Role of FDG-PET/CT in Identification of Histological Upgrade of Ductal Carcinoma in Situ (DCIS) in Needle Biopsy

AUTHORS

Na Young Jung ORCID 1 , Bong Joo Kang ORCID 2 , * , Sung Hun Kim 2 , Ie Ryung Yoo 2 , Yeon Soo Lim 1 , Won Jong Yoo 1

1 Department of Radiology, Bucheon St. Mary's Hospital, College of Medicine, the Catholic University of Korea, Seoul, South Korea

2 Department of Radiology, Seoul St. Mary's Hospital, College of Medicine, the Catholic University of Korea, Seoul, South Korea

How to Cite: Jung N Y, Kang B J, Kim S H , Yoo I R, Lim Y S, et al. Role of FDG-PET/CT in Identification of Histological Upgrade of Ductal Carcinoma in Situ (DCIS) in Needle Biopsy. Iran J Radiol. 2021;18(3):e113862. doi: 10.5812/iranjradiol.113862.

ARTICLE INFORMATION

Iranian Journal of Radiology: 18 (3); e113862
Published Online: September 11, 2021
Article Type: Research Article
Received: February 16, 2021
Revised: July 30, 2021
Accepted: August 2, 2021
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Abstract

Background: Accurate preoperative detection of the invasive components of ductal carcinoma in situ (DCIS) is essential for an appropriate treatment. 18F-fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET/CT) scan, which can indicate the metabolic activity and aggressiveness of breast cancer, may be used as one of the predictors of the invasive components of DCIS in needle biopsy.

Objectives: To determine whether the FDG-PET/CT findings are associated with the histological upgrade of DCIS in biopsy.

Methods: In this retrospective cohort, we reviewed 165 cases of DCIS in 162 patients, who underwent preoperative FDG-PET/CT examinations between April 2008 and September 2015. The clinicopathological characteristics and FDG-PET/CT findings of the patients were compared with respect to cancer invasion. The predictors of DCIS upgrade to invasive cancer were also examined. Moreover, the diagnostic performance of visual and semi-quantitative analyses of FDG-PET/CT in predicting invasion was compared. The semi-quantitative analyses were based on the maximum standardized uptake value (SUVmax), divided by the cutoff point in a receiver operating characteristic (ROC) curve analysis.

Results: The final pathological findings indicated 119 cases of pure DCIS and 46 cases of DCIS with invasion. The optimal SUVmax threshold was 1.9 in the ROC curve analysis. Young age, high SUVmax, positivity in the visual analysis of FDG-PET/CT, and large pathological tumor size were significantly more frequent in the DCIS + invasion group. The significant predictors of DCIS histological upgrade were age (P = 0.011), SUVmax (P < 0.001), visual analysis of FDG-PET/CT (P = 0.004), and pathological tumor size (P = 0.003) in the univariate analysis. In the multivariate analysis, the SUVmax (odds ratio [OR] = 3.31, P = 0.003) and tumor size (OR = 1.20, P = 0.022) were significant when the model included the SUVmax, age, and size (model 1). On the other hand, age (OR = 0.96, P = 0.032), visual analysis (OR = 4.67, P = 0.006), and tumor size (OR = 1.25, P = 0.005) were significant predictors when the model included visual analysis, age, and size (model 2). The sensitivity was significantly higher in the visual analysis, whereas the specificity, positive predictive value (PPV), and accuracy were significantly higher in the semi-quantitative analysis.

Conclusion: FDG-PET/CT is a potentially useful imaging tool to predict the upgrade of DCIS to invasive cancer.

1. Background

Ductal carcinoma in situ (DCIS) is one of the precursor lesions for invasive breast cancer. The frequency of DCIS has been increasing due to the widespread use of mammography screening and technical improvements (1-3). However, a considerable number of patients who are confirmed as DCIS in preoperative biopsy (0 - 37%) upgrade to invasive carcinoma, based on the final surgical pathological findings (4-6). Therefore, accurate diagnosis of the invasive components of DCIS is essential for appropriate surgical planning, including axillary lymph node (LN) staging. Besides, overdiagnosis and overtreatment are emerging issues in DCIS patients diagnosed via breast cancer screening. Therefore, in patients diagnosed with DCIS through biopsy, prediction of invasive cancer seems essential for selecting breast cancer treatment options (7, 8).

Multiple studies have been carried out to define the clinicopathological characteristics associated with an upgrade to invasive cancer in patients preoperatively diagnosed with DCIS (5-7, 9-15). The possible predictors include the patient’s age, palpability, tumor size, tumor grade, biopsy method, and some immunohistochemical markers. However, there is no consensus regarding the prognostic biomarkers that can be used to predict DCIS upgrades. Previous studies have demonstrated an association between the maximum standardized uptake value (SUVmax) measured with 18F-fluorodeoxyglucose (FDG)-positron emission tomography/computed tomography (PET/CT) and prognostic factors, such as histological type and grade, immunohistochemical factors, and proliferation index (16-19). It seems that the sensitivity of FDG-PET/CT is lower for DCIS than invasive ductal carcinoma (IDC) (1, 20), thereby limiting its diagnostic application for primary DCIS lesions. Nonetheless, FDG-PET/CT may be a potential tool for predicting the invasive components of DCIS in biopsy.

2. Objectives

This study aimed to evaluate whether the SUVmax and visual analysis of FDG-PET/CT were associated with the histological upgrade of DCIS in needle biopsy.

3. Patients and Methods

3.1. Patients

This retrospective cohort was approved by the institutional review board; the requirement for obtaining informed consent was waived. By reviewing the medical database, a total of 204 patients with a preoperative diagnosis of DCIS in biopsy and preoperative FDG-PET/CT scan were identified between April 2008 and September 2015. The exclusion criteria were as follows: patients who had not been treated with definitive surgery (n = 13); patients who had recently undergone an excisional biopsy (n = 7); and patients with DCIS and IDC at different sites within the same breast in biopsy, which were not separately described in the final pathology (n = 3).

During data collection, patients with at least one of the immunohistochemical parameters missing were excluded (n = 19). Five patients had two separate DCIS lesions in their breasts (three bilateral and two unilateral lesions). The three bilateral lesions were analyzed separately, while only representative unilateral lesions were included. Finally, a total of 165 cases (162 patients) were investigated in this study. The mean interval from biopsy until FDG-PET/CT scan was 13.6 days (range: 5 - 52 days).

3.2. FDG-PET/CT Protocol

All patients underwent preoperative FDG-PET/CT examinations, using a dedicated breast PET/CT scanner (Biograph Duo or Biograph True Point, Siemens Medical Solutions, Knoxville, TN, USA). The patients were asked to fast for at least six hours before the examinations. After measuring the serum glucose levels to confirm euglycemia (blood glucose < 130 mg/dL), 3.7 ~ 5.5 MBq/kg of 18F-FDG was injected as a saline infusion.

After 60 minutes of post-injection bed rest, the patients underwent a PET scan. The acquisition time was 2 - 3 minutes per bed position. All patients were in a supine position with their arms raised during the PET/CT scan. A non-contrast CT scan was acquired from the orbitomeatal line to the upper thigh (80 mAs, 130 kV, slice thickness of 5 mm and 50 mAs, 120 kV, and slice thickness of 5 mm, respectively), immediately followed by the corresponding PET scan of the same region. The CT data was used for attenuation correction, and images were reconstructed, based on the standard ordered-subset expectation maximization algorithm.

3.3. FDG-PET/CT Scan Interpretation

FDG-PET/CT scans were retrospectively interpreted by a nuclear medicine physician with 14 years of experience. All PET/CT scans were reviewed in a workstation using Syngo Fusion Package (Siemens Medical Solutions, Knoxville, TN, USA). Any lesion with FDG uptake greater than the background parenchymal uptake at the site of pathologically proven DCIS was defined as positive in the visual analysis. To find the exact location of the lesion, lesion-by-lesion correlations were examined via conventional imaging. For the semi-quantitative analysis, the SUVmax of FDG was measured by placing the regions of interest (ROIs) around the primary tumor site with perceptible FDG uptake. If no FDG uptake was perceptible in the visual analysis, the ROI for the SUVmax was drawn at the location corresponding to the tumor site, based on the conventional imaging findings. If the FDG uptake was perceptible in an axillary LN, the case was regarded as positive for axillary LN metastasis.

3.4. Histopathological Analysis

Percutaneous biopsies were performed for suspicious lesions found in the previous mammography or US image in all patients before preoperative MRI and FDG-PET/CT scan for staging. For this purpose, a US-guided 14-gauge core needle biopsy (CNB) was carried out for 138 cases, and stereotactic vacuum-assisted biopsy (VAB) was performed for 27 cases, depending on the physician’s choice (based on the radiologist’s report).

All patients underwent surgical treatment for DCIS of the breasts, including breast-conserving surgery (n = 89) and mastectomy (n = 76). The surgical pathological results were used as the reference standard. There were no cases with positive surgical margins. The reviewed histopathological findings included the size of DCIS lesion, the presence of axillary LN metastasis, estrogen receptor (ER) and progesterone receptor (PR) status, human epidermal growth factor receptor type 2 (HER-2) status, Ki-67 index, and epidermal growth factor receptor (EGFR) status of the primary tumor, based on the pathological findings. Tumor size was measured as the maximum diameter of the surgically resected specimen. Immunohistochemistry was also used to evaluate the expression of molecular markers, including ER, PR, HER2, Ki-67, and EGFR.

3.5. Statistical Analysis

Continuous variables are expressed as mean ± standard deviation (SD) and median with range, while categorical variables are expressed as number and percentage. To determine if continuous variables were normally distributed, Kolmogorov-Smirnov test was performed. Only the patient’s age showed a normal distribution. Comparisons between continuous variables were performed using independent t-test (for patient’s age) or Mann-Whitney U test (for SUVmax and tumor size), depending on the normal distribution of data. Different groups were compared using χ2 test and Fisher’s exact test regarding the biopsy method; tumor grade on biopsy; high and low SUVmax (divided by the cutoff point); visual analysis of primary tumor and axillary LNs in FDG-PET/CT; axillary LN metastasis in pathology; ER and PR status; HER2 expression; Ki-67 index; and EGFR.

Moreover, univariate and multivariate logistic regression analyses were performed to determine the effects of independent variables on cancer upgrade to invasion. The multivariate models were plotted separately for SUVmax and PET cancer detection, along with factors showing P < 0.05 in the univariate analysis (SUVmax + age + tumor size in model 1 and PET cancer detection + age + tumor size in model 2). Besides, the performance of SUVmax and visual detectability of invasive cancer were compared between the semi-quantitative analysis (divided by the cutoff point on the receiver operating characteristics [ROC] curve) and visual analysis by FDG PET/CT. All statistical analyses were performed in SAS version 9.3 (SAS Institute Inc., Cary, NC, USA), and a P-value < 0.05 was considered statistically significant.

4. Results

In this study, all patients were female, with a mean age of 52.7 ± 10.2 years (range: 26 - 82 years). The final pathology confirmed pure DCIS in 119 cases (Figure 1), DCIS with microinvasion in 20 cases, and IDC in 26 cases (Figure 2). Cases of microinvasion were included in the DCIS + invasion group, with an upgrade rate of 27.9% (46/165). Representative cases of pure DCIS and upgrade to invasive cancer are shown in Figure 1 and Figure 2, respectively.

Figure 1. A 52-year-old woman with pure ductal carcinoma in situ (DCIS) in the left breast. (A) Axial dynamic enhanced T1-weighted MRI demonstrates a segmental clumped non-mass enhancement (3.5 cm) (arrows) in the left middle inner part of the breast. (B) The FDG-PET/CT scan shows no discernible FDG uptake in the left middle inner part of the breast.
Figure 2. A 49-year-old woman with ductal carcinoma in situ (DCIS) upgraded to invasive ductal carcinoma (IDC) in the right breast. (A) Axial dynamic enhanced T1-weighted MRI demonstrates a heterogeneously enhanced mass (2.1 cm) with an irregular shape and margins (arrow) in the right middle upper part of the breast. (B) The FDG-PET/CT scan shows focal FDG uptake (arrow) in the right middle upper part of the breast with a maximum standardized uptake value (SUVmax) of 2.9.

The optimal SUVmax threshold was 1.9, based on the ROC curve analysis. The comparison of clinicopathological characteristics and FDG-PET/CT scan, according to the final pathological classification, are shown in Table 1. Young age (P = 0.008), high SUVmax (P < 0.001), positivity in the visual analysis of FDG-PET/CT (P = 0.002), and large pathological tumor size (P < 0.001) were significantly more frequent in the DCIS + invasion group as compared to the pure DCIS group.

Table 1. Comparison of the Patients’ Clinicopathological Characteristics According to the Final Pathological Classification
DCIS (n = 119)DCIS with invasion (n = 46)P-value
Age (y)
Mean ± SD54.0 ± 10.549.3 ± 8.80.008 a
Median (range)52.5 (26.0 - 82.0)49.0 (28.0 - 69.0)
Biopsy method
Core needle biopsy96 (80.7)42 (91.3)0.098
Vacuum-assisted biopsy23 (19.3)4 (8.7)
Tumor grade
1 & 255 (46.2)14 (30.4)0.065
364 (53.8)32 (69.6)
SUVmax
Mean ± SD1.9 ± 1.13.2 ± 2.5< 0.001 a
Median (range)1.6 (0.7 - 5.6)2.5 (0.7 - 13.5)
< 1.9 (cutoff point)67 (56.3)10 (21.7)< 0.001 a
≥ 1.9 (cutoff point)52 (43.7)36 (78.3)
Visual analysis of FDG-PET/CT
Negative39 (32.8)4 (8.7)0.002 a
Positive80 (67.2)42 (91.3)
FDG uptake of axillary LNs
Negative112 (94.1)42 (91.3)0.502
Positive7 (5.9)4 (8.7)
Pathological size (DCIS) (cm)
Mean ± SD2.8 ± 2.34.1 ± 2.3< 0.001 a
Median (range)2.0 (0.2 - 11.3)3.9 (0.5 - 10.0)
LN metastasis in pathology
Negative118 (99.2)44 (95.7)0.188
Positive1 (0.8)2 (4.3)
ER
Negative42 (35.3)15 (32.6)0.745
Positive77 (64.7)31 (67.4)
PR
Negative49 (41.2)17 (37.0)0.620
Positive70 (58.8)29 (63.0)
HER-2
Negative63 (52.9)21 (45.7)0.401
Positive56 (47.1)25 (54.3)
Ki-67
< 14%62 (52.1)18 (39.1)0.135
≥ 14%57 (47.9)28 (60.9)
EGFR
Negative86 (72.3)33 (71.7)0.946
Positive33 (27.7)13 (28.3)

Abbreviations: DCIS, ductal carcinoma in situ; EGFR, epidermal growth factor receptor; ER, estrogen receptor; FDG-PET/CT, 18F-fluorodeoxyglucose-positron emission tomography/computed tomography; HER-2, human epidermal growth factor receptor type 2; LN, lymph node; PR, progesterone receptor; SD, standard deviation; SUVmax, maximum standardized uptake value.

aP-value shows a significant difference between DCIS and IDC, based on Chi-square or Fisher's exact test and independent t-test or Mann-Whitney U test.

The analysis of predictive factors for DCIS upgrade is shown in Table 2. An upgrade to invasive cancer was significantly correlated with age (P = 0.011), SUVmax (P < 0.001), visual analysis of FDG-PET/CT (P = 0.004), and pathological tumor size (P = 0.003) in the univariate logistic regression analysis. In the multivariate analysis of SUVmax, age, and tumor size (model 1), the SUVmax and tumor size were found to be significant predictors. In the visual analysis with age and tumor size (model 2), all variables were found to be significant predictors.

Table 2. The Predictive Factors for the Upgrade of DCIS
Univariate analysisMultivariate analysis
Crude OR (95% CI)P-valueModel 1: SUVmax + Age + Tumor sizeModel 2: Visual detection by PET/CT + Age + Tumor size
Adjusted OR (95% CI)P-valueAdjusted OR (95% CI)P-value
Age (y)0.95 (0.92 - 0.99)0.011 a0.97 (0.93 - 1.00)0.0690.96 (0.92 - 1.00)0.032 a
Biopsy method
VAB1.0 (Reference)
CNB0.43 (0.15 - 1.29)0.134
Tumor grade of biopsy specimen
1 & 21.0 (Reference)
31.93 (0.94 - 3.96)0.074
SUVmax (≥ 1.9 as the cutoff point)4.47 (2.05 - 9.75)< 0.001 a3.53 (1.58 - 7.89)0.002 a
Visual analysis of FDG-PET/CT
Negative1.0 (Reference)1.0 (Reference)
Positive4.64 (1.61 - 13.31)0.004 a4.67 (1.55 - 14.08)0.006 a
FDG uptake of axillary LNs
Negative1.0 (Reference)
Positive1.59 (0.45 - 5.66)0.476
Pathological size (DCIS) (cm)1.25 (1.08 - 1.44)0.003 a1.20 (1.03 - 1.40)0.022 a1.25 (1.07 - 1.47)0.005 a
LN metastasis in pathology
Negative1.0 (Reference)
Positive4.44 (0.42 - 47.09)0.217
ER
Negative1.0 (Reference)
Positive1.11 (0.54 - 2.29)0.768
PR
Negative1.0 (Reference)z
Positive1.18 (0.59 - 2.38)0.636
HER-2
Negative1.0 (Reference)
Positive1.33 (0.67 - 2.63)0.408
Ki-67
< 14%1.0 (Reference)
≥ 14%1.67 (0.84 - 3.34)0.143
EGFR
Negative1.0 (Reference)
Positive1.04 (0.49 - 2.21)0.918

Abbreviations: VAB, vacuum-assisted biopsy; CNB, core needle biopsy; CI, confidence interval; DCIS, ductal carcinoma in situ; EGFR, epidermal growth factor receptor; ER, estrogen receptor; FDG-PET/CT, 18F-fluorodeoxyglucose-positron emission tomography/computed tomography; HER-2, human epidermal growth factor receptor type 2; LN, lymph node; OR, odds ratio; PR, progesterone receptor; SUVmax, maximum standardized uptake value.

aStatistically significant.

The area under the curve (AUC) was 0.72 (95% confidence interval [CI]: 0.64 - 0.81) in the semi-quantitative analysis with SUVmax and 0.62 (95% CI: 0.56 - 0.68) in the visual analysis of 18F-FDG PET/CT. The sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy of predicting DCIS upgrade to invasive cancer were 78%, 56%, 41%, 87%, and 62% in the semi-quantitative analysis with SUVmax (cutoff point: 1.9) and 91%, 33%, 34%, 91%, and 49% in the visual analysis of FDG PET/CT (Table 3). The sensitivity of visual analysis was significantly higher than that of the semi-quantitative analysis, whereas the specificity, PPV, and accuracy of the semi-quantitative analysis were significantly higher than the visual analysis.

Table 3. Comparison of the Diagnostic Performance of Visual and Semi-quantitative Analyses of FDG-PET/CT scan
Sensitivity (95% CI)Specificity (95% CI)PPV (95% CI)NPV (95% CI)Accuracy (95% CI)
Semi-quantitative analysis with SUVmax (≥ 1.9, cutoff point)0.78 (0.64-0.89)0.56 (0.47-0.65)0.41 (0.31-0.52)0.87 (0.77-0.94)0.62 (0.55-0.70)
Visual analysis 0.91 (0.79-0.98)0.33 (0.24-0.42)0.34 (0.26-0.44)0.91 (0.78-0.97)0.49 (0.41-0.57)
P-value (visual vs. semi-quantitative)0.014 a< 0.001 a0.012 a0.297<0.001 a

aP-value for differences was determined using McNemar test (sensitivity, specificity, and accuracy) or generalized score statistic (PPV and NPV).

5. Discussion

FDG-PET/CT scan is not commonly recommended for DCIS patients with a low risk of metastasis. However, we hypothesized that this modality could be a useful preoperative diagnostic tool to predict the upgrade of DCIS to invasive cancer. The tumor cell number and nodular growth pattern were associated with FDG-PET/CT (21, 22). Therefore, the FDG uptake reflects not only the biological aggressiveness of a tumor but also the tumor cell density or tumor burden of DCIS, which is considered to be associated with invasion (22).

In this study, semi-quantitative anlysis based on SUVmax and visual analysis based on the reviwer's visual judgment were performed. In clinical practice, tumors with a low SUVmax, such as DCIS, can be visually detected owing to the focal uptake pattern and relatively low background physiological absorption. Because of the low FDG uptake of DCIS, the semi-quantitative analysis has limited reliability; therefore, a more sensitive visual analysis was performed simultaneously. Some recent studies of DCIS upgrade, assessed by PET/CT scan, have conducted a visual analysis along with SUVmax measurement (22, 23). In this study, the SUVmax and visual analysis were predictors of DCIS upgrade to invasive cancer in both univariate and multivariate models, similar to previous studies (2, 4).

Moreover, in previous research, the possible predictors of the invasive components of DCIS in biopsy were the patient’s age (7, 11), palpability (5, 10), biopsy method (5, 6, 11, 13, 14), tumor grade (2, 5, 7, 11, 12, 15), pathological or imaging tumor size (5-7, 9, 11, 13, 15), and some immunohistochemical markers (2, 7, 14, 15). The patient’s age was introduced as a predictor of DCIS upgrade in some previous studies (7, 11), but not others (22). In the present study, the patient's age was a significant predictor of DCIS upgrade to invasive cancer.

Additionally, the type of biopsy method was reported as a predictive factor for the upgrade of DCIS in previous studies (5, 6, 11, 13, 14). CNB using 14-gauge needles can obtain a smaller amount of tissue than VAB with larger needles; therefore, patients undergoing US-guided CNB might have a higher upgrade rate than those undergoing mammography-guided VAB. However, in the present study, where most cases underwent US-guided CNB, the biopsy method was not significantly different between the DCIS and DCIS + invasion groups; therefore, it was not introduced as a predictor of DCIS upgrade.

In the present study, a higher nuclear grade of biopsy specimens was observed in the DCIS + invasion group as compared to the pure DCIS group (69.6% vs. 53.8%), and the difference was not statistically significant, but P value was close to <0.05 (P = 0.065). However, nuclear grade was not a significant factor associated with DCIS upgrades. Generally, there are contradictory results regarding the role of tumor grade. The tumor grade in biopsy (5, 12) and the final pathology (2, 7, 11, 12) was recognized as a significant independent predictor in some previous studies, but not in some others (9, 13, 23).

In previous studies (5-7, 11, 13, 15), tumor size was reported as one of the significant factors for DCIS upgrade. In this study, the pathological tumor size was significantly larger in the DCIS group with invasion as compared to the pure DCIS group, which is consistent with previous studies (7, 9, 13, 15). The DCIS upgrade was also significantly correlated with the pathological tumor size in the present study, similar to previous research (5, 9, 13). Moreover, in the present study, immunohistochemical markers, previously known as prognostic factors for breast cancer, were not correlated with upgrade to invasive cancer from DCIS in biopsy. Also, there are some studies on the relationship between DCIS upgrade and immunohistochemical markers (2, 7, 14, 15); however, their results are inconsistent, and consensus has not been reached. In this study, we did not find any correlation between DCIS upgrade and immunohistochemical markers, which is in line with a previous study (22).

The present findings revealed that visual and semi-quantitative analyses of FDG-PET/CT could predict DCIS upgrade preoperatively, independent of other prognostic clinicopathological factors. The SUVmax can be an objective indicator and a practical tool to predict the upgrade of DCIS. Comparison of diagnostic performance between the semi-quantitative and visual analyses showed that the visual analysis was more sensitive for detecting the invasion of DCIS; however, the overall accuracy of the semi-quantitative analysis was significantly higher than that of the visual analysis.

The main limitation of this study was its retrospective design, which could induce selection bias. Second, it was difficult in some cases to determine the correlation between the exact location of a biopsy-proven malignancy on conventional images, FDG uptake on PET/CT scan, and pathological lesion after surgery; however, we tried to find the lesion at least in the same quadrant in all cases. Third, because biopsy was performed before FDG-PET/CT scan for all patients, it could affect the PET/CT results. Finally, the menstrual cycle and menopause status, which could affect the diagnosis of FDG-PET/CT, were not considered in this study. Therefore, a well-designed prospective study is needed for further evaluation of the efficacy of FDG-PET/CT scan in detecting the invasive components of DCIS compared to other imaging modalities and pathological parameters.

5.1. Conclusion

This study demonstrated that both semi-quantitative and visual analyses of FDG uptake could preoperatively predict the risk of upgrade to invasive cancer, independent of other clinicopathological characteristics

Acknowledgements

Footnotes

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