RecruitingNot ApplicableNCT05186116

LDLT in Non Resectable Colo-rectal Cancer Liver Metastasis

Living Donor Liver Transplantation (LDLT) in Non Resectable Colo-rectal Cancer Liver Metastasis. The LIVERMORE Trial (LIVing Donor livEr tRansplant Modena cOloRectal mEtastasis) [Original Title in Italian: "Trapianto di Fegato da Donatore Vivente Per Metastasi Epatiche Non Resecabili da Adenocarcinoma Del Colon"]


Sponsor

Azienda Ospedaliero-Universitaria di Modena

Enrollment

25 participants

Start Date

Jan 1, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

This study is an interventional open label prospective study that aims to assess both overall and disease-free survival of patients treated with LDLT, partial or whole graft LT from deceased donors for unresectable CRLM. Secondary outcomes are graft survival and donor outcomes in terms of safety and quality of life. Donor selection is performed according to the currently used Institutional and National standards and protocols.


Eligibility

Min Age: 18 YearsMax Age: 77 Years

Inclusion Criteria9

  • Age ≥18.
  • Histologically confirmed colon and rectum (intraperitoneal) adenocarcinoma.
  • Pathological classification of primary tumor as pT1-3, without peritoneal tumor deposits, absence of mucinous component \>50%, confirmed R0 resection, no limitations for RAS mutations, B-RAF wild type.
  • No signs of extra hepatic metastatic disease or local recurrence according to CT scan+MRI+PET/CT scans.
  • Liver metastases not eligible for curative liver resection
  • Objective response according to RECIST 1.1 to first-line treatment, with sustained response for at least 4 months, OR disease control (complete \[CR\] or partial response \[PR\] or standard disease \[SD\]) during second- line treatment for at least 4 months.
  • Carcinoembryonic Antigen (CEA) values stable or decreasing during the enrollment prior to liver transplant.
  • Performance status, ECOG (Eastern Cooperative Oncology Group) 0-2.
  • Signed informed consent and expected cooperation of the patients for the treatment and follow-up, and national/local regulations.

Exclusion Criteria9

  • Hereditary CRC syndromes including FAP (Familial adenomatous polyposis) and Lynch syndrome.
  • Prior extra hepatic metastatic disease or primary tumor local relapse.
  • Palliative resection of primary CRC tumor.
  • Disease progression
  • Other malignancies in the previous 5 years (with exception of in situ cervical carcinoma and basal cell carcinoma; superficial bladder tumors are allowed if curatively treated).
  • Active intra-venous or alcohol abusers (patients may be eligible if abstention \> 6 months is demonstrated)
  • Active HIV infection
  • Psychiatric disorders and patient low compliance
  • Any reason why, in the judgment of the investigators, the patient should not participate (to be formally declared)

Interventions

PROCEDURELiving donor liver transplant, Split liver transplant, RAPID, DDLT

Transplantation of part of the liver from a living donor, or entire cadaveric graft


Locations(1)

Azienda Ospedaliero Universitaria di Modena

Modena, MO, Italy

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NCT05186116


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