjugate (Trop2-ADC) therapy in NSCLC patients.

Eligibility criteria

Qualifiers

adult patients (aged 18 years or order)

histologically or cytologically confirmed metastatic NSCLC previously treated with systemic therapy, supported by imaging (e.g. CT, MRI), tumor markers, or pathology reports

presence of at least one measurable lesion according to the Response Evaluation Criteria in Solid Tumors (RECIST), version 1.1

willingness to undergo serial 68Ga-MY6349 PET/CT scans before and during Trop2-ADC therapy

Disqualifiers

Evidence of significantly impaired hepatic or renal function

Estimated life expectancy of less than 3 months

Trial design

Treatments tested in this trial

  • 68Ga-MY6349 PET/CT

Treatment groups

50 Participants
are divided into 1 treatment group