PD-L1 Targeting Peptide Probe for PET Imaging of Solid Tumor

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorPeking University Cancer Hospital & Institute

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 volunteers

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 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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

40 Participants
are grouped into 1 trial group
Group A: Patients take 68Ga-cPP-BCH PET/CT before and after therapy

Trial outcomes

Primary outcomes

1

MPR

major pathological response, in the surgical pathology after neo-adjuvant immunotherapy, the proportion of active tumors was less than 10%.

Time frame
3-6 months

Secondary outcomes

1

ORR

Overall Response Rate

Time frame
3-6 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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