Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

Prevalence of germline BRCA mutations in HER2-negative metastatic breast cancer: global results from the real-world, observational BREAKOUT study

Breast Cancer Research volume 22, Article number: 114 (2020) Cite this article

Abstract

Background

The global observational BREAKOUT study investigated germline BRCA mutation (gBRCAm) prevalence in a population of patients with human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancer (MBC).

Methods

Eligible patients had initiated first-line cytotoxic chemotherapy for HER2-negative MBC within 90 days prior to enrollment. Hormone receptor (HR)-positive patients had experienced disease progression on or after prior endocrine therapy, or endocrine therapy was considered unsuitable. gBRCAm status was determined using baseline blood samples or prior germline test results. For patients with a negative gBRCAm test, archival tissue was tested for somatic BRCAm and homologous recombination repair mutations (HRRm). Details of first-line cytotoxic chemotherapy were also collected.

Results

Between March 2017 and April 2018, 384 patients from 14 countries were screened and consented to study enrollment; 341 patients were included in the full analysis set (median [range] age at enrollment: 56 [25–89] years; 256 (75.3%) postmenopausal). Overall, 33 patients (9.7%) had a gBRCAm (16 [4.7%] in gBRCA1 only, 12 [3.5%] in gBRCA2 only, and 5 [1.5%] in both gBRCA1 and gBRCA2). gBRCAm prevalence was similar in HR-positive and HR-negative patients. gBRCAm prevalence was 9.0% in European patients and 10.6% in Asian patients and was higher in patients aged ≤ 50 years at initial breast cancer (BC) diagnosis (12.9%) than patients aged > 50 years (5.4%). In patients with any risk factor for having a gBRCAm (family history of BC and/or ovarian cancer, aged ≤ 50 years at initial BC diagnosis, or triple-negative BC), prevalence was 10.4%, versus 5.8% in patients without these risk factors. HRRm prevalence was 14.1% (n = 9/64) in patients with germline BRCA wildtype.

Conclusions

Patient demographic and disease characteristics supported the association of a gBRCAm with younger age at initial BC diagnosis and family history of BC and/or ovarian cancer. gBRCAm prevalence in this cohort, not selected on the basis of risk factors for gBRCAm, was slightly higher than previous results suggested. gBRCAm prevalence among patients without a traditional risk factor for harboring a gBRCAm (5.8%) supports current guideline recommendations of routine gBRCAm testing in HER2-negative MBC, as these patients may benefit from poly(ADP-ribose) polymerase (PARP) inhibitor therapy.

Trial registration

NCT03078036.

Background

Breast cancer is the most commonly diagnosed cancer in women (excluding non-melanoma skin cancers) and is the most common cause of cancer deaths in women worldwide [1]. The breast cancer susceptibility genes (BRCA1 and BRCA2) encode proteins critically involved in the repair of DNA double-strand breaks [2]. A germline BRCA1 and/or BRCA2 mutation (gBRCAm) substantially increases the risk of developing breast and/or ovarian cancer, as well as other tumor types such as prostate and pancreatic cancer [3,4,5,6,7].

Poly(ADP-ribose) polymerase (PARP) inhibitors block DNA damage repair in cells harboring a deficiency in homologous recombination repair (HRR), including mutations in BRCA1 and BRCA2 [8]. The PARP inhibitors olaparib and talazoparib have proven effective at targeting BRCA-mutated human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancers, including in the Phase 3 OlympiAD (NCT02000622) and EMBRACA (NCT01945775) trials [9,10,11,12]. The prevalence of a gBRCAm ranges from 1.2 to 8.8% in unselected breast cancer patient populations [13,14,15,16,17,18,19]. However, limited data exist on the prevalence of a gBRCAm in patients with HER2-negative metastatic breast cancer who require treatment with a first-line systemic chemotherapy regimen. Such data would provide an estimate of the size of the patient population who may be appropriate candidates to receive treatment with a PARP inhibitor for gBRCAm metastatic breast cancer.

Here, we present data from the global observational BREAKOUT study (NCT03078036) in patients with HER2-negative metastatic breast cancer being treated with first-line chemotherapy, the primary objective of which was to estimate the prevalence of gBRCAm in this patient population.

Methods

Study design

BREAKOUT was an observational, cross-sectional study, with a nested prospective cohort component (Fig. 1). The study design was based on the Phase 3b real-world, open-label, single-arm LUCY study (NCT03286842) [20]. In the LUCY study, patients with a gBRCAm HER2-negative metastatic breast cancer were being treated with olaparib following no more than two prior lines of chemotherapy in the metastatic setting. BREAKOUT study sites were selected for their willingness to participate in the study and were requested to enroll sequential patients with HER2-negative metastatic breast cancer. See Additional file 1 for a list of participating study sites. The primary objective of BREAKOUT was to assess the prevalence of gBRCAm in a global population of patients with HER2-negative metastatic breast cancer who were not selected on the basis of risk factors for gBRCAm. For patients who tested positive for a gBRCAm, the planned secondary objectives included assessment of treatment patterns by line of therapy and prospective evaluation of clinical outcomes, including progression-free survival and overall survival.

Fig. 1
figure 1

BREAKOUT study design. BRCA, breast cancer susceptibility gene; CT, chemotherapy; gBRCAm, germline BRCA mutation; HER2, human epidermal growth factor receptor-2; HRRm, homologous recombination repair gene mutation; OS, overall survival; PFS, progression-free survival; sBRCAm, somatic BRCA mutation. *Blood/tumor testing occurred concurrently to the extent possible. †Foundation Medicine Inc. (Cambridge, Massachusetts, USA) Lynparza HRR assay was used to test for HRR gene mutations. ‡Positive: deleterious mutation; suspected deleterious. Negative: no deleterious mutation detected; no mutation detected; favor polymorphism; variant of uncertain significance; BRCA wildtype

Full size image

In order to minimize selection bias, patients were selected regardless of demographic characteristics, presence of risk factors for gBRCAm breast cancer, or previously known gBRCAm status.

For patients who tested negative for a gBRCAm (gBRCAwt), archival tumor specimens were obtained where possible, to test for somatic BRCA mutations (sBRCAm) and other HRR gene mutations, using an investigational clinical trial assay, based on the FoundationOne® CDx platform (Foundation Medicine Inc., Cambridge, Massachusetts, USA). The HRR genes evaluated were BRCA1, BRCA2, ATM, RAD51B, RAD51C, RAD51D, RAD54L, BRIP1, FANCL, PALB2, BARD1, CHEK1, CHEK2, CDK12, and PPP2R2A.

The planned sample size was 2000 patients with HER2-negative metastatic breast cancer. Study enrollment was terminated early due to poor recruitment and, therefore, only patients’ first-line cytotoxic chemotherapy regimens were collected for analysis. Data on subsequent therapies for metastatic breast cancer, progression-free survival, and overall survival were not collected due to the limited number of patients and absence of follow-up data.

Data including baseline patient demographic and disease characteristics, medical history, and treatment history were collected from individual patient records. Family history of breast and/or ovarian cancer in first- or second-degree relatives was also collected. Patients’ gBRCAm status was determined by testing baseline blood samples (in a central laboratory, or in Japan using the Myriad BRACAnalysis CDx® test) or, where available, using existing gBRCAm test results that had been obtained by local or central testing, as per local practice.

gBRCAm results were classified as positive (deleterious gBRCA1 and/or gBRCA2 mutation; genetic variant suspected deleterious), negative (gBRCAwt; genetic variant of uncertain significance; genetic variant, favor polymorphism; no mutation/deleterious mutation detected), or not determined.

Patient population

Eligible patients had started a first-line chemotherapy regimen for HER2-negative metastatic breast cancer within 90 days prior to enrollment. First-line chemotherapy was defined as the first chemotherapy given in the metastatic setting. Patients with hormone receptor (HR)-positive metastatic breast cancer had developed disease progression on or after prior endocrine therapy, or were considered unsuitable for endocrine therapy. Patients who had received prior PARP inhibitor therapy were not eligible for the study.

Statistical analysis

The full analysis set (FAS) comprised all enrolled, eligible patients who had available gBRCAm test results. An exploratory subgroup included all patients in the FAS who had been tested for sBRCAm and/or HRR gene mutations, including those whose status could not be determined (e.g., due to the sample not being evaluable).

The prevalence of a gBRCAm was determined using the number of patients who were tested and had a valid result for gBRCAm status as the denominator and the number of patients who were gBRCAm-positive as the numerator. The prevalence of a gBRCAm according to demographic variables, disease characteristics, comorbidities, and choice of first-line therapy regimens was also evaluated.

Appropriate descriptive statistics were provided for continuous and categorical variables.

Results

Between March 2017 and April 2018, 384 patients were screened and consented to study enrollment; 43 patients were excluded from the analysis—4 for whom a blood sample for gBRCAm testing was not available and 39 for not meeting prespecified eligibility criteria—resulting in 341 patients with HER2-negative metastatic breast cancer comprising the FAS (Fig. 2).

Fig. 2
figure 2

Patient disposition. FAS, full analysis set. *39 patients did not meet eligibility criteria; 29 patients had not initiated treatment with first-line systemic cytotoxic chemotherapy for metastatic breast cancer in the past 90 days and, at that time, were considered to have exhausted endocrine therapy options if hormone receptor-positive; 9 patients had no evidence of metastatic disease; and 1 patient consented after the termination of the study

Full size image

Patients were enrolled across 14 countries: Australia (n = 5), Bulgaria (n = 15), Canada (n = 8), Hungary (n = 3), Italy (n = 7), Japan (n = 44), Poland (n = 13), Russia (n = 32), South Korea (n = 45), Spain (n = 18), Taiwan (n = 15), Turkey (n = 79), the UK (n = 32), and the USA (n = 25).

gBRCAm prevalence

Of the 341 patients included in the FAS, 33 (9.7%; 95% confidence interval [CI] 6.8%, 13.3%) harbored a gBRCAm (Table 1). Mutations were detected in gBRCA1 alone in 16 patients (4.7%; 95% CI 2.7%, 7.5%), in gBRCA2 alone in 12 patients (3.5%; 95% CI 1.8%, 6.1%), and in both gBRCA1 and gBRCA2 in 5 patients (1.5%; 95% CI 0.5%, 3.4%). A total of 30 patients underwent gBRCAm testing prior to baseline; 8 (26.7%) of these patients had a gBRCAm.

Table 1 gBRCAm prevalence by region of enrollment (FAS)
Full size table

Subgroup analyses showed the prevalence of gBRCAm was 9.0% in European patients (n = 18/199; 95% CI 5.4%, 13.9%), 9.1% in North American patients (n = 3/33; 95% CI 1.9%, 24.3%), and 10.6% in Asian patients (Japan, South Korea, and Taiwan; n = 11/104; 95% CI 5.4%, 18.1%) (Table 1).

sBRCA and HRR gene mutations

In total, 64 patients with gBRCAwt who had archival breast cancer tissue were tested for HRR gene mutations and sBRCAm. The prevalence of sBRCAm was 6.3% (n = 4/64; 95% CI 1.7%, 15.2%). One patient had sBRCA1 mutation only (1.6%; 95% CI 0.0%, 8.4%) and three patients had sBRCA2 mutation only (4.7%; 95% CI 1.0%, 13.1%) (Fig. 3). The incidence of sBRCAm in patients with an existing gBRCAm was not assessed in the BREAKOUT study. The prevalence of any HRR gene mutation overall was 14.1% (n = 9/64; 95% CI 6.6%, 25.0%), including mutations in ATM (n = 2), BRCA1 (n = 1), BRCA2 (n = 3), CHEK2 (n = 1), PALB2 (n = 1), and RAD51B (n = 1) (Fig. 3).

Fig. 3
figure 3

Prevalence of sBRCAm and other HRR gene mutations (subgroup for exploratory analysis). BRCA1, breast cancer susceptibility gene 1; BRCA2, breast cancer susceptibility gene 2; HRRm, homologous recombination repair gene mutation; sBRCAm, somatic BRCA mutation; sBRCA1, somatic BRCA1 mutation; sBRCA2, somatic BRCA2 mutation

Full size image

Patient demographic and clinical characteristics

Baseline demographic and clinical characteristics for patients in the FAS are shown in Table 2. Median (range) age at enrollment was 56 (25–89) years. Median (range) age at initial breast cancer diagnosis was 40 (24–71) years in patients with a gBRCAm and 52 (24–86) years in patients with gBRCAwt.

Table 2 Baseline patient demographic and disease characteristics (FAS)
Full size table

Most patients were postmenopausal at enrollment (n = 256/340; 75.3%). The proportion of postmenopausal patients was lower in the gBRCAm group (57.6%) compared with the gBRCAwt group (77.2%). In the FAS, 58.1% of patients (n = 198/341) were postmenopausal at initial breast cancer diagnosis. Most patients with gBRCAwt were postmenopausal at initial breast cancer diagnosis (n = 186/308; 60.4%), compared with 36.4% of patients with a gBRCAm (n = 12/33).

Median time from initial breast cancer diagnosis to enrollment was 28.1 months (interquartile range 13.4–73.0) in patients with a gBRCAm and was similar at 29.9 months (interquartile range 6.3–78.2) in patients with gBRCAwt (Table 2).

Disease stage at initial breast cancer diagnosis in the FAS was stage 0 in 2.7% (n = 9/336) of patients, stage I in 9.2% (31/336) of patients, stage II in 34.8% (n = 117/336) of patients, stage III in 26.2% (n = 88/336) of patients, and stage IV in 27.1% (91/336) of patients, with similar distribution among patients with a gBRCAm (Table 2). With respect to nodal status at initial breast cancer diagnosis, in the FAS, 25.3% of patients had node stage N0 (negative) and 33.5% had node stage N1 disease. Tumor grade at initial breast cancer diagnosis was poorly differentiated in 35.1% of patients (n = 118/336) and moderately differentiated in 33.0% of patients (n = 111/336) (Table 2). In comparison with all patients in the FAS, more patients with a gBRCAm had poorly differentiated cancers (45.5%; n = 15/33) and 30.3% (n = 10/33) of patients with a gBRCAm had moderately differentiated tumors.

Overall, 52.0% (n = 156/300) of patients with gBRCAwt had received chemotherapy prior to metastatic disease, compared with 64.5% (n = 20/31) of patients with a gBRCAm, and 39.0% (n = 119/305) of patients with gBRCAwt received non-chemotherapy treatments prior to metastatic disease, compared with 30.3% (n = 10/33) of patients with a gBRCAm. Non-chemotherapy treatments included endocrine therapy (including tamoxifen, letrozole, anastrozole, exemestane, and fulvestrant), everolimus (n = 1), and bevacizumab (n = 1) (Table 2) and were mostly (77.9%) used as adjuvant therapy.

Non-chemotherapy treatments (including letrozole, fulvestrant, and exemestane) were administered for metastatic disease prior to receiving first-line chemotherapy in 24.2% (n = 8/33) of patients with a gBRCAm and 30.9% (n = 95/307) of patients with gBRCAwt.

Similar proportions of patients with a gBRCAm or gBRCAwt had HR-positive (estrogen receptor- and/or progesterone receptor-positive) versus HR-negative HER2-negative metastatic breast cancer with gBRCAwt (Table 2).

A family history of breast and/or ovarian cancer in a first- or second-degree relative was recorded for 45.5% (n = 15/33) of patients with a gBRCAm, compared with 16.6% (n = 51/307) of patients with gBRCAwt (Table 2).

Subgroup analyses by risk factors for gBRCAm

Age at initial breast cancer diagnosis

The prevalence of a gBRCAm was 12.9% (n = 22/171; 95% CI 8.2%, 18.8%) in patients aged ≤ 50 years at initial breast cancer diagnosis and was lower at 5.4% (n = 9/167; 95% CI 2.5%, 10.0%) in patients > 50 years of age at initial breast cancer diagnosis (Table 3). The prevalence of a gBRCA1 mutation was higher in patients aged ≤ 50 years at initial breast cancer diagnosis (7.6%; n = 13/171; 95% CI 4.1%, 12.6%) than in patients aged > 50 years at initial breast cancer diagnosis (1.2%; n = 2/167; 95% CI 0.1%, 4.3%), whereas prevalence of a gBRCA2 mutation was similar in patients aged ≤ 50 years and > 50 years, at 3.5% (95% CI 1.3%, 7.5%) and 3.0% (95% CI 1.0%, 6.8%), respectively.

Table 3 gBRCAm prevalence by risk factors for gBRCAm (FAS)
Full size table

Hormone receptor status

The overall prevalence of a gBRCAm was similar with respect to HR status: 9.3% (n = 20/215; 95% CI 5.8%, 14.0%) in patients with HR-positive disease (6 patients in gBRCA1 only, 10 in gBRCA2 only, and 4 in both gBRCA1 and gBRCA2) and 9.2% (n = 11/119; 95% CI 4.7%, 15.9%) in patients with HR-negative disease (9 patients in gBRCA1 only and 2 in gBRCA2 only) (Table 3). However, the prevalence of a gBRCA1 mutation was 7.6% (95% CI 3.5%, 13.9%) in patients with HR-negative metastatic breast cancer and 2.8% (95% CI 1.0%, 6.0%) in patients with HR-positive metastatic breast cancer, while a gBRCA2 mutation was more frequent in those with HR-positive metastatic breast cancer, compared with HR-negative metastatic breast cancer (4.7% [95% CI 2.3%, 8.4%] and 1.7% [95% CI 0.2%, 5.9%], respectively).

Family history of breast and/or ovarian cancer

The prevalence of a gBRCAm was higher (22.7%; n = 15/66; 95% CI 13.3%, 34.7%) in the subgroup of patients with a family history of breast and/or ovarian cancer, compared with patients without a family history of breast and/or ovarian cancer (6.6%; n = 18/274; 95% CI 3.9%, 10.2%) (Table 3). In patients with a family history of breast and/or ovarian cancer, mutations in gBRCA1 (12.1% [95% CI 5.4%, 22.5%]) and gBRCA2 (9.1% [95% CI 3.4%, 18.7%]) were more prevalent than in patients without a family history of breast and/or ovarian cancer (2.9% [95% CI 1.3%, 5.7%] and 2.2% [95% CI 0.8%, 4.7%], respectively).

Presence of ≥ 1 risk factor for having a gBRCAm

gBRCAm prevalence was 10.4% (n = 26/250; 95% CI 6.9%, 14.9%) in patients who had at least one risk factor for having a gBRCAm (family history of breast and/or ovarian cancer; age at initial breast cancer diagnosis ≤ 50 years; or triple-negative breast cancer), compared with 5.8% (n = 5/86; 95% CI 1.9%, 13.0%) in patients without any of these risk factors.

First-line chemotherapy use

Overall, most patients in the FAS received single-agent chemotherapy as their first-line chemotherapy regimen (n = 196/341; 57.5%) (Table 4), while 54.5% (n = 18/33) of patients with a gBRCAm received combination chemotherapy with ≥ 2 agents as their first-line chemotherapy regimen. Overall, the most frequently used single-agent regimens (> 10%) were paclitaxel (n = 75/196; 38.3%), capecitabine (n = 42/196; 21.4%), and docetaxel (n = 24/196; 12.2%), while the most frequently used combination regimen was paclitaxel/bevacizumab (n = 21/145; 14.5%) (see Additional file 2).

Table 4 Cytotoxic chemotherapies administered as first-line therapy for metastatic breast cancer (FAS)
Full size table

The most frequently used cytotoxic chemotherapy agent as first-line therapy, either as a single agent or in combination, regardless of gBRCAm status, was paclitaxel (n = 127/341; 37.2%), followed by cyclophosphamide (n = 60/341; 17.6%), capecitabine (n = 57/341; 16.7%), docetaxel (n = 48/341; 14.1%), carboplatin (n = 31/341; 9.1%), doxorubicin (n = 29/341; 8.5%), and gemcitabine (n = 28/341; 8.2%) (Table 4). First-line cytotoxic chemotherapy regimens are detailed in Additional file 2.

Discussion

The objectives of the BREAKOUT study were to estimate the true prevalence of gBRCAm in patients with HER2-negative metastatic breast cancer, by minimizing selection bias, and to generate observational outcome data. Outcome data, however, were not obtained from the BREAKOUT study, as the study was terminated early due to inadequate recruitment.

The estimate of gBRCAm prevalence in the observational BREAKOUT study was 9.7% (95% CI 6.8%, 13.3%) among a cohort of 341 patients with HER2-negative metastatic breast cancer being treated with first-line cytotoxic chemotherapy. Previous studies in unselected patient populations reported the prevalence of a gBRCA1m and a gBRCA2m to be between 1.2 and 8.8% [13,14,15,16,17,18,19]. In contrast, in a US study of 119 patients with HER2-negative metastatic breast cancer who were referred for mutation testing, and who likely had perceived risk factors for having a gBRCAm, the estimated prevalence was higher than that observed in the BREAKOUT population, at 24.4% [21]. Overall there were no notable differences in the prevalence of a gBRCAm with regards to HR status, sites of metastases, time from initial breast cancer diagnosis to entry into the BREAKOUT study, and physicians’ choice of first-line cytotoxic chemotherapy regimens.

In patients with at least one risk factor (family history of breast and/or ovarian cancer; age at initial breast cancer diagnosis ≤ 50 years; or triple-negative breast cancer), gBRCAm prevalence was 10.4% in the BREAKOUT study, compared with 5.8% in patients without any of these risk factors. Also of note is that approximately half of the patients with a gBRCAm in BREAKOUT (54.5%) did not have a family history of breast and/or ovarian cancer. This is notable as, although the number of patients involved is small, 5.8% is a sizeable proportion of patients whose gBRCAm could be missed if the criteria for gBRCAm testing in patients with HER2-negative metastatic breast cancer are based on the presence of risk factors, including family history of breast and/or ovarian cancer, as well as other tumor types such as prostate and pancreatic cancer [22]. Similar findings were observed in a US study in a population of patients with any-stage triple-negative breast cancer, in which 16% of patients with a gBRCAm did not have an established reason for gBRCAm testing and 10% had limited family history knowledge of breast and/or ovarian cancer at any age [23]. The data from the BREAKOUT study support the National Comprehensive Cancer Network recommendation that all patients with HER2-negative metastatic breast cancer undergo gBRCAm testing [24].

The prevalence of sBRCAm in 64 gBRCAwt patients with archival tumor tissue was 6.3% (one patient with sBRCA1 and three with sBRCA2). The prevalence of any HRR gene mutation (excluding sBRCA) in this group was 7.8%. There are very limited data that describe the prevalence of somatic or germline non-BRCA HRR gene mutations in patients with metastatic breast cancer. Data from the Cancer Genome Atlas Program (TCGA) show that ∼ 20% of basal-like breast cancers have a germline and/or somatic BRCA1 or BRCA2 variant [25]. In the ongoing PRAEGNANT (Prospective Academic Translational Research Network for the Optimization of Oncological Health Care Quality in the Adjuvant and Advanced Therapeutic Setting) registry study in Germany (NCT02338167), of 1462 patients with metastatic breast cancer receiving any therapeutic regimen who had available germline DNA from time of study entry and successful genotyping, 4.3% had a non-BRCA germline HRR gene mutation [26]. Results from the PRAEGNANT study are expected to provide further insights into the prevalence of germline HRR gene mutations and their impact on outcome [27]. In addition, the European AURORA study that is recruiting 1300 patients with metastatic breast cancer will likely generate data on the prevalence of germline and somatic HRR gene mutations and their impact on treatment outcomes [28].

This study had some limitations that could impact the generalizability of the results. With the gBRCAm testing costs covered by this observational study, investigators may have been more likely to enroll patients who were at higher risk for having a gBRCAm. However, the patient characteristics of the BREAKOUT metastatic breast cancer population, including age, menopausal status, and HR status, were similar to those described in other HER2-negative metastatic breast cancer patient populations that were unselected for gBRCAm status [29,30,31,32,33]. An additional limitation was that the BREAKOUT study excluded patients previously treated with PARP inhibitors and, therefore, participating study sites were more likely to be those in which patients had not been exposed to PARP inhibitors in clinical trials. This may have had some influence on the patient population, as well as the size and type of participating centers, and this might have contributed to the inadequate recruitment.

The smaller than planned sample size, due to the early termination of the study, had an impact on the level of precision and generalizability of the findings. The study was designed to describe the prevalence of a gBRCAm with a precision of approximately ± 2% and, with only 341 patients in the FAS, a precision of 6.5% was achieved.

The BREAKOUT study incorporated the findings of gBRCAm tests performed prior to the study if they were available. To avoid distortion by a possible overrepresentation of patients with a prior test, participating sites were instructed to enroll patients in consecutive order, regardless of the availability of prior BRCA mutation test results. In the FAS, 8.8% (n = 30) of patients were tested for gBRCAm status prior to the baseline, and of these, 8 patients (26.7%) had a gBRCAm (these patients were repeat tested at baseline).

Conclusions

The global BREAKOUT study demonstrated that 9.7% of patients with HER2-negative metastatic breast cancer who were receiving a first-line cytotoxic chemotherapy regimen had a gBRCAm and that 5.8% of the enrolled patients who had no standard risk factors had a gBRCAm.

The results help characterize the patient population who may benefit from PARP inhibitor therapy and highlight the need for broad gBRCAm testing of patients with HER2-negative metastatic breast cancer.

Availability of data and materials

Data underlying the findings described in this manuscript may be obtained in accordance with AstraZeneca’s data-sharing policy, described at https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure

Abbreviations

BC:

Breast cancer

BRCA :

Breast cancer susceptibility gene

CI:

Confidence interval

CT:

Chemotherapy

FAS:

Full analysis set

gBRCAm:

Germline BRCA mutation

gBRCAwt:

Germline BRCA wildtype

HER2:

Human epidermal growth factor receptor 2

HR:

Hormone receptor

HRR:

Homologous recombination repair

HRRm:

Homologous recombination repair gene mutation

MBC:

Metastatic breast cancer

OS:

Overall survival

PARP:

Poly(ADP-ribose) polymerase

PFS:

Progression-free survival

PRAEGNANT:

Prospective Academic Translational Research Network for the Optimization of Oncological Health Care Quality in the Adjuvant and Advanced Therapeutic Setting

sBRCAm:

Somatic BRCA mutation

sHRRm:

Somatic homologous recombination repair gene mutation

SD:

Standard deviation

References

  1. Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394–424.

    PubMed  Google Scholar 

  2. Chen CC, Feng W, Lim PX, Kass EM, Jasin M. Homology-directed repair and the role of BRCA1, BRCA2, and related proteins in genome integrity and cancer. Annu Rev Cancer Biol. 2018;2:313–36.

    Article  PubMed  Google Scholar 

  3. Heeke AL, Pishvaian MJ, Lynce F, Xiu J, Brody JR, Chen W-J, Baker TM, Marshall JL, Isaacs C. Prevalence of homologous recombination–related gene mutations across multiple cancer types. JCO Precis Oncol. 2018;2:1–13.

    Google Scholar 

  4. Ledermann JA, Drew Y, Kristeleit RS. Homologous recombination deficiency and ovarian cancer. Eur J Cancer. 2016;60:49–58.

    Article  CAS  PubMed  Google Scholar 

  5. O'Connor MJ. Targeting the DNA damage response in cancer. Mol Cell. 2015;60(4):547–60.

    Article  CAS  PubMed  Google Scholar 

  6. Iqbal J, Ragone A, Lubinski J, Lynch HT, Moller P, Ghadirian P, Foulkes WD, Armel S, Eisen A, Neuhausen SL, et al. The incidence of pancreatic cancer in BRCA1 and BRCA2 mutation carriers. Br J Cancer. 2012;107(12):2005–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Moran A, O'Hara C, Khan S, Shack L, Woodward E, Maher ER, Lalloo F, Evans DG. Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations. Familial Cancer. 2012;11(2):235–42.

    Article  CAS  PubMed  Google Scholar 

  8. AstraZeneca. Lynparza significantly reduces the risk of disease worsening or death in patients with BRCA-mutated metastatic breast cancer [press release]. 2017. https://www.astrazeneca.com/media-centre/press-releases/2017/lynparza-significantly-reduces-the-risk-of-disease-worsening-or-death-in-patients-with-BRCA-mutated-metastatic-breast-cancer-04062017.html. Accessed 26 Mar 2019.

  9. Tung NM, Robson ME, Ventz S, Santa-Maria CA, Marcom PK, Nanda R, Shah PD, Ballinger TJ, Yang ES, Melisko ME, et al. TBCRC 048: a phase II study of olaparib monotherapy in metastatic breast cancer patients with germline or somatic mutations in DNA damage response (DDR) pathway genes (Olaparib Expanded). J Clin Oncol. 2020;38.Abstract 1002.

  10. Robson M, Im S-A, Senkus E, Xu B, Domchek SM, Masuda N, Delaloge S, Li W, Tung N, Armstrong A, et al. Olaparib for metastatic breast cancer in patients with a germline BRCA mutation. N Engl J Med. 2017;377(6):523–33.

    Article  CAS  PubMed  Google Scholar 

  11. Litton JK, Rugo HS, Ettl J, Hurvitz SA, Gonçalves A, Lee K-H, Fehrenbacher L, Yerushalmi R, Mina LA, Martin M, et al. Talazoparib in patients with advanced breast cancer and a germline BRCA mutation. N Engl J Med. 2018;379(8):753–63.

    Article  CAS  PubMed  Google Scholar 

  12. Domchek SM, Postel-Vinay S, Im S-A, Park YH, Delord J-P, Italiano A, Alexandre J, You B, Bastian S, Krebs MG, et al. Olaparib and durvalumab in patients with germline BRCA-mutated metastatic breast cancer (MEDIOLA): an open-label, multicentre, phase 1/2, basket study. Lancet Oncol. 2020;21(9):1155–64.

  13. Abugattas J, Llacuachaqui M, Allende YS, Velásquez AA, Velarde R, Cotrina J, Garcés M, León M, Calderón G, de la Cruz M, et al. Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from Peru. Clin Genet. 2015;88(4):371–5.

    Article  CAS  PubMed  Google Scholar 

  14. Gomes MC, Costa MM, Borojevic R, Monteiro AN, Vieira R, Koifman S, Koifman RJ, Li S, Royer R, Zhang S, et al. Prevalence of BRCA1 and BRCA2 mutations in breast cancer patients from Brazil. Breast Cancer Res Treat. 2007;103(3):349–53.

    Article  CAS  PubMed  Google Scholar 

  15. Hernandez JEL, Llacuachaqui M, Palacio GV, Figueroa JD, Madrid J, Lema M, Royer R, Li S, Larson G, Weitzel JN, et al. Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from medellín, Colombia. Hered Cancer Clin Pract. 2014;12(1):11.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Høberg-Vetti H, Bjorvatn C, Fiane BE, Aas T, Woie K, Espelid H, Rusken T, Eikesdal HP, Listøl W, Haavind MT, et al. BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study. Eur J Hum Genet. 2016;24(6):881–8.

    Article  PubMed  Google Scholar 

  17. Li G, Guo X, Tang L, Chen M, Luo X, Peng L, Xu X, Wang S, Xiao Z, Yi W, et al. Analysis of BRCA1/2 mutation spectrum and prevalence in unselected Chinese breast cancer patients by next-generation sequencing. J Cancer Res Clin Oncol. 2017;143(10):2011–24.

    Article  CAS  PubMed  Google Scholar 

  18. Malone KE, Daling JR, Doody DR, Hsu L, Bernstein L, Coates RJ, Marchbanks PA, Simon MS, McDonald JA, Norman SA, et al. Prevalence and predictors of BRCA1 and BRCA2 mutations in a population-based study of breast cancer in white and black American women ages 35 to 64 years. Cancer Res. 2006;66(16):8297–308.

    Article  CAS  PubMed  Google Scholar 

  19. Kurian AW, Ward KC, Howlader N, Deapen D, Hamilton AS, Mariotto A, Miller D, Penberthy LS, Katz SJ. Genetic testing and results in a population-based cohort of breast cancer patients and ovarian cancer patients. J Clin Oncol. 2019;37(15):1305–15.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Gelmon KA, Fasching PA, Couch F, Gelpi JB, Delaloge S, Labidi-Galy I, Bennett J, McCutcheon S, Ano S, O'Shaughnessy J. Real-world clinical effectiveness and safety of olaparib monotherapy in HER2-negative gBRCA-mutated metastatic breast cancer: phase IIIb LUCY interim analysis. J Clin Oncol 2020;38.Abstract 1087.

  21. Bayraktar S, Gutierrez-Barrera AM, Lin H, Elsayegh N, Tasbas T, Litton JK, Ibrahim NK, Morrow PK, Green M, Valero V, et al. Outcome of metastatic breast cancer in selected women with or without deleterious BRCA mutations. Clin Exp Metastasis. 2013;30(5):631–42.

    Article  CAS  PubMed  Google Scholar 

  22. Daly MB, Pilarski R, Yurgelun MB, Berry MP, Buys SS, Dickson P, Domchek SM, Elkhanany A, Friedman S, Garber JE, et al. NCCN guidelines insights: genetic/familial high-risk assessment: breast, ovarian, and pancreatic, version 1.2020. J Natl Compr Cancer Netw. 2020;18(4):380–91.

    Article  Google Scholar 

  23. Sharma P, Klemp JR, Kimler BF, Mahnken JD, Geier LJ, Khan QJ, Elia M, Connor CS, McGinness MK, Mammen JMW, et al. Germline BRCA mutation evaluation in a prospective triple-negative breast cancer registry: implications for hereditary breast and/or ovarian cancer syndrome testing. Breast Cancer Res Treat. 2014;145(3):707–14.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. National Comprehensive Cancer Network. NCCN Clinical Practice Guidelines in Oncology - Breast Cancer v5.2020. 2020. https://www.nccn.org/professionals/physician_gls/pdf/breast.pdf. Accessed 06 Aug 2020.

  25. The Cancer Genome Atlas Network. Comprehensive molecular portraits of human breast tumors. Nature. 2012;490(7418):61–70.

    Article  PubMed Central  Google Scholar 

  26. Fasching PA, Hu C, Hart SN, Polley EC, Lee KY, Gnanolivu RD, Lilyquist J, Hartkopf AD, Taran FA, Janni W, et al. Cancer predisposition genes in metastatic breast cancer – association with metastatic pattern, prognosis, patient and tumor characteristics. Cancer Res. 2018;78.Abstract PD1-02.

  27. Fasching PA, Brucker SY, Fehm TN, Overkamp F, Janni W, Wallwiener M, Hadji P, Belleville E, Häberle L, Taran F-A, et al. Biomarkers in patients with metastatic breast cancer and the PRAEGNANT study network. Geburtshilfe Frauenheilkd. 2015;75(1):41–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Zardavas D, Maetens M, Irrthum A, Goulioti T, Engelen K, Fumagalli D, Salgado R, Aftimos P, Saini KS, Sotiriou C, et al. The AURORA initiative for metastatic breast cancer. Br J Cancer. 2014;111(10):1881–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  29. Abiltayeva A, Moore MA, Myssayev A, Adylkhanov T, Baissalbayeva A, Zhabagin K, Beysebayev E. Clinical, histopathological and molecular characteristics of metastatic breast cancer in North-Eastern Kazakhstan: a 10 year retrospective study. Asian Pac J Cancer Prev. 2016;17(10):4797–802.

    PubMed  PubMed Central  Google Scholar 

  30. Dawood S, Broglio K, Buzdar AU, Hortobagyi GN, Giordano SH. Prognosis of women with metastatic breast cancer by HER2 status and trastuzumab treatment: an institutional-based review. J Clin Oncol. 2010;28(1):92–8.

    Article  CAS  PubMed  Google Scholar 

  31. Gamucci T, Mentuccia L, Natoli C, Sperduti I, Cassano A, Michelotti A, Di Lauro L, Sergi D, Fabi A, Sarobba MG, et al. A real-world multicentre retrospective study of paclitaxel-bevacizumab and maintenance therapy as first-line for HER2-negative metastatic breast cancer. J Cell Physiol. 2017;232(6):1571–8.

    Article  CAS  PubMed  Google Scholar 

  32. Gong C, Zhao Y, Wang B, Hu X, Wang Z, Zhang J, Zhang S. Efficacy and safety of everolimus in Chinese metastatic HR positive, HER2 negative breast cancer patients: a real-world retrospective study. Oncotarget. 2017;8(35):59810–22.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Tiainen L, Tanner M, Lahdenperä O, Vihinen P, Jukkola A, Karihtala P, Paunu N, Huttunen T, Kellokumpu-Lehtinen PL. Bevacizumab combined with docetaxel or paclitaxel as first-line treatment of HER2-negative metastatic breast cancer. Anticancer Res. 2016;36(12):6431–8.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The authors wish to thank the patients, their families/caregivers, investigators, and study personnel.

Medical writing support, under the direction of the authors, was provided by Laura Fullerton-Batten, PhD, CMC Connect, McCann Health Medical Communications, funded by AstraZeneca, Cambridge, UK, in accordance with Good Publication Practice (GPP3) guidelines (Ann Intern Med. 2015;163(6):461-464).

Funding

This study was sponsored by AstraZeneca and is part of an alliance between AstraZeneca and Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA (MSD).

Author information

Authors and Affiliations

  1. Baylor University Medical Center, Texas Oncology and US Oncology, Dallas, TX, USA

    Joyce O’Shaughnessy

  2. Cancer Program at Sinai Health System, Toronto, Ontario, Canada

    Christine Brezden-Masley

  3. Ospedale San Gerardo Monza, Monza, Italy

    Marina Cazzaniga

  4. AstraZeneca Pharmaceuticals, LP, Gaithersburg, MD, USA

    Tapashi Dalvi

  5. AstraZeneca, Cambridge, UK

    Graham Walker & James Bennett

  6. NHO Shikoku Cancer Center, Matsuyama-shi, Ehime-Ken, Japan

    Shozo Ohsumi

Authors
  1. Joyce O’Shaughnessy
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Christine Brezden-Masley
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Marina Cazzaniga
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Tapashi Dalvi
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Graham Walker
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. James Bennett
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Shozo Ohsumi
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

JO’S, CB-M, MC, and SO carried out data collection, analysis, and interpretation. TD, GW, and JB carried out data analysis and interpretation. All authors drafted and revised the manuscript and approved the final draft.

Corresponding author

Correspondence to Joyce O’Shaughnessy.

Ethics declarations

Ethics approval and consent to participate

An independent ethics committee or institutional review board approved the final protocol at each study site. All patients provided written informed consent.

Consent for publication

Not applicable.

Competing interests

Dr. Joyce O’Shaughnessy has received honoraria for consulting and advisory boards from AbbVie, Agendia, Amgen, AstraZeneca, Bristol-Myers Squibb, Celgene Corporation, Eisai, Eli Lilly, Genentech, Genomic Health, GRAIL, Heron Therapeutics, Immunomedics, Ipsen Biopharmaceuticals, Jounce Therapeutics, Merck, Myriad, Novartis, Odonate Therapeutics, Pfizer, Puma Biotechnology, Roche, Seattle Genetics, and Syndax Pharmaceuticals.

Dr. Christine Brezden-Masley has received honoraria for consulting and advisory boards from Amgen, AstraZeneca, Eli Lilly, Genomic Health, Merck, Myriad, Novartis, Pfizer, Roche, and Taiho. She has received travel grants from Amgen, AstraZeneca, and Roche.

Dr. Marina Cazzaniga reports no competing interests.

Dr. Tapashi Dalvi, Dr. Graham Walker, and Dr. James Bennett are employees or contracted employees of AstraZeneca and may own stock.

Dr. Shozo Ohsumi has received honoraria for lecture fees from AstraZeneca.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Additional file 1: Table S1.

List of participating sites. This table details the sites that participated in the BREAKOUT study.

Additional file 2: Table S2.

First-line cytotoxic chemotherapy regimens in > 5% of patients (FAS). This table details first-line cytotoxic therapy regimens (single agent and combination agent).

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

O’Shaughnessy, J., Brezden-Masley, C., Cazzaniga, M. et al. Prevalence of germline BRCA mutations in HER2-negative metastatic breast cancer: global results from the real-world, observational BREAKOUT study. Breast Cancer Res 22, 114 (2020). https://doi.org/10.1186/s13058-020-01349-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13058-020-01349-9

Keywords

Breast Cancer Research

ISSN: 1465-542X

Contact us