Introduction
Breast cancer is the most frequent malignant neoplasm in women worldwide, both in new cases and in mortality1. In Mexico, Globocan 2018 estimated 27,283 new cases and 6,884 deaths2. Ductal Carcinoma In Situ (DCIS) is a heterogeneous group of pathologies with malignant proliferation of the mammarian epithelial cells that are confined inside the basal membrane of the lobular duct unit3,4. Before 1980, DCIS was considered a rare condition, fewer than 5% of all cases of breast cancer. The most common presentation of DCIS comprise microcalcifications, and the diagnosis of this pre-invasive lesion has increased during recent years due to breast-cancer screening programs with mammography, with an incidence of up to 20% 5. The prevalence of DCIS at our Institution is reported as 6.8%6.
DCIS is considered a precursor to invasive carcinoma, although not all DCIS progresses. Patients with untreated DCIS could be diagnosed with invasive breast cancer in 20-53%, according to data obtained from long-term studies. Some cases with DCIS have a slow growth disease and that never exerted an impact on health7-9. Invasive carcinoma usually developed within the first decade of the DCIS diagnosis8. Breast cancer mortality 10 years after the diagnosis of DCIS is less than 2%10.
Some factors are related to the recurrence of DCIS, such as younger age, positive surgical margins, tumor size, grade, and the presence of comedonecrosis11. Sentinel Lymph Node Biopsy (SLNB) is indicated in patients with DCIS undergoing mastectomy when there is a high suspicion of invasive carcinoma in the surgical specimen, such as younger age (less than 40 years), palpable tumor12, tumors >2.5 cm, multicentricity, extensive microcalcifications, high-grade lesions, and comedonecrosis. The upgrade or coexistence of an invasive component and/or microinvasion is reported in 25-35.9% in final surgical specimens of patients with an initial biopsy of DCIS13,14. SLNB also could be carried out in patients in whom surgery could affect lymphatic flow drainage15, with a reported procedure in 18% of SLNB in patients with DCIS who underwent conservative surgery16. The objective of the present study is to identify the clinical, radiological, and histopathological characteristics that could be predictive factors of microinvasive/invasive carcinoma in patients with an initial diagnosis of DCIS by core-needle biopsy.
Materials and Methods
This is a retrospective, cross-sectional, and analytical study that included consecutive patients with an initial diagnosis of DCIS and who were treated with surgery from January 2006 to June 2017, at a breast pathology referral institution that cares for women from an open population of the metropolitan area of Mexico City. Inclusion criteria were women aged ≥18 years, a diagnosis of DCIS performed with guided imaging or office core-needle biopsy, and treatment with mastectomy or conservative breast surgery. Patients were excluded if they underwent a previous excisional biopsy, they had incomplete information in their clinical records, and/or if they had metaplastic carcinoma in the final histopathological study. SLNB was conducted if the patient underwent mastectomy or if conservative surgery could compromise the performance of a future SLNB. At the Institution, SLNB is carried out with a double technique employing a preoperatory radiotracer and 1 ml of peri-areolar Patent Blue V (Bleu patenté V, Sodique Guerbet 2.5%; Laboratory Guerbet, 95943 Roisy CdG Cedex, France).
Analyzed variables included age, Body Mass Index (BMI), clinical aspects of the disease, breast density, imaging features and the extension of radiological lesions, tumor grade, and immunohistochemistry. DCIS grade was evaluated in the biopsy specimen and was catalogued as grade I, II, or III. Immunohistochemistry for hormonal receptor status, HER2 expression, and Ki67 was carried out on the final surgical specimen (mastectomy or conservative surgery). Positive hormonal receptor status was considered if the Estrogen Receptor (ER) or the Progesterone Receptor (PR) was ≥1%. Ki67 was classified as low if it was <20%17, this cut-off point apparently better for classifying subrogate subtypes18,19.
Patients were divided into two groups: those with an initial and final diagnosis of DCIS, and those with an initial diagnosis of DCIS and a final diagnosis of invasive or microinvasive carcinoma in the histopathological surgical specimen.
Statistical analysis
Descriptive statistics with central tendency, dispersion, measurement of frequencies, and a univariate analysis were carried out to describe the included population. Fisher exact test was used for categorical variables, while Mann–Whitney U test was utilized for differences between quantitative variables. A non-conditional logistic regression model was performed for multivariate analysis. Covariates were selected in a forward stepwise manner to identify predictive factors for invasive or microinvasive carcinoma. The study was approved by the Institutional Ethics and Research Committee. Two-sided p ≤0.05 was considered statistically significant, and the SPSS ver. 23.0 statistical software package for Windows was used.
Results
From 2006–2017, we included 334 patients in the study with an initial diagnosis of DCIS who underwent surgical treatment. Average age was 51.7 years (range, 24–98 years). Mean BMI was 27.9 ± 5.3 kg/m2, with 67% in overweight/obesity (Table 1). A family history of breast cancer in at least one first-degree member or in two second-degree members of the family was documented in 41 (12.3%) of patients. The presence of a palpable lump was documented in 117 (35%) cases, with a median tumor size of 3 cm.
Variable | Total |
---|---|
Patients | 334 |
Age (years) | 51.7 ± 10.9 |
BMI (kg/m2) | 27.9 ± 5.3 |
Normal | 110 (32.9%) |
Overweight | 131 (39.2%) |
Obesity | 93 (27.8%) |
Palpable nodule | 117 (35%) |
Palpable nodule size (cm) | 3 (0.8–7.5) |
Breast density | |
A | 19 (5.7%) |
B | 211 (63.2%) |
C | 94 (28.1%) |
D | 10 (3%) |
Presence of radiological nodule | 128 (38.3%) |
Radiological tumor size (cm) | 1.5 (0.2–7.1) |
Microcalcifications | 276 (82.6%) |
Microcalcification extension (cm) | 2.7 (0.4–12) |
Multicentricity | 117 (35%) |
Grade* | |
I | 39 (11.7%) |
II | 131 (39.2%) |
III | 164 (49.1%) |
Surgical procedure | |
Conservative surgery | 91 (27.2%) |
Mastectomy | 237 (70.9%) |
Pathological stage | |
0 | 193 (57.8%) |
I (mic) | 17 (5.1%) |
I | 57 (17.1%) |
IIA | 39 (11.7%) |
IIB | 17 (5.1%) |
IIIA | 8 (2.4% |
IIIB | 0 |
IIIC | 2 (0.6%) |
SLNB | 275 (82.3%) |
Lymph node metastasis in SLNB, n = 275 | 45 (16.3%) |
Immunohistochemistry** | |
Estrogen receptor | |
Positive | 239 (71.6%) |
Negative | 95 (28.4%) |
Progesterone receptor | |
Positive | 200 (60%) |
Negative | 134 (40%) |
HER2 (n = 239) | |
Positive | 97 (40.6%) |
Negative | 142 (59.4%) |
Ki 67 (n = 262) | |
Median expression (%) | 10% (0–85) |
Ki67 expression | |
Low (≤20%) | 214 (81.7%) |
High (>20%) | 48 (18.3%) |
Nominal variables are expressed as number and percentage. Scale variables are expressed as mean ± Standard Deviation (SD) or median with minimal-maximal values.
BMI = Body Mass index; SLNB=Sentinel Lymph Node Biopsy.
*Biopsy specimen;
**Final surgical specimen.
All patients had digital mammography and high-resolution ultrasound. According to the American College of Radiology (ACR) classification, the most frequent breast density was B type with 211 (63.2%) cases, (Table 1). Imaging findings were evaluated. The presence of a nodule or mass detected by imaging studies occurred in 128 (38.3%) of patients, with a clinical median tumor size of 1.5 cm; microcalcifications was present in 276 (82.6%), with a median extension size of 2.7 cm, and one-third of the included population had multicentric disease in radiological studies, the majority of these with a microcalcification focus (Fig. 1). In the biopsy specimen, DCIS grade III was the most frequent histopathological grade in 164 (49.1%) patients (Figs. 2-3). The most frequent surgery was mastectomy in 237 (70.9%) patients.
According to immunohistochemistry in the final surgical specimen, positive ER and PR were identified in 71.6% and 60% of patients, respectively. HER2 expression was evaluated in 239 patients. The most common HER2 status was negative expression in 142 (59.4%) patients. Determination of Ki67 has been carried out since the year 2010 at the Institution. Since that date and according to the inclusion criteria, 262 had a Ki67 evaluation. The median proliferation marker Ki67 was 10%, considered as high expression (>20%) in 48 (18.3%) patients.
After surgery, the final histopathological study of the surgical specimen identified 193 (57.8%) patients with DCIS, microinvasive carcinoma in 17 (5.1%), and invasive carcinoma in 124 (37.1%) patients. The predominant invasive pathological stages were pI and pIIA in 113 (33.8%) patients.
Sociodemographic variables did not reveal any differences between patients with final DCIS or with invasive carcinoma (Table 2). According to disease features and immunohistochemistry, the variables associated with the presence of invasion or microinvasion were the presence of a palpable lump (36.7% vs. 63.2%), and the presence of a radiological nodule (29% vs. 51%), both features with statistically significant differences. Tumor size in imaging studies also demonstrated significant differences between groups (1.2 vs. 1.75 cm, p = 0.015), and between the extension of microcalcifications (2.5 vs 3.1 cm, p <0.001). According to the core-needle biopsy device information (n=200), the thinner the cutting needle, the greater the chance of invasive component, being 29.3%, 38%, and 58.7% with 10-gauge, 11-gauge, and 14-gauge, respectively (p=0.006)
Variable | DCIS | Microinvasive/invasive carcinoma | p |
---|---|---|---|
Patients | 193 | 141 | |
Age (years) | 52.5±11.4 | 50.5±10 | 0.175 |
BMI (kg/m2) | 27.6±5.2 | 28.4±5.3 | 0.118 |
BMI (WHO classification) | 0.130 | ||
Normal | 69 (35.6%) | 41 (29.3%) | |
Overweight | 79 (40.7%) | 52 (37.1%) | |
Obesity | 46 (23.7%) | 47 (33.6%) | |
Palpable nodule, n = 117 | 43 (36.7%) | 74 (63.2%) | <0.001 |
Palpable nodule size (cm) | 3 (1–6.9) | 3 (0.8–7.5) | 0.634 |
Palpable nodule by range | 0.343 | ||
≤2 cm | 12 (27.9%) | 27 (36.5%) | |
>2 cm | 31 (72.1%) | 47 (63.5%) | |
Breast density | 0.691 | ||
A | 9 (4.6%) | 10 (7.1%) | |
B | 121 (62.4%) | 90 (64.3%) | |
C | 58 (29.9%) | 36 (25.7%) | |
D | 6 (3.1%) | 4 (2.9%) | |
Presence of radiological nodule | 56 (29%) | 72 (51%) | <0.001 |
Radiological nodule tumor size (cm) | 1.2 (0.2 – 6) | 1.7 (0.4–7.1) | 0.015 |
Microcalcifications | 159 (82.3%) | 117 (82.9%) | 0.137 |
Microcalcification size (cm) | 2.5 (0.4 –12) | 3.1 (0.4–12) | <0.001 |
Multicentricity | 60 (31.1%) | 57 (40.4%) | 0.146 |
Core-needle biopsy, n = 200 | 0.006 | ||
10-gauge | 12 (70.6%) | 5 (29.4%) | |
11-gauge | 49 (62.0%) | 30 (38.0%) | |
14-gauge | 43 (41.3%) | 61 (58.7%) | |
Grade* | 0.510 | ||
I | 26 (13.4%) | 13 (9.3%) | |
II | 75 (38.7%) | 56 (40.0%) | |
III | 93 (47.9%) | 71 (50.7%) | |
Grade I/II | 101 (52.1%) | 69 (49.3%) | |
Grade III | 93 (47.9%) | 71 (50.7%) | 0.617 |
Surgical procedure | |||
Conservative surgery | 48 (24.8%) | 0 | |
Conservative surgery + SLNB | 22 (11.4%) | 21 (14.9%) | |
Mastectomy | 4 (2%) | 1 (0.7%) | |
Mastectomy + SLNB | 115 (59.6%) | 117 (82.9%) | |
Immunohistochemistry** | |||
Estrogen receptor | 0.592 | ||
Positive | 141 (72.7%) | 98 (70%) | |
Negative | 53 (27.3%) | 42 (30%) | |
Progesterone receptor | 0.386 | ||
Positive | 120 (61.9%) | 80 (57.1%) | |
Negative | 74 (38.1%) | 60 (42.9%) | |
HER2 (n = 239) | 108 | 131 | 0.453 |
Positive | 41 (38%) | 56 (42.7%) | |
Negative | 67 (62%) | 75 (57.3%) | |
Ki 67 (n = 262) | 150 | 112 | |
Median expression (%) | 5% (0–85) | 10% (1–80) | 0.005 |
Ki67 expression | 0.425 | ||
Low (≤20%) | 125 (83.3%) | 89 (79.5%) | |
High (>20%) | 25 (16.7%) | 23 (20.5%) |
Nominal variables are expressed as number and percentage. Scale variables are expressed as mean±Standard Deviation (SD) or median with minimal-maximal values.
DCIS=Ductal Carcinoma In Situ; BMI=Body Mass Index; SLNB=Sentinel Lymph Node Biopsy;
*Biopsy specimen;
**Final surgical specimen.
Median Ki67 expression was higher in patients with invasive carcinoma (5% vs. 10%, p = 0.005), but if the comparation had employed the cut-off point of 20%, there were no differences. Other variables, such as palpable tumor size, breast density, the presence of microcalcifications, radiological multicentric disease, grade, hormonal receptor, and overexpression of HER2 had no statistically significant differences.
SLNB was carried out in 275 patients, 43 conservative surgeries, and in 232 mastectomies. Sentinel lymph node detection was 99.2%; in two patients, axillary lymph node dissection was performed because there was no migration of radiotracer nor of the blue dye, both cases without lymph node metastases at the final histopathological study. Lymph node metastasis was reported in 45 (16.3%) of the 275 cases who underwent SLNB.
In the multivariate analysis using the logistic regression model, including all variables except immunohistochemistry (n = 344), the variables considered as predictive factors for invasive/microinvasive carcinoma were the presence of a palpable nodule (OR = 4.072) and radiological multicentric disease (OR = 1.677), both with statistically significant differences (Table 3). In the logistic regression model, including all variables and immunohistochemical features (n = 170), the sole variable found associated with invasion was a palpable nodule (OR = 3.248, 95%CI = 1.642–6.421, p = 0.001).
Discussion
The presence of invasive and microinvasive carcinoma at the final histopathological study in patients with an initial diagnosis of DCIS reported in 21% and 14%, respectively20. In the present study, the prevalence of invasive carcinoma was much higher (38%), and that of microinvasive carcinoma was much lower (4.2%).
The variables identified predicting invasion were palpable nodule, high DCIS grade, and the presence of an opacity by mammography20. In the meta-analysis published by Brennan et al.13, which included 52 studies with 7,350 patients, the preoperative variables associated with the underestimation of invasive carcinoma were the presence of a palpable lesion, the use of a 14-gauge automated biopsy device, high-grade DCIS, the presence of a mammographic mass, and a BI-RADS category of 4 or 5. The underestimation of invasive carcinoma was 25.9% (95% CI = 22.5%–29.5%). When the lesion is observed as a mass, an ultrasound guided biopsy is conducted, upstaging is as high as 42.7%, with the identification of four predictive factors in order to upstage as follows: a palpable lesion; a lesion size of >2 cm; a high-grade lesion, and the use of the 14-gauge needle method21. In the present study, with 334 patients with an initial diagnosis of DCIS, upstaging with different biopsy techniques was 42.2%, and the only predictive factors identified in the present study were the presence of palpable tumor and multicentric disease in the imaging studies. Even the thinner the cutting needle, the greater the chance of invasive component, but it had no statistical significance in multivariable analysis.
There is a great deal of variability in predictive factors, both in the characteristics and in the number of features to take into account on suspecting the presence of microinvasive/invasive carcinoma and for considering a patient as a candidate for SLNB, even in conservative surgery. The more frequent variables identified in patients with DCIS as diagnosed by core-needle biopsy are palpable tumor13,20-22, the presence of a nodule or mass in imaging studies (mammogram and/or ultrasound)13,20,23, High-grade DCIS13,19,20,21,24, and a tumor size of >2 cm13,21,23-25. Some authors proposed a larger tumor size, such as Maffuz et al.26 with tumors >2.5 cm, and Yen et al.27 with ≥4 cm as a predictive factor of invasion. In the present study, after multivariate analysis, the sole two predictive factors of microinvasion/invasion were palpable tumor and the presence of multicentric disease in the imaging studies.
Other predictive factors for microinvasion that are described in the literature with less frequency are the presence of comedo-like necrosis, hormone receptor negativity, and radiological features such as a high degree of vascularization28, peri-tumoral vascular invasion, multifocality/multicentricity that correlate with larger lesions, and a tumor grade of ≥229. In the present study, multicentric disease identified in imaging studies was one of the two predictive factors in the multivariate analysis.
Younger age is also reported as a predictive factor of the invasive component. Trentin et al.23 reported an age of <40 years, a mammographic size of >2 cm, and residual lesion on post-vacuum-assisted breast biopsy mammogram, such variables being associated with the invasive component. Yen et al.27 reported 20% of invasive carcinoma at final pathology and identified four variables associated with the former: an age of ≤55 years; diagnosis by core-needle biopsy; mammographic lesion of ≥ 4 cm, and high-grade DCIS. In the present study, age was similar between groups.
For DCIS masses that underwent ultrasound-guided biopsy, predictive factors of invasion were the final BI-RADS assessment category and a high nuclear grade. With elastography, the maximal stiffness value was higher in the invasive carcinoma group30. Recently, Sun et al.31 proposed a nomogram including five independent factors associated with a histological upgrade from DCIS to invasive carcinoma. The included variables comprised the presence of high-grade DCIS, positive HER2 expression, a pattern of comedonecrosis, larger lesion size, and a higher mean of shear-wave velocity value identified by elastography, with an Area Under the Curve (AUC) of 0.896. If elastography is not included, the AUC was 0.788. This tool could be helpful in deciding which patient should undergo SLNB even in breast conservative surgery, due to the high suspicion of invasive carcinoma. The limitation of this nomogram lies in that not all DCIS lesions are visible by ultrasound, and elastography could not be performed.
Considering immunohistochemistry, in a retrospective study of 219 cases, Wan et al.19 identified that patients with DCIS with microinvasion have a lesser expression of hormonal receptors and a higher expression of HER2. In our study, hormonal receptor status and HER2 expression (in patients in whom the test was carried out), there were no differences between them. A high proliferation index based on Ki67 expression in a DCIS biopsy is considered as a risk factor for disease recurrence32, and a lack of evidence for considering this marker as a predictive factor of upstaging to invasive carcinoma, in addition to their being a controversy in terms of the cut-off point. In a recent study by Lui et al.33, upstaging to microinvasive carcinoma was associated with high-grade DCIS, large tumor size, comedonecrosis, the absence of hormonal receptors, HER2 overexpression, and a high Ki67 index (≥14%), while for invasive carcinoma, the associated variables were high-grade DCIS, large tumor size, a high Ki67 index (≥14%), and lymph node metastasis.
In the present study, Ki67 was not processed in 21.8% of the included patients, because this tumor marker has been employed at the Institution since 2010 and is usually carried out in the final histopathological surgical specimen. Even if Ki67 expression were higher in patients with a microinvasive/invasive component, we would not be able to recommend this marker as a predictive factor due to the incomplete information available on these variables.
SLNB should not be performed routinely for all patients with an initial diagnosis of DCIS. Given the low probability of positive lymph node metastasis, this one is documented approximately 1%–13%. The majority of these identified such micrometastases and detected these by immunohistochemistry20,34,35. American Society of Clinical Oncology (ASCO) guidelines36 recommended SLNB in patients with DCIS when mastectomy is performed. There are efforts to identify predictive factors of lymph node metastasis in patients with an initial diagnosis of DCIS who underwent breast conservative surgery, with published SLNB published in 18% and positive sentinel lymph node metastasis in 0.9%16. In patients with a high suspicion of the invasive component, SLNB is indicated24,33. These factors usually are the same factors as those identified by the underestimation of invasive carcinoma. Yen et al.27 recommended SLNB in younger patients, DCIS diagnosed by core- needle biopsy, or high-grade DCIS. The only variable identified as a predictive factor of positive sentinel lymph node was the presence of a palpable lesion. There is no consensus for decision-making. In a previous report deriving from our Institution of patients with as initial diagnosis of DCIS, SLNB were performed in patients undergoing mastectomy, in those with a palpable tumor, a radiological lesion of ≥5 cm, with an inadequate breast/tumor relationship, and/or in patients in whom surgery could affect lymphatic flow drainage. Patients with positive sentinel lymph nodes were younger (44.5 vs. 51 years), with more palpable tumors, larger clinical and radiological lesions, with a greater comedonecrosis pattern, more undifferentiated tumors, and fewer cases with hormonal receptors, all of these variables without statistically significant differences22. The predictive factors of nodal involvement identified by Trentin et al23 included a mammographic size of >2 cm and residual lesion in the post vacuum-assisted breast-biopsy mammogram.
Conclusions
In this retrospective study of 334 patients with an initial diagnosis of DCIS with core-needle biopsy, the global upgrade was 42.2% (38% invasive and 4.2% microinvasive carcinoma), higher than reports in the literature. In the presence of DCIS with palpable nodule and radiological multicentric disease, SLNB should be conducted due to the high probability of an upgrade and the chance of axillary lymph node metastasis, regardless of the type of surgery. Another aspect that needs to be explored in order to diminish underestimation of the invasive component is improvement in biopsy techniques to obtain more tissue samples with thicker needles.