Impact of age on breast cancer mortality and competing causes of death at 10 years follow-up in the adjuvant TEAM trial

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3086160 28 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Impact of age on breast cancer mortality and competing causes of death at 10 years follow-up in the adjuvant TEAM trial
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Aim: Due to increasing life expectancy, patients with breast cancer remain at risk of dying due to breast cancer over a long time. This study aims to assess the impact of age on breast cancer mortality and other cause mortality 10 years after diagnosis. Methods: Postmenopausal patients with hormone-receptor positive breast cancer were included in the Tamoxifen and Exemestane Adjuvant Multinational (TEAM) trial between 2001 and 2006. Age at diagnosis was categorised as <65 years (n = 3369), 65–74 years (n = 1896) and ≥75 years (n = 854). Breast cancer mortality was assessed considering other cause mortality as competing event using competing risk analysis. Results: After a median follow-up of 9.8 years (interquartile range 8.0–10.3), cumulative incidence of breast cancer mortality increased with increasing age (age <65 years, 11.7% [95% confidence interval {CI}: 10.2–13.2]; 65–74 years, 12.7% (11.2–14.2) and ≥75 years, 15.6% (13.1–18.0)). Univariate subdistribution hazard ratio (sHR) increased with increasing age (age: 65–74 years, sHR: 1.08, 95% CI: 0.92–1.27 and ≥75 years sHR: 1.30, 95% CI: 1.06–1.58, P = 0.013). Multivariable sHR adjusted for tumour and treatment characteristics increased with age but did not reach significance (age 65–74 years, sHR: 1.11, 95% CI: 0.94–1.31; ≥75 years, sHR: 1.18, 95% CI: 0.94–1.48, P = 0.055). Conclusion: Ten years after diagnosis, older age at diagnosis is associated with increasing breast cancer mortality in univariate analysis, but it did not reach significance in multivariable analysis. This is not outweighed by a substantially higher other cause mortality with older age. This underlines the need to improve the balance between undertreatment and overtreatment in older patients with breast cancer. The trial was registered in International Trial Databases (ClinicalTrials.gov NCT00279448, NCT00032136, and NCT00036270; the Netherlands Trial Registry NTR267). © 2018 Elsevier Ltd
Έτος δημοσίευσης:
2018
Συγγραφείς:
Derks, M.G.M.
Bastiaannet, E.
van de Water, W.
de Glas, N.A.
Seynaeve, C.
Putter, H.
Nortier, J.W.R.
Rea, D.
Hasenburg, A.
Markopoulos, C.
Dirix, L.Y.
Portielje, J.E.A.
van de Velde, C.J.H.
Liefers, G.J.
Περιοδικό:
EUROPEAN JOURNAL OF CANCER
Εκδότης:
Elsevier Ireland Ltd
Τόμος:
99
Σελίδες:
1-8
Λέξεις-κλειδιά:
epidermal growth factor receptor 2; exemestane; progesterone receptor; tamoxifen; androstane derivative; antineoplastic agent; estrogen receptor; exemestane; progesterone receptor, adjuvant therapy; age; aged; all cause mortality; Article; brain disease; breast cancer; cancer adjuvant therapy; cancer hormone therapy; cancer incidence; cancer mortality; cancer radiotherapy; cancer recurrence; cancer surgery; cause of death; endometrium cancer; female; follow up; heart disease; human; human epidermal growth factor receptor 2 positive breast cancer; lung disease; major clinical study; mastectomy; multicenter study (topic); postmenopause; priority journal; progesterone receptor positive breast cancer; randomized controlled trial (topic); risk assessment; second cancer; thromboembolism; adjuvant chemotherapy; age; breast; breast tumor; clinical trial; controlled study; disease free survival; metabolism; middle aged; mortality; multicenter study; pathology; phase 3 clinical trial; procedures; randomized controlled trial; surgery; survival analysis, Age Factors; Aged; Androstadienes; Antineoplastic Combined Chemotherapy Protocols; Breast; Breast Neoplasms; Cause of Death; Chemotherapy, Adjuvant; Disease-Free Survival; Female; Follow-Up Studies; Humans; Mastectomy; Middle Aged; Postmenopause; Receptors, Estrogen; Receptors, Progesterone; Survival Analysis; Tamoxifen
Επίσημο URL (Εκδότης):
DOI:
10.1016/j.ejca.2018.04.009
Το ψηφιακό υλικό του τεκμηρίου δεν είναι διαθέσιμο.