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Is the sentinel lymph node biopsy more sensitive for the identification of positive lymph nodes in breast cancer than the axillary lymph node dissection?
SpringerPlus volume 2, Article number: 275 (2013)
Since the routine clinical use of the sentinel lymph node (SLN) procedure, questions have been raised concerning an increase in the overall percentage of node-positive patients. The goal of our study was to compare the sensitivity of the SLN procedure and the axillary lymph node dissection (ALND) for the identification of positive lymph nodes in breast cancer.
The incidence of axillary node metastasis in SLNB and ALND specimens from patients undergoing operative treatment of a primary breast carcinoma was compared retrospectively.
Logistic regression models were used to analyze the effect of various predictors on the presence of positive lymph nodes. We constructed a multivariate model including the procedure and these predictors that have shown to be related to lymph node involvement in univariate analysis. The probability of finding positive lymph nodes was thus calculated in both groups correcting for relevant predictors of lymph node involvement.
The SLNB group included 830 patients, the ALND group 320. In a multivariate analysis, adjusting for the number of foci, tumor location in the breast, tumor size, LVI, ER, PR, tumor grade and histological subtype, the probability of finding positive lymph nodes was higher with SLNB procedure than with an ALND. However, this difference was not statistically significant (OR 0.7635; CI 0.5334-1.0930, p 0.1404).
For comparable tumors, SLNB procedure is at least as sensitive as ALND for detecting positive lymph nodes.
The axillary lymph node status is the most important prognostic factor in patients with early breast cancer. It is determined by patient and tumor characteristics.
To determine the axillary lymph node status, axillary lymph node dissection (ALND) has been the standard of care in patients with invasive breast cancer in order to provide correct staging of the patient and to obtain good local control. In recent years, however, sentinel lymph node (SLN) biopsy has emerged as an alternative to ALND and has become the standard treatment for axillary staging in most patients with clinically node-negative breast cancer on clinical examination, ultrasound and/or fine needle aspiration cytology (Lyman et al. 2005). The SLN procedure has been proven to be a feasible, accurate and suitable method for the staging of the axilla, while avoiding the morbidity of an ALND (Hack et al. 1999).
Since its routine clinical use, questions have been raised concerning the upstaging of a subset of node-negative patients, ranging from 5%-10% in most studies, and an increase in the overall percentage of node-positive patients due to a more detailed pathological examination of the sentinel lymph node (Tvedskov et al. 2011; Smeets & Christiaens 2005). On the other hand, the SLN procedure is associated with a false negative rate of ± 5% (Veronesi et al. 2006; Cserni et al. 2003) and thus understaging of these patients. Remarkably, axillary recurrence after a negative SLN biopsy is much lower than expected and similar to axillary recurrence after ALND (0-3%) (van der Ploeg et al. 2008; Veronesi et al. 2010; Fisher et al. 2002).
ALND is unlikely to have a therapeutic benefit for most patients with breast cancer. The value of ALND, especially in patients whose nodes are found to be tumor-free, is for accurate staging. An ALND carries the risk of understaging due to limited pathological examination of the lymph nodes, which could lead to inadequate treatment.
The goal of our study was to evaluate the sensitivity of the SLN procedure and the ALND for the identification of positive lymph nodes in breast cancer.
We hypothesized that the SLNB procedure would lead to at least equal detection rate of positive lymph nodes than an ALND when correction was performed for relevant predictors. The predictors considered were tumor size, age, number of foci, location of the tumor in the breast, tumor grade, lymphovascular invasion (LVI), histologic subtype, hormone receptor status and Her2.
Patients and methods
Data were obtained from retrospective review of the Multidisciplinary Breast Center (MBC) database from the University Hospitals Leuven (Leuven, Belgium). From 1 January 2007 until 31 December 2009, 1300 patients with a primary operable cT1-cT2N0 invasive breast carcinoma underwent resection of the primary tumor and axillary staging by SLNB and/or ALND. The indications for SLNB were described in institutional guidelines. In patients with a positive SLN, a completion ALND was performed. The local surgical treatment consisted of wide excision followed by radiotherapy or mastectomy with or without radiotherapy. In patients with a multifocal tumor, size and location of the largest focus were used for the analysis.
We excluded patients (i) treated for a local recurrence, (ii) with a carcinoma in situ, (iii) who received neo-adjuvant therapy and (iv) with primary metastatic disease.
We evaluated the association between each of the following variables and lymph node involvement: age at diagnosis, number of foci, histological tumor grade, tumor location, tumor size, histological subtype, lymphovascular invasion (LVI), ER, PR, HER-2 status and the procedure used for axillary staging (SLNB or ALND). Collection of the patients' data was approved by the local ethics committee (University Hospitals Leuven).
Sentinel lymph node localization
The sentinel lymph node (SLN) procedure was performed by injection of a radioactive (99mTc-labelled nanocolloid) tracer at the level of the tumor and Patent Blue® retroareolar. The SLNs were removed surgically using a hand-held gamma-ray detection probe.
Examination of the lymph nodes
SLNs were routinely examined by serial sectioning. Every 300 μm 2 coupes were stained, 1 with routine haematoxylin and eosin (H&E) and 1 stained immunohistochemically using cytokeratin. Lymph nodes in an ALND were examined by H&E staining using 3 sections per node. According to published guidelines, lymph nodes from lobular breast cancers, classified as lymph node negative on H&E, were additionally stained with epithelial markers.
Logistic regression models are used to analyze the effect of various predictors on the presence or absence of positive lymph nodes. Given that women with bilateral breast tumor appear twice in the data set, generalized estimating equations (GEE) are used to account for the association between the two responses from the same person.
First, we built univariate models for a number of predictors that were expected to be related to lymph node involvement. For binary or continuous predictors we calculated the odds ratio (OR) with its 95% confidence interval and the p-value. For categorical predictors with more than two levels we performed an overall test of difference between the various levels and, in case of significance, odds ratios for the pairwise comparisons between the levels. The presence of a non-linear relationship was evaluated for the continuous variables tumor size, age, and number of foci using restricted cubic splines. In a second stage, we built a multivariate model including both procedures (SLNB or ALND) and those predictors that were related to lymph node involvement in the univariate analysis or for which such a relationship has been suggested in the literature. The probability of finding positive lymph nodes was thus calculated in both groups correcting for known predictors of lymph node involvement. Two-tailed p-values were applied and p 0.05 was considered significant.
All analyses were performed using SAS software, version 9.2 of the SAS System for Windows. Copyright © 2002 SAS Institute Inc. SAS and all other SAS Institute Inc. product or service names are registered trademarks or trademarks of SAS Institute Inc., Cary, NC, USA.
A total of 1150 patients met eligibility criteria and formed the study group; 830 patients in the SLNB group, 320 patients in the ALND group. Patient and tumor characteristics are described in Table 1. Thirty-three per cent of patients in the ALND group were lymph node positive, 28% in the SLN procedure group. The percentage of clinically node-negative patients staged with SLN biopsy increased from 63% in 2007 to 86% in 2009. Tumors in the ALND group were larger (mean tumor size 27 mm versus 18 mm) and more frequently multifocal (23% versus 8%). The other characteristics were similar for both groups.
In univariate analysis, the risk of lymph node involvement was increased in the ALND group compared to that of the SLNB group. However, the difference was not significant (OR 1.2972; CI 0.9826-1.7125; p 0.0663). Furthermore, the risk was significantly related to the presence of LVI, increasing tumor size, multifocality, retroareolar or lateral tumor location in the breast, and positive hormone receptor status (ER;PR). There was no significant effect of age, tumor grade, histological subtype and HER-2 (Table 2).
In a multivariate analysis, adjusting for the number of foci, tumor location in the breast, tumor size, LVI, ER, PR, tumor grade and histological subtype, the probability of finding positive lymph nodes was now higher with SLNB procedure than with an ALND (Table 3). However, once more this difference was not statistically significant (OR 0.7635; CI 0.5334-1.0930, p 0.1404).
According to our data, SLNB with focused immunohistopathology appears to be at least as sensitive as ALND with routine lymph node analysis.
The univariate analysis did show a higher probability of detecting positive lymph nodes with an ALND. However, this is because the ALND group consists of larger and more multifocal tumors.
Our study has a few potential limitations. First, it is a retrospective study. Nowadays, it would be unethical to randomize patients between ALND and SLN biopsy because of the morbidity associated with an ALND.
Second, in our study the difference between both procedures in detecting positive lymph nodes was not significant. It might be that the sample size in our study was too small to detect small but clinically relevant differences.
Another flaw is that we did not differentiate between macro- and micrometastases. Several studies have demonstrated that intensified pathological examination of the SLNs mainly results in detection of more micrometastases (Tvedskov et al. 2011; van der Heiden-van der Loo et al. 2006). Patients with axillary lymph nodes containing micrometastases have a higher disease recurrence and a 10%-20% lower overall survival than patients with tumor-free axillary nodes (Colleoni et al. 2005; Truong et al. 2010). Thus, more accurate staging is important, even if the increase in positive nodal status is mainly due to micrometastases.
The strength of our study is the selection of a homogeneous group of patients: we compared both techniques in patients operated on in recent years and during the same time period. Additionally, only patients with a cT1-2 N0 tumor were included in the analysis as in the period 2007–2009 only these patients were candidates for a SLN procedure. Additionally, we corrected for all known predictors of lymph node involvement.
Other studies investigating the accuracy of both techniques in detecting positive lymph nodes found a stage migration of 4-10% after the introduction of the SLN biopsy (Vanderveen et al. 2006; Meiers et al. 2013; Maaskant et al. 2009; Feinstein 1985; Giuliano et al. 1995). Most of these studies included patients from two different time periods which might imply a shift in risk factors for having lymph node metastases over time. It thus becomes more difficult to compare different time periods (Tvedskov et al. 2011; van der Heiden-van der Loo et al. 2006; Vanderveen et al. 2006; Maaskant et al. 2009). The only study comparing both techniques in patients operated on during the same time period was published by Giulianio in 1995. They concluded that the SLNB increases the accuracy of axillary staging in breast cancer and can identify significantly more patients with lymph node metastases than ALND (Giuliano et al. 1995).
In addition to the main findings, we showed that positive nodal status was mainly related to the presence of LVI, increasing tumor size and multifocality, which is in accordance to the literature (Patani et al. 2007; Viale et al. 2005; Chua et al. 2001). Moreover, we showed that negative nodal status was significantly related to medial localization of the tumor in the breast. The small number of published studies that evaluated the predictive value of tumor location in the process of lymph node involvement showed similar findings to our study (Lohrisch et al. 2000; Bevilacqua et al. 2002).
Reports on the correlation between the hormone receptor status and the presence of lymph node metastases are controversial (Viale et al. 2005; Bevilacqua et al. 2002). According to our data, patients with hormone receptor positive tumors have a higher incidence of lymph node involvement in univariate analysis but not in multivariate analysis.
The results of our study are reassuring. There is a tendency to extend the indications for SLNB to the majority of patients with clinically node-negative axilla. Based on our results, a SLN biopsy provides correct staging while avoiding the morbidity of an ALND. In spite of this, there are still surgeons with a sceptic attitude to SLNB procedure. Hopefully, our data can help to persuade them to routinely implement the SLN biopsy in the surgical treatment of patients with breast cancer.
For comparable tumors, SLNB procedure is at least as sensitive as ALND for detecting positive lymph nodes.
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The authors declare that they have no competing interests.
Concept, design and manuscript writing: AS. Collection and assembly of data: EY, AR, JS. Data analysis and interpretation: AL. Final approval of manuscript: HW, RP, CVO, GF, PN, MRC. All authors read and approved the final manuscript.
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Smeets, A., Yoshihara, E., Laenen, A. et al. Is the sentinel lymph node biopsy more sensitive for the identification of positive lymph nodes in breast cancer than the axillary lymph node dissection?. SpringerPlus 2, 275 (2013). https://doi.org/10.1186/2193-1801-2-275
- Sentinel lymph node biopsy
- Axillary lymph node dissection
- Breast cancer
- Lymph nodes