Triple-negative breast cancer (TNBC) refers to any breast cancer that does not express the genes for the estrogen receptor, progesterone receptor and HER2. TNBC accounts for 10-15% of all breast cancers. These cancers tend to be more common in women aged <40 years, who are African American, or who have a BRCA1 mutation. This tumor differs from other breast cancer subtypes because it grows and spreads faster, has limited treatment options, and has a worse outcome (1,2). A previous study by the authors found that the frequency of TNBC cancers was high (29.3%), with large size, high-grade, and 70% with lymph node metastasis (3).

TNBC is unresponsive to endocrine therapy or other available targeted agents. Cytotoxic chemotherapy remains the primary treatment for TNBC disease, along with surgery and/or radiotherapy (4-6). Novel drug developments in TNBC include antibody-drug conjugates, immune checkpoint inhibitors, PARP inhibitors, and androgen receptor-targeted agents (7).

TNBC is partly a basal-like subtype, with increased expression of basal cytokeratins, such as cytokeratin (CK) 5/6, CK 17 and epidermal growth factor receptor (EGFR). Basal-like cancer occurs mainly in young women, often relapsing rapidly, with aggressive characteristics such as high-grade, high-proliferation indexes, p53 mutation, EGFR overexpression, c-MYC amplification, loss of phosphatase and tensin analog tumor suppressor gene, and the loss of function of BRCA1 (8-10). High recurrence and poor response to chemotherapy in TNBC are probably due to the presence of basal-like cancer (11).

The identification of BRCA mutations in patients with TNBC can have a significant effect on treatment. The BRCA mutation status of patients with TNBC may predict the response to treatment with inhibitors of poly (ADP ribose) polymerase (PARP) (12,13). Identification by immunohistochemistry (IHC) is a simple and reliable method to access the expression of BRCA1 protein in tumor tissues. The present study aimed to investigate the prognostic and predictive value of BRCA1 expression by using the IHC method in TNBC.

There were 100 cases of TNBC reported between 2015 and 2020 with complete clinicopathological data available. However, only 57 cases were accompanied by data on survival and therapy. Of the 57 cases studied, the mean patient age was 55.18±10.014 (32-83). Patients aged ≥50 years were more frequent (70.2%) compared with patients aged <50 years (29.8%). More patients were high-grade, advanced staged, alive, received non-platinum-based therapy, and non-specific type. The BRCA1 expression was detected in 44 cases (77.19%). The median value of the BRCA1 expression was 30, and it was used as a cut-off to categorize BRCA1 expression into negative and positive. The number of negative BRCA1 expression cases was 52.6%. Of the 48 cases studied, 72.9% were basal-like subtypes. The characteristics of the samples are presented in Table I.

Fisher's exact test analysis revealed a correlation between the expression of BRCA1 and the disease stage, as demonstrated in Table II. A negative expression of BRCA-1 was significantly associated with a more advanced disease stage (P=0.035). However, there was no correlation between the expression of BRCA-1 and other clinicopathological characteristics, such as the type of therapy.

The survival analysis of the BRCA1 expression is presented in Figs. 3 and 4. The mean survival time for patients was 100.79 weeks (minimum 17 weeks and maximum 265 weeks). The results of the survival analysis demonstrated that neither BRCA1 expression (P=0.150; Fig. 3) nor stage (P=0.091; Fig. 4) were significant prognostic factors in patients with TNBC.

In the present study, the mean age of patients with TNBC at diagnosis was 55.18±10.014 years. The number of patients aged >50 years was high (70.2%). Previous studies concluded that TNBC more frequently occurred at the age of ≤40 years, especially among African-Americans (16-18), and mostly has a poorer prognosis than other breast cancer subtypes (1-3). The present study found that 75.4% of TNBC cases were high-grade and 82.5% were advanced stage. In total, 60-80% of TNBC cases are basal-like subtypes with poor prognoses because they tended to recur and were resistant to therapy (19-21). Our cases were also dominated by basal-like subtypes (72.9%); of these cases, 63% were high-grade, 74% were advanced-stage, and 52.6% succumbed.

The prevalence of BRCA mutations differs across various ethnic groups. Previous studies on BRCA1/2 mutations in TNBC predominantly focused on Caucasian populations. Studying within the Asian population is crucial, as Asian patients with breast cancer manifest the disease at a younger age compared with their Caucasian counterparts. The frequency of BRCA1/2 mutations in Korean patients with non-familial high-risk breast cancer and familial breast cancer was 17.8 and 21.7%, respectively (22). The prevalence of BRCA1/2 mutations in patients with familial breast cancer and early-onset breast cancer in China ranged from 8-13.5% and from 8.7-11.4%, respectively (23). A study of Japanese patients with familial breast cancer indicated that 15-31.8% expressed mutations in the BRCA1/2 genes (24).

Several methods are available for detecting BRCA1 and BRCA2 dysfunction. Identification through IHC is a simple and reliable method to assess the expression of the BRCA1 protein in tumor tissues. Using the IHC method, cancer with positive BRCA1 expression in the present study was 47.4%. BRCA1-positive expression reported by other studies was 17.5% (25) and 20.5%, (15) possibly due to differences in the method and cut-off value of the BRCA1 expression. Previous research used the cystoscope method, and BRCA1 was considered positive if the score was ≥4(25). Meanwhile, other groups used the cut-off value research of 20% and found that a cut-off of 20% is improved for avoiding missing variants and has a lower false positive rate compared with a cut-off of 10% (0.14 vs. 6.82%) (15,26).

In the present study, a negative BRCA1 expression was correlated with advanced-stage cancer, but not with other clinicopathological characteristics. Altered BRCA1 expression was significantly associated with high-grade and advanced-stage breast carcinoma; however, there was no correlation of the BRCA1 expression with clinicopathological parameters (15,25). A previous study proved that reduced BRCA1 expression was associated with high-grade tumors, negative hormone receptors and HER2 status (27). Differences in the number of samples, method and type of antibody used influence these controversial results.

In the present study, basal-like and non-basal-like subtype cancers tended to have a positive BRCA1 expression and were not statistically significant. This result differed from those of a previous study wherein positive BRCA1 expression correlated with basal-like tumors (27). In relation to mutation, basal-like breast cancer did not improve the estimate of BRCA1 mutation risk (12).

Chemotherapy in TNBC can be platinum- or non-platinum-based, including taxane, and anthracycline, among others. The number of patients treated with non-platinum-based treatment was higher (64.9%) than that of patients treated with platinum-based treatment (35.1%). The therapy type did not correlate with the BRCA1 expression. However, the mutation status of BRCA1 in patients with TNBC was considered essential as it influences the treatment choice. Patients with TNBC with BRCA1 mutation respond well to platinum-based therapy and PARP inhibitors (12,13,28). It was necessary to investigate the relation between the BRCA1 expression at the protein level and its mutation status considering that protein detection is markedly simpler, cheaper and visible in different laboratories in developing countries, such as Indonesia.

The disease stage did not act as a prognostic factor for patients with TNBC in the present study. It was recently concluded that the advanced stage was related to significant overall and disease-free survival reduction (29). Another study confirmed that young patients with TNBC have a higher pathological stage and worse long-term survival than young patients with other breast cancer subtypes (30). The present study has several limitations that need to be addressed in future studies. Only 57 cases were included due to difficulty in obtaining survival and therapy data and challenges in reaching the patients. Transportation costs could constrain the distance from the patient's house; therefore, check-ups were irregular. In addition, limited therapy options for TNBC and national health insurance are occasionally not easily accessible. Therefore, further study using a more significant number of cases is needed to elaborate on the prognostic significance of the disease stage in Indonesian patients with TNBC.

The BRCA1 expression in the present study did not act as a prognostic factor for TNBC cancer. A 20% cut-off was employed for the BRCA1 expression, considering the lack of a standard consensus on the cut-off point (15). The present study focuses on the Indonesian population as it is currently an underexplored topic, especially within the Indonesian demographic. Consequently, the current study can significantly impact future research using samples from the Southeast Asian region, specifically the Indonesian population. Comprehensive research must therefore be conducted to determine the standard value of BRCA1 expression, especially when later BRCA1 protein expression can be applied to determine the treatment choice in patients with TNBC.

In conclusion, the present study concluded that a negative BRCA1 expression was correlated with the advanced stage of Indonesian patients with TNBC, albeit it was not a prognostic factor.