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Early Results of Omitting Completion Axillary Lymph Node Dissection in Sentinel Lymph Node Metastas

Advances in Breast Cancer Research
 Vol.2No.4(2013), Article ID:36730,7 pages DOI:10.4236/abcr.2013.24021

Junko Honda1, Hisashi Matsuoka1, Chieko Hirose1, Taeko Nagao2, Takahiro Yoshida2, Masako Takahashi3, Issei Imoto4, Mitsunori Sasa3*

1Department of Surgery, National Hospital Organization Higashitokushima Medical Center, Tokushima, Japan

2Department of Oncological and Regenerative Surgery, Institute of Health Biosciences, The University of Tokushima Graduate Scholl, Tokushima, Japan

3Department of Surgery, Tokushima Breast Care Clinic, Tokushima, Japan

4Department of Human Genetics, Institute of Health Biosciences, The University of Tokushima Graduate School, Tokushima, Japan

Email: *breast@mb.tcn.ne.jp

Copyright © 2013 Junko Honda 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.

Received July 21, 2013; revised August 20, 2013; accepted August 28, 2013

Keywords: Axillary Lymph Node Dissection; Breast Cancer; Sentinel Node Biopsy

ABSTRACT

Background: We investigated the early results of omitting completion axillary lymph node dissection (ALND) for axillary node metastasis-negative (N0), sentinel node (SN) metastasis-positive breast cancer patients. Patients and Methods: 489 patients had invasive N0 breast cancer treated without completion ALND, regardless of their SN metastasis status. Analyses included the associations between the SN metastasis status, clinicopathological findings and recurrence, between recurrence and clinicopathological findings, and recurrence-free survival. Results: 430 patients were SN biopsy (SNB)-negative, and 59 were SNB-positive. The SNB-positive patients received significantly more potent adjuvant therapy than the SNB-negative patients. Median follow-up was 3.7 years, and the axillary node recurrence was seen in 6 patients (1.2%) and recurrence in 21 patients. The SN status showed no associations with the clinicopathological findings or recurrence. Univariate analysis showed recurrence was associated with absence of hormonal therapy, ER-negative, PgR-negative, HER2-positive or triple-negative (TNBC) disease, a tumor ≥2.1 cm and higher nuclear grade. Multivariate analysis showed recurrence was associated with absence of hormonal therapy and a tumor ≥2.1 cm. Cox proportional hazards model showed recurrence was extremely early in ER-negative and TNBC patients. Conclusion: Completion ALND can be skipped in N0 breast cancer patients even if they are SNB-positive, but adjuvant therapy is essential.

1. Introduction

Sentinel lymph node biopsy (SNB) has been used as a standard procedure for the management of early breast cancer patients who have no clinical axillary lymph node metastasis (N0) [1,2]. If the SN is negative, axillary dissection (ALND) can be omitted, but if the SN is positive for metastasis, completion ALND is generally warranted [3]. However, after release of the results of the American College of Surgeon’s Oncology Group (ACOSOG) Z0011 randomized clinical trial [4], the National Comprehensive Cancer Network’s (NCCN) Practice Guidelines issued in 2012 recommended avoidance of completion ALND as an option in selected SNB-positive cases [5].

Since March 2003, which predates that NCCN recommendation, we have been omitting the completion ALND in N0 patients even if they are SNB-positive. The scientific basis for that policy is as follows: 1) First, in the case of axillary node micrometastasis, it was reported that the incidence of axillary recurrence is low even when completion ALND is not performed, and the survival results do not differ between the dissected and non-dissected patient groups [6-8], and 2) then, even in the case of overt axillary metastasis, it was shown that rescue surgery was feasible and there was no effect on survival [6-8]. Therefore, since 2003 we obtain written informed consent and then skip ALND in selected SNB-positive cases. To date, the median follow-up period for our patients has been over 3.7 years, and we think that our data are of value for assessing lymph node recurrence. Accordingly, we report here the results of our comparative analysis of SNB-positive patients who did not undergo completion ALND and SNB-negative patients. We compared the two patient groups in regard to the clinicopathological findings and recurrence, tested for associations between recurrence and the clinicopathological findings, and also analyzed the recurrence-free survival.

2. Patients and Methods

We identified the SN using CT-lymphography (CTLG) combined with dye-staining [9,10] because our institution is not equipped with RI facilities. Clinicopathological studies to determine the metastatic status of SNs were performed on 2-mm sections of hematoxylin-eosin (HE)- stained surgical permanent specimens. SNB-positive cases were treated by one of two methods chosen in accordance with each patient’s expressed desire after written informed consent had been obtained. That is, when the SNB was positive for metastasis following the surgery, the patient was allowed to choose one of two treatment options: 1) performance of completion ALND, followed by performance of adjuvant therapy, or 2) performance of appropriate adjuvant therapy, including axillary radiation therapy, with repeat performance of dissection at the time of any overt recurrence. For patients whose SNB was negative for metastasis, adjuvant therapy was decided on the basis of the subtype classification of the primary lesion. This study was carried out after its design had been approved by the Ethics Committee of National Hospital Organization Higashi-Tokushima Medical Center.

From March 2003 through September 2012, our hospital treated 663 primary breast cancer patients by performing axillary surgery that was limited to SNB. This study enrolled 489 of those patients who had invasive ductal carcinoma, while 46 patients who had undergone preoperative chemotherapy, 102 patients with ductal carcinoma in situ and 26 patients with a special pathological subtype of disease were excluded.

Recurrent breast cancer can have various presentations: axillary lymph node recurrence, recurrence in other lymph nodes (i.e., the ipsilateral supraclavicular, subclavicular and internal mammary nodes), distant recurrence, recurrence in the ipsilateral breast and recurrence in the contralateral breast. For this study, contralateral breast cancer recurrence was considered to be development of a new lesion and thus excluded from the category of “recurrence”.

The clinicopathological findings were analyzed for associations with the SNB status, i.e., positive or negative for metastasis. Recurrence was also analyzed for association with the status of SN metastasis. Moreover, for all recurrent events (excluding contralateral breast cancer recurrence), the status of recurrence and the clinicopathological findings were analyzed for associations and recurrence-free survival was also analyzed.

For statistical analyses of the data, Fisher’s exact test was used to analyze for associations between the status of SN metastasis (positive vs. negative) and the clinicopathological findings, including recurrence. Clinicopathological characteristics that showed possible association with recurrence in univariate analysis, were analyzed by multivariate analysis using logistic regression analysis. Recurrence-free survival was analyzed using the Cox proportional hazards model, taking into account several covariates. Statistical tests provided two-sided p values, and a significance level of p < 0.05 was used. Statistical analyses were carried out using the R statistical environment version 2.13.0 (http://www.r-project.org/).

3. Results

3.1. Demographic Data for the 489 Enrolled Patients and Comparison of Pathological Findings in SNB-Negative Patients and SNB-Positive Patients

The age range was 29 - 85 years (median: 55 y), with 33% being ≤49 yo and 67% being ≥50 yo. The number of biopsied lymph nodes per patient was 1 - 3, with a mean of 1.7. Receptor analyses indicated that the rates of ERpositive, PgR-positive, HER2-positive and triple-negative (TNBC) patients were 80%, 70%, 6% and 11%, respectively. The tumor size was ≤2 cm in 86% of the patients, while 62% were nuclear grade 1. The surgical procedure was breast-conserving therapy in 91% of the patients. SNB-negative patients numbered 430 (87.9%), while 59 patients (12.1%) were SNB-positive. Table 1 shows that comparative analysis of the clinicopathological characteristics as a function of the SNB-negative/-positive status found no statistically significant differences.

3.2. Comparison of Adjuvant Therapy in SNB-Negative and SNB-Positive Patients

Table 2 shows the results of comparison of the types of adjuvant therapy administered to the SNB-negative and SNB-positive patients. Axillary radiation was administered to 18 of the 59 SNB-positive patients, but to none of the 430 SNB-negative patients. Chemotherapy was administered to 34 of the 59 SNB-positive patients and to 38 of the 430 SNB-negative patients. Finally, hormonal therapy was administered to a majority of the patients, regardless of the status of SN metastasis. It is thus clear that the SNB-positive patients received more potent adjuvant therapies, i.e., axillary radiation and chemotherapy, compared with the SNB-negative patients.

3.3. Events of Recurrence

Table 3 compiles the data on the events of recurrence (some overlapping exists). The median follow-up period was 3.7 years, and recurrence was documented in 21 patients. The types of recurrence were distant metastatic events in 10 patients (2.0%), axillary node recurrence in 6 patients (1.2%), recurrence in other nodes in 3 patients (0.6%) and recurrence in the ipsilateral breast in 7 patients (1.4%). No recurrence was seen in 468 patients.

Table 1. Comparison of clinicopathological findings in SNB-negative patients and SNB-positive patients (excluding data for unknown cases).

*Score of 3+ in immunohistochemistry or fluorescence in situ hybridization-positive. ER: estrogen receptor; PgR: progesterone receptor; HER2: human epidermal growth factor receptor 2; NS: not significant.

However, after exclusion of 17 patients with contralateral breast events, 451 patients were considered to have had no events of recurrence and were used for the subsequent analyses.

3.4. Comparison of Events of Recurrence in SNB-Negative and SNB-Positive Patients

Table 4 shows the comparison of the recurrences in the SNB-negative and SNB-positive patients. No statistically

Table 2. Comparison of adjuvant therapy SNB-negative patients and SNB-positive patients.

NS: not significant.

Table 3. Events of recurrence (includes some overlapping).

*Other nodes include ipsilateral supraclavicular, subclavicular and internal mammary nodes.

Table 4. Comparison of events of recurrence in SNB-negative and SNB-positive patients.

NS: not significant.

significant associations were found between any of the types of recurrences and the status of SN metastasis.

3.5. Clinical and Pathological Findings as a Function of the Recurrence Status

Table 5 shows the associations between the status of recurrences and the clinicopathological findings evaluated by univariate analysis using Fisher’s exact test and by multivariate analysis using logistic regression analysis. The univariate analysis found statistically significant associations between recurrence and each of the following clinicopathological findings: no hormonal therapyER-negative, PgR-negative, HER2-positive, TNBC, a tumor size of ≥2.1 cm and a higher nuclear grade. The multivariate analysis found that recurrence was significantly more frequent in patients who had not undergone hormonal therapy or had a tumor size of ≥2.1 cm.

3.6. Multivariate Analysis of All Recurrence-Free Survival

Table 6 shows the results of multivariate analysis performed using the Cox proportional hazards model to examine for associations between the recurrence-free survival and the clinicopathological findings. The results

Table 5. Clinicopathological findings as a function of the recurrence status (excluding data for unknown cases).

*Recurrence includes locoregional events and distant metastasis events. **Score of 3+ in immunohistochemistry or fluorescence in situ hybridization positive. ER: estrogen receptor; PgR: progesterone receptor; HER2: human epidermal growth factor receptor 2; NS: not significant.

Table 6. Multivariate analysis of all recurrence-free survival.

*Score of 3+ in immunohistochemistry or fluorescence in situ hybridization positive. ER: estrogen receptor; PgR: progesterone receptor; HER2: human epidermal growth factor receptor 2.

showed that recurrence took place significantly early in patients who had not undergone hormonal therapy, were ER-negative, HER2-positive or TNBC, or had a tumor size of ≥2.1 cm. In particular, recurrence was extremely early in ER-negative (odds ratio of 58.82) and TNBC (odds ratio of 46.12) patients.

4. Discussion

A randomized clinical trial was started in 2001 with the aim of demonstrating the non‑inferiority of non-performance of completion ALND in breast cancer patients with an SN positive for metastasis (IBCSG Trial 23-01) [11]. No significant differences were found in terms of the axillary recurrence rate, recurrence-free survival rate or overall survival rate. The Z0011 randomized trial also reported the appropriateness of avoidance of completion ALND even in T1-2 N0 patients who were SNB-positive [4]. The cohort research report released by the U.S.A. National Cancer Data Base also found that although ALND was skipped for about 20% of SNB-positive cases in actual clinical settings, the 5-year axillary recurrence rate was only 1% [12]. Reflecting those findings, the NCCN Practice Guidelines issued in 2012 states that avoidance of completion ALND is an option for SNBpositive breast cancer patients who satisfy the criteria set forth in the Z0011 study [5].

Since 2003, with approval from our Ethics Committee, we have been obtaining written informed consent and then omitting ALND in N0 patients even if they are SNB-positive. The median follow-up period for our patients has reached 3.7 years. Since it was reported that most events of axillary recurrence in N0 patients without completion ALND occur within 3 years after surgery [6,13], we felt that our present data were at least good for the relationship between that therapeutic approach and disease recurrence. Our analysis of those data showed a 1.2% incidence rate for axillary recurrence in N0 breast cancer patients who underwent only SNB. That recurrence rate is comparable to the rates reported by others [12,14-16], and we think that it sufficiently guarantees safety in regard to axillary recurrence. In addition, we found no statistically significant differences between the status of SN metastasis and the site of recurrence, although the axillary recurrence rate was slightly higher in patients who had been SNB-positive. All other sites showed no difference. Our present results provide further evidence of the reliability of the Z0011 study results [4] and the NCCN Practice Guidelines recommendation [5]. Taking into consideration the facts that rescue surgery can still be carried out in the case of axillary recurrence and that suitable adjuvant therapy is administered to N0 patients even if they are SNB-positive, we think that it is possible to omit completion ALND in these patients.

Next, we analyzed for associations between recurrence and the patients’ background factors. Most of the patients in our present series received adjuvant therapies based on their disease subtype. In addition, with a median follow-up of only 3.7 years, this study can be considered short-term. Our univariate analysis found that, with regard to adjuvant treatment, recurrence was significantly more frequent in patients who had not undergone hormonal therapy. This finding seems to mean that patients who did not receive hormonal therapy were negative for both ER and PgR. With regard to the malignancy of breast cancer, our results showed significantly higher incidences of recurrence in patients who were ER-negative, PgR-negative, HER2-positive or TNBC, or had a larger tumor size or a higher nuclear grade. In addition, our multivariate analysis found that recurrence was significantly more frequent in patients who had not undergone hormonal therapy or had a larger tumor size. That is, when adjuvant therapy was administered to N0 patients in consideration of their disease subtype, negative status for both ER and PgR and the larger tumor size can be considered independent poorer predictors of recurrence in the early postoperative stage. There is a possibility that the tumor size became an independent predictor of recurrence, exactly because it had not been taken into account when deciding the adjuvant therapy for our patients. Moreover, it is possible that the cohort negative for both ER and PgR (which includes TNBC) includes a population whose disease has an especially high degree of malignancy. Our data also indicates that recurrence occurs very early in ER-negative and TNBC patients. It has been proposed that various types are included in TNBC [17], and it will be necessary to identify the highly-malignant subtypes having various surrogate markers and establish appropriate therapeutic approaches for them.

We selected chemotherapy plus hormonal therapy for SNB-positive patients even when they had the luminal A subtype. At present, it is thought that chemotherapy is not necessary for the luminal A subtype if the number of metastatic lymph nodes is small [18]. Accordingly, it is possible that we administered unnecessary chemotherapy for our SNB-positive patient group. This warrants further investigation in the future.

The small number of analyzed cases and the rather short duration of follow-up are other limitations of this study. Also, this study analyzed the clinicopathological characteristics of invasive N0 breast cancer patients for association with recurrence, but did not analyze with regard to survival. In the future, we are willing to perform further analyses, including of the relationship between omitting completion ALND and the survival results, in a larger number of patients over a longer follow-up period.

5. Conclusion

This study found that completion ALND could be omitted for N0 breast cancer patients even if they were SNB-positive, and provided that appropriate adjuvant therapy was administered. Also, when suitable adjuvant therapy was administered to N0 patients, even during the course of short-term observation recurrence was significantly more common in patients who were hormone recaptor-negative or had a large tumor, those results were shown to be unrelated to whether or not there had been SN metastasis.

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NOTES

*Corresponding author.

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