Evidence map›Paper›PMID 36249030›Full record

ArticleFrontiers in oncology2022

Clonal evolution characteristics and reduced dimension prognostic model for non-metastatic metachronous bilateral breast cancer.

Lingyu Li, Jiaxuan Li, Jiwei Jia, Hua He, Mingyang Li, Xu Yan, Qing Yu, Hanfei Guo, Hong Wang, Zheng Lv and 3 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Lingyu LiCancer Center, The First Hospital of Jilin University, Changchun, China.
Jiaxuan LiCancer Center, The First Hospital of Jilin University, Changchun, China.
Jiwei JiaSchool of Mathematics, Jilin University, Changchun, China.
Hua HeCancer Center, The First Hospital of Jilin University, Changchun, China.
Mingyang LiCollege of Electronic Science and Engineering, Jilin University, Changchun, China.
Xu YanCancer Center, The First Hospital of Jilin University, Changchun, China.
Qing YuDepartment of Translational Medicine, Geneplus-Beijing, Beijing, China.
Hanfei GuoCancer Center, The First Hospital of Jilin University, Changchun, China.
Hong WangCancer Center, The First Hospital of Jilin University, Changchun, China.
Zheng LvCancer Center, The First Hospital of Jilin University, Changchun, China.
Haishuang SunCancer Center, The First Hospital of Jilin University, Changchun, China.
Guidong LiaoSchool of Mathematics, Jilin University, Changchun, China.
Jiuwei CuiCancer Center, The First Hospital of Jilin University, Changchun, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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 ( 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.

Indexed as

clonal evolutionmetachronous bilateral breast cancernomogramprognostic evaluationSEER database

Identifiers

PMID36249030
PMCPMC9559188

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.