Are mammographic density phenotypes associated with breast cancer treatment response and clinical outcomes? A systematic review and meta-analysis

被引:13
|
作者
Kanbayti, Ibrahem H. [1 ,2 ]
Rae, William I. D. [2 ]
McEntee, Mark E. [2 ,3 ]
Ekpo, Ernest U. [2 ,4 ]
机构
[1] King Abdulaziz Univ, Fac Appl Med Sci, Diagnost Radiog Technol Dept, Jeddah, Saudi Arabia
[2] Univ Sydney, Fac Hlth Sci, Discipline Med Radiat Sci, Sydney, NSW, Australia
[3] Brookfield Hlth Sci, Dept Med Roinn Slainte, UG Aras Watson 12, Cork T12 AK54, Ireland
[4] Labs & Res Ctr, Orange Radiol, Calabar, Nigeria
关键词
Mammographic breast density; Breast cancer; Cancer treatment interventions; Patient outcomes; NEOADJUVANT CHEMOTHERAPY; TAMOXIFEN TREATMENT; RISK; RECURRENCE; REDUCTION; IMPACT; CLASSIFICATION; RADIOTHERAPY; RALOXIFENE; PREDICTOR;
D O I
10.1016/j.breast.2019.07.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mammographic density (MD) increases breast cancer (BC) risk, however, its association with patient outcomes is unclear. We examined the association of baseline MD (BMD), and MD reduction (MDR) following BC treatment with patient outcomes. Six databases (CINAHL, Scopus, PubMed, Web of Science, MEDLINE, and Embase) were used to identify relevant articles. The PRISMA strategy was used to extract relevant details. Study quality and risk of bias were assessed using the "Quality In Prognosis Studies" (QUIPS) tool. A Meta-analysis and pooled risk estimates were performed. Results showed that BMD is associated with contralateral breast cancer (CBC) risk (HR = 1.9; 95%CI: 1.3-3.0, p = 0.0007), recurrence (HR = 2.0; 95%CI: 1.0-4.0, p = 0.04), and mortality (HR =1.4; 95%CI: 1.1-1.9, p = 0.003). No association was found between BMD and prognosis (HR = 3.2; 95%CI: 0.9-11.2, p = 0.06). Data on risk estimates (95% CI) from BMD for survival [RR: 1.75; 0.99-3.1 to 2.4; 1.4-4.1], ipsilateral BC [HR: 1; 0.6-1.6 to 3; 1.2-7.5], and treatment response (OR, 1.8; 0.98-3.3) are limited. MDR showed no association with mortality (HR = 0.5; 95%CI: 0.2-1.2, p = 0.13). MDR is associated with a reduced risk of recurrence [HR/RR: 0.35; 0.17-0.68 to 1.33; 0.67-2.65)], however data on MDR and outcomes such as mortality [HR/RR: 0.5; 0.27 -0.93 to 0.59; 0.22-0.88], and CBC risk [RR/HR: 0.53; 0.24-0.84 to 1.3; 0.6-2.7] are limited. Evidence, although sparse, demonstrates that high BMD is associated with an increased risk of recurrence, CBC, and mortality. Conversely, MDR is associated with a reduced risk of BC recurrence, CBC, and BC-related mortality. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:62 / 76
页数:15
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