Investigation of Lymph Node Biology in Kidney Cancer
Characterizing the Tumor-draining Lymph Nodes and Other Immune Sites in Renal Cell Carcinoma
Yale University
10 participants
Jan 30, 2026
INTERVENTIONAL
Conditions
Summary
The purpose of this pilot study is to investigate the phenotype, anti-tumor effector functions, and TCR repertoire of T cells isolated from patient tumor draining lymph nodes (TDLNs) to understand T cell priming and trafficking patterns in Renal Cell Carcinoma (RCC). Data and biospecimen collected will be used for current and future research projects involving the study of kidney cancer biology and related medical conditions. We will use this valuable resource to ask clinically relevant translational questions that pertain to biomarker discovery/validation, identification of novel therapeutic targets, and to better understand the genetic and biological basis of the various kidney cancers.
Eligibility
Inclusion Criteria2
- Candidates for inclusion include adult patients with either a known or suspected kidney cancer referred to Yale Genitourinary Oncology providers in the Yale Urology, Medical Oncology and Radiation Oncology or Nephrology Departments. These individuals will be receiving clinical evaluation/medical treatment/surgery/procedures at Yale New Haven Hospital or the Smilow Cancer Hospital.
- Participant eligibility will be determined by study investigators and will be offered protocol details. Interested participants will be invited to participate by study investigators. Consent will be obtained by study investigators or other authorized study personnel. Any potential adult participants with known or suspected kidney cancers with a renal mass who are patients of non-study physicians will be invited to participate by study personal only with the approval of their treating physician.
Exclusion Criteria3
- Participants under the age of 18. Children will not be enrolled on the study.
- Participants known to be pregnant or actively breastfeeding.
- Iodine allergy hypersensitivity.
Interventions
A peripheral blood sample will be collected at the time of surgery.
Extra tumor which is left over following clinical diagnoses will be collected.
Extra normal tissue which is left over following clinical diagnoses will be collected.
Draining lymph nodes which have been identified by the surgeon visually, potentially using a tracer (injection of up to 5mg of ICG into the peritumor kidney) will be collected.
Regional lymph nodes which have been deemed as non-draining by the surgeon will be collected.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT07038733