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Article

Optimal Breast Density Characterization Using a Three-Dimensional Automated Breast Densitometry System

by
Reika Yoshida
1,2,*,
Takenori Yamauchi
2,
Sadako Akashi-Tanaka
1,
Misaki Matsuyanagi
1,
Kanae Taruno
1,
Terumasa Sawada
1,
Akatsuki Kokaze
2 and
Seigo Nakamura
1
1
Department of Breast Surgical Oncology, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan
2
Department of Hygiene, Public Health and Preventive Medicine, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan
*
Author to whom correspondence should be addressed.
Curr. Oncol. 2021, 28(6), 5384-5394; https://doi.org/10.3390/curroncol28060448
Submission received: 26 October 2021 / Revised: 9 December 2021 / Accepted: 12 December 2021 / Published: 14 December 2021
(This article belongs to the Section Surgical Oncology)
Browse Figures
Review Reports Versions Notes

Abstract

:
Dense breasts are a risk factor for breast cancer. Assessment of breast density is important and radiologist-dependent. We objectively measured mammographic density using the three-dimensional automatic mammographic density measurement device Volpara™ and examined the criteria for combined use of ultrasonography (US). Of 1227 patients who underwent primary breast cancer surgery between January 2019 and April 2021 at our hospital, 441 were included. A case series study was conducted based on patient age, diagnostic accuracy, effects of mammography (MMG) combined with US, size of invasion, and calcifications. The mean density of both breasts according to the Volpara Density Grade (VDG) was 0–3.4% in 2 patients, 3.5–7.4% in 55 patients, 7.5–15.4% in 173 patients, and ≥15.5% in 211 patients. Breast density tended to be higher in younger patients. Diagnostic accuracy of MMG tended to decrease with increasing breast density. US detection rates were not associated with VDG on MMG and were favorable at all densities. The risk of a non-detected result was high in patients without malignant suspicious calcifications. Supplementary use of US for patients without suspicious calcifications on MMG and high breast density, particularly ≥25.5%, could improve the breast cancer detection rate.

1. Introduction

Merely repeating mammography (MMG) examination in women with dense breasts may not reveal abnormal findings, resulting in a delayed breast cancer diagnosis, which has become a global issue [1,2,3,4,5,6,7,8]. Despite reports suggesting that the combined use of ultrasonography (US) and MMG is effective in detecting breast cancer [8,9,10], performing US for a vast number of individuals warranting screening is impossible.
Dense breasts are considered a strong risk factor for breast cancer. Statistical surveys on differences in mammographic density distribution due to racial differences indicated a higher frequency of denser breasts in Asians than in Westerners [1,11,12,13,14]. Even among Asians, mammographic density tends to be higher among Chinese than among Malay and Indian women [11] and is higher among Japanese women than among European and American women [15].
Previous reports indicate that a higher the breast density is associated with a higher incidence of breast cancer among Japanese women. However, although one of the causes of high breast density among Asians is a low BMI, and the cause of high breast density is different from that of Europeans, the incidence of breast cancer between Asians and Europeans is not appreciably different [16,17].
Mammographic density on MMG is classified into four categories according to the Breast Imaging-Reporting and Data System proposed by the American College of Radiology (ACR BI-RADS) as a global standard [18]. Nonetheless, this assessment depends on visual examination by a radiologist; thus, interpretations vary among clinicians [19]. A previous report demonstrated that for MMG screening tests performed at different times, 20% of women were classified by the same radiologist into different BI-RADS density categories [20]. Additionally, no clear criteria for the combined use of US and MMG have been proposed.
Several methods for the objective calculation of mammographic density from electronic MMG data have been investigated [21,22,23,24,25]. Volpara™ (Volpara Health Technologies, Wellington, New Zealand) is a three-dimensional automated breast densitometry system with unified assessment criteria for mammographic density. A significant positive correlation between breast densities determined by digital MMG software, such as Volpara, and those determined by radiologists has been reported [21,22,23,24,25].
Considering this background, we objectively measured mammographic density in Japanese women using the computer-based mammographic density measurement software Volpara and examined the diagnostic accuracy according to Volpara results. We examined objective and specific selection criteria for patients who should be screened with US in addition to MMG to improve the effective diagnostic rate in breast cancer screening.

2. Materials and Methods

2.1. Study Design

Patients who underwent breast cancer surgery between January 2019 and April 2021 in our hospital were reviewed. The exclusion criteria were as follows: (1) patients without MMG images obtained in our hospital, (2) patients whose tumors were breast cancer recurrences following partial mammectomy, and (3) patients with occult breast cancer and Paget’s disease. Patients with bilateral breast cancer were regarded as two independent cases. We conducted a case series study based on patients’ age, diagnostic accuracy, diagnostic category by MMG (with ≥3 being malignant), effects of detection by the combined use of US and MMG, pathological classification, preoperative hormone therapy/neoadjuvant chemotherapy, size of invasion, and presence of calcifications. The study was conducted according to the guidelines of the Declaration of Helsinki and was approved by the Showa University Institutional Review Board (No. 3371). Because all participants in this study were patients with breast cancer, patients whose condition was deemed malignant or benign by both MMG and US were considered as “detected” and “non-detected”, respectively.

2.2. Study Content and Investigated Items

In our hospital, Senographe Essential (GE Medical Systems, Chicago, IL, USA) is used for MMG, LOGIQ E9 (GE Medical Systems) is utilized for US, and Volpara version 1.5.3 (Volpara Health Technologies) is used as the three-dimensional automatic mammographic density measurement device.
Volpara uses digital MMG raw data to perform a three-dimensional analysis of the breasts to calculate the volume and density of fat and mammographic density in each breast. Mammographic density is defined as the ratio (%) of the mammographic density volume divided by the entire breast volume, which is an objective and reproducible result using the average density of both breasts. The measured density was adapted to the four ACR BI-RADS categories (A: fatty; B: scattered; C: heterogeneously dense; and D: extremely dense) [16], which are widely used worldwide, and was shown in terms of Volpara Density Grade (VDG): a–d. Furthermore, the average density in both breasts was defined as follows: 0–3.4%, VDG: a; 3.5–7.4%, VDG: b; 7.5–15.4%, VDG: c; and ≥15.5%, VDG: d.

2.3. Statistical Analysis

Patients’ age, breast density (%) as measured by Volpara, and size of invasion were assessed as continuous variables. Given that as a normal distribution could not be assumed, between-group differences were tested using the Mann–Whitney U test, whereas significant differences between multiple groups were examined using the Kruskal–Wallis test. Multiple comparisons were performed using the pairwise Wilcoxon test and p-value correction with Holm’s method. The degree of correlation was assessed based on the Spearman’s rank correlation coefficient. Furthermore, the presence of calcifications, VDG, presence of invasion, diagnosis by MMG, and diagnosis by US were assessed as categorical variables, and the relationship between categorical variables was assessed using Fisher’s exact test. The Cochran–Armitage test was used for trend analysis. Confounding factors were adjusted and analyzed using logistic regression analysis for diagnostic accuracy and non-detected rate.
As the size of invasion was determined using the pathological specimen after surgery, it was examined in 385 patients, except in patients who received neoadjuvant chemotherapy or preoperative hormone therapy and patients for whom all lesions had been removed by biopsy.

3. Results

Of the 1227 patients reviewed, 441 met the inclusion criteria and were included for further analyses. Table 1 presents the breakdown of background data for these 441 patients. The median age was 56 years, the median Volpara density was 14.7%, and the median size of invasion was 12.5 mm. Of all patients, 81.4% and 89.1% were categorized as “detected” by MMG and US, respectively.

3.1. Volpara Density by Age and Relationship between VDG and Age

A negative correlation between age and VDG was observed (p = −0.47, p < 0.001). Patients were classified based on VDG as follows: VDG: a, 2 (0.5%); VDG: b, 55 (12.5%); VDG: c, 173 (39.2); and VDG: d, 211 (47.8%). As there were two patients in category a, subsequent analyses were conducted by including them in VDG: b, such that there were 57, 173, and 211 patients in VDG: a + b, c, and d, respectively. We identified no significant difference in age between VDG: a, b, and c, but significant differences were observed between VDG: a, b, and d as well as between c and d (Figure 1).
Figure 2 shows the proportion of VDG according to age. VDG: d tended to be more common at younger ages (p < 0.001). The proportion of VDG: c and d, which would be regarded as dense breasts, accounted for 96.3% (106/110) of patients aged <40 years, 91.2% (94/103) of patients in their 40s, 75% (63/84) of patients in their 50s, and 84.7% (121/144) of patients aged ≥60 years.

3.2. Relationship between VDG and Diagnostic Accuracy

The diagnostic accuracy of MMG was 81.4% (359/441) among all patients (84.2% [48/57], 84.2% [148/173], and 77.3% [163/211] for patients in VDG: a + b, c, and d, respectively), highlighting a significant trend in which the diagnostic accuracy decreased with increasing VDG (p = 0.0284).
The diagnostic accuracy of US was 89.1% (393/441) among all patients (87.7% [40/57], 89.6% [155/173], and 89.1% [188/211] for patients in VDG: a + b, c, and d, respectively), indicating no difference in the diagnostic accuracy among VDG categories.
Ten patients in our study had non-detected conditions by both MMG and US. One of these ten patients was revealed to have cancer, as shown by biopsy conducted as a precaution because of a mild increase in calcifications. Another patient being monitored for a fibroadenoma-like mass by follow-up US was also diagnosed with cancer, as revealed by a biopsy performed due to a mild increase in the tumor size. The cancers on the contralateral breast in the remaining eight patients were accidentally determined by preoperative magnetic resonance imaging (MRI).

3.3. Diagnostic Accuracy by US for Patients Whose Tumors Were Non-Detected by MMG According to VDG

The diagnostic accuracy of US among patients in whom breast cancer was non-detected by MMG was 87.8% for all such patients, 88.9% in VDG: a + b, 76.0% in VDG: c, and 93.8% in VDG: d. No correlation with VDG was observed.

3.4. Impact of VDG on the Relationship between Non-Detected Cases by MMG and Presence of Invasion

The diagnostic accuracy of MMG was not significantly associated with the presence of invasion in all VDG groups (p > 0.05). The comparison of the size of invasion between the non-detected and detected groups indicated that the size of invasion was significantly smaller in the non-detected group than in the detected group in both complete patient populations (p < 0.01) and the VDG: c group (p < 0.05). A nonsignificant trend for a smaller size of invasion was observed in the VDG: a + b group (p < 0.1), and no significant difference was noted in the VDG: d group (p = 0.21) (Figure 3).

3.5. Difference in Non-Detected Rate between Cases with and without Calcifications Requiring MMG Differentiation by VDG

Of 192 patients with malignant suspicious calcifications (suspicious calcifications), 5.2% (10/192) were non-detected on MMG, whereas 28.9% (72/249) of 249 patients without calcifications had non-detected results on MMG (Table 2). The risk of a non-detected result was 7.4 times greater among patients without suspicious calcifications (p < 0.001).
The MMG results of all patients were categorized into four groups (“MMG correct diagnosis group with suspicious calcifications”, “MMG non-detected group with suspicious calcifications”, “MMG correct diagnosis group without suspicious calcifications”, and “MMG non-detected group without suspicious calcifications”), and their VDG results were compared. This comparison indicated that patients in the “MMG non-detected group without suspicious calcifications” and “MMG correct diagnosis group without suspicious calcifications” had a significantly higher mammographic density (Figure 4).
Logistic regression analysis of age, VDG, and suspicious calcifications was conducted for non-detected patients, revealing that VDG and the presence of suspicious calcifications were significant risk factors for a non-detected result. The risk of a non-detected result was 1.07 times greater when the VDG increased by 1%, increasing to 9.2 times when calcifications showed no malignant findings (Table 3). In particular, the non-detected rate increased sharply when VDG was ≥25.5% (Figure 4).

4. Discussion

The results of our study suggest that the combined use of US would be beneficial in patients without suspicious calcifications by MMG and classified as Volpara density of VDG: d or higher (in particular, those ≥ 25.5%). When these classifications were applied to the present results, the combined use of US increased the detection sensitivity to 95.8% (23/24) from 25% (6/24) with MMG alone.
As mentioned earlier, merely repeating MMG examinations in women with dense breasts can lead to masking and oversight of abnormal findings, resulting in a delay in breast cancer diagnosis [1,2,3,4,5,6,7]. Several studies using various supplemental modalities have been conducted to resolve this problem.
In the United States, breast cancer screening using MMG for women with fatty breasts showed a sensitivity of 80%; nonetheless, the diagnostic accuracy significantly decreased to 30% in women with extremely dense breasts [26]. As such, testing with MMG alone has been suggested to be insufficient for dense breasts. Thus far, the combined use of US and MMG has been proposed to overcome this shortcoming. Previous reports indicated that 89% of patients diagnosed with invasive breast cancer tested positive on MMG. However, the rate of detection increased to 98% through the combined use of US [27], the rate of detection of breast masses with a small size of invasion also increased through the combined use of US and MMG [28]. Invasive breast cancer can be detected early by using both strategies for screening women with dense breasts [29]. Furthermore, the sensitivity was significantly higher when both MMG and US were used for women with dense breasts (77.5%) than when MMG alone was used (50%) [30]. The J-START, a large randomized controlled trial conducted in Japan to examine the usefulness of adding US to MMG examinations for women in their 40s with a high prevalence of dense breasts [31,32], demonstrated that the combined use of US and MMG increased the rate of breast cancer detection by 1.5-fold, as compared with the use of MMG alone. Furthermore, the combined use of US resulted in increased sensitivity, regardless of breast density, indicating that combined US is the best method for these women. In addition, for patients with suspicious calcification and already considered malignancy, combined US is very helpful in determining abnormal findings in other sites, enlargement of axillary lymph nodes, invasion of the pectoralis major muscle, and treatment strategy. However, combined use of US in all cases is difficult due to a shortage of human resources, increases in false positive case, and poor cost-effectiveness.
Recently, reports have demonstrated the utility of combined use of various supplemental modalities such as three-dimensional automated breast ultrasound (ABUS), MRI, and digital breast tomosynthesis (DBT) for MMG screening.
ABUS is a highly reproducible and operator-independent imaging method. The addition of ABUS to MMG screening increased the sensitivity of detecting invasive ductal carcinomas in dense breasts by approximately 40% [33,34]. ABUS includes computer-aided detection as auxiliary software, which can reduce the reading time without compromising the screening accuracy [35,36]. A study conducted in 2021 compared screening with MMG alone and with ABUS in 1165 women with dense breasts and reported that ABUS combined with MMG increased the sensitivity by 31.8% [37]. Future challenges include further examination of cost-effectiveness and, as with portable US (i.e., handheld US), reducing the risk of false positives [38].
In recent years, contrast-enhanced spectral MMG has also been performed. There is also the accelerating research field of radiomics, which seeks to integrate and combine information from multiple imaging diagnoses, such as CT, MRI, and US, and analyze it using AI to improve the rate of correct diagnosis. This has the potential to improve diagnostic performance even in dense breasts [39].
The DENSE trial, a randomized controlled trial of MRI screening in the Netherlands, compared the incidence of interval cancers over 2 years in 40,373 women between 50 and 75 years with normal MMG screening results and VDG: d breast density. Participants were divided into two groups: those who underwent screening with MMG only and those who underwent screening with both MRI and MMG. The results revealed that cancer was detected at an earlier stage in the group with combined MRI and MMG. However, the biggest drawback of this test was that it requires the use of contrast media [40]. Although MRI has an extremely high cancer detection rate, it is very time-consuming and expensive for screening. In contrast, AB-MRI is less expensive, time-consuming, and less complicated than MRI, while maintaining the same diagnostic performance [36,41]. The use of DBT in combination with MMG screening for invasive cancer significantly improves both the sensitivity and specificity of detection [42,43,44]. Nonetheless, Lowry et al. reported that women with extremely dense breasts did not benefit appreciably from the addition of DBT [45]. Studies comparing DBT and AB-MRI with respect to cost-effectiveness have reported that AB-MRI is recommended if the cost is below a certain amount [46]. The eight cases in which preoperative MRI incidentally revealed contralateral breast cancer may indicate the potential usefulness of this AB-MRI.
As mentioned above, the optimal modality for breast cancer screening remains a topic of discussion. Most previous studies on dense breasts were based on visual judgement rather than objective values acquired by automated measurements. Therefore, the results of this study, for which specific numerical values were used as the prognostic criteria, are considered objective and meaningful.
Previous reports indicated that an increase in mammographic density reduces MMG sensitivity in patients without suspicious calcifications [10,47]. In another report, the addition of DBT for dense breasts did not improve early breast cancer detection without calcifications [48]. However, there are only a few studies from which conclusions can be drawn. According to the present study results, the risk of a non-detected result was 7.4-fold greater in patients without suspicious calcifications.
This study has some limitations. Given that this was a case series study, VDG (≥25.5%) should be confirmed by validation studies from actual clinical practice. Furthermore, because this study examined patients diagnosed with cancer, it was impossible to examine false negatives among patients who were not diagnosed with cancer or to examine interval cancer. In addition, there was an imbalance in sample sizes among the four VDG classifications, with only 2 out of 441 patients belonging to the group VDG: a, which is rare among Japanese women [15]. The widespread use of Volpara, other breast densitometry software and large-scale analyses at multiple centers [15] could enable a more accurate analysis of mammographic density according to ethnicity.

5. Conclusions

Active use of US in combination with MMG for patients without suspicious calcifications on MMG and a Volpara density classification of VDG: d (particularly for those ≥25.5%) could help improve the rate of effective breast cancer diagnosis. For such women, supplemental US is an efficient choice in breast cancer screening. A larger study is needed to validate these findings.

Author Contributions

Conceptualization, methodology, R.Y. and S.N.; formal analysis, R.Y. and T.Y.; data curation, M.M. and T.S.; writing—original draft preparation, R.Y.; writing—review and editing, S.A.-T., K.T., A.K. and S.N. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and was approved by the Showa University Institutional Review Board (No. 3371).

Informed Consent Statement

Informed consent was obtained from all the study participants. All the data have been anonymized to protect the identity of the participants of the study.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

We would like to thank the patients who participated in this study.

Conflicts of Interest

The authors declare no conflict of interest.

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Curroncol 28 00448 g001 550
Figure 1. Relationship between Volpara Density Grade and age.
Figure 1. Relationship between Volpara Density Grade and age.
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Figure 2. Volpara Density Grade (VDG) according to age.
Figure 2. Volpara Density Grade (VDG) according to age.
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Figure 3. Size of invasion in the non-detected and detected groups, as shown by mammography.
Figure 3. Size of invasion in the non-detected and detected groups, as shown by mammography.
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Figure 4. Risk factors for non-detected results and flow diagram leading to a non-detected result. VDG—Volpara Density Grade.
Figure 4. Risk factors for non-detected results and flow diagram leading to a non-detected result. VDG—Volpara Density Grade.
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Table
Table 1. Breakdown of the patient population (N = 441).
Table 1. Breakdown of the patient population (N = 441).
Characteristic Value
Age 56 [47, 70]
Volpara density 14.7% [9.2, 20.7]
Suspicious calcificationsYes193 (43.8%)
No248 (56.2%)
MMG category1.2 (non-detected)82 (18.6%)
3.4.5 (detected)359 (81.4%)
US category1.2 (non-detected)48 (10.9%)
3.4.5 (detected)393 (89.1%)
Neoadjuvant chemotherapy/preoperative hormone therapyYes55 (12.5%)
No386 (87.5%)
InvasionYes354 (80.3%)
No87 (19.7%)
Size of invasion 12.5 mm [5, 22]
Method of diagnosisSymptomatic81 (18.4%)
Screening147 (33.3%)
Referred129 (29.3%)
Others84 (19%)
MMG, mammography; US, ultrasonography. Presented statistics: Median [25%, 75%]; n (%).
Table
Table 2. Non-detected rate by MMG in patients with and without suspicious calcifications.
Table 2. Non-detected rate by MMG in patients with and without suspicious calcifications.
CharacteristicsDiagnosis by MMG Only
Suspicious calcifications DetectedNon-detected
Yes18210 (5.2%)
No17772 (28.9%)
MMG, mammography; p < 0.001.
Table
Table 3. Risk factors for non-detected results by MMG (logistic regression analysis).
Table 3. Risk factors for non-detected results by MMG (logistic regression analysis).
Characteristics Odds Ratio95% Confidence Intervalp
Age 0.990.97–1.010.3
VDG 1.071.04–1.11<0.001
Suspicious calcificationsYes1.00 (reference)
No9.24.68–19.85<0.001
VDG—Volpara Density Grade.
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Yoshida, R.; Yamauchi, T.; Akashi-Tanaka, S.; Matsuyanagi, M.; Taruno, K.; Sawada, T.; Kokaze, A.; Nakamura, S. Optimal Breast Density Characterization Using a Three-Dimensional Automated Breast Densitometry System. Curr. Oncol. 2021, 28, 5384-5394. https://doi.org/10.3390/curroncol28060448

AMA Style

Yoshida R, Yamauchi T, Akashi-Tanaka S, Matsuyanagi M, Taruno K, Sawada T, Kokaze A, Nakamura S. Optimal Breast Density Characterization Using a Three-Dimensional Automated Breast Densitometry System. Current Oncology. 2021; 28(6):5384-5394. https://doi.org/10.3390/curroncol28060448

Chicago/Turabian Style

Yoshida, Reika, Takenori Yamauchi, Sadako Akashi-Tanaka, Misaki Matsuyanagi, Kanae Taruno, Terumasa Sawada, Akatsuki Kokaze, and Seigo Nakamura. 2021. "Optimal Breast Density Characterization Using a Three-Dimensional Automated Breast Densitometry System" Current Oncology 28, no. 6: 5384-5394. https://doi.org/10.3390/curroncol28060448

APA Style

Yoshida, R., Yamauchi, T., Akashi-Tanaka, S., Matsuyanagi, M., Taruno, K., Sawada, T., Kokaze, A., & Nakamura, S. (2021). Optimal Breast Density Characterization Using a Three-Dimensional Automated Breast Densitometry System. Current Oncology, 28(6), 5384-5394. https://doi.org/10.3390/curroncol28060448

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