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. 2013 Sep 26;19(3):173-81.
doi: 10.1016/j.rpor.2013.08.007. eCollection 2014 May.

Clinicopathological features and prognosis of triple negative breast cancer in Kuwait: A comparative/perspective analysis

Affiliations

Clinicopathological features and prognosis of triple negative breast cancer in Kuwait: A comparative/perspective analysis

Mohammed S Fayaz et al. Rep Pract Oncol Radiother. .

Abstract

Aim: The aim of this study was to determine the incidence of TNBC in Kuwait, to analyze the clinicopathologic features and prognosis of this type of breast cancer, and compare it with reports from other regions of the world.

Background: Triple negative breast cancer (TNBC) is defined as a subtype that is negative for estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 (HER2). There is a growing evidence of the heterogeneity of such entity on the molecular level that may cause discrete outcomes.

Methods: We analyzed the clinicopathologic features of 363 TNBC cases which were diagnosed in Kuwait from July 1999 to June 2009. The disease-free survival (DFS) and overall survival (OS) were analyzed by Kaplan-Meier method. Comparison was done with reports from USA, Europe, Middle and Far East.

Results: Among 2986 patients diagnosed with breast cancer in Kuwait, 363 patients (12.2%) were TNBC. The median age was 48 years, 57.2% had lymph nodes (LN) metastasis, 56.9% were of grade III tumor and 41.9% had stage II disease. 81% developed recurrences and 75% of deaths occurred by 2.5 years after treatment. There is marked variation of clinicopathologic features according to country of patients' cohort.

Conclusion: The incidence of TNBC in our study is similar to other studies. TNBC patients showed an early major recurrence surge peaking at approximately year 2.5. Regional variation of clinicopathologic features indicates a need for molecular studies to define underlying molecular features and its impact on survival.

Keywords: Breast cancer; Clinicopathological; Epidemiology; Triple negative; Variation.

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Figures

Fig. 1
Fig. 1
DFS and OS of all study cohor (cumulative and by stage).

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