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Number of negative lymph nodes can predict survival of breast cancer patients with four or more positive lymph nodes after postmastectomy radiotherapy
Radiation Oncology volume 9, Article number: 284 (2014)
This study was conducted to assess the prognostic value of the number of negative lymph nodes (NLNs) in breast cancer patients with four or more positive lymph nodes after postmastectomy radiotherapy (PMRT).
This retrospective study examined 605 breast cancer patients with four or more positive lymph nodes who underwent mastectomy. A total of 371 patients underwent PMRT. The prognostic value of the NLN count in patients with and without PMRT was analyzed. The log-rank test was used to compare survival curves, and Cox regression analysis was performed to identify prognostic factors.
The median follow-up was 54 months, and the overall 8-year locoregional recurrence-free survival (LRFS), distant metastasis-free survival (DMFS), disease-free survival (DFS), and overall survival (OS) were 79.8%, 50.0%, 46.8%, and 57.9%, respectively. The optimal cut-off points for NLN count was 12. Univariate analysis showed that the number of NLNs, lymph node ratio (LNR) and pN stage predicted the LRFS of non-PMRT patients (p < 0.05 for all). Multivariate analysis showed that the number of NLNs was an independent prognostic factor affecting the LRFS, patients with a higher number of NLNs had a better LRFS (hazard ratio = 0.132, 95% confidence interval = 0.032-0.547, p =0.005). LNR and pN stage had no effect on LRFS. PMRT improved the LRFS (p < 0.001), DMFS (p = 0.018), DFS (p = 0.001), and OS (p = 0.008) of patients with 12 or fewer NLNs, but it did not any effect on survival of patients with more than 12 NLNs. PMRT improved the regional lymph node recurrence-free survival (p < 0.001) but not the chest wall recurrence-free survival (p = 0.221) in patients with 12 or fewer NLNs.
The number of NLNs can predict the survival of breast cancer patients with four or more positive lymph nodes after PMRT.
The purpose of postmastectomy radiotherapy (PMRT) is to improve survival by eliminating potential occult lesions in the chest wall and lymphatic drainage area. The status of axillary lymph nodes is an important factor that affects the choice to use PMRT. PMRT is a standard adjuvant postoperative therapy for patients with four or more positive lymph nodes -. The local recurrence rate (LRR) of patients with four or more positive lymph nodes who did not receive PMRT was 11.9-59% -. Thus, about 40% of patients with four or more positive lymph nodes do not benefit from PMRT. At present, there is a trend for oncologists to use individualized treatments for different breast cancer patients. However, it is still difficult to predict which patients with four or more positive lymph nodes will benefit from PMRT.
In breast cancer patients, there is a critical correlation between the status and dissection of axillary lymph nodes, especially with regard to the number of removed lymph nodes (RLNs) ,. The total number of RLNs includes positive lymph nodes and negative lymph nodes (NLNs), so this number may not be a reliable clinical indicator. In addition, due to the different pathological features of lymph nodes, there may be different numbers of occult lesions in the different numbers of NLNs. In theory, removal of more NLNs may reduce the overall risk of occult lesions and thereby improve patient survival. If the number of NLNs is relatively small, the possible presence of occult lesions may increase the LRR. Previous research reported that the number of NLNs might affect the prognosis of breast cancer patients ,. However, the usefulness of the number of NLNs in predicting outcome after PMRT has not yet been reported. We hypothesized that the number of NLNs affects the LRR of breast cancer patients with four or more positive lymph nodes and thereby affects the outcome of PMRT. The current study is a retrospective analysis that investigated the predictive value of the number of NLNs in breast cancer patients with four or more positive axillary lymph nodes after PMRT.
Materials and methods
We retrospectively evaluated 605 breast cancer patients who were received mastectomy at the Sun Yat-sen University Cancer Center between January 1998 and December 2007. All included patients were females who: (i) had pathologically confirmed diagnoses of unilateral invasive breast cancer; (ii) received mastectomy and axillary lymph node dissection (at least I-II levels) with 10 or more lymph nodes; (iii) had stage pT1-4 N2-3 M0 cancer according to the 7th edition of the American Joint Committee on Cancer/Union for International Cancer Control (AJCC/UICC) tumor node metastasis (TNM) staging system; (iv) the tumor was completely removed and the margins were negative; (v) no neoadjuvant chemotherapy was administered before surgery, and receive at least 4 cycles of postoperative adjuvant chemotherapy; (vi) complete immunohistochemistry results including estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2), and endocrine therapy was administered when indicated.
Clinical and pathological factors and lymph node status
Patient clinicopathological and immunohistochemical factors including age, menstrual status, pT stage, pN stage, NLN count, lymph node ratio (LNR), ER, PR, HER2, breast cancer subtypes (BCS), and PMRT. ER and PR positivity were defined by the presence of more than 1% positive cells based on immunohistochemistry results; HER2 positivity was defined as 3+ or 2+ with confirmation by fluorescence in situ hybridization (FISH). The BCS were not determined according to the criteria developed in the St. Gallen International Breast Cancer Conference because immunohistochemistry results for Ki-67 were not available for some patients . Thus, the categorization of BCS was based on ER, PR, and HER2 status as follows: luminal A (ER+ and/or PR+, and HER2-), luminal B (ER+ and/or PR+, and HER2+), HER-2 + (ER-, PR-, and HER2+), and triple negative (TN) (ER-, PR-, and HER2-).
We identified the pT/pN stages according to the 7th edition of the AJCC/UICC TNM staging system. Stage pN2 was defined by metastases in 4–9 lymph nodes and stage pN3 by metastases in 10 or more lymph nodes. The number of removed NLNs was obtained by subtracting the number of positive lymph nodes from the total number of removed axillary lymph nodes. LNR classifications were based on the report by Vinh-Hung et al.  and our previously reported ,. Patients were classified into 3 groups with LNR 0.01-0.20, LNR 0.21 - 0.65, and LNR > 0.65.
Adjuvant chemotherapy was administered to all patients for a median of 6 cycles (range: 4–8 cycles), with 29 patients (4.8%) receiving a regimen consisting of cyclophosphamide, methotrexate, and 5-fluorouracil (CMF), and 576 (95.2%) receiving regimens with anthracycline and/or taxane. All patients were recommended for PMRT, but the patient made the final decision over whether to proceed. Of the 234 patients (38.7%) did not receive PMRT due to economic and social factors. A total of 371 patients (61.3%) received PMRT within 6 months after surgery. The PMRT was delivered mainly to the ipsilateral chest wall, supra- and infra-clavicular lymph node regions. The total radiation dose was 46–50 Gy in 23–25 fractions. The chest wall was treated with 6 MV X-ray with opposed tangential fields or 6–9 Mev electron beam, with the use of tissue compensation membrane of 0.5–1 cm when needed. Single-field irradiation was performed for the supra- and infra-clavicular lymph drainage regions with 6 MV X-ray combined with 12–15 Mev. Patients with tumours positive for the ER or PR (or both) received endocrine therapy, mainly with tamoxifen or aromatase inhibitors.
Follow-up and survival endpoints
Follow-up was performed once every 3 to 6 months. Locoregional recurrence-free survival (LRFS) was the primary endpoint. Distant metastasis-free survival (DMFS), disease free survival (DFS), and overall survival (OS) were the secondary endpoints. Locoregional recurrence refers to pathologically confirmed recurrence at the ipsilateral chest wall, supraclavicular and subclavian lymph nodes, axillary lymph nodes, or internal mammary lymph nodes. Distant metastasis refers to recurrence at a site distant from the primary cancer based on two imaging examinations or by pathologic assessment. OS was calculated as the time from the date of diagnosis to the date of death from any cause or to the date of last follow-up.
All data were analyzed using the SPSS statistical software package (version 16.0; IBM Corporation, Armonk, NY, USA). The χ2 and Fisher’s exact probability tests were used to analyze differences in the qualitative data. Cut-off point analyses were then performed to determine whether there was a cut-off NLN number that was related to the greatest difference in LRFS. The optimum cut-off point for the NLNs was determined by use of the receiver operating characteristic (ROC) curve. Calculation of survival rates were plotted by the Kaplan-Meier method and compared using the log-rank test. To determine the effect of the number of NLNs on LRFS, we performed univariate and multivariate Cox regression model analysis. The variables with p-values less than 0.05 by univariate analyses were included in the multivariate analyses. A p-value less than 0.05 was considered statistically significant.
Patient clinicopathologic data and status of lymph node dissection
A total of 605 patients were enrolled and 371 patients (61.3%) underwent PMRT. Table 1 shows the clinicopathologic data of the enrolled patients. Except for the greater use of PMRT in patients with pN3 disease, there were no significant differences between the PMRT and non-PMRT groups.
The median number of RLNs in the entire cohort was 18 (range: 10–73); the median number in the non-PMRT group and the PMRT group were 18 (range: 10–45) and 18 (range: 10–73), respectively. The median number of NLNs in the non-PMRT group and the PMRT group was 8 (25th percentile: 5, 75th percentile: 12; range, 0–39) and 7 (25th percentile: 4, 75th percentile: 12; range: 0–36), respectively.
The median follow-up time of all patients was 54 months (range: 6–138 months). A total of 91 patients had locoregional recurrence, and the 5-year LRFS and 8-year LRFS were 83.3% and 79.8%, respectively. Two hundred forty-seven patients had distant metastases and the 5-year DMFS and 8-year DMFS were 58.3% and 50.0%, respectively. The 5-year DFS and 8-year DFS were 55.1% and 46.8%, respectively. One hundred ninety-six patients died and the 5-year OS and 8-year OS of these patients were 69.9% and 57.9%, respectively.
Identification of optimal cut-off points of NLNs
The optimal cut-off points of NLNs were analyzed for non-PMRT patients using ROC curve. The results showed that 12 was the optimal cut-off point for NLNs (Area Under roc Curve = 0.644, p = 0.001) (Figure 1). Therefore, the optimal cutoff value of 12 was validated as a prognostic factor for analysis of the clinical effect of the number of NLNs.
The NLN count was associated with pT stage (p = 0.003), pN stage (p < 0.001), and LNR (p < 0.001), but was not associated with age, menstrual status, ER status, PR status, HER2 status, and BCS (all, p > 0.05) (Additional file 1: Table S1).
Analysis of prognostic factors affecting LRFS in patients without PMRT
Univariate analysis of non-PMRT patients showed that the NLN count, LNR, menstruation status, pT stage, and pN stage were prognostic factors that affected LRFS (p < 0.05) (Table 2).
Multivariate analysis showed that the number of NLNs was an independent prognostic factor for LRFS. Patients with a higher number of NLNs had a better LRFS (hazard ratio [HR]: 0.132, 95% confidence interval [CI]: 0.032-0.547, p = 0.005), but pN stage and LNR did not affect LRFS (p > 0.05). In addition, menopausal status and pT stage were also independent risk factors for LRFS (p < 0.05 for both) (Table 2).
In patients without PMRT, a higher number of NLNs was correlated with a better LRFS (p < 0.001), DMFS (p = 0.017), DFS (p = 0.003), and OS (p = 0.012) using the log-rank test (Figure 2).
Prognostic value of the number of NLNs in patients undergoing PMRT
Compared to non-PMRT patients, PMRT patients had better outcomes, with significantly improved LRFS (p < 0.001), DMFS (p = 0.012), DFS (p = 0.001), and OS (p = 0.013)..
Subgroup analysis showed that different numbers of NLNs could predict the outcome in patients received PMRT. PMRT improved the LRFS (p < 0.001), DMFS (p = 0.018), DFS (p = 0.001), and OS (p = 0.008) of patients with 12 or fewer NLNs. However, PMRT had no effect on LRFS (p = 0.500), DMFS (p = 0.204), DFS (p = 0.199), and OS (p = 0.653) of patients with more than 12 NLNs (Table 3 and Figure 3).
We examined the prognostic effect of the number of NLNs according to local (chest wall) or regional (regional lymph node) recurrences in patients with and without PMRT. In patients with 12 or fewer NLNs, PMRT did not improved the chest wall recurrence, the 8-year chest wall recurrence-free survival was 84.7% and 89.8%, respectively (p = 0.221). However, PMRT improved the regional recurrence with the 8-year regional recurrence-free survival was 90.1% and 70.1%, respectively (p < 0.001). In patients with more than 12 NLNs, PMRT without any effect on survival of chest wall recurrence (p = 0.803) and regional recurrence (p = 0.331).
In the present study, we investigated the prognostic value of the number of NLNs in breast cancer patients with four or more positive lymph nodes. The results indicate that the number of NLNs can be used to predict the outcome of PMRT in breast cancer patients.
Total number of RLNs include positive lymph nodes, so use of this number may only have limited prognostic value in identification of breast cancer patients that would benefit from PMRT. Thus, Karlsson et al. found that the number of NLNs is an independent risk factor for LRFS; the LRR of patients with 10 or more NLNs was significantly lower than that of patients with fewer than 10 NLNs, and the difference was especially significant in patients with positive lymph nodes . Kuru reported better OS of patients with more than 15 NLNs . We used Cox multivariate analysis, with NLN count, LNR, and pN stage as covariates, and found that the number of NLNs was an independent prognostic factor for LRFS, but that LNR and pN stage had no significant effect on prognosis. These results suggest that the number of NLNs may be a better indicator of axillary lymph node status in breast cancer patients.
At present, the mechanism underlying why the number of NLNs can be used to predict the survival of breast cancer patients is still unclear. However, previous studies showed that this relationship might be explained by “stage migration” or by the host’s immune response to tumor cells and the molecular biology of tumor cells -. For example, a study of colorectal cancer patients found that the lymphocyte response to the tumor was related to patient survival .
The LRR of breast cancer is an important factor used to guide the selection of PMRT. The status of axillary lymph nodes has been always one of the main factors used to guide selection of PMRT. PMRT remains the standard therapy for breast cancer patients who have four or more positive lymph nodes. PMRT can eliminate residual occult lesions in the ipsilateral chest wall and lymph drainage area, and thereby improve survival. PMRT improves the prognosis of breast cancer patients with 4 or more positive axillary lymph nodes . Our subgroup analysis showed that the LRR was relatively low in patients with a higher number of NLNs, and that PMRT provided no obvious benefit for these patients. In addition, we also found that PMRT improved locoregional control by reducing nodal recurrences but without any effect on local control in the chest wall in patients with a fewer number of NLNs. This supports our hypothesis that patients with fewer NLNs may have more residual lesions, which increases the rate of locoregional recurrence. However, for patients with more NLNs, surgery can reduce the number of residual lesions, and these patients do not benefit significantly from PMRT.
The American College of Surgeons Oncology Group (ACOSOG) Z0011 trial reported that axillary lymph node dissection did not affect the local recurrence and survival rates of patients without positive sentinel lymph nodes or with 1–2 positive sentinel lymph nodes after breast-conserving therapy ,. Thus, axillary lymph node dissection is unnecessary in these patients ,. However, the St. Gallen International Breast Cancer Conference (2013) reported that axillary lymph node dissection was necessary for cases who did not receive radiotherapy and for those with 3 or more metastases in the sentinel lymph nodes . Thus, the status of axillary lymph nodes is an important indicator that affects the prognosis of breast cancer patients and is useful in guiding therapy. In the present study, the number of NLNs significantly affected prognosis and could be used to predict the outcome of radiotherapy. Therefore, when the status of axillary lymph nodes can be accurately determined, axillary lymph node dissection is a very important procedure for patients with positive axillary lymph nodes. In particular axillary lymph node dissection can reduce the risk of occult lesions, allows some patients to omit radiotherapy and thereby avoid radiation injury -, and thereby improves patient quality of life and prolongs survival.
We need to recognize the limitations of the present study. First, this study is a single-center retrospective study and is not representative of the breast cancer population at large. In addition, the optimal number of NLNs in present study is different from the number in other studies. This may be related to differences in the clinical characteristics of the patient populations, use of different surgical procedures, and analysis by different statistical method. However, based on the relationship between the number of NLNs and host immune response ,, sufficient attention should be paid to differences in individual patient immune status. Ultimately, multicenter prospective studies should be performed to verify the value of the number of NLNs in breast cancer patients to determine the most appropriate cut-off point. Finally, patients enrolled in the current study did not undergo trastuzumab therapy. Recent studies reported that trastuzumab reduces the rate of locoregional recurrence ,.
In conclusion, the results of the present study show that the number of NLNs is a prognostic factor for LRFS in breast cancer patients with four or more positive lymph nodes after mastectomy. Patients with more NLNs have lower LRR, and the number of NLNs can predict the outcome of PMRT. PMRT might represent for certain patients with a lower number of NLNs, but not in patients with a higher number of NLNs. Future prospective studies are needed to confirm these results.
Local recurrence rate
Removed lymph nodes
Negative lymph nodes
Lymph node ratio
Human epidermal growth factor receptor 2
Breast cancer subtpye
Fluorescence in situ hybridization
American Joint Committee on Cancer/Union for International Cancer Control
Tumor node metastasis
Locoregional recurrence-free survival
Distant metastasis-free survival
Disease free survival
American College of Surgeons Oncology Group
McGale P, Taylor C, Correa C, Cutter D, Duane F, Ewertz M, Gray R, Mannu G, Peto R, Whelan T, Wang Y, Wang Z, Darby S: Effect of radiotherapy after mastectomy and axillary surgery on 10-year recurrence and 20-year breast cancer mortality: meta-analysis of individual patient data for 8135 women in 22 randomised trials. Lancet 2014, 383: 2127-2135. 10.1016/S0140-6736(14)60488-8
Wenz F, Sperk E, Budach W, Dunst J, Feyer P, Fietkau R, Haase W, Harms W, Piroth MD, Sautter-Bihl ML, Sedlmayer F, Souchon R, Fussl C, Sauer R: DEGRO practical guidelines for radiotherapy of breast cancer IV: radiotherapy following mastectomy for invasive breast cancer. Strahlenther Onkol 2014, 190: 705-714. 10.1007/s00066-014-0687-0
Jagsi R: Progress and controversies: radiation therapy for invasive breast cancer. CA Cancer J Clin 2014; 64:135-152.
Nagao T, Kinoshita T, Tamura N, Hojo T, Morota M, Kagami Y: Locoregional recurrence risk factors in breast cancer patients with positive axillary lymph nodes and the impact of postmastectomy radiotherapy. Int J Clin Oncol 2013, 18: 54-61. 10.1007/s10147-011-0343-y
Nielsen HM, Overgaard M, Grau C, Jensen AR, Overgaard J: Loco-regional recurrence after mastectomy in high-risk breast cancer–risk and prognosis. An analysis of patients from the DBCG 82 b&c randomization trials. Radiother Oncol 2006, 79: 147-155. 10.1016/j.radonc.2006.04.006
Wu SG, He ZY, Li Q, Li FY, Lin Q, Lin HX, Guan XX: Predictive value of breast cancer molecular subtypes in Chinese patients with four or more positive nodes after postmastectomy radiotherapy. Breast 2012, 21: 657-661. 10.1016/j.breast.2012.07.004
Somner JE, Dixon JM, Thomas JS: Node retrieval in axillary lymph node dissections: recommendations for minimum numbers to be confident about node negative status. J Clin Pathol 2004, 57: 845-848. 10.1136/jcp.2003.015560
Wiznia LE, Lannin DR, Evans SB, Hofstatter EW, Horowitz NR, Killelea BK, Tsangaris TN, Chagpar AB: The number of lymph nodes dissected in breast cancer patients influences the accuracy of prognosis. Ann Surg Oncol 2014, 21: 389-394. 10.1245/s10434-013-3308-8
Karlsson P, Cole BF, Price KN, Coates AS, Castiglione-Gertsch M, Gusterson BA, Murray E, Lindtner J, Collins JP, Holmberg SB, Fey MF, Thürlimann B, Crivellari D, Forbes JF, Gelber RD, Goldhirsch A, Wallgren A: The role of the number of uninvolved lymph nodes in predicting locoregional recurrence in breast cancer. J Clin Oncol 2007, 25: 2019-2026. 10.1200/JCO.2006.09.8152
Kuru B: Prognostic significance of total number of nodes removed, negative nodes removed, and ratio of positive nodes to removed nodes in node positive breast carcinoma. Eur J Surg Oncol 2006, 32: 1082-1088. 10.1016/j.ejso.2006.06.005
Goldhirsch A, Winer EP, Coates AS, Gelber RD, Piccart-Gebhart M, Thürlimann B, Senn HJ: Personalizing the treatment of women with early breast cancer: highlights of the St Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2013. Ann Oncol 2013, 24: 2206-2223. 10.1093/annonc/mdt303
Vinh-Hung V, Verkooijen HM, Fioretta G, Neyroud-Caspar I, Rapiti E, Vlastos G, Deglise C, Usel M, Lutz JM, Bouchardy C: Lymph node ratio as an alternative to pN staging in node-positive breast cancer. J Clin Oncol 2009, 27: 1062-1068. 10.1200/JCO.2008.18.6965
Wu SG, Chen Y, Sun JY, Li FY, Lin Q, Lin HX, He ZY: Using the lymph nodal ratio to predict the risk of locoregional recurrence in lymph node-positive breast cancer patients treated with mastectomy without radiation therapy. Radiat Oncol 2013, 8: 119. 10.1186/1748-717X-8-119
Wu SG, He ZY, Li Q, Sun JY, Li FY, Lin Q, Lin HX, Guan XX: Prognostic value of metastatic axillary lymph node ratio for Chinese breast cancer patients. PLoS One 2013, 8: e61410. 10.1371/journal.pone.0061410
Schaapveld M, de Vries EG, van der Graaf WT, Otter R, de Vries J, Willemse PH: The prognostic effect of the number of histologically examined axillary lymph nodes in breast cancer: stage migration or age association? Ann Surg Oncol 2006, 13: 465-474. 10.1245/ASO.2006.02.020
Johnson PM, Porter GA, Ricciardi R, Baxter NN: Increasing negative lymph node count is independently associated with improved long-term survival in stage IIIB and IIIC colon cancer. J Clin Oncol 2006, 24: 3570-3575. 10.1200/JCO.2006.06.8866
Pagès F, Berger A, Camus M, Sanchez-Cabo F, Costes A, Molidor R, Mlecnik B, Kirilovsky A, Nilsson M, Damotte D, Meatchi T, Bruneval P, Cugnenc PH, Trajanoski Z, Fridman WH, Galon J: Effector memory T cells, early metastasis, and survival in colorectal cancer. N Engl J Med 2005, 353: 2654-2666. 10.1056/NEJMoa051424
Morris M, Platell C, Iacopetta B: Tumor-infiltrating lymphocytes and perforation in colon cancer predict positive response to 5-fluorouracil chemotherapy. Clin Cancer Res 2008, 14: 1413-1417. 10.1158/1078-0432.CCR-07-1994
Jagsi R, Pierce L: Postmastectomy radiation therapy for patients with locally advanced breast cancer. Semin Radiat Oncol 2009, 19: 236-243. 10.1016/j.semradonc.2009.05.009
Giuliano AE, McCall L, Beitsch P, Whitworth PW, Blumencranz P, Leitch AM, Saha S, Hunt KK, Morrow M, Ballman K: Locoregional recurrence after sentinel lymph node dissection with or without axillary dissection in patients with sentinel lymph node metastases: the American College of Surgeons Oncology Group Z0011 randomized trial. Ann Surg 2010, 252: 426-432. discussion 432–3
Giuliano AE, Hunt KK, Ballman KV, Beitsch PD, Whitworth PW, Blumencranz PW, Leitch AM, Saha S, McCall LM, Morrow M: Axillary dissection vs no axillary dissection in women with invasive breast cancer and sentinel node metastasis: a randomized clinical trial. JAMA 2011, 305: 569-575. 10.1001/jama.2011.90
Abo-Madyan Y, Aziz MH, Aly MM, Schneider F, Sperk E, Clausen S, Giordano FA, Herskind C, Steil V, Wenz F, Glatting G: Second cancer risk after 3D-CRT, IMRT and VMAT for breast cancer. Radiother Oncol 2014, 110: 471-476. 10.1016/j.radonc.2013.12.002
Darby SC, Ewertz M, McGale P, Bennet AM, Blom-Goldman U, Brønnum D, Correa C, Cutter D, Gagliardi G, Gigante B, Jensen MB, Nisbet A, Peto R, Rahimi K, Taylor C, Hall P: Risk of ischemic heart disease in women after radiotherapy for breast cancer. N Engl J Med 2013, 368: 987-998. 10.1056/NEJMoa1209825
McGale P, Darby SC, Hall P, Adolfsson J, Bengtsson NO, Bennet AM, Fornander T, Gigante B, Jensen MB, Peto R, Rahimi K, Taylor CW, Ewertz M: Incidence of heart disease in 35,000 women treated with radiotherapy for breast cancer in Denmark and Sweden. Radiother Oncol 2011, 100: 167-175. 10.1016/j.radonc.2011.06.016
Panoff JE, Hurley J, Takita C, Reis IM, Zhao W, Sujoy V, Gomez CR, Jorda M, Koniaris L, Wright JL: Risk of locoregional recurrence by receptor status in breast cancer patients receiving modern systemic therapy and post-mastectomy radiation. Breast Cancer Res Treat 2011, 128: 899-906. 10.1007/s10549-011-1495-1
Kiess AP, McArthur HL, Mahoney K, Patil S, Morris PG, Ho A, Hudis CA, McCormick B: Adjuvant trastuzumab reduces locoregional recurrence in women who receive breast-conservation therapy for lymph node-negative, human epidermal growth factor receptor 2-positive breast cancer. Cancer 2012, 118: 1982-1928. 10.1002/cncr.26484
This work was supported by grants from the National Natural Science Foundation of China (No. 81402527), the Sci-Tech Office of Guangdong Province (No. 2013B021800157) and the Education Scientific Research Project of Young Teachers in Fujian Province (No. JB13131).
The authors declare that they have no competing interests.
SGW, JYS, and JZ carried out the data collection and writing of the manuscript; SGW helped to conceive the study; YB and ZYH contributed to the design of the study; QL and FYL helped to collect data, ZH, HXL and FYL participated in statistical analysis. All authors read and approved the final manuscript.
San-Gang Wu, Jia-Yuan Sun, Juan Zhou contributed equally to this work.
Electronic supplementary material
Additional file 1: Table S1: Characteristics of breast cancer patients according to different number of negative lymph nodes in patients without postmastectomy radiotherapy. (DOC 50 KB)
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Wu, SG., Sun, JY., Zhou, J. et al. Number of negative lymph nodes can predict survival of breast cancer patients with four or more positive lymph nodes after postmastectomy radiotherapy. Radiat Oncol 9, 284 (2014). https://doi.org/10.1186/s13014-014-0284-5
- Breast cancer
- Negative lymph nodes