<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lin KY</submitter><funding>Science and Technology Innovation Joint Foundation of Fujian Province</funding><funding>Fujian Medical University Qihang Fund Graduate Innovation Project</funding><funding>National Natural Science Foundation of China</funding><funding>Major Research Projects for Young and Middle-aged Researchers of Fujian Provincial Health Care Commission</funding><pagination>1190</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10696803</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Routine clinical staging for hepatocellular carcinoma (HCC) incorporates liver function, general health, and tumor morphology. Further refinement of prognostic assessments and treatment decisions may benefit from the inclusion of tumor biological marker alpha-fetoprotein (AFP) and systemic inflammation indicator C-reactive protein (CRP).&lt;h4>Methods&lt;/h4>Data from a multicenter cohort of 2770 HCC patients undergoing hepatectomy were analyzed. We developed the PACE risk score (Prognostic implications of AFP and CRP Elevation) after initially assessing preoperative AFP and CRP's prognostic value. Subgroup analyzes were performed in BCLC cohorts A and B using multivariable Cox analysis to evaluate the prognostic stratification ability of the PACE risk score and its complement</pubmed_abstract><journal>BMC cancer</journal><pubmed_title>Prognostic implications of alpha-fetoprotein and C-reactive protein elevation in hepatocellular carcinoma following resection (PACE): a large cohort study of 2770 patients.</pubmed_title><pmcid>PMC10696803</pmcid><funding_grant_id>2022QH2030</funding_grant_id><funding_grant_id>2021ZQNZD013</funding_grant_id><funding_grant_id>62275050</funding_grant_id><funding_grant_id>2019Y9108</funding_grant_id><pubmed_authors>Li YT</pubmed_authors><pubmed_authors>Zheng SM</pubmed_authors><pubmed_authors>Zheng LF</pubmed_authors><pubmed_authors>Tang SC</pubmed_authors><pubmed_authors>Lin ZW</pubmed_authors><pubmed_authors>You PH</pubmed_authors><pubmed_authors>Lin KC</pubmed_authors><pubmed_authors>Chen QJ</pubmed_authors><pubmed_authors>Wang XM</pubmed_authors><pubmed_authors>Lin KY</pubmed_authors><pubmed_authors>Zhang JX</pubmed_authors><pubmed_authors>Fu J</pubmed_authors><pubmed_authors>Zeng YY</pubmed_authors><pubmed_authors>Yang T</pubmed_authors><pubmed_authors>Wu MM</pubmed_authors><pubmed_authors>Lu Q</pubmed_authors><pubmed_authors>Guo LB</pubmed_authors><pubmed_authors>Zhou WP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prognostic implications of alpha-fetoprotein and C-reactive protein elevation in hepatocellular carcinoma following resection (PACE): a large cohort study of 2770 patients.</name><description>&lt;h4>Background&lt;/h4>Routine clinical staging for hepatocellular carcinoma (HCC) incorporates liver function, general health, and tumor morphology. Further refinement of prognostic assessments and treatment decisions may benefit from the inclusion of tumor biological marker alpha-fetoprotein (AFP) and systemic inflammation indicator C-reactive protein (CRP).&lt;h4>Methods&lt;/h4>Data from a multicenter cohort of 2770 HCC patients undergoing hepatectomy were analyzed. We developed the PACE risk score (Prognostic implications of AFP and CRP Elevation) after initially assessing preoperative AFP and CRP's prognostic value. Subgroup analyzes were performed in BCLC cohorts A and B using multivariable Cox analysis to evaluate the prognostic stratification ability of the PACE risk score and its complement</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Dec</publication><modification>2025-04-22T20:12:02.451Z</modification><creation>2024-10-18T07:31:00.424Z</creation></dates><accession>S-EPMC10696803</accession><cross_references><pubmed>38053048</pubmed><doi>10.1186/s12885-023-11693-6</doi></cross_references></HashMap>