<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7</volume><submitter>Yan WT</submitter><pubmed_abstract>Whether circulating tumor cells (CTCs) can be used as an indicator of treatment response in breast cancer (BC) needs to be clarified. We addressed this issue by a meta-analysis. PubMed, EMBase and Cochrane library databases were searched in June 2016. Effect measures were estimated as pooled risk ratio (RR), odds ratio (OR) or mean difference by fixed- or random-effect models, according to heterogeneity of included studies. In total, 50 studies with 6712 patients were recruited. Overall analysis showed that there was a significant reduction of CTC-positive rate (RR = 0.68, 95% CI: 0.61-0.76, P &lt; 0.00001) after treatment. Subgroup analyses revealed that neoadjuvant treatment, adjuvant treatment, metastatic treatment or combination therapy could reduce the CTC-positive rate, but surgery could not; moreover, the reduction was only found in HER2+ or HER2- patients but not in the triple-negative ones. Reduction of CTC-positive rate was associated with lower probability of disease progression (OR = 0.54, 95% CI: 0.33-0.89, P = 0.01) and longer overall survival period (mean difference = 11.61 months, 95% CI: 8.63-14.59, P &lt; 0.00001) as well as longer progression-free survival period (mean difference = 5.07 months, 95% CI: 2.70-7.44, P &lt; 0.0001). These results demonstrate that CTC status can serve as an indicator to monitor the effectiveness of treatments and guide subsequent therapies in BC.</pubmed_abstract><journal>Scientific reports</journal><pagination>43464</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5364512</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Circulating tumor cell status monitors the treatment responses in breast cancer patients: a meta-analysis.</pubmed_title><pmcid>PMC5364512</pmcid><pubmed_authors>Jiang J</pubmed_authors><pubmed_authors>Chen Q</pubmed_authors><pubmed_authors>Cui X</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Cui YH</pubmed_authors><pubmed_authors>Yan WT</pubmed_authors><pubmed_authors>Li YF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Circulating tumor cell status monitors the treatment responses in breast cancer patients: a meta-analysis.</name><description>Whether circulating tumor cells (CTCs) can be used as an indicator of treatment response in breast cancer (BC) needs to be clarified. We addressed this issue by a meta-analysis. PubMed, EMBase and Cochrane library databases were searched in June 2016. Effect measures were estimated as pooled risk ratio (RR), odds ratio (OR) or mean difference by fixed- or random-effect models, according to heterogeneity of included studies. In total, 50 studies with 6712 patients were recruited. Overall analysis showed that there was a significant reduction of CTC-positive rate (RR = 0.68, 95% CI: 0.61-0.76, P &lt; 0.00001) after treatment. Subgroup analyses revealed that neoadjuvant treatment, adjuvant treatment, metastatic treatment or combination therapy could reduce the CTC-positive rate, but surgery could not; moreover, the reduction was only found in HER2+ or HER2- patients but not in the triple-negative ones. Reduction of CTC-positive rate was associated with lower probability of disease progression (OR = 0.54, 95% CI: 0.33-0.89, P = 0.01) and longer overall survival period (mean difference = 11.61 months, 95% CI: 8.63-14.59, P &lt; 0.00001) as well as longer progression-free survival period (mean difference = 5.07 months, 95% CI: 2.70-7.44, P &lt; 0.0001). These results demonstrate that CTC status can serve as an indicator to monitor the effectiveness of treatments and guide subsequent therapies in BC.</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Mar</publication><modification>2026-05-05T16:56:21.224Z</modification><creation>2019-03-27T02:39:29Z</creation></dates><accession>S-EPMC5364512</accession><cross_references><pubmed>28337998</pubmed><doi>10.1038/srep43464</doi></cross_references></HashMap>