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Identification of Novel High Quality Methylated DNA Markers in Renal Tumors: Whole Methylome Discovery, Tissue Validation, and Feasibility Testing In Blood and Urine, The INQUIRE Study

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Mayo Clinic

Status

Active, not recruiting

Conditions

Kidney Oncocytoma
Urothelial Carcinoma
Clear Cell Papillary Renal Tumor
Clear Cell Renal Cell Carcinoma
Chromophobe Renal Cell Carcinoma
Papillary Renal Cell Carcinoma

Treatments

Other: Non-Interventional Study

Study type

Observational

Funder types

Other

Identifiers

NCT06339138
NCI-2024-00971 (Registry Identifier)
17-010944 (Other Identifier)

Details and patient eligibility

About

This study is being done to collect blood, tissue and urine samples to identify a novel high quality methylated DNA marker in patients with renal tumors.

Full description

PRIMARY OBJECTIVES:

I. In tissue, to discover and validate DNA methylation markers (MDMs) for detection of malignant renal and urothelial tumors.

II. In blood, to assess the accuracy of candidate MDMs from above for detection of malignant renal and urothelial tumors.

OUTLINE: This is an observational study.

Participants may undergo blood, urine, and tissue sample collection on study. Participants' medical records are also reviewed.

Enrollment

589 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • CASE TISSUE:

    • Patient has a histological diagnosis of primary clear cell RCC, papillary cell RCC, clear cell papillary RCC, chromophobe RCC, oncocytoma, or urothelial cell carcinoma
    • Age >= 18 years
  • CASE BLOODS AND URINE:

    • Patient has a histological diagnosis of primary clear cell RCC, papillary cell RCC, chromophobe RCC, oncocytoma, or urothelial cell carcinoma
    • Age >= 18 years
  • HEALTHY CONTROL BLOODS AND URINE:

    • Patients has undergone negative hematuria workups (defined as negative abdominal imaging and negative cystoscopy
    • Age >= 18 years

Exclusion criteria

  • CASE TISSUE:

    • Patient has von Hippel-Lindau disease (VHL), Hereditary leiomyomatosis and renal cell cancer (HLRCC), Hereditary papillary renal carcinoma (HPRC), or Birt-Hogg-Dube syndrome (BHD)
    • The current target pathology is a recurrence
    • Patient has undergone any prior radiation therapy to target lesion prior to surgery
    • Patient has received chemotherapy class drugs in the 5 years prior to surgery
    • Patient has had any transplants prior to surgery
    • Patient has confirmation of Lynch Syndrome, is presumed to have Lynch Syndrome, or has familial cancer syndrome X
    • Patient has Nephritis (Glomerulus or Interstitial), Poly Cystic Kidney Disease, Glomerulonephropathies or Acquired Renal Kidney Disease
  • RENAL CONTROL TISSUE:

    • Patient has von Hippel-Lindau disease (VHL), Hereditary leiomyomatosis and renal cell cancer (HLRCC), Hereditary papillary renal carcinoma (HPRC), or Birt-Hogg-Dube syndrome (BHD).
    • Patient has inflammation, atypia, or hyperplasia of the parenchyma
    • Patient has a current or past history of renal cancer.
    • Patient has undergone any prior radiation therapy to target lesion prior to surgery
    • Patient has received chemotherapy class drugs in the 5 years prior to surgery
    • Patient has had any transplants prior to surgery
    • Patient has confirmation of Lynch Syndrome, is presumed to have Lynch Syndrome, or has familial cancer syndrome X
    • Patient has Nephritis (Glomerulus or Interstitial), Poly Cystic Kidney Disease, Glomerulonephropathies or Acquired Renal Kidney Disease
  • UROTHELIAL CONTROL TISSUE:

    • Patient has von Hippel-Lindau disease (VHL), Hereditary leiomyomatosis and renal cell cancer (HLRCC), Hereditary papillary renal carcinoma (HPRC), or Birt-Hogg-Dubé syndrome (BHD)
    • Patient has inflammation, atypia, or hyperplasia of the urothelium
    • Patient has a current or past history of urothelial cancer
    • Patient has undergone any prior radiation therapy to target lesion prior to surgery
    • Patient has received chemotherapy class drugs in the 5 years prior to surgery
    • Patient has had any transplants prior to surgery
    • Patient has confirmed or presumed lynch
  • CASE BLOODS AND URINE:

    • Patient has known primary cancer outside of the kidney within the last 5 years prior to plasma and urine collection (not including basal cell or squamous cell skin cancers)
    • Patient has had surgery to completely or partially remove current target pathology
    • Patient has undergone any prior radiation therapy to target lesion prior to plasma and urine collection
    • Patient has received chemotherapy class drugs in the 5 years prior to plasma and urine collection
    • Patient has had any transplants prior to plasma and urine collection
    • Patient has confirmed or presumed lynch
    • Patient has von Hippel-Lindau disease (VHL), Hereditary leiomyomatosis and renal cell cancer (HLRCC), Hereditary papillary renal carcinoma (HPRC), or Birt-Hogg-Dubé syndrome (BHD)
  • HEALTHY CONTROL BLOODS AND URINE:

    • Patient has known primary cancer outside of the urothelium within the last 5 years prior to plasma and urine collection (not including basal cell or squamous cell skin cancers)
    • Current target pathology is a recurrence
    • Patient has undergone prior radiation therapy in the 5 years prior to plasma and urine collection
    • Patient has received chemotherapy class drugs in the 5 years prior to plasma and urine collection
    • Patient has had any transplants prior to plasma and urine collection
    • Patient has von Hippel-Lindau disease (VHL), Hereditary leiomyomatosis and renal cell cancer (HLRCC), Hereditary papillary renal carcinoma (HPRC), or Birt-Hogg-Dube syndrome (BHD)
    • Patient has confirmed or presumed lynch
    • Gross urinary incontinence
    • Patient has undergone cystectomy

Trial design

589 participants in 1 patient group

Observational
Description:
Participants may undergo blood, urine, and tissue sample collection on study. Participants' medical records are also reviewed.
Treatment:
Other: Non-Interventional Study

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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