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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03291028
Other study ID # GU-118
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 27, 2017
Est. completion date December 2024

Study information

Verified date March 2024
Source Fox Chase Cancer Center
Contact Matthew Zibelman, MD
Phone 215 214 1515
Email matthew.zibelman@fccc.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a comparative study using resected/ biopsied tumors samples collected from renal cell carcinoma and urothelial carcinoma patients who underwent surgical removal of lesions, followed by immune checkpoint blockade (ICB) treatment targting programmed cell death 1 (PD1) but developed new lesions later were also removed and stored in the biosample repository (BSR). The histology and genomic analysis of the pre-treatment and metastatic samples from the same patient would be used to find out the changes that may have lead to metastasis. Also, metastatic samples from ICB naive patients would be collected and compared with those from ICB treated patients to find out if the metastasis in treated patients was due to development of reistance.


Recruitment information / eligibility

Status Recruiting
Enrollment 16
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Eligible patients will include retrospectively identified patients with RCC or UC who have received treatment with ICB and achieved clinical benefit but subsequently developed a solitary new/progressive lesion that was removed surgically. Patients with other tumor types who otherwise meet criteria may be included at a later time - Additionally, a group of patients with RCC who have undergone a metastasectomy but who did not receive treatment with ICB will be identified. These patients may be approached for study participation to serve as a comparator group Exclusion Criteria: -

Study Design


Intervention

Biological:
Immune checkpoint inhibitor targeting PD1
RCC and UC patients treated with immune checkpoint blockade

Locations

Country Name City State
United States Fox Chase Cancer Center - Philadelphia Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Fox Chase Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Histopathological characterization of samples from ICB treated patients To characterize differences in histopathology and patterns of genomic expression between baseline tumors and metastases exhibiting divergent growth kinetics ("escape" metastases) in patients treated with immune checkpoint blockade (ICB) 18 months
Primary Genomic characterization of samples from ICB treated patients To characterize expression of different genes between baseline tumors and metastases exhibiting divergent growth kinetics ("escape" metastases) in patients treated with immune checkpoint blockade (ICB) 18 months
Secondary Histopathological characterization of samples from patients treated with targeted or observational therapy To characterize differences in histopathology between baseline tumors and metastases in patients with RCC treated with observation or targeted therapy. 18 months
Secondary Comparison of Histopathological characteristics of metastatic samples from ICB naive and treated patients To characterize differences in histopathology and patterns of genomic expression between "escape" metastases in patients treated with ICB from patients treated with targeted therapy or observation. 18 months
Secondary Genomic characterization of samples from patients treated with targeted or observational therapy To characterize differences in patterns of genomic expression between baseline tumors and metastases in patients with RCC treated with observation or targeted therapy 18 months
Secondary Comparison of genomic characteristics of metastatic samples from ICB naive and treated patients To characterize differences in patterns of genomic expression between "escape" metastases in patients treated with ICB from patients treated with targeted therapy or observation. 18 months
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