AI Article Synopsis

  • Liver transplantation (LT) is being explored as a curative option for patients with unresectable colorectal cancer liver metastasis (CRLM), particularly in selected individuals.
  • A case study highlights the first domino LT where a liver from a 30-year-old woman with heterozygous familial hypercholesterolemia (FH) was successfully transplanted to a 44-year-old woman with advanced sigmoid cancer and liver metastases.
  • The domino recipient showed positive outcomes, maintaining normal LDL-C levels and no cancer recurrence after 31 months, indicating that domino LT from donors with heterozygous FH can be a viable treatment for specific CRLM cases.

Article Abstract

Liver transplantation (LT) is a potential curative treatment for unresectable colorectal cancer liver metastasis (CRLM). Familial hypercholesterolemia (FH) is an inherited condition characterized by elevated low-density lipoprotein cholesterol (LDL-C) levels. Liver transplantation is offered for selected cases, and an explanted liver can be used as a domino graft. We report the first report of domino LT for unresectable CRLM using a liver from a patient with heterozygous FH. The domino donor was a 30-year-old female with a history of heterozygous FH. She had failed medical therapies for FH, including plasmapheresis; therefore, she underwent living donor LT as a treatment for FH. The explanted liver was transplanted to the domino recipient. She has been doing well with normal LDL-C levels. The domino recipient was a 44-year-old female with a history of stage 4 sigmoid cancer with liver metastases, for which she underwent laparoscopic sigmoid colectomy and right hepatectomy. She developed unresectable lesions in the remnant left lobe, which were controlled well with chemotherapy; therefore, she underwent domino LT. She is doing well without recurrence at the 31-month follow-up. Domino LT from a donor with heterozygous FH is feasible for strictly selected patients with unresectable CRLM.

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Source
http://dx.doi.org/10.1016/j.transproceed.2023.07.012DOI Listing

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