Validation of CTS5 on a Retrospective Cohort of Real-Life Pre- and Postmenopausal Patients Diagnosed With Estrogen Receptor-Positive Breast Cancers: Is It Prognostic?


Journal

Clinical breast cancer
ISSN: 1938-0666
Titre abrégé: Clin Breast Cancer
Pays: United States
ID NLM: 100898731

Informations de publication

Date de publication:
02 2021
Historique:
received: 03 03 2020
revised: 23 06 2020
accepted: 24 06 2020
pubmed: 25 7 2020
medline: 26 11 2021
entrez: 25 7 2020
Statut: ppublish

Résumé

More than 50% of estrogen receptor (ER)-positive breast cancer (BC) distant recurrences (DR) develop after the completion of 5 years of adjuvant endocrine therapy (ET). Its extension is beneficial on disease-free survival and overall survival but increases therapy-related side effects. Selecting patients who could benefit the most from an extended regimen has become an increasing need. Clinical Treatment Score at 5 Years (CTS5) is a prognostic tool using clinicopathologic data to estimate DR risk after 5 years of ET for ER CTS5 was calculated for 603 patients diagnosed with ER Median follow-up was 8 years (range, 6-26 years). The 426 postmenopausal women were categorized by CTS5 as follows: 152 low risk, 139 intermediate risk, and 135 high risk. LDR rates were 3.9%, 7.2%, and 15.6%, respectively. CTS5 results were prognostic for LDR: patients with CTS5-high showed a fourfold risk of developing an LDR compared to patients with CTS5-low (hazard ratio, 4.48; 95% confidence interval, 1.80-11.1). The same analysis was conducted for the 177 premenopausal women: 88 low risk, 40 intermediate risk, and 49 high risk. LDR rate were 5.6%, 7.5%, and 20.4%, respectively, proving CTS5 to be prognostic for premenopausal patients as well (CTS5-high vs. CTS5-low: hazard ratio, 3.40; 95% confidence interval, 1.06-11.0). CTS5 was shown to be prognostic of the risk of LDR in our population of real-life pre- and postmenopausal patients. Our results support its use in clinical practice to better tailor the prescription of extended ET.

Sections du résumé

BACKGROUND
More than 50% of estrogen receptor (ER)-positive breast cancer (BC) distant recurrences (DR) develop after the completion of 5 years of adjuvant endocrine therapy (ET). Its extension is beneficial on disease-free survival and overall survival but increases therapy-related side effects. Selecting patients who could benefit the most from an extended regimen has become an increasing need. Clinical Treatment Score at 5 Years (CTS5) is a prognostic tool using clinicopathologic data to estimate DR risk after 5 years of ET for ER
PATIENTS AND METHODS
CTS5 was calculated for 603 patients diagnosed with ER
RESULTS
Median follow-up was 8 years (range, 6-26 years). The 426 postmenopausal women were categorized by CTS5 as follows: 152 low risk, 139 intermediate risk, and 135 high risk. LDR rates were 3.9%, 7.2%, and 15.6%, respectively. CTS5 results were prognostic for LDR: patients with CTS5-high showed a fourfold risk of developing an LDR compared to patients with CTS5-low (hazard ratio, 4.48; 95% confidence interval, 1.80-11.1). The same analysis was conducted for the 177 premenopausal women: 88 low risk, 40 intermediate risk, and 49 high risk. LDR rate were 5.6%, 7.5%, and 20.4%, respectively, proving CTS5 to be prognostic for premenopausal patients as well (CTS5-high vs. CTS5-low: hazard ratio, 3.40; 95% confidence interval, 1.06-11.0).
CONCLUSION
CTS5 was shown to be prognostic of the risk of LDR in our population of real-life pre- and postmenopausal patients. Our results support its use in clinical practice to better tailor the prescription of extended ET.

Identifiants

pubmed: 32703705
pii: S1526-8209(20)30152-X
doi: 10.1016/j.clbc.2020.06.008
pii:
doi:

Substances chimiques

Receptors, Estrogen 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e53-e62

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Andrea Villasco (A)

Academic Division of Gynecology and Obstetrics, Mauriziano Hospital, University of Turin, Turin, Italy. Electronic address: andrea.villasco@unito.it.

Francesca Agnelli (F)

School of Medicine, University of Turin, Turin, Italy.

Marta D'Alonzo (M)

Academic Division of Gynecology and Obstetrics, Mauriziano Hospital, University of Turin, Turin, Italy.

Francesca Accomasso (F)

Academic Division of Gynecology and Obstetrics, Mauriziano Hospital, University of Turin, Turin, Italy.

Piero Sismondi (P)

Academic Division of Gynecology and Obstetrics, Mauriziano Hospital, University of Turin, Turin, Italy.

Nicoletta Biglia (N)

Academic Division of Gynecology and Obstetrics, Mauriziano Hospital, University of Turin, Turin, Italy.

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