J Cancer 2020; 11(9):2509-2517. doi:10.7150/jca.38976 This issue Cite

Research Paper

Decision-making of Adjuvant Chemotherapy for Breast Cancer Patients with Discordant Risk Classifications between Clinical-Pathological Factors and 21-gene Recurrence Score

Weiqi Gao1, Lin Lin2, Xiaochun Fei3, Xiaosong Chen1✉, Kunwei Shen1✉

1. Comprehensive Breast Health Center, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China
2. Department of clinical laboratory, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China
3. Department of pathology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China

Citation:
Gao W, Lin L, Fei X, Chen X, Shen K. Decision-making of Adjuvant Chemotherapy for Breast Cancer Patients with Discordant Risk Classifications between Clinical-Pathological Factors and 21-gene Recurrence Score. J Cancer 2020; 11(9):2509-2517. doi:10.7150/jca.38976. https://www.jcancer.org/v11p2509.htm
Other styles

File import instruction

Abstract

Background: Clinical-pathological factors and 21-gene recurrence score (RS) influence adjuvant chemotherapy (ACT) decision for early breast cancer patients. We investigated the decision-making of ACT in patients with discordant risk classifications of clinical-pathological factors and RS.

Methods: Patients with hormonal receptor (HR)+/ human epidermal growth factor receptor 2 (HER2)-, early breast cancer, who underwent 21-gene RS testing were identified from Ruijin Hospital (RJBC) and the Surveillance, Epidemiology, and End Results (SEER) database. According to Adjuvant! Online and RS (≤25 or >25), discordant risk classifications were defined as: clinical low-risk/ RS high-risk (C-low/ RS-high) and clinical high-risk/ RS low-risk (C-high/RS-low). McNemar's test was used to assess the changes between pre- and post-RS recommendations. Breast cancer-specific survival (BCSS) was estimated using the Kaplan-Meier methods.

Results: Among 727 RJBC patients, the C-low/RS-high group and the C-high/RS-low group represented 19.7% and 21.3% of the cohort. After receiving 21-gene RS results, treatment recommendations were changed for 22.1% patients with discordant risk classifications: ACT rate increased from 41.9% to 75.5% in the C-low/RS-high group and decreased from 63.9% to 60.0% in the C-high/RS-low group. Among 2958 patients from the SEER cohort, 18.4% of the C-high/RS-low group and 59.2% of the C-low/RS-high group received ACT. There was no significant difference in the estimated 3-year BCSS between ACT or not among the C-low/RS-high group (p=0.708) and the C-high/RS-low groups (p=0.391).

Conclusion: For patients with discordant risk classifications, physicians were apt to adopt the 21-gene RS rather than routine clinical-pathological factors to guide ACT selection.

Keywords: breast cancer, Adjuvant! Online, 21-gene recurrence score, discordant risk, adjuvant chemotherapy


Citation styles

APA
Gao, W., Lin, L., Fei, X., Chen, X., Shen, K. (2020). Decision-making of Adjuvant Chemotherapy for Breast Cancer Patients with Discordant Risk Classifications between Clinical-Pathological Factors and 21-gene Recurrence Score. Journal of Cancer, 11(9), 2509-2517. https://doi.org/10.7150/jca.38976.

ACS
Gao, W.; Lin, L.; Fei, X.; Chen, X.; Shen, K. Decision-making of Adjuvant Chemotherapy for Breast Cancer Patients with Discordant Risk Classifications between Clinical-Pathological Factors and 21-gene Recurrence Score. J. Cancer 2020, 11 (9), 2509-2517. DOI: 10.7150/jca.38976.

NLM
Gao W, Lin L, Fei X, Chen X, Shen K. Decision-making of Adjuvant Chemotherapy for Breast Cancer Patients with Discordant Risk Classifications between Clinical-Pathological Factors and 21-gene Recurrence Score. J Cancer 2020; 11(9):2509-2517. doi:10.7150/jca.38976. https://www.jcancer.org/v11p2509.htm

CSE
Gao W, Lin L, Fei X, Chen X, Shen K. 2020. Decision-making of Adjuvant Chemotherapy for Breast Cancer Patients with Discordant Risk Classifications between Clinical-Pathological Factors and 21-gene Recurrence Score. J Cancer. 11(9):2509-2517.

This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
Popup Image