<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(1)</volume><submitter>Selmani Z</submitter><pubmed_abstract>Breast cancers expressing high levels of Ki67 are associated with poor outcomes. Oncotype DX test was designed for ER+/HER2- early-stage breast cancers to help adjuvant chemotherapy decision by providing a Recurrent Score (RS). RS measures the expression of 21 specific genes from tumor tissue, including Ki67. The primary aim of this study was to assess the agreement between Ki67&lt;sub>RNA&lt;/sub> obtained with Oncotype DX RS and Ki67&lt;sub>IHC&lt;/sub>. Other objectives were to analyze the association between the event free survival (EFS) and the expression level of Ki67&lt;sub>RNA&lt;/sub>; and association between RS and Ki67&lt;sub>RNA&lt;/sub>. Herein, we report a low agreement of 0.288 by Pearson correlation coefficient test between Ki67&lt;sub>IHC&lt;/sub> and Ki67&lt;sub>RNA&lt;/sub> in a cohort of 98 patients with early ER+/HER2- breast cancers. Moreover, Ki67&lt;sub>RNA&lt;/sub>&lt;sup>high&lt;/sup> tumors were significantly associated with the occurrence of events (p = 0.03). On the other hand, we did not find any association between Ki67&lt;sub>IHC&lt;/sub> and EFS (p = 0.26). We observed a low agreement between expression level of Ki67&lt;sub>RNA&lt;/sub> and Ki67 protein labelling by IHC. Unlike Ki67&lt;sub>IHC&lt;/sub> and independently of the RS, Ki67&lt;sub>RNA&lt;/sub> could have a prognostic value. It would be interesting to better assess the prognosis and predictive value of Ki67&lt;sub>RNA&lt;/sub> measured by qRT-PCR. The Ki67&lt;sub>RNA&lt;/sub> in medical routine could be a good support in countries where Oncotype DX is not accessible.</pubmed_abstract><journal>Scientific reports</journal><pagination>3617</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8901910</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Low correlation between Ki67 assessed by qRT-PCR in Oncotype Dx score and Ki67 assessed by Immunohistochemistry.</pubmed_title><pmcid>PMC8901910</pmcid><pubmed_authors>Curtit E</pubmed_authors><pubmed_authors>Dobi E</pubmed_authors><pubmed_authors>Feugeas JP</pubmed_authors><pubmed_authors>Meneveau N</pubmed_authors><pubmed_authors>Bazan F</pubmed_authors><pubmed_authors>Pivot X</pubmed_authors><pubmed_authors>Overs A</pubmed_authors><pubmed_authors>Selmani Z</pubmed_authors><pubmed_authors>Meynard G</pubmed_authors><pubmed_authors>Algros MP</pubmed_authors><pubmed_authors>Molimard C</pubmed_authors><pubmed_authors>Borg C</pubmed_authors><pubmed_authors>Mansi L</pubmed_authors><pubmed_authors>Paillard MJ</pubmed_authors><pubmed_authors>Pretet JL</pubmed_authors><pubmed_authors>Viot J</pubmed_authors><pubmed_authors>Chaigneau L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Low correlation between Ki67 assessed by qRT-PCR in Oncotype Dx score and Ki67 assessed by Immunohistochemistry.</name><description>Breast cancers expressing high levels of Ki67 are associated with poor outcomes. Oncotype DX test was designed for ER+/HER2- early-stage breast cancers to help adjuvant chemotherapy decision by providing a Recurrent Score (RS). RS measures the expression of 21 specific genes from tumor tissue, including Ki67. The primary aim of this study was to assess the agreement between Ki67&lt;sub>RNA&lt;/sub> obtained with Oncotype DX RS and Ki67&lt;sub>IHC&lt;/sub>. Other objectives were to analyze the association between the event free survival (EFS) and the expression level of Ki67&lt;sub>RNA&lt;/sub>; and association between RS and Ki67&lt;sub>RNA&lt;/sub>. Herein, we report a low agreement of 0.288 by Pearson correlation coefficient test between Ki67&lt;sub>IHC&lt;/sub> and Ki67&lt;sub>RNA&lt;/sub> in a cohort of 98 patients with early ER+/HER2- breast cancers. Moreover, Ki67&lt;sub>RNA&lt;/sub>&lt;sup>high&lt;/sup> tumors were significantly associated with the occurrence of events (p = 0.03). On the other hand, we did not find any association between Ki67&lt;sub>IHC&lt;/sub> and EFS (p = 0.26). We observed a low agreement between expression level of Ki67&lt;sub>RNA&lt;/sub> and Ki67 protein labelling by IHC. Unlike Ki67&lt;sub>IHC&lt;/sub> and independently of the RS, Ki67&lt;sub>RNA&lt;/sub> could have a prognostic value. It would be interesting to better assess the prognosis and predictive value of Ki67&lt;sub>RNA&lt;/sub> measured by qRT-PCR. The Ki67&lt;sub>RNA&lt;/sub> in medical routine could be a good support in countries where Oncotype DX is not accessible.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-04T20:50:09.606Z</modification><creation>2025-04-04T20:50:09.606Z</creation></dates><accession>S-EPMC8901910</accession><cross_references><pubmed>35256657</pubmed><doi>10.1038/s41598-022-07593-7</doi></cross_references></HashMap>