Computer-assisted quantification of tumor-associated collagen signatures to improve the prognosis prediction of breast cancer

Abstract Background Collagen fibers play an important role in tumor initiation, progression, and invasion. Our previous research has already shown that large-scale tumor-associated collagen signatures (TACS) are powerful prognostic biomarkers independent of clinicopathological factors in invasive br...

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Autores principales: Gangqin Xi, Lida Qiu, Shuoyu Xu, Wenhui Guo, Fangmeng Fu, Deyong Kang, Liqin Zheng, Jiajia He, Qingyuan Zhang, Lianhuang Li, Chuan Wang, Jianxin Chen
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Publicado: BMC 2021
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spelling oai:doaj.org-article:aae68bb767024f68b8bf835a36b4b62a2021-11-21T12:16:06ZComputer-assisted quantification of tumor-associated collagen signatures to improve the prognosis prediction of breast cancer10.1186/s12916-021-02146-71741-7015https://doaj.org/article/aae68bb767024f68b8bf835a36b4b62a2021-11-01T00:00:00Zhttps://doi.org/10.1186/s12916-021-02146-7https://doaj.org/toc/1741-7015Abstract Background Collagen fibers play an important role in tumor initiation, progression, and invasion. Our previous research has already shown that large-scale tumor-associated collagen signatures (TACS) are powerful prognostic biomarkers independent of clinicopathological factors in invasive breast cancer. However, they are observed on a macroscale and are more suitable for identifying high-risk patients. It is necessary to investigate the effect of the corresponding microscopic features of TACS so as to more accurately and comprehensively predict the prognosis of breast cancer patients. Methods In this retrospective and multicenter study, we included 942 invasive breast cancer patients in both a training cohort (n = 355) and an internal validation cohort (n = 334) from one clinical center and in an external validation cohort (n = 253) from a different clinical center. TACS corresponding microscopic features (TCMFs) were firstly extracted from multiphoton images for each patient, and then least absolute shrinkage and selection operator (LASSO) regression was applied to select the most robust features to build a TCMF-score. Finally, the Cox proportional hazard regression analysis was used to evaluate the association of TCMF-score with disease-free survival (DFS). Results TCMF-score is significantly associated with DFS in univariate Cox proportional hazard regression analysis. After adjusting for clinical variables by multivariate Cox regression analysis, the TCMF-score remains an independent prognostic indicator. Remarkably, the TCMF model performs better than the clinical (CLI) model in the three cohorts and is particularly outstanding in the ER-positive and lower-risk subgroups. By contrast, the TACS model is more suitable for the ER-negative and higher-risk subgroups. When the TACS and TCMF are combined, they could complement each other and perform well in all patients. As expected, the full model (CLI+TCMF+TACS) achieves the best performance (AUC 0.905, [0.873–0.938]; 0.896, [0.860–0.931]; 0.882, [0.840–0.925] in the three cohorts). Conclusion These results demonstrate that the TCMF-score is an independent prognostic factor for breast cancer, and the increased prognostic performance (TCMF+TACS-score) may help us develop more appropriate treatment protocols.Gangqin XiLida QiuShuoyu XuWenhui GuoFangmeng FuDeyong KangLiqin ZhengJiajia HeQingyuan ZhangLianhuang LiChuan WangJianxin ChenBMCarticleBreast cancerMultiphoton imagingTACS corresponding microscopic featuresPrognosisMedicineRENBMC Medicine, Vol 19, Iss 1, Pp 1-16 (2021)
institution DOAJ
collection DOAJ
language EN
topic Breast cancer
Multiphoton imaging
TACS corresponding microscopic features
Prognosis
Medicine
R
spellingShingle Breast cancer
Multiphoton imaging
TACS corresponding microscopic features
Prognosis
Medicine
R
Gangqin Xi
Lida Qiu
Shuoyu Xu
Wenhui Guo
Fangmeng Fu
Deyong Kang
Liqin Zheng
Jiajia He
Qingyuan Zhang
Lianhuang Li
Chuan Wang
Jianxin Chen
Computer-assisted quantification of tumor-associated collagen signatures to improve the prognosis prediction of breast cancer
description Abstract Background Collagen fibers play an important role in tumor initiation, progression, and invasion. Our previous research has already shown that large-scale tumor-associated collagen signatures (TACS) are powerful prognostic biomarkers independent of clinicopathological factors in invasive breast cancer. However, they are observed on a macroscale and are more suitable for identifying high-risk patients. It is necessary to investigate the effect of the corresponding microscopic features of TACS so as to more accurately and comprehensively predict the prognosis of breast cancer patients. Methods In this retrospective and multicenter study, we included 942 invasive breast cancer patients in both a training cohort (n = 355) and an internal validation cohort (n = 334) from one clinical center and in an external validation cohort (n = 253) from a different clinical center. TACS corresponding microscopic features (TCMFs) were firstly extracted from multiphoton images for each patient, and then least absolute shrinkage and selection operator (LASSO) regression was applied to select the most robust features to build a TCMF-score. Finally, the Cox proportional hazard regression analysis was used to evaluate the association of TCMF-score with disease-free survival (DFS). Results TCMF-score is significantly associated with DFS in univariate Cox proportional hazard regression analysis. After adjusting for clinical variables by multivariate Cox regression analysis, the TCMF-score remains an independent prognostic indicator. Remarkably, the TCMF model performs better than the clinical (CLI) model in the three cohorts and is particularly outstanding in the ER-positive and lower-risk subgroups. By contrast, the TACS model is more suitable for the ER-negative and higher-risk subgroups. When the TACS and TCMF are combined, they could complement each other and perform well in all patients. As expected, the full model (CLI+TCMF+TACS) achieves the best performance (AUC 0.905, [0.873–0.938]; 0.896, [0.860–0.931]; 0.882, [0.840–0.925] in the three cohorts). Conclusion These results demonstrate that the TCMF-score is an independent prognostic factor for breast cancer, and the increased prognostic performance (TCMF+TACS-score) may help us develop more appropriate treatment protocols.
format article
author Gangqin Xi
Lida Qiu
Shuoyu Xu
Wenhui Guo
Fangmeng Fu
Deyong Kang
Liqin Zheng
Jiajia He
Qingyuan Zhang
Lianhuang Li
Chuan Wang
Jianxin Chen
author_facet Gangqin Xi
Lida Qiu
Shuoyu Xu
Wenhui Guo
Fangmeng Fu
Deyong Kang
Liqin Zheng
Jiajia He
Qingyuan Zhang
Lianhuang Li
Chuan Wang
Jianxin Chen
author_sort Gangqin Xi
title Computer-assisted quantification of tumor-associated collagen signatures to improve the prognosis prediction of breast cancer
title_short Computer-assisted quantification of tumor-associated collagen signatures to improve the prognosis prediction of breast cancer
title_full Computer-assisted quantification of tumor-associated collagen signatures to improve the prognosis prediction of breast cancer
title_fullStr Computer-assisted quantification of tumor-associated collagen signatures to improve the prognosis prediction of breast cancer
title_full_unstemmed Computer-assisted quantification of tumor-associated collagen signatures to improve the prognosis prediction of breast cancer
title_sort computer-assisted quantification of tumor-associated collagen signatures to improve the prognosis prediction of breast cancer
publisher BMC
publishDate 2021
url https://doaj.org/article/aae68bb767024f68b8bf835a36b4b62a
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