<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>65(10)</volume><submitter>Malapelle U</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Sanger sequencing (SS) of PCR products is still the most frequent method to test colorectal cancer for KRAS mutations in routine practice.&lt;h4>Methods&lt;/h4>An audit of SS on 1720 routine cases was carried out, taking into account age, gender, specimen type (resection vs biopsies), tumour site (primary vs metastasis), tumour stage, neoplastic cells abundance (>30% vs &lt;30%) and fixation type (buffered formalin vs simple formalin). In a subset of 50 wild-type (WT) patients correlations between SS findings and response rate (RR), progression-free survival (PFS) and overall survival (OS) were also evaluated.&lt;h4>Results&lt;/h4>The tests were informative in 1691 cases (98.3%). Mutations were detected in 671 cases (39.6%). No significant differences in mutation rates were observed wi</pubmed_abstract><journal>Journal of clinical pathology</journal><pagination>940-4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3461636</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Sanger sequencing in routine KRAS testing: a review of 1720 cases from a pathologist's perspective.</pubmed_title><pmcid>PMC3461636</pmcid><pubmed_authors>de Luca C</pubmed_authors><pubmed_authors>Sparano L</pubmed_authors><pubmed_authors>Troncone G</pubmed_authors><pubmed_authors>Carlomagno C</pubmed_authors><pubmed_authors>Bellevicine C</pubmed_authors><pubmed_authors>Maiello FM</pubmed_authors><pubmed_authors>Riccio P</pubmed_authors><pubmed_authors>Nappi O</pubmed_authors><pubmed_authors>Salatiello M</pubmed_authors><pubmed_authors>Rispo E</pubmed_authors><pubmed_authors>Vita G</pubmed_authors><pubmed_authors>Malapelle U</pubmed_authors><pubmed_authors>De Stefano A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sanger sequencing in routine KRAS testing: a review of 1720 cases from a pathologist's perspective.</name><description>&lt;h4>Background&lt;/h4>Sanger sequencing (SS) of PCR products is still the most frequent method to test colorectal cancer for KRAS mutations in routine practice.&lt;h4>Methods&lt;/h4>An audit of SS on 1720 routine cases was carried out, taking into account age, gender, specimen type (resection vs biopsies), tumour site (primary vs metastasis), tumour stage, neoplastic cells abundance (>30% vs &lt;30%) and fixation type (buffered formalin vs simple formalin). In a subset of 50 wild-type (WT) patients correlations between SS findings and response rate (RR), progression-free survival (PFS) and overall survival (OS) were also evaluated.&lt;h4>Results&lt;/h4>The tests were informative in 1691 cases (98.3%). Mutations were detected in 671 cases (39.6%). No significant differences in mutation rates were observed wi</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Oct</publication><modification>2025-04-18T11:34:44.151Z</modification><creation>2019-03-27T00:58:33Z</creation></dates><accession>S-EPMC3461636</accession><cross_references><pubmed>22872705</pubmed><doi>10.1136/jclinpath-2012-200773</doi></cross_references></HashMap>