Bone mineral density in breast cancer patients treated with adjuvant letrozole, tamoxifen, or sequences of letrozole and tamoxifen in the BIG 1-98 study (SAKK 21/07)

Autor: Jens Huober, Anita Giobbie-Hurder, J. Lüthi, G. Berthod, A. Schönenberger, O. Pagani, M. Simcock, Peter Brauchli, C. Genton, Khalil Zaman, S. Aebi, Beat Thürlimann
Přispěvatelé: Swiss Group for Clinical Cancer Research (SAKK)
Jazyk: angličtina
Rok vydání: 2017
Předmět:
Oncology
musculoskeletal diseases
medicine.medical_specialty
Bone density
medicine.drug_class
medicine.medical_treatment
Osteoporosis
Aged
Aged
80 and over

Antineoplastic Combined Chemotherapy Protocols/adverse effects
Antineoplastic Combined Chemotherapy Protocols/therapeutic use
Bone Density/drug effects
Breast Neoplasms/drug therapy
Female
Hip/pathology
Hip/radiography
Humans
Lumbar Vertebrae/pathology
Lumbar Vertebrae/radiography
Middle Aged
Multivariate Analysis
Nitriles/administration & dosage
Osteoporosis/chemically induced
Osteoporosis/radiography
Postmenopause
Randomized Controlled Trials as Topic
Retrospective Studies
Tamoxifen/administration & dosage
Triazoles/administration & dosage
610 Medicine & health
Breast Neoplasms
Breast cancer
Bone Density
Internal medicine
Antineoplastic Combined Chemotherapy Protocols
Nitriles
medicine
Bone mineral
Hip
Lumbar Vertebrae
Aromatase inhibitor
business.industry
Letrozole
Hormone replacement therapy (menopause)
Hematology
Triazoles
medicine.disease
Radiography
Tamoxifen
business
medicine.drug
Zdroj: Annals of Oncology, vol. 23, no. 6, pp. 1474-1481
Zaman, K; Thürlimann, B; Huober, J; Schönenberger, A; Pagani, O; Lüthi, J; Simcock, M; Giobbie-Hurder, A; Berthod, G; Genton, C; Brauchli, P; Aebi, S (2012). Bone mineral density in breast cancer patients treated with adjuvant letrozole, tamoxifen, or sequences of letrozole and tamoxifen in the BIG 1-98 study (SAKK 21/07). Annals of oncology, 23(6), pp. 1474-1481. Oxford University Press 10.1093/annonc/mdr448
DOI: 10.1093/annonc/mdr448
Popis: BACKGROUND The risk of osteoporosis and fracture influences the selection of adjuvant endocrine therapy. We analyzed bone mineral density (BMD) in Swiss patients of the Breast International Group (BIG) 1-98 trial [treatment arms: A, tamoxifen (T) for 5 years; B, letrozole (L) for 5 years; C, 2 years of T followed by 3 years of L; D, 2 years of L followed by 3 years of T]. PATIENTS AND METHODS Dual-energy X-ray absorptiometry (DXA) results were retrospectively collected. Patients without DXA served as control group. Repeated measures models using covariance structures allowing for different times between DXA were used to estimate changes in BMD. Prospectively defined covariates were considered as fixed effects in the multivariable models. RESULTS Two hundred and sixty-one of 546 patients had one or more DXA with 577 lumbar and 550 hip measurements. Weight, height, prior hormone replacement therapy, and hysterectomy were positively correlated with BMD; the correlation was negative for letrozole arms (B/C/D versus A), known osteoporosis, time on trial, age, chemotherapy, and smoking. Treatment did not influence the occurrence of osteoporosis (T score < -2.5 standard deviation). CONCLUSIONS All aromatase inhibitor regimens reduced BMD. The sequential schedules were as detrimental for bone density as L monotherapy.
Databáze: OpenAIRE