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

Qualifiers

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 design

Treatments tested in this trial

  • Not listed

Trial groups

40 Participants
are grouped into 1 trial group

Locations

This trial has no locations

Sponsors and collaborators

Peking University Cancer Hospital & Institute

Lead sponsor