Pathology Research InternationalVolume 2011 (2011), Article ID 504940, 7 pagesdoi:10.4061/2011/504940

Review Article

Issues Related to Sentinel Lymph Node Assessment in the Management of Breast Cancer—What Are Relevant in Pathology Reports?

Patricia Tai,¹ Kurian J. Joseph,² and Edward Yu³

¹Department of Radiation Oncology, Allan Blair Cancer Center, SK, Canada S4T 7T1²Department of Oncology, Cross Cancer Center, AB, Canada T6G 1Z2³Radiation Oncology Division, London Regional Cancer Program, ON, Canada N5A 4L6

Received 12 September 2010; Accepted 19 January 2011

Academic Editor: Sunati Sahoo

Copyright © 2011 Patricia Tai et al. Patricia Tai et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Most cancer centers now perform sentinel node (SN) biopsies. The limited number of SNs sampled compared with an axillary dissection has allowed more comprehensive lymph node analysis resulting in increased detection of micrometastases. Many node-negative cases are now reclassified as micrometastatic. Recent research on SN biopsy focuses on whether axillary dissection is always necessary when the SN is positive. Some subgroups of patients have a higher risk of more nodal metastases when completion axillary dissections were performed. This paper summarizes the different studies and examines what are the clinically relevant items to report on SN node pathology: volume or size of nodal metastasis, location within the node, extranodal extension, number of involved SN(s) and non-SN(s), total number of SN, and total number of nodes on axillary dissection, if performed.

1. Introduction

Breast cancer is estimated to have an incidence of 22,700 and will cause 5400 cancer deaths among females in Canada in 2009 as per Canadian Cancer Society Statistics [1]. Better prognostic factors to aid oncologists in making treatment decision will benefit a significant number of patients. The nodal staging of breast cancer generally involved a level I and II axillary dissection. To reduce the risk of surgical complications, sentinel node (SN) biopsy has been widely used in the last decade.

Nodal ratio (absolute number of involved nodes/number of nodes resected) was recently proposed to have a greater prognostic value than absolute number of involved nodes [2–7]. Since the paper by Woodward et al. [8] from the International Nodal Ratio (NR) Working Group, there are a few more studies confirming this [9]. In a recent study, relapse free and overall survival rates were not different according to the absolute number of involved nodes (, , resp.) [10], but on multivariate analysis, the NR was an independent prognostic factor for relapse free and overall survival (Hazard ratio, HR = 4.246, ; HR = 7.764, ), respectively.

Different dividing lines for NR have been used in the literature. Our previous work showed a survival benefit for regional nodal radiotherapy (RT) when the NR of axillary nodes is 0.25 or more [11]. In this study, patients were categorized into three NR groups; low (LNR, ≤25%), medium (MNR, >25% to ≤75%) and high (HNR, >75%) nodal involvement. This categorization follows previous literature using British Columbia data [2] and American data [8, 12]. Truong et al. found that 25% is a good dividing line for grouping [2].

With sentinel node (SN) mapping technique, the minimum number of nodes required for accurate staging becomes less. This is because SN biopsy technique uses radio-isotope and dye to guide the search for first drainage node(s) accurately. SN biopsy correctly identifies the involved node which could be missed by axillary node dissection without any guidance [13]. Analysis of frozen section of SNs is an accurate method for metastasis detection, allowing axillary dissection when positive at the same operative setting [14].

Controversies of sentinel node assessment abound. This paper aims to summarize and analyze the current management of breast cancer following SN biopsy. Recommendations to target readers (clinical oncologists and pathologists) are suggested.

2. Material and Methods

A search of PubMed and the proceedings of the American Society for Therapeutic Radiology and Oncology (ASTRO) and American Society of Clinical Oncology (ASCO) annual meeting books was performed and selected relevant articles and abstracts pertinent to SN assessment and prognostic relevance.

3. Results and Discussion

The limited number of SNs compared with an axillary dissection has allowed more comprehensive lymph node analysis resulting in increased detection of micrometastases. Many women previously classified as node-negative are now reclassified as having micrometastatic nodal involvement. As a result, our nodal classification and cancer staging have evolved to recognize the continuum of nodal tumor burden rather than a simplistic dichotomous stratification [15]. The pathologist is expected to mount, stain, and microscopically examine serial sections of the SN using hematoxylin and eosin (H&E) staining. Despite recommendations from the College of American Pathologists and the American Society of Clinical Oncology, heterogeneity in the approach to SN evaluation exists. What is needed is adherence to a standardized evaluation protocol. The most important aspect of the SN examination is careful attention to slicing the SN with thickness no more than 2.0 mm and correct embedding of the slices to assure all macrometastases larger than 2.0 mm are identified.

3.1. Is Minimal Lymph Node Involvement Clinically Relevant?

There is an ongoing debate concerning the clinical implications of micrometastases in the SN. Many observational studies have been published but results do not justify conclusions. Bulte et al. [18] of Netherlands looked at the subgroup of patients with micrometastases () :  3 (7.9%) patients developed distant recurrence. In the group with a tumour-free sentinel node (), 17 (3.4%) distant recurrence and 3 (0.6%) combined regional and distant recurrence were observed. The rates of distant recurrence between the node-negative and micrometastatic cases are not significantly different (Chi-square test, ). However, the authors reported that the result may be limited by small sample size. Despite the lack of statistical significance of outcome of pN1mi in reference 18, to an individual patient the worse outcome is still clinically important.

Indeed other studies show that the prognosis of patients with pN1mi is significantly worse compared to node-negative patients, in terms of regional and distant recurrence rates [19]. The worse prognosis was further confirmed by a large SEER database study [20]: breast cancer specific survival (BCSS) and overall survival with pNmi disease progressively declined with increasing number of positive nodes and increasing NR.

In the MIRROR (Micrometastases and ITCs: Relevant and Robust or Rubbish?) study, almost all participating pathology laboratories used a protocol in which the SN was serially sectioned at least every 150 μm and at a minimum of three levels, with the use of keratin immunohistochemical (IHC) staining if the H&E staining was negative. In contrast, the nonSNs were macroscopically sectioned every 2 to 5 mm, and one section per slice was stained with H&E. The aim was to evaluate the relationship, if any, between ITCs or micrometastases in the regional lymph nodes and clinical outcome in patients who had undergone an SN procedure and who did or did not receive systemic adjuvant therapy. They found that adjuvant treatment helped to lower the risk of disease events [21]. The median followup was 5.1 years. This agrees with large studies that included women who received a diagnosis before the SN era; micrometastases, defined as 2 mm or smaller in diameter and including ITCs, were associated with reduced overall survival [22–25]. In these studies, however, the axillary nodes were examined by means of H&E staining at just one level. Thus, we cannot compare these studies with the MIRROR study, which involved a detailed examination of the SN. The few previous studies of SNs were limited by small samples, lack of multivariate analyses, or short followup [26–28].

It is noteworthy that for patients with minimal nodal involvement, the disease-free survival (DFS) was initially similar but started to fall after the third year compared to node-negative results [29]. Patients with pN1a and pN1mi/pN0i+, when compared with patients with pN0 disease, were more often prescribed anthracycline-containing chemotherapy (39.1% versus 33.2% versus 6.1%, resp., ) and were less likely to receive endocrine therapy alone (9.8% versus 19.4% versus 41.9%, resp., ). On multivariate analysis, a statistically significant difference in DFS and in the risk of distant metastases was observed for patients with pN1a versus pN0 disease (HR = 2.04; 95% CI, 1.46 to 2.86; for DFS; HR = 2.32; 95% CI, 1.42 to 3.80; for distant metastases) and for patients with pN1mi/pN0i+ versus pN0 disease (HR = 1.58; 95% CI, 1.01 to 2.47; for DFS; HR = 1.94; 95% CI, 1.04 to 3.64; for distant metastases).

In summary, Table 2 shows that pN1mi patients consistently have an HR for events of 1.5 versus node-negative patients. Hence despite smaller studies with shorter followup showing no significant difference in outcome [18, 30], with the best available evidence at the present time, the authors of this paper felt that pN1mi patients tend to have worse outcome than node-negative patients.

Table 1: Definition of minimal pathologic lymph node involvement in American Joint Committee on Cancer (AJCC) Staging Manual, seventh edition (2010) [16, 17].

pN0(i−)
No regional lymph node metastases histologically, negative immunohistochemistry (IHC)

pN0(i+)
Malignant cells in regional lymph node(s) no greater than 0.2 mm (detected by H&E or IHC including isolated tumor cell clusters (ITC))

pN0(mol−)
No regional lymph node metastases histologically, negative molecular findings (RT-PCR, reverse transcriptase/polymerase chain reaction)

pN0(mol+)
Positive molecular findings (RT-PCR), but no regional lymph node metastases detected by histology or IHC

pN1
Micrometastases; or metastases in 1–3 axillary lymph nodes; and/or in internal mammary nodes with metastases detected by sentinel lymph node biopsy but not clinically detected

pN1mi
Micrometastases (greater than 0.2 mm and/or more than 200 cells, but none greater than 2.0 mm)

Table 2: Important studies on micrometastatic nodes in breast cancer.

Author
Study
Median FU
Patient number
Conclusion

Bulte et al. [18]
7 hospitals in Netherlands
3.8 years
503 pN0 38 pNmi
Local relapse—5(1.0%) versus 1(2.6%)Regional relapse—0% versus 0%Distant relapse—17(3.4%) versus 3(7.9%)Combined locoregional relapse—1(0.2%) versus 0%Combined regional and distant relapse—3(0.6%) versus 0% (n.s., see text for details)

Hainsworth et al. [19]
St Vincent's Hospital, Australia
6.6 years
31/343 occult node metastases found on IHC, plus 10 found on H&E
Among the 31 patients, presence of occult metastases in 2 or more nodes was associated with decreased DFS and OS ()

Truong et al. [20]
Surveillance Epidemiology and End Results database
7.3 years
62,551 pT1–2pN0-: 57,980 pN0, 1818 pNmi, 2753 pNmac >2 mm but <2 cm
10-year BCSS (82.3% versus 91.9%) and OS (68.1% versus 75.7%) in pNmi compared to pN0. (s.s.)

Colleoni et al. [29]
Italian medical oncology department
4.2 years
1959 pT1-3, pN0, pN1mi or pN0i+), or pN1a (single positive node) and M0
pN1mi/pN0i+ versus pN0 disease: HR = 1.58; 95% CI, 1.01 to 2.47; for DFS; HR = 1.94; 95% CI, 1.04 to 3.64; for distant metastases.

de Boer et al. [21]
Dutch cohort study of all centers in Netherlands (MIRROR study)
5.1 years
(a) 856 Nmi/ITC without adjuvant therapy, (b) 995 Nmi/ITC with adjuvant therapy, (c) 856 node-negative
Disease events: (a) for Nmi: HR 1.56 (95% CI:1.15-2.13; for ITC:HR 1.50 (95% CI:1.15-1.94) (b) HR 0.57 (95% CI:0.45-0.73)

Houvenaeghel et al. [33]
A French center
—
SN involvement in 388 times (55.4%) by H&E, 312 times by IHC
May omit additional ALND for pT1a and pT1b tumors, and pT1a-c tumors corresponding to tubular, colloidal or medullary cancers

ALND: axilllary lymph node dissection; DFS: disease-free survival; FU: followup; n.s.: statistically nonsignificant; OS: overall survival; SNB: sentinel node biopsy; s.s.: statistically nonsignificant.

Table 3: Summary of results of American College of Surgeons Oncology Group (ACOSOG) Z0011 study.

ALND
SN biopsy
values

5-year in-breast recurrence
3.7%
2.1%
.16

5-year nodal recurrence
0.6%
13%
.44

5-year overall survival
91.9%
92.5%
.24

5-year disease-free survival
82.2%
83.8%
.13

In our institute, medical oncologists tend to treat patients with micrometastases (0.2–2 mm node) with adjuvant systemic treatment, while the treatment for nodal metastases <0.2 mm is still debatable. For patients with nodal metastasis ≤2 mm including ITC, the use of nodal radiotherapy is controversial. A muticenters trial for these patients with enough followup duration, and to stratify tumor size, grade and nodal ratio may provide further insight to the role of nodal radiotherapy.

3.2. Completion Axillary Dissection after a Positive SN Biopsy

Another area of recent research on SN biopsy focuses on whether axillary lymph node dissection (ALND) is always necessary when the SN is positive [31]—what is the probability of further nodal metastases in the axilla? Here we examine the available research studies on this issue.

A study of 159 stage T1 or T2 breast cancer patients speculated that axillary dissection can be avoided in those patients diagnosed of micrometastasis in the SN [32]. Completion ALND was performed when micro or macrometastases were found in the SN. A total of 40 patients (25%) showed infiltration of the SN. This infiltration was only by micrometastasis in 17 of them (10.7%). Of these 17 patients, only 2 (11.8%) showed macrometastasis in the lymphadenectomy specimens.

3.2.1. Which Patients Can Be Safely Selected to Forgo Completion ALND?

Table 2 shows that if micrometastasis is found in a SN, omission of additional ALND may be envisaged by Houvenaeghel et al. with minimal risk for pT1a and pT1b tumors, and pT1a-b-c tumors corresponding to tubular, colloidal, or medullary cancers [33].

A study from São Paulo of 1,000 successive patients with SN biopsy from 1998 to 2008 put this issue into context [34]. The mean age was 57.6 years and mean tumor size was 1.85 cm. A total of 72.2% SN were negative and 27.8% were positive, but in 61.9% of the cases, the SN was the only positive one, with 78.4% having macrometastases, 17.3% micrometastases and 4.3% ITCs. After 54 months of followup, there were no recurrences in patients with ITCs, but one local recurrence and two systemic recurrences were observed in the micrometastases group, as well as four local and 30 distant metastases in the macrometastases group. Among the clinical parameters studied, only tumor size was correlated with metastatic involvement in axillary lymph nodes. The size of the metastases and the number of positive SN also directly increased the possibility of systemic recurrence.

Volume of disease in the SN is a significant predictor of additional nodal metastasis. In a Memorial Sloan-Kettering Cancer Center study of 505 patients, 251 pN0(i+) and 254 pN1mi: 12% of pN0(i+) and 20% pN1mi had additional nonSN disease [35]. On multivariate analyses including eight variables, only lymphovascular invasion (odds ratio > 2.2, ) and volume of nodal metastasis as assessed by any method of measurement (method of detection, AJCC, and cell count) were significantly correlated with additional nonSN disease (,  and , resp.).

More pathologic risk factors were investigated in another study of 128 patients who had a positive SN biopsy in 2005–2007 [36]. The metastases in each SN were assessed according to their location within the node (subcapsular, mixed subcapsular and parenchymal, parenchymal, multifocal or extensive) and metastatic infiltration of perinodal tissue was also reported. The strong predictors of the axillary lymph node metastasis included the SN metastasis diameter (7.6 versus 4.4 mm) and size classified according to WHO classification (ITC 0 versus 100%, micrometastasis 23.5 versus 76.5%, macrometastasis 51.9 versus 48.1%). The SN metastases with a diameter of above 3 mm were associated with approximately twice more frequent ALN metastases. If there is extensive SN metastasis, the highest percentage of ALN metastases was found (65 versus 35%). The weak predictors of ALN metastases were: primary tumor diameter (>2 cm), immunohistochemical HER2 positive status, infiltration of sentinel perinodal tissue by metastasis, histological primary tumour grade.

Two other important concepts to select patients for completion ALND to mention are nomograms and nodal ratio. Nomograms or other scoring systems have been used to predict the chance of involvement of nonSNs after a single involved SN is found [37, 38]. The nodal ratio concept has been extended to SN biopsy. More than one positive SN and a ratio of positive SN(s) to total SN(s) of greater than 0.5 were found to be predictors for additional axillary nodal involvement in both univariate and multivariate analyses [39]. The number of positive SNs and the SN nodal ratio is an indication of total tumor burden in the SNs and may be a reflection of the propensity of the tumor for further lymphatic invasion in the axillary basin.

3.2.2. What Is the Significance of IHC Positivity in SN Which Is H&E Negative?

The surgeons at the St Vincent’s University Hospital in Dublin, Ireland performed SN mapping for breast cancer from January 1st, 2000 to December 31st, 2006 [40]. All SNs were assessed by serial H&E and IHC sections. Patients with micrometastases (0.2–2 mm) underwent completion ALND. Patients with ITC (<0.2 mm) were individually discussed and an ALND was performed selectively based on additional clinicopathological criteria and patient preference. Patients were followed for a median of 27 months (range 12–72 months). 1076 patients who underwent SN were included for analysis. The experience is unique as it demonstrates the breakdown of cases into each category: 211 (20%) had a positive SN biopsy using H&E. Forty-nine patients (5%) had a negative SN on H&E which was positive on IHC. Of these, 15 had micrometastases and underwent an ALND. Two had further axillary nodal disease. ITC were found in the remaining 34 patients. Sixteen of these patients underwent an ALND. Five of this group had further nodal disease. Therefore, micrometastases and ITCs, detected only by IHC analysis of SNs, are associated with further positive nodes in the axilla in up to 15% of patients. However, more research is needed and IHC is not yet the standard procedure in most pathology departments.

3.3. Effect on Survival of Completion ALND

Completion ALND remains the gold standard for patients with a tumor-involved SN. ALND achieves regional control, but its effect on survival remains controversial. The American College of Surgeons Oncology Group (ACOSOG) Z0011 study randomized clinically node-negative patients who underwent SN biopsy and had 1 or 2 SN with metastases detected by H&E to ALND or no further axillary surgery [41]. Ineligibility criteria were SN metastasis detected by IHC, 3 or more SN positive, third field RT for nodal RT or accelerated partial breast irradiation (APBI). Both groups have tangent breast RT plus systemic therapy (which can be hormone or chemotherapy). The 446 patients with SN biopsy alone and 445 patients with SN biopsy plus ALND were similar in prognostic factors. Median followup is 6.2 years. Table 4 summarizes the results.

Table 4: Summary of important aspects of a standard pathology report—this would enable oncologists to make individual decision on management, including completion ALND and adjuvant systemic treatment.

Primary tumor

    Multifocal or multicentric

    In-situ component

    Grade

    Necrosis

    Lymphovascular invasion

    Margin

    Histologic subtype

    Immunohistochemical HER2, ER, PR

    Involvement of nipple or skeletal muscle

    Abnormalities of surrounding breast tissue

NODE

    Volume or size of nodal metastasis

    Location within the node

    Extranodal extension

    Number of involved sentinel node

    Number of involved nonsentinel node

    Total number of sentinel node

    Total number of nodes on axillary dissection, if performed

So despite the widely held belief that ALND improves survival, no significant difference was recognized by this study of SN node-positive women. Although the study closed early because of low accrual/event rate, it is the largest phase III study of ALND for node-positive women, and it demonstrates no trend toward clinical benefit of ALND for patients with limited nodal disease and given adjuvant systemic therapy.

Based on the above evidence, the authors of this paper believe that when the estimated risk of nonSN involvement is low enough, a completion ALND is not necessary. Even if there is further involved nonSN(s), they may be treated by systemic therapy or tangent field RT which covers level I and some level II axillary nodes. The survival benefit from radiation is best explained by the prevention of an isolated loco-regional recurrence, which could serve as a source of fatal distant metastases and parallels the difference in the total incidence of distant metastases [42].

3.4. Important Aspects of a Standard Pathology Report

See Table 4.

4. Conclusion

We have summarized the studies and analyzed them as a whole to draw the following conclusions. Misleading studies due to small patient numbers and short followup have clouded the issue of poor outcome of pN1mi before. The authors of this paper felt that pN1mi patients have worse outcome than node-negative patients. Patients with micrometastases or ITC benefit from adjuvant systemic treatment as evident from de Boer et al. [21].

When the estimated risk of nonSN involvement is low enough, a completion ALND is not necessary. Even if there is further involved nonSN(s), they may be treated by systemic therapy or tangent field RT which covers level I and some level II axillary nodes. In the ACOSOG study, for clinically node-negative patients who underwent SN biopsy and had 1 or 2 SN with metastases detected by H&E, completion ALND would not affect local recurrence, OS or DFS [41]. Hence provided patients had limited nodal disease and receive adjuvant systemic treatment, completion ALND after SN biopsy is not warranted.

References

http://www.cancer.ca/.

P. T. Truong, E. Berthelet, J. Lee, H. A. Kader, and I. A. Olivotto, “The prognostic significance of the percentage of positive/dissected axillary lymph nodes in breast cancer recurrence and survival in patients with one to three positive axillary lymph nodes,” Cancer, vol. 103, no. 10, pp. 2006–2014, 2005.

M. Voordeckers, V. Vinh-Hung, J. van de Steene, J. Lamote, and G. Storme, “The lymph node ratio as prognostic factor in node-positive breast cancer,” Radiotherapy and Oncology, vol. 70, no. 3, pp. 225–230, 2004.

B. C. H. van der Wal, R. M. J. M. Butzelaar, S. van der Meij, and M. A. Boermeester, “Axillary lymph node ratio and total number of removed lymph nodes: predictors of survival in stage I and II breast cancer,” European Journal of Surgical Oncology, vol. 28, no. 5, pp. 481–489, 2002.

Y. Nieto, P. J. Cagnoni, E. J. Shpall, X. Xu, J. Murphy, J. Vredenburgh, N. J. Chao, S. I. Bearman, and R. B. Jones, “A predictive model for relapse in high-risk primary breast cancer patients treated with high-dose chemotherapy and autologous stem-cell transplant,” Clinical Cancer Research, vol. 5, no. 11, pp. 3425–3431, 1999.

L. J. Megale Costa, H. Prado Soares, H. Amaral Gaspar, L. Garcia Trujillo, P. Xavier Santi, R. Sarmento Pereira, T. L. de Santana, F. Nunes Pinto, and A. Del Giglio, “Ratio between positive lymph nodes and total dissected axillaries lymph nodes as an independent prognostic factor for disease-free survival in patients with breast cancer,” American Journal of Clinical Oncology, vol. 27, no. 3, pp. 304–306, 2004.

J. Martinez-Trufero, A. Artal-Cortes, M. Zorrilla, et al., “New distinctive features on the study of prognostic factors in patients with locally advanced breast cancer (LABC) treated with neoadjuvant chemotherapy (NAC),” Proceedings of the American Society of Clinical Oncology, vol. 20, abstract 3069, 2001.

W. A. Woodward, V. Vinh-Hung, N. T. Ueno, C. C. Yee, M. Royce, P. Tai, G. Vlastos, A. M. Wallace, G. N. Hortobagyi, and Y. Nieto, “Prognostic value of nodal ratios in node-positive breast cancer,” Journal of Clinical Oncology, vol. 24, no. 18, pp. 2910–2916, 2006.

E. Yildirim and U. Berberoglu, “Lymph node ratio is more valuable than level III involvement for prediction of outcome in node-positive breast carcinoma patients,” World Journal of Surgery, vol. 31, no. 2, pp. 276–289, 2007.

B. Keam, S. A. Im, H. J. Kim, D. Y. Oh, J. H. Kim, S. H. Lee, E. K. Chie, W. Han, D. W. Kim, N. Cho, W. K. Moon, T. Y. Kim, I. A. Park, D. Y. Noh, D. S. Heo, S. W. Ha, and Y. J. Bang, “Clinical significance of axillary nodal ratio in stage II/III breast cancer treated with neoadjuvant chemotherapy,” Breast Cancer Research and Treatment, vol. 116, no. 1, pp. 153–160, 2009.

P. Tai, K. Joseph, E. Sadikov, S. Mahmood, F. Lien, and E. Yu, “Nodal ratios in node-positive breast cancer-long-term study to clarify discrepancy of role of supraclavicular and axillary regional radiotherapy,” International Journal of Radiation Oncology Biology Physics, vol. 68, no. 3, pp. 662–666, 2007.

S. A. Joslyn and B. R. Konety, “Effect of axillary lymphadenectomy on breast carcinoma survival,” Breast Cancer Research and Treatment, vol. 91, no. 1, pp. 11–18, 2005.

K. A. Vanderveen, P. D. Schneider, V. P. Khatri, J. E. Goodnight, and R. J. Bold, “Upstaging and improved survival of early breast cancer patients after implementation of sentinel node biopsy for axillary staging,” Annals of Surgical Oncology, vol. 13, no. 11, pp. 1450–1456, 2006.

J. C. Tille, J. F. Egger, M. C. Devillaz, G. Vlastos, and M. F. Pelte, “Frozen section in axillary sentinel lymph nodes for diagnosis of breast cancer micrometastasis,” Anticancer Research, vol. 29, no. 11, pp. 4711–4716, 2009.

D. L. Weaver, “Pathology evaluation of sentinel lymph nodes in breast cancer: protocol recommendations and rationale,” Modern Pathology, vol. 23, no. 2, pp. S26–S32, 2010.

American Joint Committee on Cancer (AJCC) Cancer Staging Manual, Springer, New York, NY, USA, 7th edition, 2010.

D. F. Hayes, “Tumor node metastasis (TNM) staging classification for breast cancer,” in UpToDate, B. D. Rose, Ed., UpToDate, Waltham, Mass, USA, 2010.

C. S. E. Bulte, M. van der Heiden-van der Loo, and A. Hennipman, “Axillary recurrence rate after tumour negative and micrometastatic positive sentinel node procedures in breast cancer patients, a population based multicenter study,” European Journal of Surgical Oncology, vol. 35, no. 1, pp. 25–31, 2009.

P. J. Hainsworth, J. J. Tjandra, R. G. Stillwell, D. Machet, M. A. Henderson, G. C. Rennie, I. F. C. McKenzie, and R. C. Bennett, “Detection and significance of occult metastases in node-negative breast cancer,” British Journal of Surgery, vol. 80, no. 4, pp. 459–463, 1993.

P. T. Truong, V. Vinh-Hung, G. Cserni, W. A. Woodward, P. Tai, and G. Vlastos, “The number of positive nodes and the ratio of positive to excised nodes are significant predictors of survival in women with micrometastatic node-positive breast cancer,” European Journal of Cancer, vol. 44, no. 12, pp. 1670–1677, 2008.

M. de Boer, C. H. M. van Deurzen, J. A. A. M. van Dijck, G. F. Borm, P. J. van Diest, E. M. M. Adang, J. W. R. Nortier, E. J. T. Rutgers, C. Seynaeve, M. B. E. Menke-Pluymers, P. Bult, and V. C. G. Tjan-Heijnen, “Micrometastases or isolated tumor cells and the outcome of breast cancer,” The New England Journal of Medicine, vol. 361, no. 7, pp. 653–663, 2009.

S. L. Chen, F. M. Hoehne, and A. E. Giuliano, “The prognostic significance of micrometastases in breast cancer: a SEER population-based analysis,” Annals of Surgical Oncology, vol. 14, no. 12, pp. 3378–3384, 2007.

D. Grabau, M. B. Jensen, F. Rank, and M. Blichert-Toft, “Axillary lymph node micrometastases in invasive breast cancer: national figures on incidence and overall survival,” APMIS, vol. 115, no. 7, pp. 828–837, 2007.

G. P. Kuijt, A. C. Voogd, L. V. van de Poll-Franse, L. J. E. E. Scheijmans, M. W. P. M. van Beek, and R. M. H. Roumen, “The prognostic significance of axillary lymph-node micrometastases in breast cancer patients,” European Journal of Surgical Oncology, vol. 31, no. 5, pp. 500–505, 2005.

D. C. Maibenco, G. W. Dombi, T. Y. Kau, and R. K. Severson, “Significance of micrometastases on the survival of women with T1 breast cancer,” Cancer, vol. 107, no. 6, pp. 1234–1239, 2006.

Y. G. Fan, Y. Y. Tan, C. T. Wu, P. Treseler, Y. Lu, C. W. Chan, S. Hwang, C. Ewing, L. Esserman, E. Morita, and S. P. L. Leong, “The effect of sentinel node tumor burden on non-sentinel node status and recurrence rates in breast cancer,” Annals of Surgical Oncology, vol. 12, no. 9, pp. 705–711, 2005.

C. E. Cox, J. V. Kiluk, A. I. Riker, J. M. Cox, N. Allred, D. C. Ramos, E. L. Dupont, V. Vrcel, N. Diaz, and D. Boulware, “Significance of sentinel lymph node micrometastases in human breast cancer,” Journal of the American College of Surgeons, vol. 206, no. 2, pp. 261–268, 2008.

P. D. Gobardhan, S. G. Elias, E. V. E. Madsen, V. Bongers, H. J. M. Ruitenberg, C. I. Perre, and T. van Dalen, “Prognostic value of micrometastases in sentinel lymph nodes of patients with breast carcinoma: a cohort study,” Annals of Oncology, vol. 20, no. 1, pp. 41–48, 2009.

M. Colleoni, N. Rotmensz, G. Peruzzotti, P. Maisonneuve, G. Mazzarol, G. Pruneri, A. Luini, M. Intra, P. Veronesi, V. Galimberti, R. Torrisi, A. Cardillo, A. Goldhirsch, and G. Viale, “Size of breast cancer metastases in axillary lymph nodes: clinical relevance of minimal lymph node involvement,” Journal of Clinical Oncology, vol. 23, no. 7, pp. 1379–1389, 2005.

A. J. Maaskant-Braat, L. V. van de Poll-Franse, A. C. Voogd, et al., “SN micrometastases in breast cancer do not affect prognosis, a population-based study,” Breast Cancer Research and Treatment. In press.

L. H. Sobin and C. Wittekind, Eds., TNM Classification of Malignant Tumours, Wiley-Liss, New York, NY, USA, 6th edition, 2002.

J. M. Cordero García, M. Delgado Portela, A. M. García Vicente, J. P. Pilkington Woll, M. A. Palomar Muñoz, V. M. Poblete García, M. E. Bellón Guardia, R. Pardo García, L. Rabadán Ruiz, and A. M. Soriano Castrejón, “Micrometastasis in the sentinel node and axillary lymph node macrometastasis in breast cancer,” Revista Espanola de Medicina Nuclear, vol. 29, no. 3, pp. 122–126, 2010.

G. Houvenaeghel, C. Nos, H. Mignotte, J. M. Classe, S. Giard, P. Rouanet, F. P. Lorca, J. Jacquemier, and V. J. Bardou, “Micrometastases in sentinel lymph node in a multicentric study: predictive factors of nonsentinel lymph node involvement—Groupe des Chirurgiens de la Federation des Centres de Lutte Contre Le Cancer,” Journal of Clinical Oncology, vol. 24, no. 12, pp. 1814–1822, 2006.

E. M. Barbosa, A. A. R. F. Francisco, J. T. Araujo Neto, E. M. F. Alves, M. G. M. Tavares, and J. C. S. Góes, “Clinicopathological predictor factors of axillary involvement in patients with metastatic breast cancer in the sentinel lymph node,” Revista Brasileira de Ginecologia e Obstetricia, vol. 32, no. 3, pp. 144–149, 2010.

S. Kumar, M. Bramlage, L. M. Jacks, J. I. Goldberg, S. M. Patil, D. D. Giri, and K. J. van Zee, “Minimal disease in the sentinel lymph node: how to best measure sentinel node micrometastases to predict risk of additional non-sentinel lymph node disease,” Annals of Surgical Oncology, vol. 17, no. 11, pp. 2909–2919, 2010.

W. P. Olszewski, A. Szumera-Ciećkiewicz, J. Piechocki, E. Towpik, and W. T. Olszewski, “The characteristics of the sentinel lymph node metastasis in predicting the axillary lymph node status in patients with breast carcinoma,” Polish Journal of Pathology, vol. 60, no. 3, pp. 138–143, 2009.

K. J. van Zee, D. M. E. Manasseh, J. L. B. Bevilacqua, S. K. Boolbol, J. V. Fey, L. K. Tan, P. I. Borgen, H. S. Cody, and M. W. Kattan, “A nomogram for predicting the likelihood of additional nodal metastases in breast cancer patients with a positive sentinel node biopsy,” Annals of Surgical Oncology, vol. 10, no. 10, pp. 1140–1151, 2003.

E. Barranger, C. Coutant, A. Flahault, Y. Delpech, E. Darai, and S. Uzan, “An axilla scoring system to predict non-sentinel lymph node status in breast cancer patients with sentinel lymph node involvement,” Breast Cancer Research and Treatment, vol. 91, no. 2, pp. 113–119, 2005.

Y. Y. Tan, Y. G. Fan, Y. Lu, S. Hwang, C. Ewing, L. Esserman, E. Morita, P. Treseler, and S. P. L. Leong, “Ratio of positive to total number of sentinel nodes predicts nonsentinel node status in breast cancer patients,” Breast Journal, vol. 11, no. 4, pp. 248–253, 2005.

S. M. Giobuin, D. O. Kavanagh, E. Myers, A. O. Doherty, C. M. Quinn, T. Crotty, D. Evoy, and E. McDermott, “The significance of immunohistochemistry positivity in sentinel nodes which are negative on haematoxylin and eosin in breast cancer,” European Journal of Surgical Oncology, vol. 35, no. 12, pp. 1257–1260, 2009.

A. E. Giuliano, L. M. McCall, P. D. Beitsch, et al., “ACOSOG Z0011: a randomized trial of axillary node dissection in women with clinical T1-2 N0 M0 breast cancer who have a positive SN,” Journal of Clinical Oncology, vol. 28, p. 18s, abstract CRA506, 2010.

O. Abe, R. Abe, K. Enomoto, K. Kikuchi, H. Koyama, H. Masuda, Y. Nomura, K. Sakai, K. Sugimachi, T. Tominaga, J. Uchino, M. Yoshida, J. L. Haybittle, C. Davies, V. J. Harvey, T. M. Holdaway, R. G. Kay, B. H. Mason, J. F. Forbes, N. Wilcken, M. Gnant, R. Jakesz, M. Ploner, H. M. A. Yosef, C. Focan, J. P. Lobelle, U. Peek, G. D. Oates, J. Powell, M. Durand, L. Mauriac, A. Di Leo, S. Dolci, M. J. Piccart, M. B. Masood, D. Parker, J. J. Price, P. S.G.J. Hupperets, S. Jackson, J. Ragaz, D. Berry, G. Broadwater, C. Cirrincione, H. Muss, L. Norton, R. B. Weiss, H. T. Abu-Zahra, S. M. Portnoj, M. Baum, J. Cuzick, J. Houghton, D. Riley, R. E. Mansel, N. H. Gordon, H. L. Davis, A. Beatrice, J. Mihura, A. Naja, Y. Lehingue, P. Romestaing, J. B. Dubois, T. Delozier, J. Mace Lesec'h, P. Rambert, L. Petruzelka, O. Pribylova, J. R. Owen, N. Harbeck, F. Jänicke, C. Meisner, P. Meier, A. Howell, G. C. Ribeiro, R. Swindell, J. Burrett, M. Clarke, R. Collins, S. Darby, C. Davies, P. Elphinstone, V. Evans, J. Godwin, R. Gray, C. Harwood, C. Hicks, D. Jackson, S. James, E. MacKinnon, P. McGale, T. McHugh, G. Mead, P. Morris, J. Oulds, R. Peto, C. Taylor, Y. Wang, J. Albano, C. F. De Oliveira, H. Gervásio, J. Gordilho, H. Johansen, H. T. Mouridsen, R. S. Gelman, J. R. Harris, I. C. Henderson, C. L. Shapiro, P. Christiansen, B. Ejlertsen, H. T. Mouridsen, S. Møller, M. Overgaard, B. Carstensen, T. Palshof, H. J. Trampisch, O. Dalesio, E. G.E. de Vries, S. Rodenhuis, H. van Tinteren, R. L. Comis, N. E. Davidson, R. Gray, N. Robert, G. Sledge, D. C. Tormey, W. Wood, D. Cameron, U. Chetty, P. Forrest, W. Jack, J. Rossbach, J. G.M. Klijn, A. D. Treurniet-Donker, W. L.J. van Putten, A. Costa, U. Veronesi, H. Bartelink, L. Duchateau, C. Legrand, R. Sylvester, J. A. van der Hage, C. J.H. van de Velde, M. P. Cunningham, R. Catalano, R. H. Creech, J. Bonneterre, P. Fargeot, P. Fumoleau, P. Kerbrat, M. Namer, W. Jonat, M. Kaufmann, M. Schumacher, G. Von Minckwitz, G. Bastert, H. Rauschecker, R. Sauer, W. Sauerbrei, A. Schauer, M. Schumacher, A. de Schryver, L. Vakaet, M. Belfiglio, A. Nicolucci, F. Pellegrini, M. Sacco, M. Valentini, C. S. McArdle, D. C. Smith, E. Galligioni, F. Boccardo, A. Rubagotti, D. M. Dent, C. A. Gudgeon, A. Hacking, A. Erazo, J. Y. Medina, M. Izuo, Y. Morishita, H. Takei, I. S. Fentiman, J. L. Hayward, R. D. Rubens, D. Skilton, H. Scheurlen, M. Kaufmann, D. Von Fournier, U. Dafni, G. Fountzilas, P. Klefstrom, C. Blomqvist, T. Saarto, R. Margreiter, B. Asselain, R. J. Salmon, J. R. Vilcoq, R. Arriagada, C. Hill, A. Laplanche, M. G. Lê, M. Spielmann, P. Bruzzi, E. Montanaro, R. Rosso, M. R. Sertoli, M. Venturini, D. Amadori, J. Benraadt, M. Kooi, A. O. van de Velde, J. A. van Dongen, J. B. Vermorken, M. Castiglione, F. Cavalli, A. Coates, J. Collins, J. Forbes, R. D. Gelber, A. Goldhirsch, J. Lindtner, K. N. Price, C. M. Rudenstam, H. J. Senn, J. M. Bliss, C. E.D. Chilvers, R. C. Coombes, E. Hall, M. Marty, R. Borovik, G. Brufman, H. Hayat, E. Robinson, N. Wigler, G. Bonadonna, T. Camerini, G. de Palo, M. Del Vecchio, F. Formelli, P. Valagussa, A. Martoni, F. Pannuti, G. Cocconi, A. Colozza, R. Camisa, K. Aogi, S. Takashima, O. Abe, T. Ikeda, K. Inokuchi, K. Kikuchi, K. Sawa, H. Sonoo, S. Korzeniowski, J. Skolyszewski, M. Ogawa, J. Yamashita, J. Bonte, R. Christiaens, R. Paridaens, W. van den Bogaert, P. Martin, S. Romain, T. Hakes, C. A. Hudis, L. Norton, R. Wittes, G. Giokas, D. Kondylis, B. Lissaios, R. de La Huerta, M. G. Sainz, R. Altemus, K. Cowan, D. Danforth, A. Lichter, M. Lippman, J. O'Shaughnessy, L. J. Pierce, S. Steinberg, D. Venzon, J. A. Zujewski, A. Paradiso, M. de Lena, F. Schittulli, J. D. Myles, J. L. Pater, K. I. Pritchard, T. Whelan, Y. Nomura, S. Anderson, G. Bass, A. Brown, J. Bryant, J. Costantino, J. Dignam, B. Fisher, C. Redmond, S. Wieand, N. Wolmark, M. Baum, I. M. Jackson, M. K. Palmer, J. N. Ingle, V. J. Suman, N. O. Bengtsson, H. Jonsson, L. G. Larsson, J. P. Lythgoe, R. Swindell, M. Kissin, B. Erikstein, E. Hannisdal, A. B. Jacobsen, J. E. Varhaug, B. Erikstein, S. Gundersen, M. Hauer-Jensen, H. Høst, A. B. Jacobsen, R. Nissen-Meyer, R. W. Blamey, A. K. Mitchell, D. A. L. Morgan, J. F.R. Robertson, M. Di Palma, G. Mathé, J. L. Misset, R. M. Clark, M. Levine, K. I. Pritchard, T. Whelan, K. Morimoto, K. Sawa, Y. Takatsuka, E. Crossley, A. Harris, D. Talbot, M. Taylor, G. Cocconi, B. Di Blasio, V. Ivanov, V. Semiglazov, J. Brockschmidt, M. R. Cooper, H. Ueo, C. I. Falkson, R. A'Hern, S. Ashley, T. J. Powles, I. E. Smith, J. R. Yarnold, J. C. Gazet, N. Corcoran, N. Deshpande, L. Di Martino, P. Douglas, A. Hacking, H. Høst, A. Lindtner, G. Notter, A. J.S. Bryant, G. H. Ewing, L. A. Firth, J. L. Krushen-Kosloski, R. Nissen-Meyer, L. Foster, W. D. George, H. J. Stewart, P. Stroner, P. Malmström, T. R. Möller, S. Rydén, I. Tengrup, L. Tennvall-Nittby, J. Carstenssen, M. Dufmats, T. Hatschek, B. Nordenskjöld, M. Söderberg, J. T. Carpenter, K. Albain, J. Crowley, S. Green, S. Martino, C. K. Osborne, P. M. Ravdin, U. Glas, U. Johansson, L. E. Rutqvist, T. Singnomklao, A. Wallgren, M. Castiglione, A. Goldhirsch, R. Maibach, H. J. Senn, B. Thürlimann, H. Brenner, A. Hercbergs, M. Yoshimoto, G. DeBoer, A. H.G. Paterson, K. I. Pritchard, J. W. Meakin, T. Panzarella, K. I. Pritchard, Y. Shan, Y. F. Shao, X. Wang, D. B. Zhao, Z. M. Chen, H. C. Pan, J. Bahi, M. Reid, M. Spittle, G. P. Deutsch, F. Senanayake, D. L.W. Kwong, A. R. Bianco, C. Carlomagno, M. de Laurentiis, S. de Placido, A. U. Buzdar, T. Smith, J. Bergh, L. Holmberg, G. Liljegren, J. Nilsson, M. Seifert, P. Sevelda, C. C. Zielinsky, R. B. Buchanan, M. Cross, G. T. Royle, J. A. Dunn, R. K. Hills, M. Lee, J. M. Morrison, D. Spooner, A. Litton, R. T. Chlebowski, and H. Caffier, “Effects of radiotherapy and of differences in the extent of surgery for early breast cancer on local recurrence and 15-year survival: an overview of the randomised trials,” The Lancet, vol. 366, no. 9503, pp. 2087–2106, 2005.