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Locoregional treatment for colorectal liver metastases aiming for precision medicine

In patients with colorectal liver metastases (CLM), surgery is potentially curative. The use of novel surgical techniques and complementary percutaneous ablation allows for curative‐intent treatment even in marginally resectable cases. Resection is used as part of a multidisciplinary approach, which...

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Autores principales: Maki, Harufumi, Jain, Anish J., Haddad, Antony, Lendoire, Mateo, Chun, Yun Shin, Vauthey, Jean‐Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10319606/
https://www.ncbi.nlm.nih.gov/pubmed/37416742
http://dx.doi.org/10.1002/ags3.12689
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author Maki, Harufumi
Jain, Anish J.
Haddad, Antony
Lendoire, Mateo
Chun, Yun Shin
Vauthey, Jean‐Nicolas
author_facet Maki, Harufumi
Jain, Anish J.
Haddad, Antony
Lendoire, Mateo
Chun, Yun Shin
Vauthey, Jean‐Nicolas
author_sort Maki, Harufumi
collection PubMed
description In patients with colorectal liver metastases (CLM), surgery is potentially curative. The use of novel surgical techniques and complementary percutaneous ablation allows for curative‐intent treatment even in marginally resectable cases. Resection is used as part of a multidisciplinary approach, which for nearly all patients will include perioperative chemotherapy. Small CLM can be treated with parenchymal‐sparing hepatectomy (PSH) and/or ablation. For small CLM, PSH results in better survival and higher rates of resectability of recurrent CLM than non‐PSH. For patients with extensive bilateral distribution of CLM, two‐stage hepatectomy or fast‐track two‐stage hepatectomy is effective. Our increasing knowledge of genetic alterations allows us to use them as prognostic factors alongside traditional risk factors (e.g. tumor diameter and tumor number) to select patients with CLM for resection and guide surveillance after resection. Alteration in RAS family genes (hereafter referred to as “RAS alteration”) is an important negative prognostic factor, as are alterations in the TP53, SMAD4, FBXW7, and BRAF genes. However, APC alteration appears to improve prognosis. RAS alteration, increased number and diameter of CLM, and primary lymph node metastasis are well‐known risk factors for recurrence after CLM resection. In patients free of recurrence 2 y after CLM resection, only RAS alteration is associated with recurrence. Thus, surveillance intensity can be stratified by RAS alteration status after 2 y. Novel diagnostic instruments and tools, such as circulating tumor DNA, may lead to further evolution of patient selection, prognostication, and treatment algorithms for CLM.
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spelling pubmed-103196062023-07-06 Locoregional treatment for colorectal liver metastases aiming for precision medicine Maki, Harufumi Jain, Anish J. Haddad, Antony Lendoire, Mateo Chun, Yun Shin Vauthey, Jean‐Nicolas Ann Gastroenterol Surg Review Articles In patients with colorectal liver metastases (CLM), surgery is potentially curative. The use of novel surgical techniques and complementary percutaneous ablation allows for curative‐intent treatment even in marginally resectable cases. Resection is used as part of a multidisciplinary approach, which for nearly all patients will include perioperative chemotherapy. Small CLM can be treated with parenchymal‐sparing hepatectomy (PSH) and/or ablation. For small CLM, PSH results in better survival and higher rates of resectability of recurrent CLM than non‐PSH. For patients with extensive bilateral distribution of CLM, two‐stage hepatectomy or fast‐track two‐stage hepatectomy is effective. Our increasing knowledge of genetic alterations allows us to use them as prognostic factors alongside traditional risk factors (e.g. tumor diameter and tumor number) to select patients with CLM for resection and guide surveillance after resection. Alteration in RAS family genes (hereafter referred to as “RAS alteration”) is an important negative prognostic factor, as are alterations in the TP53, SMAD4, FBXW7, and BRAF genes. However, APC alteration appears to improve prognosis. RAS alteration, increased number and diameter of CLM, and primary lymph node metastasis are well‐known risk factors for recurrence after CLM resection. In patients free of recurrence 2 y after CLM resection, only RAS alteration is associated with recurrence. Thus, surveillance intensity can be stratified by RAS alteration status after 2 y. Novel diagnostic instruments and tools, such as circulating tumor DNA, may lead to further evolution of patient selection, prognostication, and treatment algorithms for CLM. John Wiley and Sons Inc. 2023-05-18 /pmc/articles/PMC10319606/ /pubmed/37416742 http://dx.doi.org/10.1002/ags3.12689 Text en © 2023 The Authors. Annals of Gastroenterological Surgery published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Gastroenterological Surgery. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Articles
Maki, Harufumi
Jain, Anish J.
Haddad, Antony
Lendoire, Mateo
Chun, Yun Shin
Vauthey, Jean‐Nicolas
Locoregional treatment for colorectal liver metastases aiming for precision medicine
title Locoregional treatment for colorectal liver metastases aiming for precision medicine
title_full Locoregional treatment for colorectal liver metastases aiming for precision medicine
title_fullStr Locoregional treatment for colorectal liver metastases aiming for precision medicine
title_full_unstemmed Locoregional treatment for colorectal liver metastases aiming for precision medicine
title_short Locoregional treatment for colorectal liver metastases aiming for precision medicine
title_sort locoregional treatment for colorectal liver metastases aiming for precision medicine
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10319606/
https://www.ncbi.nlm.nih.gov/pubmed/37416742
http://dx.doi.org/10.1002/ags3.12689
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