<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>48</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Xia B</submitter><funding>Science and Technology Commission of Shanghai Municipality</funding><funding>Shanghai Shenkang Hospital Development Center</funding><funding>National Natural Science Foundation of China</funding><pubmed_abstract>&lt;b>Background:&lt;/b> To investigate whether the radiomics signature (Rad-score) of DCE-MRI images obtained in triple-negative breast cancer (TNBC) patients before neoadjuvant chemotherapy (NAC) is associated with disease-free survival (DFS). Develop and validate an intuitive nomogram based on radiomics signatures, MRI findings, and clinicopathological variables to predict DFS. &lt;b>Methods:&lt;/b> Patients (&lt;i>n&lt;/i> = 150) from two hospitals who received NAC from August 2011 to May 2017 were diagnosed with TNBC by pathological biopsy, and follow-up through May 2020 was retrospectively analysed. Patients from one hospital (&lt;i>n&lt;/i> = 109) were used as the training group, and patients from the other hospital (&lt;i>n&lt;/i> = 41) were used as the validation group. ROIs were drawn on 1.5 T MRI T1W enhancement images of the whole volume of the tumour obtained with a 3D slicer. Radiomics signatures predicting DFS were identified, optimal cut-off value for Rad-score was determined, and the associations between DFS and radiomics signatures, MRI findings, and clinicopathological variables were analysed. A nomogram was developed and validated for individualized DFS estimation. &lt;b>Results:&lt;/b> The median follow-up time was 53.5 months, and 45 of 150 (30.0%) patients experienced recurrence and metastasis. The optimum cut-off value of the Rad-score was 0.2528, which stratified patients into high- and low-risk groups for DFS in the training group (&lt;i>p&lt;/i>&lt;0.001) and was validated in the external validation group. Multivariate analysis identified three independent indicators: multifocal/centric disease status, pCR status, and Rad-score. A nomogram based on these factors showed discriminatory ability, the C-index of the model was 0.834 (95% CI, 0.761-0.907) and 0.868 (95% CI, 0.787-949) in the training and the validation groups, respectively, which is better than clinicoradiological nomogram(training group: C-index = 0.726, 95% CI = 0.709-0.743; validation group: C-index = 0.774,95% CI = 0.743-0.805). &lt;b>Conclusion:&lt;/b> The Rad-score derived from preoperative MRI features is an independent biomarker for DFS prediction in patients with TNBC to NAC, and the combined radiomics nomogram improved individualized DFS estimation.</pubmed_abstract><journal>Frontiers in genetics</journal><pagination>783513</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8632946</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Combined Nomogram Model to Predict Disease-free Survival in Triple-Negative Breast Cancer Patients With Neoadjuvant Chemotherapy.</pubmed_title><pmcid>PMC8632946</pmcid><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Qian Z</pubmed_authors><pubmed_authors>Shao Z</pubmed_authors><pubmed_authors>Gu Y</pubmed_authors><pubmed_authors>Zhou S</pubmed_authors><pubmed_authors>You C</pubmed_authors><pubmed_authors>Xia B</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Xiao Q</pubmed_authors><pubmed_authors>Chai W</pubmed_authors><view_count>48</view_count></additional><is_claimable>false</is_claimable><name>A Combined Nomogram Model to Predict Disease-free Survival in Triple-Negative Breast Cancer Patients With Neoadjuvant Chemotherapy.</name><description>&lt;b>Background:&lt;/b> To investigate whether the radiomics signature (Rad-score) of DCE-MRI images obtained in triple-negative breast cancer (TNBC) patients before neoadjuvant chemotherapy (NAC) is associated with disease-free survival (DFS). Develop and validate an intuitive nomogram based on radiomics signatures, MRI findings, and clinicopathological variables to predict DFS. &lt;b>Methods:&lt;/b> Patients (&lt;i>n&lt;/i> = 150) from two hospitals who received NAC from August 2011 to May 2017 were diagnosed with TNBC by pathological biopsy, and follow-up through May 2020 was retrospectively analysed. Patients from one hospital (&lt;i>n&lt;/i> = 109) were used as the training group, and patients from the other hospital (&lt;i>n&lt;/i> = 41) were used as the validation group. ROIs were drawn on 1.5 T MRI T1W enhancement images of the whole volume of the tumour obtained with a 3D slicer. Radiomics signatures predicting DFS were identified, optimal cut-off value for Rad-score was determined, and the associations between DFS and radiomics signatures, MRI findings, and clinicopathological variables were analysed. A nomogram was developed and validated for individualized DFS estimation. &lt;b>Results:&lt;/b> The median follow-up time was 53.5 months, and 45 of 150 (30.0%) patients experienced recurrence and metastasis. The optimum cut-off value of the Rad-score was 0.2528, which stratified patients into high- and low-risk groups for DFS in the training group (&lt;i>p&lt;/i>&lt;0.001) and was validated in the external validation group. Multivariate analysis identified three independent indicators: multifocal/centric disease status, pCR status, and Rad-score. A nomogram based on these factors showed discriminatory ability, the C-index of the model was 0.834 (95% CI, 0.761-0.907) and 0.868 (95% CI, 0.787-949) in the training and the validation groups, respectively, which is better than clinicoradiological nomogram(training group: C-index = 0.726, 95% CI = 0.709-0.743; validation group: C-index = 0.774,95% CI = 0.743-0.805). &lt;b>Conclusion:&lt;/b> The Rad-score derived from preoperative MRI features is an independent biomarker for DFS prediction in patients with TNBC to NAC, and the combined radiomics nomogram improved individualized DFS estimation.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2024-02-15T21:07:29.129Z</modification><creation>2022-02-11T13:53:27.875Z</creation></dates><accession>S-EPMC8632946</accession><cross_references><pubmed>34868273</pubmed><doi>10.3389/fgene.2021.783513</doi></cross_references></HashMap>