Does the 21-gene recurrence score have clinical utility in HR+/HER2+breast cancer?

被引:2
作者
Bilani, Nadeem [2 ]
Crowley, Fionnuala [2 ]
Mohanna, Mohamed [1 ]
Itani, Mira [1 ]
Yaghi, Marita [1 ]
Saravia, Diana [1 ]
Jabbal, Iktej [1 ]
Dominguez, Barbara [1 ]
Liang, Hong [1 ]
Nahleh, Zeina [1 ]
机构
[1] Cleveland Clin Florida, Maroone Canc Ctr, Dept Hematol & Oncol, Weston, FL 33331 USA
[2] Icahn Sch Med Mt Sinai Morningside West, Dept Internal Med, New York, NY 10029 USA
关键词
HER2-POSITIVE BREAST-CANCER; SIGNATURE;
D O I
10.1016/j.breast.2022.09.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The 21-gene recurrence score assay has been validated as a predictive biomarker in early-stage HR+ and HER2-breast cancer. It is not indicated for use in HER2+ disease based on national guidelines. In this study, we assessed the value of 21-gene recurrence score (RS), or OncotypeDX (ODX), testing in HR+/HER2+ breast cancer.We used the National Cancer Database to identify patients with stages I-II, HR+/HER2+ breast cancer who received multi-gene testing with ODX. We then explored the prognostic and predictive value of this biomarker through various forms of survival modeling.ODX testing was performed in n = 5,280 patients. N = 2,678 patients (50.7%) had a RS < 26, while n = 2,602 (49.3%) had a RS >= 26. In Kaplan-Meier survival modeling for patients with recurrence scores < 26, there was no significant difference in overall survival (p = 0.445) between patients receiving different systemic treatment regimens. However, when recurrence scores were >= 26, there was a statistically-significant difference in overall survival between systemic treatment regimens (p < 0.001). 5-year overall survival was highest (97.4%) for patients receiving triple therapy (anti-HER2 with chemotherapy and endocrine therapy), followed by those receiving dual therapy with endocrine and anti-HER2 (96.7%), and endocrine with chemotherapy (94.9%). Patients receiving endocrine therapy alone exhibited the lowest 5-year overall survival (88.5%).Results: Analysis from this large national cancer registry suggests that multigene testing may have predictive value in treatment selection for patients with early-stage, HR+/HER2+ breast cancer. Prospective trials are warranted to identify subgroups of patients with HR+/HER2+ breast cancer who can be spared anti-HER2 treatments and cytotoxic chemotherapy.
引用
收藏
页码:49 / 53
页数:5
相关论文
共 24 条
[1]   Treatment of HER2-positive breast cancer: current status and future perspectives [J].
Arteaga, Carlos L. ;
Sliwkowski, Mark X. ;
Osborne, C. Kent ;
Perez, Edith A. ;
Puglisi, Fabio ;
Gianni, Luca .
NATURE REVIEWS CLINICAL ONCOLOGY, 2012, 9 (01) :16-32
[2]   Biomarker analysis of the NeoSphere study: pertuzumab, trastuzumab, and docetaxel versus trastuzumab plus docetaxel, pertuzumab plus trastuzumab, or pertuzumab plus docetaxel for the neoadjuvant treatment of HER2-positive breast cancer [J].
Bianchini, Giampaolo ;
Kiermaier, Astrid ;
Bianchi, Giulia Valeria ;
Im, Young-Hyuck ;
Pienkowski, Tadeusz ;
Liu, Mei-Ching ;
Tseng, Ling-Ming ;
Dowsett, Mitch ;
Zabaglo, Lila ;
Kirk, Sarah ;
Szado, Tania ;
Eng-Wong, Jennifer ;
Amler, Lukas C. ;
Valagussa, Pinuccia ;
Gianni, Luca .
BREAST CANCER RESEARCH, 2017, 19
[3]  
Bilani N, 2021, GLOBAL WOMENS HLTH
[4]  
Conte PF, 2019, AM SOC CLIN ONCOLOGY
[5]  
DeSantis CE, 2019, CA-CANCER J CLIN, V2019
[6]   HER2-amplified breast cancer: mechanisms of trastuzumab resistance and novel targeted therapies [J].
Gajria, Devika ;
Chandarlapaty, Sarat .
EXPERT REVIEW OF ANTICANCER THERAPY, 2011, 11 (02) :263-275
[7]  
Greenblatt K., 2021, STATPEARLS
[8]   Adjuvant abemaciclib combined with endocrine therapy for high-risk early breast cancer: updated efficacy and Ki-67 analysis from the monarchE study [J].
Harbeck, N. ;
Rastogi, P. ;
Martin, M. ;
Tolaney, S. M. ;
Shao, Z. M. ;
Fasching, P. A. ;
Huang, C. S. ;
Jaliffe, G. G. ;
Tryakin, A. ;
Goetz, M. P. ;
Rugo, H. S. ;
Senkus, E. ;
Testa, L. ;
Andersson, M. ;
Tamura, K. ;
Del Mastro, L. ;
Steger, G. G. ;
Kreipe, H. ;
Hegg, R. ;
Sohn, J. ;
Guarneri, V ;
Cortes, J. ;
Hamilton, E. ;
Andre, V ;
Wei, R. ;
Barriga, S. ;
Sherwood, S. ;
Forrester, T. ;
Munoz, M. ;
Shahir, A. ;
San Antonio, B. ;
Nabinger, S. C. ;
Toi, M. ;
Johnston, S. R. D. ;
O'Shaughnessy, J. .
ANNALS OF ONCOLOGY, 2021, 32 (12) :1571-1581
[9]   HER2+breast cancer treatment and cardiotoxicity: monitoring and management [J].
Jerusalem, Guy ;
Lancellotti, Patrizio ;
Kim, Sung-Bae .
BREAST CANCER RESEARCH AND TREATMENT, 2019, 177 (02) :237-250
[10]   Biomarkers in Her2-Positive Disease [J].
Klocker, Eva Valentina ;
Suppan, Christoph .
BREAST CARE, 2020, 15 (06) :586-593