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Minimally Invasive versus Open Liver Resection for Stage I/II Hepatocellular Carcinoma
SIMPLE SUMMARY: The type of surgical approach for the treatment of hepatocellular carcinoma is unclear. This study compared minimally invasive to open liver resections using the National Cancer Database. The results showed a similar overall survival with improved perioperative outcomes, but higher r...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507639/ https://www.ncbi.nlm.nih.gov/pubmed/34638285 http://dx.doi.org/10.3390/cancers13194800 |
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author | Birgin, Emrullah Kaslow, Sarah R. Hetjens, Svetlana Correa-Gallego, Camilo Rahbari, Nuh N. |
author_facet | Birgin, Emrullah Kaslow, Sarah R. Hetjens, Svetlana Correa-Gallego, Camilo Rahbari, Nuh N. |
author_sort | Birgin, Emrullah |
collection | PubMed |
description | SIMPLE SUMMARY: The type of surgical approach for the treatment of hepatocellular carcinoma is unclear. This study compared minimally invasive to open liver resections using the National Cancer Database. The results showed a similar overall survival with improved perioperative outcomes, but higher rates of positive resection margins in patients with minimally invasive liver resections. The higher rate of residual tumors requires further investigation. ABSTRACT: Minimally invasive liver resection (MILR) is increasingly used as a surgical treatment for patients with hepatocellular carcinoma (HCC). However, there is no large scale data to compare the effectiveness of MILR in comparison to open liver resection (OLR). We identified patients with stage I or II HCC from the National Cancer Database using propensity score matching techniques. Overall, 1931 (66%) and 995 (34%) patients underwent OLR or MILR between 2010 and 2015. After propensity matching, 5-year OS was similar in the MILR and OLR group (51.7% vs. 52.8%, p = 0.766). MILR was associated with lower 90-day mortality (5% vs. 7%, p = 0.041) and shorter length of stay (4 days vs. 5 days, p < 0.001), but higher rates of positive margins (6% vs. 4%, p = 0.001). An operation at an academic institution was identified as an independent preventive factor for a positive resection margin (OR 0.64: 95% CI 0.43–0.97) and 90-day mortality (OR 0.61; 95% CI 0.41–0.91). MILR for HCC is associated with similar overall survival to OLR, with the benefit of improved short term postoperative outcomes. The increased rate of positive margins after MILR requires further investigation, as do the differences in perioperative outcomes between academic and nonacademic institutions. |
format | Online Article Text |
id | pubmed-8507639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85076392021-10-13 Minimally Invasive versus Open Liver Resection for Stage I/II Hepatocellular Carcinoma Birgin, Emrullah Kaslow, Sarah R. Hetjens, Svetlana Correa-Gallego, Camilo Rahbari, Nuh N. Cancers (Basel) Article SIMPLE SUMMARY: The type of surgical approach for the treatment of hepatocellular carcinoma is unclear. This study compared minimally invasive to open liver resections using the National Cancer Database. The results showed a similar overall survival with improved perioperative outcomes, but higher rates of positive resection margins in patients with minimally invasive liver resections. The higher rate of residual tumors requires further investigation. ABSTRACT: Minimally invasive liver resection (MILR) is increasingly used as a surgical treatment for patients with hepatocellular carcinoma (HCC). However, there is no large scale data to compare the effectiveness of MILR in comparison to open liver resection (OLR). We identified patients with stage I or II HCC from the National Cancer Database using propensity score matching techniques. Overall, 1931 (66%) and 995 (34%) patients underwent OLR or MILR between 2010 and 2015. After propensity matching, 5-year OS was similar in the MILR and OLR group (51.7% vs. 52.8%, p = 0.766). MILR was associated with lower 90-day mortality (5% vs. 7%, p = 0.041) and shorter length of stay (4 days vs. 5 days, p < 0.001), but higher rates of positive margins (6% vs. 4%, p = 0.001). An operation at an academic institution was identified as an independent preventive factor for a positive resection margin (OR 0.64: 95% CI 0.43–0.97) and 90-day mortality (OR 0.61; 95% CI 0.41–0.91). MILR for HCC is associated with similar overall survival to OLR, with the benefit of improved short term postoperative outcomes. The increased rate of positive margins after MILR requires further investigation, as do the differences in perioperative outcomes between academic and nonacademic institutions. MDPI 2021-09-25 /pmc/articles/PMC8507639/ /pubmed/34638285 http://dx.doi.org/10.3390/cancers13194800 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Birgin, Emrullah Kaslow, Sarah R. Hetjens, Svetlana Correa-Gallego, Camilo Rahbari, Nuh N. Minimally Invasive versus Open Liver Resection for Stage I/II Hepatocellular Carcinoma |
title | Minimally Invasive versus Open Liver Resection for Stage I/II Hepatocellular Carcinoma |
title_full | Minimally Invasive versus Open Liver Resection for Stage I/II Hepatocellular Carcinoma |
title_fullStr | Minimally Invasive versus Open Liver Resection for Stage I/II Hepatocellular Carcinoma |
title_full_unstemmed | Minimally Invasive versus Open Liver Resection for Stage I/II Hepatocellular Carcinoma |
title_short | Minimally Invasive versus Open Liver Resection for Stage I/II Hepatocellular Carcinoma |
title_sort | minimally invasive versus open liver resection for stage i/ii hepatocellular carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507639/ https://www.ncbi.nlm.nih.gov/pubmed/34638285 http://dx.doi.org/10.3390/cancers13194800 |
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