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Transplantation of Reconstructed Renal Allografts Following Ex-Vivo Partial Nephrectomy

Primary Purpose

Renal Cell Carcinoma

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Donor Radical and Partial Nephrectomy
Kidney Transplantation
Laparoscopic Radical Nephrectomy
Sponsored by
Case Comprehensive Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Cell Carcinoma focused on measuring Radical Nephrectomy, Renal Allograft, Ex-Vivo Partial Nephrectomy

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: For Donors: Adults > 50 years Willing and able to understand and sign informed consent 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 Patient who is a candidate for partial nephrectomy for cT1a 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. Functional considerations: o Normal baseline renal function, with eGFR > 80 ml/min/1.73 m2 No proteinuria on urine dipstick (negative/trace considered negative) 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)2 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 PN based on surgeon judgment Tumor is cT1a which is defined as ≤ 4cm and confined Reconstructed kidney is likely to provide NBGFR for the recipient of >30 ml/min/1.73 m2. This can be estimated as (global GFR)(SRFipsilateral) 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. For Recipients: Age >60 Able to understand and willing to sign informed consent Presence of ESRD or CKD5 with likely progression to ESRD Does not have potential living donor Not likely to receive a more "ideal" donor kidney due to significant comorbidities and/or age Exclusion Criteria: For Donors: Known familial RCC syndrome Functional considerations: o < 50 years of age Preoperative GFR < 80 ml/min/1.73 m2 Proteinuria on urine dipstick or urinalysis (≥1+ considered positive) 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)2 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 or other Tumor characteristics on pre-operative cross-sectional imaging: o Tumor has infiltrative features Tumor is > 4cm (does not meet criteria for cT1a stage) Regional lymphadenopathy, branch or main renal vein invasion, or other imaging findings suggestive of locally advanced disease 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 High-risk features on renal mass biopsy (if obtained) or intraoperative pathology o Malignant non-RCC pathology o Rhabdoid or sarcomatoid differentiation o Grade 4 o Positive or concerning margins during tumor excision Must be deemed appropriate living donor candidate per the standard living donor selection process at the Cleveland Clinic o 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. For Recipients: • 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)14 or chronic hepatitis15 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. Improved methods of cancer prognostication are available on a cancer-specific basis.16 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.

Sites / Locations

  • Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

cT1a Radical Nephrectomy + Donor Kidney Transplantation

Arm Description

Radical nephrectomy will be used to remove a cT1a renal mass in an altruistic kidney donor. The kidney obtained from the radical nephrectomy participant with the cT1a mass removed will be transplanted to the recipient using an allograft.

Outcomes

Primary Outcome Measures

Safety and Feasibility of Radical Nephrectomy for a Small Renal Mass
Safety and feasibility as determined by peri-operative adverse events of the following Grade 3-5 CTCAE v5.0 outcomes within 30 days of surgery: i. Anemia ii. Acute kidney injury
Safety and feasibility for Renal Transplant Participants Receiving a Reconstructed Donor Kidney
Safety and feasibility as determined by peri-operative adverse events of the following Grade 3-5 CTCAE v5.0 outcomes within 30 days of surgery: i. Anemia ii. Renal hemorrhage iii. Kidney anastomotic leak iv. Urinary fistula

Secondary Outcome Measures

Surgical Outcomes for a Radical Nephrectomy for a Small Renal Mass
a. Intermediate term surgical outcomes as determined by adverse events of the following Grade 3-5 CTCAE v5.0 outcomes within 180 days of surgery: i. Anemia ii. Acute kidney injury iii. Wound infection iv. Infection and infestations - Urinary tract infection, abscess
Functional Outcomes for a Radical Nephrectomy for a Small Renal Mass
Renal function as determined by: i. Post-operative baseline GFR >45 ml/min/1.73m2 at time of follow up ii. GFR >45 ml/min/1.73m2 at one year after radical nephrectomy
Oncologic Outcomes for a Radical Nephrectomy for a Small Renal Mass
c. Oncologic outcomes as determined by local or distant recurrence of malignancy within one year of follow up
Surgical Outcomes for a Renal Transplant Recipient After Ex-vivo Partial Nephrectomy
Intermediate term surgical outcomes as determined by adverse events of the following Grade 3-5 CTCAE v5.0 outcomes within 180 days of surgery: i. Anemia ii. Renal hemorrhage iii. Kidney anastomotic leak iv. Urinary fistula v. Wound infection vi. Infection and infestations - Other, Urinary tract infection, abscess, bacteremia
Functional Outcomes for a Renal Transplant Recipient After Ex-vivo Partial Nephrectomy
Renal function as determined by: i. Delayed-graft function ii. Nadir post-transplant GFR iii. GFR measured at one year follow up
Oncologic Outcomes for a Renal Transplant Recipient After Ex-vivo Partial Nephrectomy
c. Oncologic outcomes as determined by local or distant recurrence of malignancy within one year of follow up, diagnosed by one year follow up CT imaging or other method used to determine presence of recurrent malignancy
Participant Attitudes/Decision Making Surrounding Altruistic Kidney Donation
Participant attitudes and decision making surrounding altruistic donation as a component of surgery for a renal mass will be determined by a survey provided to participants at a preoperative visit prior to surgery and at the 12 month follow-up visit.
Participant Attitudes/Decision Making Surrounding Transplant Recipients
Participant attitudes and decision-making surrounding receipt of a kidney that previously had a small renal mass will be determined by a survey provided to participants at a preoperative visit prior to surgery and at the 12-month follow-up visit.

Full Information

First Posted
February 2, 2023
Last Updated
August 15, 2023
Sponsor
Case Comprehensive Cancer Center
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1. Study Identification

Unique Protocol Identification Number
NCT05725421
Brief Title
Transplantation of Reconstructed Renal Allografts Following Ex-Vivo Partial Nephrectomy
Official Title
Oncologic, Functional and Surgical Outcomes for Patients Undergoing Radical Nephrectomy for Low-Risk Renal Cell Carcinoma and Recipients of Reconstructed Renal Allografts Following Ex-Vivo Partial Nephrectomy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 2024 (Anticipated)
Primary Completion Date
July 2024 (Anticipated)
Study Completion Date
July 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Case Comprehensive Cancer Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This study is designed to investigate a novel approach to offer more ESRD participants the benefits associated with renal transplantation by increasing the supply of available allografts

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Cell Carcinoma
Keywords
Radical Nephrectomy, Renal Allograft, Ex-Vivo Partial Nephrectomy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
cT1a Radical Nephrectomy + Donor Kidney Transplantation
Arm Type
Experimental
Arm Description
Radical nephrectomy will be used to remove a cT1a renal mass in an altruistic kidney donor. The kidney obtained from the radical nephrectomy participant with the cT1a mass removed will be transplanted to the recipient using an allograft.
Intervention Type
Procedure
Intervention Name(s)
Donor Radical and Partial Nephrectomy
Intervention Description
Donor participants will undergo laparoscopic radical nephrectomy (RN) . Donor kidney then will undergo cold perfusion and ex-vivo partial nephrectomy (PN) with cold ischemia. During PN, careful inspection of tumor will be performed to ensure it is well-encapsulated. If any infiltrative features (versus well encapsulated tumor) are noted intraoperatively then transplant will not be performed. Multiple surgical margins will be sent (either frozen section or standard with priority). If final margins are positive or concerning, then transplant will not be performed. Biopsies of the tumor will be performed and sent to pathology (either frozen section or standard with priority).
Intervention Type
Procedure
Intervention Name(s)
Kidney Transplantation
Intervention Description
The donor kidney will remain on ice while pathologic analysis is performed, and transplant recipient surgery is initiated (if pathologic analysis satisfactory). Cold ischemia with delay for pathology will have minimal functional impact in this setting based on extensive prior experience with renal transplantation where kidneys are routinely kept hypothermic for several hours prior to transplantation.
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic Radical Nephrectomy
Intervention Description
Radical nephrectomy consists of the removal of the kidney together with the perirenal fat and regional lymph nodes. The transperitoneal approach allows early control of the renal vessels.
Primary Outcome Measure Information:
Title
Safety and Feasibility of Radical Nephrectomy for a Small Renal Mass
Description
Safety and feasibility as determined by peri-operative adverse events of the following Grade 3-5 CTCAE v5.0 outcomes within 30 days of surgery: i. Anemia ii. Acute kidney injury
Time Frame
Within 30 days of surgery
Title
Safety and feasibility for Renal Transplant Participants Receiving a Reconstructed Donor Kidney
Description
Safety and feasibility as determined by peri-operative adverse events of the following Grade 3-5 CTCAE v5.0 outcomes within 30 days of surgery: i. Anemia ii. Renal hemorrhage iii. Kidney anastomotic leak iv. Urinary fistula
Time Frame
Within 30 days of surgery
Secondary Outcome Measure Information:
Title
Surgical Outcomes for a Radical Nephrectomy for a Small Renal Mass
Description
a. Intermediate term surgical outcomes as determined by adverse events of the following Grade 3-5 CTCAE v5.0 outcomes within 180 days of surgery: i. Anemia ii. Acute kidney injury iii. Wound infection iv. Infection and infestations - Urinary tract infection, abscess
Time Frame
Within 180 days of surgery
Title
Functional Outcomes for a Radical Nephrectomy for a Small Renal Mass
Description
Renal function as determined by: i. Post-operative baseline GFR >45 ml/min/1.73m2 at time of follow up ii. GFR >45 ml/min/1.73m2 at one year after radical nephrectomy
Time Frame
1 year after surgery
Title
Oncologic Outcomes for a Radical Nephrectomy for a Small Renal Mass
Description
c. Oncologic outcomes as determined by local or distant recurrence of malignancy within one year of follow up
Time Frame
Up to 1 year after surgery
Title
Surgical Outcomes for a Renal Transplant Recipient After Ex-vivo Partial Nephrectomy
Description
Intermediate term surgical outcomes as determined by adverse events of the following Grade 3-5 CTCAE v5.0 outcomes within 180 days of surgery: i. Anemia ii. Renal hemorrhage iii. Kidney anastomotic leak iv. Urinary fistula v. Wound infection vi. Infection and infestations - Other, Urinary tract infection, abscess, bacteremia
Time Frame
Within 180 days of surgery
Title
Functional Outcomes for a Renal Transplant Recipient After Ex-vivo Partial Nephrectomy
Description
Renal function as determined by: i. Delayed-graft function ii. Nadir post-transplant GFR iii. GFR measured at one year follow up
Time Frame
1 year after surgery
Title
Oncologic Outcomes for a Renal Transplant Recipient After Ex-vivo Partial Nephrectomy
Description
c. Oncologic outcomes as determined by local or distant recurrence of malignancy within one year of follow up, diagnosed by one year follow up CT imaging or other method used to determine presence of recurrent malignancy
Time Frame
Up to 1 year after surgery
Title
Participant Attitudes/Decision Making Surrounding Altruistic Kidney Donation
Description
Participant attitudes and decision making surrounding altruistic donation as a component of surgery for a renal mass will be determined by a survey provided to participants at a preoperative visit prior to surgery and at the 12 month follow-up visit.
Time Frame
1 year after surgery
Title
Participant Attitudes/Decision Making Surrounding Transplant Recipients
Description
Participant attitudes and decision-making surrounding receipt of a kidney that previously had a small renal mass will be determined by a survey provided to participants at a preoperative visit prior to surgery and at the 12-month follow-up visit.
Time Frame
1 year after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: For Donors: Adults > 50 years Willing and able to understand and sign informed consent 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 Patient who is a candidate for partial nephrectomy for cT1a 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. Functional considerations: o Normal baseline renal function, with eGFR > 80 ml/min/1.73 m2 No proteinuria on urine dipstick (negative/trace considered negative) 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)2 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 PN based on surgeon judgment Tumor is cT1a which is defined as ≤ 4cm and confined Reconstructed kidney is likely to provide NBGFR for the recipient of >30 ml/min/1.73 m2. This can be estimated as (global GFR)(SRFipsilateral) 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. For Recipients: Age >60 Able to understand and willing to sign informed consent Presence of ESRD or CKD5 with likely progression to ESRD Does not have potential living donor Not likely to receive a more "ideal" donor kidney due to significant comorbidities and/or age Exclusion Criteria: For Donors: Known familial RCC syndrome Functional considerations: o < 50 years of age Preoperative GFR < 80 ml/min/1.73 m2 Proteinuria on urine dipstick or urinalysis (≥1+ considered positive) 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)2 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 or other Tumor characteristics on pre-operative cross-sectional imaging: o Tumor has infiltrative features Tumor is > 4cm (does not meet criteria for cT1a stage) Regional lymphadenopathy, branch or main renal vein invasion, or other imaging findings suggestive of locally advanced disease 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 High-risk features on renal mass biopsy (if obtained) or intraoperative pathology o Malignant non-RCC pathology o Rhabdoid or sarcomatoid differentiation o Grade 4 o Positive or concerning margins during tumor excision Must be deemed appropriate living donor candidate per the standard living donor selection process at the Cleveland Clinic o 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. For Recipients: • 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)14 or chronic hepatitis15 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. Improved methods of cancer prognostication are available on a cancer-specific basis.16 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mohamed Eltemamy, MD
Phone
216-296-3693
Email
Eltemam@ccf.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohamed Eltemamy, MD
Organizational Affiliation
Cleveland Clinic: Glickman Urological and Kidney Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mohamed Eltemamy, MD
Phone
216-296-3693
Email
Eltemam@ccf.org
First Name & Middle Initial & Last Name & Degree
Mohamed Eltemamy, MD

12. IPD Sharing Statement

Learn more about this trial

Transplantation of Reconstructed Renal Allografts Following Ex-Vivo Partial Nephrectomy

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