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A simple prognostic scoring system for patients receiving transarterial embolisation for hepatocellular cancer

BACKGROUND: The prognosis for patients with hepatocellular cancer (HCC) undergoing transarterial therapy (TACE/TAE) is variable. METHODS: We carried out Cox regression analysis of prognostic factors using a training dataset of 114 patients treated with TACE/TAE. A simple prognostic score (PS) was de...

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Autores principales: Kadalayil, L., Benini, R., Pallan, L., O'Beirne, J., Marelli, L., Yu, D., Hackshaw, A., Fox, R., Johnson, P., Burroughs, A. K., Palmer, D. H., Meyer, T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023407/
https://www.ncbi.nlm.nih.gov/pubmed/23857958
http://dx.doi.org/10.1093/annonc/mdt247
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author Kadalayil, L.
Benini, R.
Pallan, L.
O'Beirne, J.
Marelli, L.
Yu, D.
Hackshaw, A.
Fox, R.
Johnson, P.
Burroughs, A. K.
Palmer, D. H.
Meyer, T.
author_facet Kadalayil, L.
Benini, R.
Pallan, L.
O'Beirne, J.
Marelli, L.
Yu, D.
Hackshaw, A.
Fox, R.
Johnson, P.
Burroughs, A. K.
Palmer, D. H.
Meyer, T.
author_sort Kadalayil, L.
collection PubMed
description BACKGROUND: The prognosis for patients with hepatocellular cancer (HCC) undergoing transarterial therapy (TACE/TAE) is variable. METHODS: We carried out Cox regression analysis of prognostic factors using a training dataset of 114 patients treated with TACE/TAE. A simple prognostic score (PS) was developed, validated using an independent dataset of 167 patients and compared with Child–Pugh, CLIP, Okuda, Barcelona Clinic Liver Cancer (BCLC) and MELD. RESULTS: Low albumin, high bilirubin or α-fetoprotein (AFP) and large tumour size were associated with a two- to threefold increase in the risk of death. Patients were assigned one point if albumin <36 g/dl, bilirubin >17 μmol/l, AFP >400 ng/ml or size of dominant tumour >7 cm. The Hepatoma arterial-embolisation prognostic (HAP) score was calculated by summing these points. Patients were divided into four risk groups based on their HAP scores; HAP A, B, C and D (scores 0, 1, 2 and >2, respectively). The median survival for the groups A, B, C and D was 27.6, 18.5, 9.0 and 3.6 months, respectively. The HAP score validated well with the independent dataset and performed better than other scoring systems in differentiating high- and low-risk groups. CONCLUSIONS: The HAP score predicts outcomes in patients with HCC undergoing TACE/TAE and may help guide treatment selection, allow stratification in clinical trials and facilitate meaningful comparisons across reported series.
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spelling pubmed-40234072014-10-01 A simple prognostic scoring system for patients receiving transarterial embolisation for hepatocellular cancer Kadalayil, L. Benini, R. Pallan, L. O'Beirne, J. Marelli, L. Yu, D. Hackshaw, A. Fox, R. Johnson, P. Burroughs, A. K. Palmer, D. H. Meyer, T. Ann Oncol Original Articles BACKGROUND: The prognosis for patients with hepatocellular cancer (HCC) undergoing transarterial therapy (TACE/TAE) is variable. METHODS: We carried out Cox regression analysis of prognostic factors using a training dataset of 114 patients treated with TACE/TAE. A simple prognostic score (PS) was developed, validated using an independent dataset of 167 patients and compared with Child–Pugh, CLIP, Okuda, Barcelona Clinic Liver Cancer (BCLC) and MELD. RESULTS: Low albumin, high bilirubin or α-fetoprotein (AFP) and large tumour size were associated with a two- to threefold increase in the risk of death. Patients were assigned one point if albumin <36 g/dl, bilirubin >17 μmol/l, AFP >400 ng/ml or size of dominant tumour >7 cm. The Hepatoma arterial-embolisation prognostic (HAP) score was calculated by summing these points. Patients were divided into four risk groups based on their HAP scores; HAP A, B, C and D (scores 0, 1, 2 and >2, respectively). The median survival for the groups A, B, C and D was 27.6, 18.5, 9.0 and 3.6 months, respectively. The HAP score validated well with the independent dataset and performed better than other scoring systems in differentiating high- and low-risk groups. CONCLUSIONS: The HAP score predicts outcomes in patients with HCC undergoing TACE/TAE and may help guide treatment selection, allow stratification in clinical trials and facilitate meaningful comparisons across reported series. Oxford University Press 2013-10 2013-07-14 /pmc/articles/PMC4023407/ /pubmed/23857958 http://dx.doi.org/10.1093/annonc/mdt247 Text en © The Author 2013. Published by Oxford University Press on behalf of the European Society for Medical Oncology. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Kadalayil, L.
Benini, R.
Pallan, L.
O'Beirne, J.
Marelli, L.
Yu, D.
Hackshaw, A.
Fox, R.
Johnson, P.
Burroughs, A. K.
Palmer, D. H.
Meyer, T.
A simple prognostic scoring system for patients receiving transarterial embolisation for hepatocellular cancer
title A simple prognostic scoring system for patients receiving transarterial embolisation for hepatocellular cancer
title_full A simple prognostic scoring system for patients receiving transarterial embolisation for hepatocellular cancer
title_fullStr A simple prognostic scoring system for patients receiving transarterial embolisation for hepatocellular cancer
title_full_unstemmed A simple prognostic scoring system for patients receiving transarterial embolisation for hepatocellular cancer
title_short A simple prognostic scoring system for patients receiving transarterial embolisation for hepatocellular cancer
title_sort simple prognostic scoring system for patients receiving transarterial embolisation for hepatocellular cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023407/
https://www.ncbi.nlm.nih.gov/pubmed/23857958
http://dx.doi.org/10.1093/annonc/mdt247
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