<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li P</submitter><funding>Guangdong Provincial Science and Technology Foundation of China</funding><funding>National Natural Science Foundation of China</funding><pagination>e6813</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10935875</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(5)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>TFE3 immunohistochemistry (TFE3-IHC) is controversial in the diagnosis of TFE3-rearranged renal cell carcinoma (TFE3-rearranged RCC). This study is to investigate the accuracy and sensitivity of IHC and establish a predictive model to diagnose TFE3-rearranged RCC.&lt;h4>Methods&lt;/h4>Retrospective analysis was performed by collecting IHC and fluorescence in situ hybridization (FISH) results from 228 patients. IHC results were evaluated using three scoring systems. Scoring system 1 is graded based on nuclear staining intensity, scoring system 2 is graded based on the percentage of stained tumor cell nuclei, and scoring system 3 is graded based on both the nuclear staining intensity and the percentage. We collected patients' IHC results and clinical information. Important varia</pubmed_abstract><journal>Cancer medicine</journal><pubmed_title>A nomogram based on TFE3 IHC results and clinical factors as a preliminary screening scheme for TFE3-rearranged renal cell carcinoma.</pubmed_title><pmcid>PMC10935875</pmcid><funding_grant_id>81872094</funding_grant_id><funding_grant_id>2017B020227004</funding_grant_id><funding_grant_id>81972376</funding_grant_id><funding_grant_id>81725016</funding_grant_id><funding_grant_id>81772718</funding_grant_id><funding_grant_id>2017A030313538</funding_grant_id><funding_grant_id>81602219</funding_grant_id><pubmed_authors>Chen M</pubmed_authors><pubmed_authors>Cao J</pubmed_authors><pubmed_authors>Xu Q</pubmed_authors><pubmed_authors>Mumin MA</pubmed_authors><pubmed_authors>Deng Q</pubmed_authors><pubmed_authors>Liao B</pubmed_authors><pubmed_authors>Li P</pubmed_authors><pubmed_authors>Huang K</pubmed_authors><pubmed_authors>Jiang Z</pubmed_authors><pubmed_authors>Zhu J</pubmed_authors><pubmed_authors>Liang H</pubmed_authors><pubmed_authors>Luo J</pubmed_authors><pubmed_authors>Cao Y</pubmed_authors><pubmed_authors>Chen W</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>A nomogram based on TFE3 IHC results and clinical factors as a preliminary screening scheme for TFE3-rearranged renal cell carcinoma.</name><description>&lt;h4>Background&lt;/h4>TFE3 immunohistochemistry (TFE3-IHC) is controversial in the diagnosis of TFE3-rearranged renal cell carcinoma (TFE3-rearranged RCC). This study is to investigate the accuracy and sensitivity of IHC and establish a predictive model to diagnose TFE3-rearranged RCC.&lt;h4>Methods&lt;/h4>Retrospective analysis was performed by collecting IHC and fluorescence in situ hybridization (FISH) results from 228 patients. IHC results were evaluated using three scoring systems. Scoring system 1 is graded based on nuclear staining intensity, scoring system 2 is graded based on the percentage of stained tumor cell nuclei, and scoring system 3 is graded based on both the nuclear staining intensity and the percentage. We collected patients' IHC results and clinical information. Important varia</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-07-15T14:57:23.465Z</modification><creation>2026-07-06T03:09:21.532Z</creation></dates><accession>S-EPMC10935875</accession><cross_references><pubmed>38477529</pubmed><doi>10.1002/cam4.6813</doi></cross_references></HashMap>