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Clinical Treatment Score Post-5 Years (CTS5) and Late Recurrence Risk in Hormone Receptor-Positive, HER2-Positive Breast Cancer

Authors
 Saranya Chumsri  ;  Tanmayi Pai  ;  Yaohua Ma  ;  Zhuo Li  ;  Angelica Gil  ;  Alvaro Moreno-Aspitia  ;  Gerardo Colon-Otero  ;  Katherine L Pogue-Geile  ;  Priya Rasgoti  ;  Soonmyung Paik  ;  Edith A Perez  ;  E Aubrey Thompson 
Citation
 JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, Vol.22(7) : 463-468, 2024-09 
Journal Title
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK
ISSN
 1540-1405 
Issue Date
2024-09
MeSH
Adult ; Aged ; Biomarkers, Tumor / metabolism ; Breast Neoplasms* / drug therapy ; Breast Neoplasms* / metabolism ; Breast Neoplasms* / mortality ; Breast Neoplasms* / pathology ; Female ; Humans ; Middle Aged ; Neoplasm Recurrence, Local* / epidemiology ; Neoplasm Recurrence, Local* / pathology ; Prognosis ; Receptor, ErbB-2* / metabolism ; Receptors, Estrogen / metabolism ; Receptors, Progesterone* / metabolism ; Risk Assessment / methods ; Risk Factors ; Trastuzumab / therapeutic use
Abstract
Background: The Clinical Treatment Score post-5 years (CTS5) is a risk stratification tool used to determine the risk of late recurrence in hormone receptor-positive (HR+), HER2-negative breast cancer (BC). Limited data exist on its use in HR+, HER2-positive (HER2+) BC.

Patients and methods: CTS5 was evaluated in HR+, HER2+ BC in the North Central Cancer Treatment Group (NCCTG) N9831 (Alliance) and NSABP B-31 (NRG) trials.

Results: A total of 1,862 patients with HR+, HER2+ BC without recurrence 5 years after enrollment were included. Overall, the CTS5 score was significantly associated with recurrence-free survival (RFS), with a hazard ratio (HR) of 1.35 (95% CI, 1.12-1.63; P=.002), but did not reach statistical significance in patients who received trastuzumab (n=829; HR, 1.29; 95% CI, 0.98-1.71; P=.07). CTS5 risk category was not significantly associated with RFS. In patients who received trastuzumab, other variables used in CTS5, including patient age and tumor size, were not significantly associated with RFS. N3 was significantly associated with worse outcomes (HR, 1.86; 95% CI, 1.09-3.17; P=.02) compared with N0-N1. Paradoxically, higher tumor grade was associated with better outcomes after 5 years in the multivariate analysis (HR, 0.71; 95% CI, 0.50-1.00; P=.05). The incidence of recurrences or deaths between years 5 to 10 was 10.6% in the CTS5 low-risk category, 5.6% in the intermediate-risk category, and 9.8% in the high-risk category.

Conclusions: The CTS5 model does not accurately predict the risk of late recurrence in HR+, HER2+ BC treated with adjuvant trastuzumab in the N9831 and B-31 trials. This study underlines the need to develop a new prognostic model to better delineate the risk of late recurrence in patients with HR+, HER2+ BC receiving adjuvant trastuzumab.

Clinicaltrials: gov identifiers: NCT00005970 (NCCTG N9831) and NCT00004067 (NRG/NSABP B-31).
Files in This Item:
T992024802.pdf Download
DOI
10.6004/jnccn.2024.7015
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
Yonsei Authors
Paik, Soon Myung(백순명) ORCID logo https://orcid.org/0000-0001-9688-6480
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/201697
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