Molybdenum Target X-ray in Early Breast Carcinoma Diagnosis … – Dove Medical Press

Introduction

Breast carcinoma (BC), a common heterogeneous tumor that threatens womens physical and mental health all over the world, is influenced by age, obesity, smoking, alcohol consumption, family history, and use of oral contraceptives.13 Worldwide, there are approximately 2.1 million females diagnosed as BC each year and 630,000 associated deaths.4 Early diagnosis of BC, of no doubt, is conducive to improving survival outcomes and the probability of successful treatment in such patients.5 Moreover, early monitoring is of great value in understanding BC progression and predicting the treatment response, allowing for effective and timely adjustment of treatment.57 Thus, exploring the early diagnosis of BC is beneficial to reduce mortality in BC patients and improve the chance of survival.

Molybdenum target X-ray is an imaging technique that uses molybdenum target X-ray machine to take pictures of the patients breast in oblique and axial planes, which can obtain information about the shape, margin, density, calcification and axillary lymph nodes (LNs) of the patients breast mass.8 This examination technique has the advantages of non-invasiveness and high resolution, with important guiding value in early diagnosis and prognosis evaluation of BC.9 But it also has some shortcomings such as poor penetrability and difficulty in distinguishing deep and high lesions, which limits its diagnostic accuracy (ACC) in breast lesions and pathological properties.10,11 High-frequency color Doppler flow imaging (CDFI) is another imaging inspection system that collects information such as the location, size, relationship with surrounding tissues and blood flow of the lesions by examining the lesions in different planes of the breast, which can effectively determine the nature of the lesions and distinguish the benign and malignant breast tumors.12,13 This technique can also be applied to assess the response of tumor xenografts in nude mice to early antiangiogenic therapy.14 Its drawbacks lie in the difficulty in distinguishing small lesions with unclear echoes and microcalcifications (MCs), as well as the difficulty in screening for ductal carcinoma in situ.15 Molybdenum target X-ray has good diagnostic ability for early lesion morphology and microcalcification foci of BC, which can just make up for the shortcomings of CDFI.16 Therefore, we believe that the combination of the two may have a synergistic effect on the early diagnosis of BC.

At present, the clinical application of molybdenum target X-ray plus CDFI in early diagnosis of BC is rarely reported. We speculate that the two approaches can synergistically improve the diagnosis efficiency in early diagnosis of BC, so we conduct relevant research and report it as follows.

One hundred and two cases of suspected early-stage BC (ESBC) examined by molybdenum target X-ray and CDFI and treated in the Henan Provincial Peoples Hospital were selected. Patients general data (age, course of disease, tumor diameter, etc.) can be found in Table 1. This retrospective study was approved by the Medical Research Ethics Committee of Henan Provincial Peoples Hospital. This study was conducted in accordance with the Declaration of Helsinki. As this study is a retrospective study, the data are anonymous and informed consent is not required.

Table 1 General Information

Inclusion criteria: female patients with unilateral disease; palpable breast mass that appeared for the first time, with the presence of symptoms such as nipple inversion, galactorrhea, and breast pain; patients with calcification; voluntary inspection by molybdenum target X-ray and CDFI; complete clinical data and no deliberate concealment of clinical history.

Exclusion criteria: pregnant or lactating women; other malignancies; presence of pleural effusion as indicated by the imaging examination; heart, lung, kidney dysfunction or immune deficiency; contraindications for molybdenum target X-ray and CDFI examinations.

All patients were examined by molybdenum target X-ray and CDFI, using the methods described below.

(1) Molybdenum target X-ray inspection: Before the examination, the medical staff explained the relevant principles of the inspection and the precautions in the examination process, so as to improve patients compliance with medical examinations. A full-field digital mammography system with a flat panel detector was used for inspection. X-ray photographs of both breasts were taken in the oblique and axial planes, and local compression and amplification or tangential photographs were taken if necessary to record the shape and quantity of the lesions and their relationship with the surrounding tissues.

(2) CDFI (AlokaProsoundAlpha7, linear probe): The patient was placed in a supine position with arms raised and breasts and armpits fully exposed. Using a superficial probe with a frequency adjusted to 5.013.0 MHz, examinations in the longitudinal, transverse, and multi-sectional directions were performed on different quadrants of the breast with the nipple as the center, and the size, position, morphology, aspect ratio, and internal echo of the breast mass were observed. The CDFI images were then observed, including the presence or absence of blood flow in and around the lesion and the blood flow morphology. Blood flow classification was carried out by referring to the Adler semi-quantitative method.

Molybdenum target X-ray and CDFI were performed by two clinically experienced operators, and the inspection results were jointly reviewed by two experienced radiologists, neither of whom was aware of the purpose of the study and other variables. For details, please refer to Figures 1 and 2 for the molybdenum target X-ray and CDFI examination of two patients tested positive for B.

Figure 1 Results of a patient tested positive for breast carcinoma. (A and B). Molybdenum target X-ray results. (C and D). High-frequency color Doppler flow imaging (CDFI) results.

Figure 2 Results of another patient tested positive for breast carcinoma. (A and B). Molybdenum target X-ray results. (C and D). High-frequency color Doppler flow imaging (CDFI) results.

(1) Taking pathological examination as the gold standard, the positive detection rate (PDR), positive predictive value (PPV), negative predictive value (NPV), sensitivity (SEN), specificity (SPE), and ACC of molybdenum target X-ray and CDFI in differentiating suspected ESBC patients were compared and analyzed.

(2) CDFI and molybdenum target X-ray imaging features, mainly including masses, MCs, axillary LN metastases, and abnormalities in blood flow signals or vascular signs, were compared.

In this study, SPSS 21.0 was used for data analysis. The meanSEM was used to describe continuous variables, and the t-test was used for inter-group comparisons. Categorical variables, indicated by the ratios (percentages), were compared between groups by the 2 test. Statistical significance was declared if the P value was < 0.05.

The average age of the patients with suspected ESBC was (48.4410.18) years, the course of disease was (3.630.58) months, and the tumor diameter was (2.830.48) cm; the lesion was found on the left side in 62 (60.78%) and the right side in 40 cases (39.22%).The details are given in Table 1.

Using pathological findings as the gold standard, we collected data related to molybdenum target X-ray diagnosis of ESBC. The PDR, PPV, NPV, SEN, SPE, and ACC of molybdenum target X-ray in diagnosing ESBC were found to be 25.49%, 65.00%, 41.94%, 41.94%, 65.00%, and 50.98%, respectively (Table 2).

Table 2 Molybdenum Target X-Ray Inspection Results

Similarly, we statistically analyzed the relevant data of CDFI in the diagnosis of ESBC with pathological findings as the gold standard. Through further calculation, we found that the PDR, PPV, NPV, SEN, SPE, and ACC of CDFI in the diagnosis of ESBC were 47.06%, 87.27%, 70.21%, 77.42%, 82.50%, and 79.41, respectively (Table 3).

Table 3 CDFI Inspection Results

Data analysis of molybdenum target X-ray + CDFI in the diagnosis of ESBC showed that the PDR, PPV, NPV, SEN, SPE, and ACC of the joint diagnosis were 53.92%, 94.83%, 84.09%, 88.71%, 92.50%, and 90.20%, respectively (Table 4).

Table 4 Results of the Joint Inspection by Molybdenum Target X-Ray Plus CDFI

The diagnostic value of molybdenum target X-ray and CDFI in ESBC, either alone or in combination, was comparatively analyzed. CDFI was found to have higher PDR, PPV, NPV, SEN, and ACC (P<0.05) and comparable SPE (P<0.01) than molybdenum target X-ray. While molybdenum target X-ray + CDFI contributed to markedly higher indexes mentioned above than molybdenum target X-ray (P<0.01), and higher ACC than CDFI (P<0.001), as shown in Table 5.

Table 5 Diagnostic Data of Molybdenum Target X-Ray and CDFI (%)

The imaging results of masses, MCs, axillary LN metastases, and abnormalities in blood flow signals or vascular signs were statistically analyzed. CDFI was significantly superior to molybdenum target X-ray in distinguishing tumor, axillary LN metastases, and blood flow signal or vascular sign abnormalities (P<0.05), while molybdenum target X-ray had markedly better performance in identifying MCs than CDFI (P<0.05), as shown in Table 6.

Table 6 Imaging Results of Molybdenum Target X-Ray and CDFI

Early diagnosis of BC has been shown to improve patient survival by up to 20%.17 Most BC patients present with advanced disease at diagnosis, which is associated with a high risk of metastasis and recurrence even after tumor resection.18 Although pathological testing is the golden standard for determining BC staging, this test is lowly accepted by some patients.19 Therefore, an effective, reliable and highly accepted screening technique for ESBC is particularly needed to help BC patients improve their survival outcomes.

Molybdenum target X-ray, CDFI, and magnetic resonance imaging (MRI) are commonly used imaging techniques for the early diagnosis of BC, which is conducive to improving ESBC screening efficiency.20 Of them, MRI is not suitable for early BC screening due to its disadvantages such as high cost, complicated procedure, and overdiagnosis.21 A great number of studies have explored the application of molybdenum target X-ray and CDFI in diagnosing BC. Tailaiti G et al,9 for example, found that the molybdenum target X-ray features of invasive BC are related to immune indexes such as estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2, which can reflect pathological information like nipple depression, axillary LN enlargement and maximum tumor diameter. Hu et al22 pointed out that molybdenum target X-ray combined with dynamic contrast-enhanced MRI can improve the diagnostic efficiency of BC of different molecular types (Luminal-A/B, HER2-positive, and triple negative BC) compared with their single use. In addition, the response of BC patients to chemotherapy can be evaluated by using the resistivity index, pulsatility index, and maximum flow rate of CDFI, facilitating the prediction of the efficacy of treatment schemes and the clinical outcomes of patients.23 Rjosk-Dendorfer et al24 also reported that CDFI plus high-resolution compression elastography can improve the diagnostic ACC of benign and malignant breast masses. Li et al25 proposed that CDFI combined with strain elastography can enhance the screening efficiency of B-ultrasound for benign and malignant non-mass breast lesions. In our research, CDFI and CDFI + molybdenum target X-ray showed markedly higher PDR (47.06%, 53.92% vs 25.49%), PPV (87.27%, 94.83% vs 65.00%), and NPV (70.21%, 84.09% vs 41.94%) than molybdenum target X-ray alone. Furthermore, the SEN (88.71% vs 41.94%), SPE (92.50% vs 65.00%), and ACC (90.20% vs 50.98%) of the joint examination were notably higher compared with molybdenum target X-ray, and the ACC (90.20% vs 79.41%) was also obviously higher compared to CDFI. Two conclusions can be drawn from the above data. First, the combined examination by molybdenum target X-ray and CDFI can significantly improve the diagnostic ACC (compared with any single examination) in the 102 patients with suspected ESBC, with significant superiority over molybdenum target X-ray in other indicators such as PDR, PPV, NPV, SEN, and SPE. Second, the above diagnostic data of CDFI, except for SPE, are significantly better than those of molybdenum target X-ray. The frequency of CDFI used in this study ranges from 5.0MHz to 13.0MHz, with relatively high spatial resolution, which helps to display anomalies from the superficial to the deep plane of the breast while providing better image quality.26 In addition, the superiority of CDFI may lie in its ability to present clear anatomical layers of the lesion through acoustic impedance differences, thus helping to determine the elasticity and activity of the lesion. Moreover, CDFI is less affected by external interference and gland density, which is conducive to reducing the missed diagnosis rate. The higher diagnostic ACC of the combination of the two methods may be related to their synergistic improvement in the early diagnosis of BC. Breast masses, axillary LN metastases, abnormal blood flow signals or vascular signs, and MCs are common symptoms in women with BC and are helpful in identifying breast malignancies.27 In imaging examinations in this study, CDFI screened significantly more cases of masses, axillary LN metastases, and blood flow signal or vascular sign abnormalities than molybdenum target X-ray, while molybdenum target X-ray detected significantly greater number of cases of MCs than CDFI, suggesting that the two can complement each other in screening early pathological features of BC. Evidence has shown that CDFI can show information such as subcutaneous mammary gland, internal fine structure of each layer, tumor margins and internal echo characteristics, while revealing the blood flow and axillary LNs in the breast tumor to help identify the nature of the tumor. However, the image of micro-calcified foci displayed by CDFI is a spot-like strong echo with no distinct features, which may explain the inferior diagnostic advantage of CDFI in micro-calcified foci over molybdenum target X-ray.

This study has several limitations that need to be carefully considered and refined. First, this study is a small sample analysis and the sampling range is not samples without specific clinical suspicion, which may affect the accuracy of the research results to some extent. Second, as a single-center study, there may be information collection bias. Third, mammography or ultrasonic elastography was not included in the comparative analysis, and the findings would be more comprehensive if the analysis data in this aspect could be supplemented. In the future, this study will be gradually improved based on the above aspects, such as expanding the sample size and sampling range and supplementing mammography-related data.

CDFI significantly outperforms molybdenum target X-ray for early diagnosis of BC. The combination of the two can significantly improve diagnostic ACC for ESBC and provide more comprehensive clinical information for early diagnosis of BC.

This Study Did Not Receive Any Funding in Any Form.

The authors declare no competing interests in this work.

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Molybdenum Target X-ray in Early Breast Carcinoma Diagnosis ... - Dove Medical Press