Kidney Transplantation after Ex-vivo Partial Nephrectomy for Small Renal Mass
This clinical trial evaluates the effect of transplanting the kidney of a low-risk renal cell cancer patient into a patient with kidney failure (end stage renal disease [ESRD]) after the kidney tumor has been removed. ESRD occurs when a patient requires dialysis because their kidney function is no longer adequate to keep them alive. Transferring a healthy kidney from a donor to the patient for the purpose of replacing one of the failing kidneys of the patient (kidney transplant) is the treatment of choice for patients with ESRD and those that receive a transplant have a better quality of life and live longer than those who remain on dialysis. However, the wait for a transplant can be years due to the limited number of kidneys available for transplant and many do not ever receive a transplant. Standard treatment for patients with low-risk renal cell cancer is removal of the kidney tumor (partial nephrectomy). Patients may choose to donate their kidney at the time of partial nephrectomy. This may increase the number kidneys available for transplant. This trial is being done to explore another option for kidney transplantation and to increase the number of options available for kidney donors (patients who have small kidney tumor that needs to be treated).
Inclusion Criteria
- DONOR: Adults > 50 years
- DONOR: Willing and able to understand and sign informed consent
- DONOR: Must have high-quality pre-operative cross-sectional imaging (CT or MRI) to determine tumor characteristics and perform parenchymal volume analysis for split renal function
- DONOR: Patient who is a candidate for partial nephrectomy for cT1a or cT1b mass who understands that partial nephrectomy is standard of care for such mass but wishes to be an altruistic kidney donor (primary incentive is altruism) via radical nephrectomy with loss of the entire kidney
- DONOR: Normal baseline renal function, with estimated glomerular filtration rate (eGFR) > 80 ml/min/1.73 m^2
- DONOR: No proteinuria on urine dipstick (negative/trace considered negative)
- DONOR: Predicted new baseline GFR (NBGFR) following radical nephrectomy would be ≥ 45 * NBGFR will be calculated using a previously described equation based on split renal function (SFR) and renal functional compensation (RFC) * NBGFR = global GFR x (SRFcontralateral from PVA) x 1.25 (average amount of RFC in adults)
- DONOR: Tumor characteristics on pre-operative cross-sectional imaging: * Tumor appears well-encapsulated * Tumor appears amenable to ex-vivo partial nephrectomy with reconstruction that will leave ≥ 75% of the functioning parenchyma intact and well vascularized * Low risk of complications for the recipient after ex-vivo partial nephrectomy (PN) based on surgeon judgment taking into account tumor size and location * Tumor is cT1a or cT1b which is defined as ≤ 7cm and confined * Reconstructed kidney is likely to provide NBGFR for the recipient of > 30 ml/min/1.73 m^2. This can be estimated as (global GFR)(SRF ipsilateral) x 0.75 (estimate that at least 75% of the function will be saved during ex vivo tumor excision and reconstruction). Of note most such kidneys will experience some positive functional compensation but this might be mitigated by a small amount of functional loss related to ischemia. Most studies suggest that this will really be an underestimate of the final GFR in the recipient in the majority of cases
- RECIPIENT: Age > 60
- RECIPIENT: Able to understand and willing to sign informed consent
- RECIPIENT: Presence of ESRD or chronic kidney disease stage 5 (CKD5) with likely progression to ESRD
- RECIPIENT: Does not have potential living donor
- RECIPIENT: Not likely to receive a more “ideal” donor kidney due to significant comorbidities and/or age
Exclusion Criteria
- DONOR: Known familial renal cell carcinoma (RCC) syndrome
- DONOR: < 50 years of age
- DONOR: Preoperative GFR < 80 ml/min/1.73 m^2
- DONOR: Proteinuria on urine dipstick or urinalysis (≥ 1+ considered positive)
- DONOR: Predicted new baseline GFR (NBGFR) following radical nephrectomy would be < 45 * NBGFR would be calculated using previously described equation based on split renal function (SFR) and renal functional compensation (RFC) * NBGFR = global GFR x (SRFcontralateral from PVA) x 1.25 (average amount of RFC in adults after radical nephrectomy [RN])
- DONOR: Comorbidities with risk of deteriorating renal function: * Hypertension requiring three or more anti-hypertensives * Diabetes mellitus requiring insulin or with end organ damage * Morbid obesity * History of nephrolithiasis with > one stone or > one surgical intervention for stone disease in the past
- DONOR: Tumor characteristics on pre-operative cross-sectional imaging: * Tumor has infiltrative features * Tumor is > 7cm (does not meet criteria for cT1a or cT1b stage) * Regional lymphadenopathy, branch or main renal vein invasion, or other imaging findings suggestive of locally advanced disease
- DONOR: Kidney characteristics on pre-operative cross-sectional imaging: * More than one renal artery unless can be readily and safely reconstructed * More than one renal vein unless can be readily and safely reconstructed * Duplicated collecting system unless can be readily and safely reconstructed
- DONOR: High-risk features on renal mass biopsy (if obtained) or intraoperative pathology * Malignant non-RCC pathology * Rhabdoid or sarcomatoid differentiation * Grade 4 * Positive or concerning margins during tumor excision
- DONOR: Must be deemed appropriate living donor candidate per the standard living donor selection process at the Cleveland Clinic * All altruistic living donors undergo a complete evaluation by medical providers and social workers ensuring that they are appropriate candidates to undergo this procedure. This evaluation includes direct query into any history of psychiatric comorbidities and/or substance abuse. If present, this prompts a formal evaluation by psychiatry prior to confirmation of donor candidacy
- RECIPIENT: Traditional contraindications to kidney transplantation at the Cleveland Clinic would apply, including the following directly from the Transplant Care Pathway: * Active, untreated bacterial, fungal, or viral infections. Once treated, patients may be reconsidered. Patients with human immunodeficiency virus (HIV) or chronic hepatitis infections will be evaluated on an individual basis * Active malignancy, except non-melanoma skin cancer and other selected low-grade, low-stage cancers (e.g., bladder, kidney, prostate). The American Society of Transplant (AST) clinical practice guidelines published in 2001 are dated and generally not followed in this era. Improved methods of cancer prognostication are available on a cancer-specific basis. An acceptable disease-free waiting period may be needed prior to transplantation depending on the cancer type (stage/grade) and treatment modality. Expert opinion from an oncological specialist may be needed to facilitate decisions about wait-listing or performance of a transplant * Medical non-adherence, substance abuse or behaviors leading to a failure to achieve a therapeutic physician/transplant team-patient alliance * Life expectancy of less than five years independent of renal disease * Advanced circulatory disease (cardiac, cerebral, peripheral), pulmonary disease or other non-renal conditions such that transplantation would pose a significant risk for morbidity/mortality * Obesity with body mass index (BMI) > 38, or an abdominal wall configuration that in the judgment of the evaluating surgeon poses undue complication risk * Active nicotine abuse (in any form) * Poor functional status independent of renal disease * Considering the average waiting times for a deceased donor kidney is more than 3 years, only transplant candidates 72 years or younger will be accepted for evaluation. Suitable candidates may remain on the waiting list up to the age of 75-year-old. They will be delisted if no transplantation has occurred * Cumulative burden of disease defined as multiple medical conditions that on their own may not preclude listing but that in combination are deemed not suitable by the transplant selection committee
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT05725421.
Locations matching your search criteria
United States
Ohio
Cleveland
PRIMARY OBJECTIVES:
I. To determine safety and feasibility of patients undergoing radical nephrectomy for a small renal mass in the context of altruistic kidney donation.
Ia. Safety and feasibility as determined by peri-operative adverse events of the following grade 3-5 Common Terminology Criteria for Adverse Events (CTCAE) version (v) 5.0 outcomes within 30 days of surgery:
Iai. Anemia;
Iaii. Acute kidney injury.
II. To determine safety and feasibility for renal transplant patients receiving a reconstructed kidney after ex-vivo partial nephrectomy for a small renal mass.
IIa. Safety and feasibility as determined by peri-operative adverse events of the following grade 3-5 CTCAE v 5.0 outcomes within 30 days of surgery:
IIai. Anemia;
IIaii. Renal hemorrhage;
IIaiii. Kidney anastomotic leak;
IIaiv. Urinary fistula.
SECONDARY OBJECTIVES:
I. To determine the surgical, functional, and oncologic outcomes for patients who undergo radical nephrectomy for a small renal mass in the context of altruistic kidney donation.
Ia. Intermediate term surgical outcomes as determined by adverse events of the following grade 3-5 CTCAE v 5.0 outcomes within 180 days of surgery:
Iai. Anemia;
Iaii. Acute kidney injury;
Iaiii. Wound infection;
Iaiv. Infection and infestations-urinary tract infection, abscess.
Ib. Renal recovery as determined by:
Ibi. Post-operative baseline glomerular filtration rate (GFR) > 45 ml/min/1.73m^2 at time of follow up.
Ibii. GFR > 45 ml/min/1.73m^2 at one year after radical nephrectomy.
Ic. Oncologic outcomes as determined by local or distant recurrence of malignancy within one year of follow up.
II. To determine the surgical, functional, and oncologic outcomes for renal transplant recipients of a reconstructed kidney after ex-vivo partial nephrectomy for a small renal mass.
IIa. Intermediate term surgical outcomes as determined by adverse events of the following grade 3-5 CTCAE v 5.0 outcomes within 180 days of surgery:
IIai. Anemia;
IIaii. Renal hemorrhage;
IIaiii. Kidney anastomotic leak;
IIaiv. Urinary fistula;
IIav. Wound infection;
IIavi. Infection and infestations-other, Uurinary tract infection, abscess, bacteremia.
IIb. Renal recovery as determined by:
IIbi. Delayed-graft function;
IIbii. Nadir post-transplant GFR;
IIbiii. GFR measured at one year follow up.
IIc. Oncologic outcomes as determined by local or distant recurrence of malignancy within one year of follow up.
IIci. Diagnosed by one year follow up computed tomography (CT) imaging or other method used to determine presence of recurrent malignancy.
TERTIARY OBJECTIVES:
I. To understand patient attitudes and decision making surrounding altruistic donation as a component of surgery for a renal mass.
II. To understand patient attitudes and decision-making surrounding receipt of a kidney that previously had a small renal mass.
OUTLINE: Patients are assigned to 1 of 2 arms.
ARM I (DONOR): Patients undergo radical nephrectomy on study. Additionally, patients undergo CT or magnetic resonance imaging (MRI) at baseline and urine and blood sample collection throughout the study.
ARM II (RECIPIENT): Patients undergo kidney transplantation on study. Additionally, patients undergo CT and/or MRI and blood sample collection throughout the study.
After completion of study treatment, donors are followed up at days 2-4, 7-60, 90-365 and at day 365. Recipients are followed up at days 2-6, up to day 30, days 30-90, days 90-180, days 180-365 and at day 365.
Trial PhaseNo phase specified
Trial Typetreatment
Lead OrganizationCase Comprehensive Cancer Center
Principal InvestigatorMohamed Eltemamy
- Primary IDCASE13822
- Secondary IDsNCI-2025-03581
- ClinicalTrials.gov IDNCT05725421