About this trial
The objective of this study is to construct a noninvasive approach using radiolabbled peptide 68Ga-cPP-BCH PET/CT to detect the PD-L1 expression of tumor lesion in patients with lung cancer, melanoma and other solid tumor to identify patients benefiting from anti-PD-(L)1 treatment.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Aged 18-75, male and female, with ECOG score of 0 or 1;
Subjects with lung cancer, melanoma, or other solid tumors scheduled for immunotherapy or combined immunotherapy;
underwent PD-L1 IHC examination before therapy;
The expected survival was more than 26 weeks;
Disqualifiers
The function of liver and kidney was seriously abnormal;
Preparation for pregnant, pregnant and lactating women;
Inability to lie flat for half an hour;
Suffering from claustrophobia or other mental disorders;
Trial population
patients with lung cancer, melanoma or other solid tumors scheduled for immunotherapy or combined immunotherapy; underwent PD-L1 IHC examination before therapy
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
MPR
major pathological response, in the surgical pathology after neo-adjuvant immunotherapy, the proportion of active tumors was less than 10%.
Secondary outcomes
ORR
Overall Response Rate
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: