Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03819569
Other study ID # LCCC 1834
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date October 30, 2018
Est. completion date December 30, 2025

Study information

Verified date October 2023
Source UNC Lineberger Comprehensive Cancer Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Purpose: The purpose of this study is to evaluate the role of renal mass biopsy on decision-making for patients presenting with clinical T1 kidney tumors. This study also incorporates integrated biomarker study to compare the genomic data obtained through biopsy tissue to genomic information from surgical data.


Description:

Primary Objective 1. To compare the decisional conflict between patients who undergo renal mass biopsy during their evaluation for SRMs versus those who do not. 2. To validate the concordance of RNA sequencing (RNAseq) and genomic-based risk stratification molecular biomarkers between renal biopsy tissue and surgical (nephrectomy) specimen tissue. Secondary objective 1. To characterize the impact of biopsy on patient reported anxiety and uncertainty, assessment of cancer care communication, and satisfaction with cancer care.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 265
Est. completion date December 30, 2025
Est. primary completion date December 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 95 Years
Eligibility Inclusion Criteria: - Ages 18 - 95 - Have a small renal mass =7 cm on cross-sectional radiologic study evaluated at the University of North Carolina (UNC) Urology or the UNC Cancer Hospital. - Has voluntarily provided signed informed consent to participate and HIPAA authorization for the release of personal health information - Willing and able to complete patient-reported outcome questionnaires - Willing to have extra cores taken for research during the standard-of-care biopsy procedure - Willing to allow surgical specimens to be used for research - Willing to undergo a blood draw to evaluate for circulating tumor DNA Exclusion Criteria - Has staging information indicating locally advanced or metastatic disease. - Presence of transplant kidney - Unwilling or unable to complete informed consent - Previous biopsy of small renal mass.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Small Renal Mass Biopsy
Subjects will receive a small renal mass biopsy prior to making a treatment decision
Other:
No Small Renal Mass Biopsy
Subjects will not receive a small renal mass biopsy prior to making a treatment decision

Locations

Country Name City State
United States UNC Lineberger Comprehensive Cancer Center Chapel Hill North Carolina

Sponsors (1)

Lead Sponsor Collaborator
UNC Lineberger Comprehensive Cancer Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Decisional Conflict Decisional conflict scale between patients who undergo renal mass biopsy, and who do not will be compared. Decisional conflict scale is a validated, 16-item instrument that measures personal perceptions of decision-making. It yields a total score from 0 to 100 (higher scores indicate more decisional conflict) and sub-scores for perceptions of uncertainty, informed values clarity, support, and effectiveness in decision-making. Baseline, 1-3 months (before treatment)
Primary Receipt of nephrectomy The proportion of patients undergoing nephrectomy (radical and partial nephrectomy) between patients who undergo renal mass biopsy versus those who do not will be compared. 1-3 months (index treatment), 2 years
Primary Genomic mutations comparison Molecular subtype (ccA vs ccB) and the presence of genomic mutations between the renal mass biopsy and the surgical nephrectomy specimen will be compared. 2 years
Secondary Patient-reported anxiety Patient-reported anxiety will be assessed using the Short Form PROMIS Anxiety scale. Short Form PROMIS Anxiety is a validated 4-item survey of generalized anxiety, consisting of 5 questions, each scored using a 5-point Likert scale. High scores reflect better results. Baseline, 1-3 months (before treatment), 6, 12, 18, 24 months
Secondary Patient-reported cancer worry Patient-reported cancer worry will be assessed using the Brief Worry Scale which is a 4 questions assessment designed to measure the relationship between worry and an event or behavior. This study will use the brief worry scale to measure the relationship between worry and the diagnosis of a small renal mass. Baseline, 1-3 months (before treatment), 6, 12, 18, 24 months
Secondary Patient-Reported Risk Perception Patient-reported Risk Perception will be assessed using 2 two-question instrument to assign a numeric risk score for patients regarding incidental renal lesions, which may facilitate accurate risk comprehension. Baseline, 1-3 months (before treatment)
Secondary Patient-reported uncertainty Patient-reported uncertainty will be assessed using the Short-Form Mishel Uncertainty of Illness Scale which is a validated instrument that measures the patient's perception of the uncertainty of symptoms, diagnosis, treatment, and prognosis as well as the uncertainty subscale of the Decisional Conflict Scale. The scores are summed to yield a total score with a higher score indicating greater uncertainty. baseline, 1-3 months (before treatment)
Secondary Patient-reported regret about the decision Patient-reported regret about the decision will be assessed using the Decisional regret scale. Decisional Regret scale is a 5-item regret scale that measures distress or remorse after a healthcare decision. The short form consists of 5 questions, each scored using a 5-point Likert scale, indicating a number from 1 (Strongly Agree) to 5 (Strongly Disagree). 6, 12, 18, 24 months
Secondary Patient-reported health-related quality of life Patient-reported health-related quality of life will be assessed using The PROMIS Global Health scale is an 8-item, validated survey that represents five core PROMIS domains (physical function, pain, fatigue, emotional distress, social health). Higher score indicating better quality of life. Baseline, 1-3 months (before treatment), 6, 12, 18, 24 months
Secondary Patient reported assessment of communication in cancer care The validated 6-item Short-Form for Patient-Centered Communication-Cancer Scale. This is a validated, 6-item instrument that measures the patient's perspective on communication in cancer care. It incorporates questions relating to exchanging information, fostering relationships, making decisions, responding to emotions, enabling self-efficacy, and managing uncertainty. Each item is scored 1-5, and the overall score is an average of 6 questions, with 5 indicating the most satisfaction. A high score indicates better communication. Baseline, 1-3 months (before treatment)
Secondary Receipt of any intervention (ablation, radiation therapy, nephrectomy) The proportion of patients undergoing ablation, radiation therapy, nephrectomy between patients who undergo renal mass biopsy versus those who do not will be compared 1-3 months (index treatment), 2 years
See also
  Status Clinical Trial Phase
Completed NCT01950923 - Sildenafil Citrate Before Surgery in Improving Kidney Function in Patients With Kidney Cancer Phase 1
Withdrawn NCT01688414 - Imaging During Surgery in Diagnosing Patients With Prostate, Bladder, or Kidney Cancer N/A
Recruiting NCT05387863 - Decision Aid (DA) for Renal Patients N/A
Recruiting NCT06056505 - Virtual Interactive 3D Modelling to Improve Outcomes in Robotic-Assisted Partial Nephrectomy N/A
Recruiting NCT01967407 - IReversible Electroporation of Kidney Tumors Before Partial Nephrectomy. Phase 1/Phase 2
Terminated NCT00960063 - A Study of Robatumumab (SCH 717454, MK-7454) in Combination With Different Treatment Regimens in Pediatric Participants With Advanced Solid Tumors (P05883, MK-7454-006) Phase 1
Recruiting NCT05890781 - Engineering Immune Organoids to Study Pediatric Cancer N/A
Completed NCT05015179 - Mixed Reality Technology in Laparoscopic Partial Nephrectomy N/A
Completed NCT00019630 - Liposomal Doxorubicin in Treating Children With Refractory Solid Tumors Phase 1
Completed NCT01908166 - Ultrasound Elastography in Diagnosing Patients With Kidney or Liver Solid Focal Lesions N/A
Recruiting NCT05728957 - Renal Mass Biopsy, PEER, and 99mTc-sestamibi SPECT/CT for Patients With Clinically Localized Renal Tumors