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Continued value of the serum alpha-fetoprotein test in surveilling at-risk populations for hepatocellular carcinoma

BACKGROUNDS AND AIMS: Because of the known limitations of ultrasonography (US) alone, we re-evaluated whether complimentary testing for serum alpha-fetoprotein (AFP) is helpful in surveilling for hepatocellular carcinoma (HCC) in high-risk populations. METHODS: We included, from a hospital-based can...

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Autores principales: An, Jihyun, Kim, Ha Il, Chang, Seheon, Shim, Ju Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7449471/
https://www.ncbi.nlm.nih.gov/pubmed/32845895
http://dx.doi.org/10.1371/journal.pone.0238078
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author An, Jihyun
Kim, Ha Il
Chang, Seheon
Shim, Ju Hyun
author_facet An, Jihyun
Kim, Ha Il
Chang, Seheon
Shim, Ju Hyun
author_sort An, Jihyun
collection PubMed
description BACKGROUNDS AND AIMS: Because of the known limitations of ultrasonography (US) alone, we re-evaluated whether complimentary testing for serum alpha-fetoprotein (AFP) is helpful in surveilling for hepatocellular carcinoma (HCC) in high-risk populations. METHODS: We included, from a hospital-based cancer registry, 1,776 asymptomatic adults who were surveilled biannually with the AFP test and US and eventually diagnosed with HCC between 2007 and 2015. Based on the screening results, these patients were divided into three groups: AFP (positive for AFP only; n = 298 [16.8%]), US (positive for US only; n = 978 [55.0%]), and AFP+US (positive for both; n = 500 [28.2%]). We compared the outcomes of the three groups, calculating the survival of the AFP group both as observed survival and as survival corrected for lead-time. RESULTS: In terms of tumor-related factors, the separate AFP and US groups were more likely to have early stage HCC and to receive curative treatments than the combined AFP+US group (Ps<0.05). The AFP group had significantly better overall and cancer-specific survival than the AFP+US group after adjusting for covariates (adjusted hazard ratios [HRs] 0.68 and 0.62, respectively). In analyses correcting for lead-time in the AFP group (doubling time 120 days), the respective adjusted HRs for the AFP group were unchanged (0.74 and 0.67), but they were no longer significant after additional adjustment for tumor stage and curative treatment (0.87 and 0.81). CONCLUSIONS: HCC cases detected by the AFP test without abnormal ultrasonic findings appear to have better survival, possibly as a result of stage migration and the resulting cures. Complementary AFP surveillance, together with US, could be helpful for at-risk patients.
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spelling pubmed-74494712020-09-02 Continued value of the serum alpha-fetoprotein test in surveilling at-risk populations for hepatocellular carcinoma An, Jihyun Kim, Ha Il Chang, Seheon Shim, Ju Hyun PLoS One Research Article BACKGROUNDS AND AIMS: Because of the known limitations of ultrasonography (US) alone, we re-evaluated whether complimentary testing for serum alpha-fetoprotein (AFP) is helpful in surveilling for hepatocellular carcinoma (HCC) in high-risk populations. METHODS: We included, from a hospital-based cancer registry, 1,776 asymptomatic adults who were surveilled biannually with the AFP test and US and eventually diagnosed with HCC between 2007 and 2015. Based on the screening results, these patients were divided into three groups: AFP (positive for AFP only; n = 298 [16.8%]), US (positive for US only; n = 978 [55.0%]), and AFP+US (positive for both; n = 500 [28.2%]). We compared the outcomes of the three groups, calculating the survival of the AFP group both as observed survival and as survival corrected for lead-time. RESULTS: In terms of tumor-related factors, the separate AFP and US groups were more likely to have early stage HCC and to receive curative treatments than the combined AFP+US group (Ps<0.05). The AFP group had significantly better overall and cancer-specific survival than the AFP+US group after adjusting for covariates (adjusted hazard ratios [HRs] 0.68 and 0.62, respectively). In analyses correcting for lead-time in the AFP group (doubling time 120 days), the respective adjusted HRs for the AFP group were unchanged (0.74 and 0.67), but they were no longer significant after additional adjustment for tumor stage and curative treatment (0.87 and 0.81). CONCLUSIONS: HCC cases detected by the AFP test without abnormal ultrasonic findings appear to have better survival, possibly as a result of stage migration and the resulting cures. Complementary AFP surveillance, together with US, could be helpful for at-risk patients. Public Library of Science 2020-08-26 /pmc/articles/PMC7449471/ /pubmed/32845895 http://dx.doi.org/10.1371/journal.pone.0238078 Text en © 2020 An et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
An, Jihyun
Kim, Ha Il
Chang, Seheon
Shim, Ju Hyun
Continued value of the serum alpha-fetoprotein test in surveilling at-risk populations for hepatocellular carcinoma
title Continued value of the serum alpha-fetoprotein test in surveilling at-risk populations for hepatocellular carcinoma
title_full Continued value of the serum alpha-fetoprotein test in surveilling at-risk populations for hepatocellular carcinoma
title_fullStr Continued value of the serum alpha-fetoprotein test in surveilling at-risk populations for hepatocellular carcinoma
title_full_unstemmed Continued value of the serum alpha-fetoprotein test in surveilling at-risk populations for hepatocellular carcinoma
title_short Continued value of the serum alpha-fetoprotein test in surveilling at-risk populations for hepatocellular carcinoma
title_sort continued value of the serum alpha-fetoprotein test in surveilling at-risk populations for hepatocellular carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7449471/
https://www.ncbi.nlm.nih.gov/pubmed/32845895
http://dx.doi.org/10.1371/journal.pone.0238078
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