Adjuvant Aromatase Inhibitors or Tamoxifen Following Chemotherapy for Perimenopausal Breast Cancer Patients.


Journal

Journal of the National Cancer Institute
ISSN: 1460-2105
Titre abrégé: J Natl Cancer Inst
Pays: United States
ID NLM: 7503089

Informations de publication

Date de publication:
02 11 2021
Historique:
received: 26 11 2020
revised: 29 03 2021
accepted: 10 05 2021
pubmed: 9 6 2021
medline: 25 2 2022
entrez: 8 6 2021
Statut: ppublish

Résumé

The benefit of adjuvant aromatase inhibitors (AI) vs tamoxifen has been investigated in randomized clinical trials for premenopausal and postmenopausal patients with early, estrogen receptor-positive (ER+) breast cancer. The optimal endocrine treatment for chemotherapy-treated perimenopausal women, who generally develop chemotherapy-induced amenorrhea, is uncertain. All Dutch women who received adjuvant chemotherapy and endocrine treatment for stage I-III, ER+ (>10% positive cells), invasive breast cancer diagnosed between 2004 and 2007 were identified through the Netherlands Cancer Registry. Included women were considered perimenopausal based on an age at diagnosis of 45 to 50 years (n = 2295). For each patient, AI treatment duration relative to total endocrine treatment duration was calculated. Predominantly tamoxifen-treated patients (AI < 25%) were compared with those receiving AI and tamoxifen for a similar duration (AI 25%-75%) and those mostly using AI (AI > 75%). Adjusted hazard ratios (HRs) for recurrence-free survival (RFS) and overall survival were calculated using time-dependent Cox regression. After an average follow-up of 7.6 years, 377 RFS events occurred. Women mostly receiving AI (AI > 75%) had the best RFS (adjusted HR = 0.63, 95% confidence interval = 0.46 to 0.86) followed by those receiving AI 25% to 75% (adjusted HR = 0.85, 95% confidence interval = 0.65 to 1.12) compared with predominantly tamoxifen-treated women. Trend analyses showed that every 10% increase in AI-endocrine treatment ratio reduced RFS event risk by 5% (2-sided Ptrend = .002). In total, 236 deaths occurred; hazard ratios for overall survival showed similar trends. These results suggest that the best adjuvant endocrine treatment for chemotherapy-treated, ER+ breast cancer patients diagnosed aged 45-50 years consists of mainly AI followed by a switch strategy and mainly tamoxifen.

Sections du résumé

BACKGROUND
The benefit of adjuvant aromatase inhibitors (AI) vs tamoxifen has been investigated in randomized clinical trials for premenopausal and postmenopausal patients with early, estrogen receptor-positive (ER+) breast cancer. The optimal endocrine treatment for chemotherapy-treated perimenopausal women, who generally develop chemotherapy-induced amenorrhea, is uncertain.
METHODS
All Dutch women who received adjuvant chemotherapy and endocrine treatment for stage I-III, ER+ (>10% positive cells), invasive breast cancer diagnosed between 2004 and 2007 were identified through the Netherlands Cancer Registry. Included women were considered perimenopausal based on an age at diagnosis of 45 to 50 years (n = 2295). For each patient, AI treatment duration relative to total endocrine treatment duration was calculated. Predominantly tamoxifen-treated patients (AI < 25%) were compared with those receiving AI and tamoxifen for a similar duration (AI 25%-75%) and those mostly using AI (AI > 75%). Adjusted hazard ratios (HRs) for recurrence-free survival (RFS) and overall survival were calculated using time-dependent Cox regression.
RESULTS
After an average follow-up of 7.6 years, 377 RFS events occurred. Women mostly receiving AI (AI > 75%) had the best RFS (adjusted HR = 0.63, 95% confidence interval = 0.46 to 0.86) followed by those receiving AI 25% to 75% (adjusted HR = 0.85, 95% confidence interval = 0.65 to 1.12) compared with predominantly tamoxifen-treated women. Trend analyses showed that every 10% increase in AI-endocrine treatment ratio reduced RFS event risk by 5% (2-sided Ptrend = .002). In total, 236 deaths occurred; hazard ratios for overall survival showed similar trends.
CONCLUSIONS
These results suggest that the best adjuvant endocrine treatment for chemotherapy-treated, ER+ breast cancer patients diagnosed aged 45-50 years consists of mainly AI followed by a switch strategy and mainly tamoxifen.

Identifiants

pubmed: 34101806
pii: 6292098
doi: 10.1093/jnci/djab091
pmc: PMC8562974
doi:

Substances chimiques

Antineoplastic Agents, Hormonal 0
Aromatase Inhibitors 0
Tamoxifen 094ZI81Y45

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1506-1514

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press.

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Auteurs

Gwen M H E Dackus (GMHE)

Division of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Department of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands.

Katarzyna Jóźwiak (K)

Department of Epidemiology and Biostatistics, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Institute of Biostatistics and Registry Research, Brandenburg Medical School, Neuruppin, Germany.

Gabe S Sonke (GS)

Department of Medical Oncology, Netherlands Cancer Institute, the Netherlands.

Elsken van der Wall (E)

Division Cancer Center, University Medical Center Utrecht, Utrecht, the Netherlands.

Paul J van Diest (PJ)

Department of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands.

Sabine Siesling (S)

Department of Research, Netherlands Comprehensive Cancer Organization, Utrecht, the Netherlands.
Department of Health Technology and Services Research (HTSR), University of Twente, Enschede, the Netherlands.

Michael Hauptmann (M)

Department of Epidemiology and Biostatistics, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Institute of Biostatistics and Registry Research, Brandenburg Medical School, Neuruppin, Germany.

Sabine C Linn (SC)

Division of Molecular Pathology, Netherlands Cancer Institute, Amsterdam, the Netherlands.
Department of Pathology, University Medical Center Utrecht, Utrecht, the Netherlands.
Department of Medical Oncology, Netherlands Cancer Institute, the Netherlands.

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