Living Donor Liver Transplantation for CRC Liver Metastases

NCT ID: NCT05175092

Last Updated: 2023-11-21

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-11-30
• Study Completion Date: 2030-12-31

Brief Summary

This study will test the safety and efficacy of living donor liver transplant after standard-of-care chemotherapy for participants with non-resectable liver metastases (LM) from colorectal cancer. 25 donor-recipient pairs will be enrolled (50 participants). Donors will be on study for 2 years and recipients will be on study for up to 5 years.

Detailed Description

This study is a single center, open-label study available to male and female adults with CRC LM that are deemed to be "unresectable" and who are receiving standard of care chemotherapy. Participants will be worked up for LDLT while continuing to receive chemotherapy and, if deemed eligible for surgery, will stop chemotherapy 4 weeks prior to receiving a living donor transplant. Recipients will be followed for 5 years (for safety, survival and disease recurrence for purposes of study data collection). They will continue to be monitored for safety, survival and disease recurrence indefinitely as part of University of Wisconsin (UW) Health's Organ Transplant Program care standards. Living liver donors will be followed for 2 years after transplant surgery for safety monitoring as part of this study.

Recruitment will be done in two stages. The first stage will be a pilot study of 5 recipients to determine if LDLT is a suitable treatment for patients with non-resectable LM. If, after 3 years of follow-up, the overall survival is greater than 60%, stage two recruitment will commence. Thus, an interim analysis will be done for the first 5 recipients prior to requiring a larger number of subjects. Stage two recruitment will focus on accruing a total of up to 20 additional recipients to be analyzed.

The control group will consist of any potential recipients that sign the informed consent and are enrolled in the study but do not undergo LDLT due to a lack of an eligible donor. These participants will be referred back to their medical oncologists to receive standard of care chemotherapy, and will continue to be followed as the control group.

Patients who sign the informed consent and are enrolled in the study with an eligible live donor but do not undergo LDLT due to disease progression or a contraindication is established for undergoing LT (exclusion criteria) will also be referred back to their medical oncologists to receive standard of care chemotherapy. This group will be followed as part of the intent to treat cohort.

Conditions

Liver Metastasis Colon Cancer

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Intent to Treat: LDLT

Living Donor Liver Transplantation

Group Type: EXPERIMENTAL

Living Donor Liver Transplantation

Intervention Type: PROCEDURE

The LDLT will be performed by the UW Division of Transplantation in accordance with the standard of care for this operation.

Control Group

Enrolled but does not receive LDLT

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Living Donor Liver Transplantation

The LDLT will be performed by the UW Division of Transplantation in accordance with the standard of care for this operation.

Intervention Type: PROCEDURE

Other Intervention Names

LDLT

Eligibility Criteria

Inclusion Criteria

In order to be eligible to participate in this study, a potential recipient must meet all of the following criteria prior to transplant procedure:

• Male or female, aged 18 - 65 years old inclusive, at study entry
• Willing and able to provide written informed consent
• Reside in the United States
• Negative serum pregnancy test for women of childbearing potential

• Eastern Cooperative Oncology Group (ECOG) : 0 or 1 at all times prior to LDLT
• Biopsy-proven colorectal LM
• Tumor must have the following characteristics

• Non-resectable LM (by consensus of three hepatobiliary (HPB) surgeons). All potential recipients will be presented at Multidisciplinary Tumor Rounds for discussion of treatment options
• Synchronous or Metachronous disease
• R0 resection can be achieved by total hepatectomy
• Primary CRC tumor stage is ≤T3 and ≤N2
• Oslo score of 0-1. The Oslo Score summarizes 4 negative predictive factors for overall survival after liver transplantation for CRLM where each factor is assigned 1 point; maximal diameter of the largest lesion >5.5 cm, pre-transplant CEA level >80 μg/L, progressive disease at time of liver transplant and interval from diagnosis to transplant <2 years
• The patient has undergone first-line "standard of care" chemotherapy for a minimum of 3 months (at the time of screening), with demonstrated stability or regression of LM based on RECIST v 1.1 criteria
• The only site of metastases is the liver (Staging CT scans are clear of metastases)

• At least one ABO compatible living donor has been identified, and has completed an intake history which, upon review by the Living Donor team, is deemed acceptable and demonstrates no obvious contraindications to donation (Altruistic donors will not be accepted for the study).
• Complete colonoscopy within the 12 months prior to potential recipient's inclusion, showing no signs of local recurrence
• Prior authorization by private insurance as a single payer exception is required. This will be discussed on a case-by-case basis with the insurance providers and the Transplant Financial Group
• Creatinine clearance greater than or equal to 50 ml/min
• Absolute neutrophil count greater than or equal to 1,500/uL
• Child-Pugh score of A
• Meets criteria to undergo a liver transplantation

Exclusion Criteria

A potential recipient who meets any of the following criteria will be excluded from participation in this study:

• Substance abuse, medical, psychological or social conditions that may interfere with the potential recipient's participation in the study or evaluation of the study results
• Known or suspected allergy to any agent given in association with this trial
• Any condition that is unstable or which could jeopardize the safety of the potential recipient and his/her compliance in the study
• Pregnant or breast-feeding patients

• Previous or concurrent cancer that is distinct in primary site or histology from adenocarcinoma, except ductal carcinoma in situ, cervical carcinoma in situ, localized prostate cancer, treated basal cell carcinoma, superficial bladder tumors (Ta, Tis & T1). Any cancer curatively treated 5 years prior to entry is permitted
• Progression of LM at any time point prior to transplant surgery
• LM show no major vascular invasion: no vena cava involvement and no porta hepatis involvement as seen on scans (including PET-CT), or through endoscopic ultrasound and exploratory laparotomy sampling of porta hepatis lymph nodes
• BRAF+ mutation or microsatellite instability of either primary tumor or LM

• Renal dysfunction with an estimated creatinine clearance of less than 50 ml/min
• Pulmonary insufficiency (history of chronic obstructive pulmonary disease and FEV1 /FVC < 75%)
• History of cardiac disease:

• Congestive heart failure > New York Heart Association (NYHA) class 2
• Non-revascularized coronary artery disease
• Uncontrolled hypertension (two systolic blood pressure readings greater than 150 in past 2 visits)
• Uncontrolled infection(s) as defined per surgeon, subject may be on antibiotics at time of transplant
• Severe liver dysfunction (Child-Pugh Score of B or C will be excluded)
• History of solid organ transplantation

Donor eligibility criteria:

In order to be eligible to participate in this study, a potential donor must meet all of the following criteria prior to transplant procedure:

• Willing and able to provide informed consent
• Upon review by the Living Donor team, is deemed acceptable and demonstrates no obvious contraindications to donation
• Not an altruistic donor
• Before transplant surgery, must be approved as a liver donor by UW Health Transplant Program

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Wisconsin, Madison

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

David P Al-Adra, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Wisconsin, Madison

Locations

University of Wisconsin School of Medicine and Public Health

Madison, Wisconsin, United States

Countries

United States

Other Identifiers

2021-0021

Identifier Type: OTHER

Identifier Source: secondary_id

A539742

Identifier Type: OTHER

Identifier Source: secondary_id

Protocol Version 7/15/2022

Identifier Type: OTHER

Identifier Source: secondary_id

UW20113

Identifier Type: -

Identifier Source: org_study_id