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Comparing Genetic Risk and Clinical Risk Classification in Luminal-like Breast Cancer Patients Using a 23-Gene Classifier.
Huang, Chi-Cheng; Chen, Ting-Hao; Liu, Liang-Chih; Huang, Chiun-Sheng; Liang, Ji-An; Hsu, Yu-Chen; Hsieh, Chia-Ming; Huang, Sean-Lin; Shih, Kuan-Hui; Tseng, Ling-Ming.
Afiliação
  • Huang CC; Comprehensive Breast Health Center, Department of Surgery, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
  • Chen TH; Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei 106170, Taiwan.
  • Liu LC; Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei 106170, Taiwan.
  • Huang CS; Amwise Diagnostics Pte. Ltd., Singapore 069547, Singapore.
  • Liang JA; Department of General Surgery, China Medical University Hospital, Taichung 40454, Taiwan.
  • Hsu YC; College of Medicine, China Medical University, Taichung 40402, Taiwan.
  • Hsieh CM; Department of Surgery, National Taiwan University Hospital, Taipei 300600, Taiwan.
  • Huang SL; Department of Radiation Oncology, China Medical University Hospital, Taichung 40454, Taiwan.
  • Shih KH; Department of General Surgery, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chia-Yi 60002, Taiwan.
  • Tseng LM; Department of General Surgery, Taiwan Adventist Hospital, Taipei 105520, Taiwan.
Cancers (Basel) ; 14(24)2022 Dec 19.
Article em En | MEDLINE | ID: mdl-36551748
ABSTRACT

Background:

A 23-gene classifier has been developed based on gene expression profiles of Taiwanese luminal-like breast cancer. We aim to stratify risk of relapse and identify patients who may benefit from adjuvant chemotherapy based on genetic model among distinct clinical risk groups.

Methods:

There were 248 luminal (hormone receptor-positive and human epidermal growth factor receptor II-negative) breast cancer patients with 23-gene classifier results. Using the modified Adjuvant! Online definition, clinical high/low-risk groups were tabulated with the genetic model. The primary endpoint was a recurrence-free interval (RFI) at 5 years.

Results:

There was a significant difference between the high/low-risk groups defined by the 23-gene classifier for the 5-year prognosis of recurrence (16 recurrences in high-risk and 3 recurrences in low-risk; log-rank test p < 0.0001). Among the clinically high-risk group, the 5-year RFI of high risk defined by the 23-gene classifier was significantly higher than that of the low-risk group (15 recurrences in high-risk and 2 recurrences in low-risk; log-rank test p < 0.0001).

Conclusion:

This study showed that 23-gene classifier can be used to stratify clinically high-risk patients into distinct survival patterns based on genomic risks and displays the potentiality to guide adjuvant chemotherapy. The 23-gene classifier can provide a better estimation of breast cancer prognosis which can help physicians make a better treatment decision.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article