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Clonal evolution characteristics and reduced dimension prognostic model for non-metastatic metachronous bilateral breast cancer.
Li, Lingyu; Li, Jiaxuan; Jia, Jiwei; He, Hua; Li, Mingyang; Yan, Xu; Yu, Qing; Guo, Hanfei; Wang, Hong; Lv, Zheng; Sun, Haishuang; Liao, Guidong; Cui, Jiuwei.
Affiliation
  • Li L; Cancer Center, The First Hospital of Jilin University, Changchun, China.
  • Li J; Cancer Center, The First Hospital of Jilin University, Changchun, China.
  • Jia J; School of Mathematics, Jilin University, Changchun, China.
  • He H; National Applied Mathematical Center (Jilin), Changchun, China.
  • Li M; Cancer Center, The First Hospital of Jilin University, Changchun, China.
  • Yan X; College of Electronic Science and Engineering, Jilin University, Changchun, China.
  • Yu Q; Cancer Center, The First Hospital of Jilin University, Changchun, China.
  • Guo H; Department of Translational Medicine, Geneplus-Beijing, Beijing, China.
  • Wang H; Cancer Center, The First Hospital of Jilin University, Changchun, China.
  • Lv Z; Cancer Center, The First Hospital of Jilin University, Changchun, China.
  • Sun H; Cancer Center, The First Hospital of Jilin University, Changchun, China.
  • Liao G; Cancer Center, The First Hospital of Jilin University, Changchun, China.
  • Cui J; School of Mathematics, Jilin University, Changchun, China.
Front Oncol ; 12: 963884, 2022.
Article in En | MEDLINE | ID: mdl-36249030
Background: How to evaluate the prognosis and develop overall treatment strategies of metachronous bilateral breast cancer (MBBC) remains confused in clinical. Here, we investigated the correlation between clonal evolution and clinical characteristics of MBBC; we aim to establish a novel prognostic model in these patients. Methods: The data from Surveillance, Epidemiology, and End Results (SEER) database and the First Hospital of Jilin University were analyzed for breast cancer-specific cumulative mortality (BCCM) by competing risk model. Meanwhile, whole-exome sequencing was applied for 10 lesions acquired at spatial-temporal distinct regions of five patients from our own hospital to reconstruct clonal evolutionary characteristics of MBBC. Then, dimensional-reduction (DR) cumulative incidence function (CIF) curves of MBBC features were established on different point in diagnostic interval time, to build a novel DR nomogram. Results: Significant heterogeneity in genome and clinical features of MBBC was widespread. The mutational diversity of contralateral BC (CBC) was significantly higher than that in primary BC (PBC), and the most effective prognostic MATH ratio was significantly correlated with interval time (R 2 = 0.85, p< 0.05). In SEER cohort study (n = 13,304), the interval time was not only significantly affected the BCCM by multivariate analysis (p< 0.000) but determined the weight of clinical features (T/N stage, grade and ER status) on PBC and CBC in prognostic evaluation. Thus, clinical parameters after DR based on interval time were incorporated into the nomogram for prognostic predicting BCCM. Concordance index was 0.773 (95% CI, 0.769-0.776) in training cohort (n = 8,869), and 0.819 (95% CI, 0.813-0.826) in validation cohort (n = 4,435). Conclusions: Bilateral heterogeneous characteristics and interval time were determinant prognostic factors of MBBC. The DR prognostic nomogram may help clinicians in prognostic evaluation and decision making.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Front Oncol Year: 2022 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: Front Oncol Year: 2022 Document type: Article Affiliation country: Country of publication: