ABSTRACT
Introduction: The use of axillary marking prior to Neoadjuvant Systemic Therapy (NST) is a controversial matter regarding patients with positive Lymph Nodes (LN). Several methods were tested to make possible the decrease of false negative rate in comparison to sentinel lymph node adding more accuracy to the results. This study aims to evaluate the oncological outcomes in patients who had undergone selective axillary dissection with 4% carbon marking before TSN.
Methods: A prospective study was performed with cT1-T4, cN1-N2 breast cancer patients classified as suspected LNs undergoing concomitant 4% carbon marking. After TSN, targeted LNs were identified and resected associated to the sentinel lymph node (SLN) biopsy. The oncological outcomes pointed out were overall survival (OS), causespecific survival (CSS), distant disease-free survival (DDFS), axillary recurrence (AR) and local recurrence (LR).
Results: A total of 168 patients were evaluated for a median period of 49 months. The axillary emptying was reached in 89 (50.6%) cases. Five of 168 patients (2.9%) had axillary recurrence (AR). There was a significant link between axillary emptying and AR (0 vs. 6% p = 0.012). The DDFS was 140/168 (83.3%), OS 158/168 (94%) and CSS 158/163 (96.9%).
Conclusion: The use of carbon marking in selective axillary dissection is a reliable low-cost method with simple execution. Among the oncological outcomes AR may not be considered for post downstaging axillary evaluation analysis since it is a rare event and not necessarily related to OS or DDFS.
Keywords:
Breast Neoplasms; Sentinel Lymph Node; Carbon; Neoplasm Staging; Neoadjuvant Therapy
RESUMO
Introdução: O uso de marcadores na axila antes da terapia sistêmica neoadjuvante (TSN) é um tema controverso em mulheres com linfonodos (LN) acometidos. Diversos marcadores foram utilizados resultando em uma redução da taxa de falso negativo ao comparar com o linfonodo sentinela, melhorando a acurácia. Este estudo tem como propósito analisar os resultados oncológicos em mulheres que passaram por dissecção axilar seletiva com marcação prévia à terapia sistêmica neoadjuvante (TSN) usando carvão a 4% e sua relação com o LN sentinela.
Métodos: Foram selecionadas pacientes diagnosticadas com carcinoma invasivo de mama, apresentando estágios clínicos T1-4 e N1-2 submetidas à análise de LNs suspeitos e marcação pré TSN com carvão a 4%. Após o tratamento neoadjuvante, os LNs indicados com carvão foram excisados em um mesmo procedimento com o linfonodo sentinela. Os desfechos sobrevida global (SG), sobrevida específica (SE), sobrevida livre de doença a distância (SLDD), recidiva axilar (RA) e recidiva local (RL) foram catalogados.
Resultados: Para a análise entre linfonodos marcados e linfonodo sentinela 176 pacientes foram incluídas com taxa de identificação de 95,4% do LN marcado. Para os desfechos oncológicos, cento e sessenta e oito pacientes foram analisadas em 49 meses de tempo mediano. O esvaziamento axilar foi omitido em 89 (50,6%) casos. Cinco/168 (2,9%) tiveram RA. Houve relação entre linfadenectomia axilar e RA (0 vs. 6% p=0,012). A SLDD foi 140/168 (83,3%), SG 158/168 (94%) e SE 158/163 (96,9%).
Conclusões: O carvão se destaca como um marcador confiável, acessível e prático para dissecção axilar seletiva. O evento RA não deve ser utilizada para análise após TSN uma vez que é um evento raro e não está relacionada a SG ou SLDD diretamente.
Palavras-chave:
Tratamento Neoadjuvante; Câncer de Mama; Biópsia do Linfonodo Sentinel; Cirurgia Axilar; Dissecção Axilar Seletiva
INTRODUCTION
Axillary examinations prior to neoadjuvant systemic therapy (NST) are a useful tool for staging and conducting the treatment of breast carcinoma1-3. However, after clinical response in previously compromised lymph nodes, there were uncertainties that limited the use of sentinel lymph nodes (SLN) due to its high false negative rate and low identification rate4,5. Tactics such as increasing the number of biopsied lymph nodes, applying immunohistochemistry, and using two ways to map the sentinel lymph node have rendered a false negative rate of less than 10%6-8. In these studies, all patients underwent lymphadenectomy, and it was not possible to evaluate the oncological outcomes in the preservation setting, and did not provide data on axillary recurrence (AR).
AR in women who had their axillary status reduced from positive to negative after NST is between 1.4 - 2.6%9,10. However, the evaluation of this outcome is not sufficient in the face of the new demand to lower false negative rates with the introduction of adjuvant drugs when complete pathological responses are not obtained11-13.
Applying techniques to mark a suspicious lymph node before NST and excising it afterwards increases the reliability of axillary evaluation without the need for lymphadenectomy, with false negative rates ranging from 1.4 to 4.2%14-16. Some of the barriers to the use of metal clips in these methods are cost, the need for interventional radiology before surgery, and the possibility of permanence of the clip after surgery in few patients17-20. In search of new, cheaper methodologies or with less technical difficulty, other materials were used for lymph node marking, such as magseed®21, Radar/Infrared22, clips visible on ultrasound14, and lymph node pigmentation through ink or carbon23-25.
Carbon has been used as a marker for non-palpable lesions in the breast for a long time26,27 and has been efficient in pre-NST lymph node marking, with lymph node identification rates between 96.4 and 100%23-25. The advantages reported in this technique include the ease of intraoperative identification and the non-need for an invasive localization procedure, thus reducing the burden on the patient by avoiding the use of radioactive materials.
This analysis aims to observe the oncological results in women undergoing selective axillary dissection in association with the sentinel lymph node and to evaluate its safety, as well as to evaluate the relationship between the sentinel lymph node and the marked lymph node prior to systemic therapy.
METHODS
This study is a prospective cohort of longitudinal nature, conducted with a single group of patients who underwent selective axillary dissection combined with SLN biopsy, in the context of invasive breast carcinoma with clinical evidence of axillary involvement and who underwent neoadjuvant therapy. The procedures were performed in both public and private health facilities located in Curitiba, Paraná, during the period from July 2014 to January 2019.
We selected patients diagnosed with invasive breast carcinoma confirmed by anatomopathological analysis, with clinical stages T1-4 and N1-2. We excluded from the study patients who had distant metastases at the time of diagnosis, histology other than invasive breast carcinoma, history of surgical breast biopsy and/or previous axillary surgical procedures, history of other malignant neoplasms, clinical contraindications to radiotherapy, inflammatory carcinomas, and inability to adhere to regular medical follow-up.
Since this was an analysis of axillary evaluation in patients with suspicious axillary lymph nodes, we also excluded cases of breast carcinoma with clinically negative axillae. Thus, there were no cases of T1 N0 breast cancer. As SLN is contraindicated in cases of inflammatory carcinoma, patients with this clinical presentation also did not participate in the study.
The information collected was organized in Excel® spreadsheets, 2020 version. Quantitative variables were summarized using measures of central tendency and dispersion. Categorical variables were arranged in frequency and percentage. We sued the chi-square test for comparative analysis between subgroups. To analyze the time to oncological events, Kaplan-Meier curves were made. The study of similarity and causality between the results was conducted with the Log-rank test. Values of p<0.05 were considered statistically significant. Statistical analysis was performed using the Stata/SS software, version 14.1 (StataCorp LP, United States).
The project was approved by the Ethics in Research Committee of the Federal University under number 510304.7.0000.0096.
Lymph node marking and surgery
Prior to neoadjuvant therapy, the patients underwent ultrasonographic evaluation of the axilla on the same side of the tumor. When any suspicious lymph node was identified during this evaluation, fine-needle aspiration was performed to collect cytological material (Figure 1). In the case of identification of more than one suspicious lymph node, we prioritized the evaluation of the largest diameter lymph node. In the same intervention, we performed peri-lymph node marking using a 4% carbon suspension.
Axillary recurrence according to axillary preservation or dissection. AD = axillary dissection.
After completion of systemic treatment, the patients underwent a reassessment to determine the extent of locoregional response to treatment, and subsequently underwent surgical intervention. During the surgical procedure, after the administration of anesthesia, we injected 1-2ml of Patent Blue Dye V in the periareolar region of the breast, followed by an approach to the armpit. During this procedure, we identified and removed lymph nodes stained with patent blue dye, as well as those previously marked with 4% carbon suspension (Figure 2).
During surgery, we conducted a pathological evaluation by freezing, and thus the patients were directed to axillary emptying or not. If the intraoperative pathological result was positive, indicating the presence of cancer cells, lymphadenectomy was performed, with the removal of at least 10 lymph nodes from the axillary chain, visualizing the anatomical structures that limit Berg’s levels 1 and 2. On the other hand, if the result was negative, indicating the absence of cancer cells, the intervention in the armpit was terminated.
After the surgical intervention, the specimens were immersed in vials containing 10% formaldehyde, where they remained for a period of more than 24 hours. Then, they were sectioned along their longitudinal axis into slices of up to 2 mm thickness and processed for histological analysis, including microtomy (with a 4-micrometer cut) and staining with hematoxylin and eosin.
For the cytological analysis prior to the systemic neoadjuvant treatment, the material obtained through fine needle aspiration puncture (FNA) was deposited on slides, dried in air, and then stained by the May-Grünwald-Giemsa method, being covered with coverslips. The analyses were performed using a Nikon Eclipse E200 microscope (Nikon Corporation, Tokyo, Japan) at magnifications of 40x, 100x and 400x. This process allowed a detailed evaluation of the morphological and cytological characteristics of the samples, contributing to a more accurate understanding of the condition of the tissues and cells studied.
Follow-up
We gathered relevant data for statistical analysis from the medical records on the clinical stage, as defined by the TNM28 system, as well as on the tumor and axillary anatomopathological classification, in addition to the immunohistochemistry results.
We collected data on the axillary stage at two moments: before neoadjuvant systemic therapy, by means of imaging tests, categorized with the prefix “c”; and after surgery and systemic therapy, through the result of the final pathology, categorized with the prefix “yp”.
For a precise correlation between elapsed time and oncological outcomes, we recorded the dates of surgery, of event of interest, and of last visit. Follow-up was done through two medical consultations per year for the first two years and one annual consultation until ten years from the date of surgery.
RESULTS
Between July 2014 and January 2019, 181 women underwent axillary marking prior to neoadjuvant treatment. We excluded five patients due to lack of adequate data and eight due to loss to follow-up. The final number of patients analyzed was 176 for lymph node identification in the two methods employed and 168 for oncological outcomes. Six individuals did not have their immunohistochemistry data categorized. The demographic characteristics of the study cohort are presented in Table 1.
Regarding axillary dissection, this procedure was omitted in 89 cases (50.6%), while clinical suspicions were confirmed in 113 cases (64.2%) by FNA.
Events analyzed included local recurrence (LR), axillary recurrence (AR), distant disease-free survival (DDFS), overall survival (OS), and breast cancer specific survival (SS). We excluded four patients from the analysis due to the lack of data on breast cancer deaths on their death certificates.
We included 176 patients in the analysis of the detection rate of the carbon-labeled lymph nodes and the sentinel lymph node. The sentinel lymph node (SLN) detection method was unsuccessful in 31 (17.6%) cases, while the carbon-labeled lymph node (CLLN) was not identified in eight (4.5%) procedures. We observed coincidence between the sentinel and carbon-labeled lymph nodes in 93 of 176 (52.8%) patients, whereas there was no coincidence in 44 (25%) cases. At least one of the methods was not identified in 39 (22.1%) procedures. None of the surgeries had no lymph node identified by both methods. The lymph node identification rate according to the method is shown in Table 2.
Table 3 presents the frequency and percentages of cases according to the anatomopathological results of the SLN and the CLLN, categorizing the lymph nodes not found as positive in the “yes/not found” category and as negative in the “no” category for neoplasm-free lymph nodes. This grouping was carried out with the aim of evaluating the decision on axillary lymphadenectomy after pathological analysis, given that, in the absence of lymph nodes evaluated, axillary lymphadenectomy is indicated. When condensing the lymph nodes not found with the positive lymph nodes, the sample agreement was 148 in 176 cases (81.4%), with a Kappa agreement coefficient of 0.67 (95% CI 0.56 -0.78), indicating a good agreement.
Frequency and percentages of anatomopathological results and methods of lymph node identification considering a node not found as positive.
The distribution of oncological outcomes, percentages, and the mean and median duration of follow-up are detailed in Table 4. In the group of patients examined, with a median follow-up time of 49 months, we observed a statistically significant association between axillary dissection and the incidence of axillary recurrence (0/85 0% vs. 5/83 6%, p=0.012). Graph 1 shows the evolution of axillary recurrence over time, comparing individuals who underwent axillary lymphadenectomy and those who did not. We identified seven local recurrence (LR) events in 168 patients analyzed, corresponding to a rate of 4.1%.
The most prevalent oncological outcome was distant recurrence. DFS was observed in 140 of 168 patients (83.3%). The most frequent site of recurrence was bone, occurring in nine of 28 cases (32.1%), followed by the lung, present in seven of 28 cases (25%). We identified a significant association between distant recurrence and involvement of at least one lymph node after neoadjuvant therapy (11.3% vs. 23.9%, p=0.027), as well as between distant recurrence and axillary dissection (10.5% vs. 22.9%, p=0.025).
During follow-up, there were 10 deaths among the 168 patients analyzed, of which five were secondary to breast carcinoma and five had an undetermined cause. The analysis of the clinical stage proved to be the main factor related to lower OS and SS, with statistical significance (log-rank test, p<0.05), as illustrated in Graph 2. In addition, we observed an association between a decrease in OS in women who underwent lymphadenectomy compared with those who did not (97.6% vs. 90.4%, p=0.035), as shown in Table 5.
The difficulties in locating and obtaining death certificates, together with the insufficiency of information when finally found, became a considerable obstacle to determining the causes of death not recorded in the study, which significantly compromised the analysis of the outcome of specific overall survival.
In the pre-NST clinical classification, 147 (87.5%) women were categorized as cN1 and 21 (12.5%) as cN2, after excluding the patients due to loss to follow-up. In the cN1 subgroup, the occurrence of the most relevant oncological outcomes was three (2%) for AR, 127 (86.4%) for DFS, and 140 (95.2%) for OS. When comparing the main oncological outcomes between the cN1 and cN2 subgroups, we observed a significant association in the DFS outcome, favoring the cN1 group (86.4% vs. 62.9%, p<0.05).
DISCUSSION
We present the application of carbon as a marker for axillary lymph nodes before NST and its association with sentinel lymph nodes, aiming to improve the rates of false negatives in evaluations after neoadjuvant systemic therapy, following the approach adopted in the Target Axillary Dissection Study15. In addition, our study reveals the oncological outcomes in a mean follow-up period of 49 months in women undergoing selective axillary dissection using 4% carbon as a marker, presenting a pioneering contribution to this field of research.
We selected carbon as a material for lymph node marking due to its characteristics of being static, non-absorbable, and inert, making it suitable for the intended purpose, since it is not susceptible to migration29. In addition to its technical advantages, there are also associated economic benefits. Marking for non-palpable lesions with carbon is more economical compared with metallic wire when performed in the same biopsy procedure30. This advantage becomes even more evident when compared with metal clip, with an approximate cost of US$ 70 (US$ 60 for ultrasound-guided biopsy and marking procedure, and US$ 10 for 4% carbon) in the Brazilian context23. In addition, carbon offers an alternative to the use of I125 seed, which presents potential risks related to radiation exposure and requires specialized equipment and trained personnel for implantation and removal31. Like the metal clip, the seeds may shift slightly after implantation, which may make it difficult to locate the lesion during surgery32-35. The rate of identification of carbon as a marker in our study was 95.4%, higher than the rate of metal clip6,15.
We observed higher distant recurrence in patients with greater pre-NST axillary involvement (13.6% vs. 38.1% - p<0.05) when comparing cN1 with cN2. It is important to note that correct staging before the start of treatment is an important tool in determining prognosis, in addition to immunohistochemistry, histological grade, and genomic platform28, although post-NST involvement is important in the choice of adjuvant treatment11,12.
Axillary recurrence is an uncommon outcome and, therefore, should not be considered as the primary event in the analysis of axillary management. In patients with negative axillary status or lymph node micrometastases, the axillary recurrence rate at a 42-month follow-up is only 0.7%36, being more frequent in the first 24 months of follow-up37,38. It is relevant to note that women who underwent axillary lymphadenectomy often have worse prognosis28,38-40, 6% of our sample submitted to lymphadenectomy had regional recurrence, while there was no AR in the group that underwent conservative axillary surgery. This is because the number of lymph nodes affected is inversely associated with breast cancer-specific survival (SS) and overall survival (OS), with the persistence of regional disease being the main reason for lymphadenectomy.
The decision about performing axillary dissection can be improved by lymph node labeling prior to neoadjuvant chemotherapy. The lack of agreement between the carbon-labeled lymph node and the sentinel lymph node does not necessarily alter the decision on axillary lymphadenectomy. For example, even if they do not match, both lymph nodes may be positive, leading to the decision to evacuate the axilla. We observed a rate of agreement in the decision to axillary dissection in 148 out of 176 cases (81.4%), with a Kappa coefficient of 0.67 (95% CI 0.56-0.78), indicating a good agreement when considering the broad decision. However, the high rate of SLN non-identification, 17.6% in this cohort, can be attenuated with pre-systemic therapy marking.
This study has some limitations. The sample is not homogeneous, since some patients underwent axillary dissection due to preoperative clinical suspicion that was not confirmed in the anatomopathological examination. The small number of patients limits the evaluation of subgroups. In addition, it lacked a control group according to the criteria of the ACOZOG Z1071 study, i.e., with double labeling and removal of at least three lymph nodes6. Moreover, post-neoadjuvant therapies were not performed at the time of study recruitment, so one of the doubts about the benefit of reducing false negatives in the axillary evaluation cannot be tested.
The addition of other drugs after neoadjuvant therapy has become the target of research and, when selecting patients who need more therapy, one chooses those who did not have a complete pathological response due to the worse prognosis in this scenario41-44. As a result, the use of PARP45 inhibitors and CDK 4/613 inhibitors is already part of the arsenal of therapies that can be individualized for patients without a complete pathologic response to the treatment of early breast cancer. New studies should be designed to evaluate if the reduction of false negatives in axillary evaluation after selective axillary dissection has an impact on these patients.
CONCLUSION
The use of carbon as a marker in selective axillary dissection is a reliable, low-cost, and easily identifiable material in 95.4% of axillary surgeries. The rate of AR in patients submitted to pre-systemic therapy 4% carbon labeling at 49 months of follow-up was 2.9%. Among oncological events, AR should not be used for axillary evaluation analysis after downstaging, since it is a rare event and is not necessarily related to OS or DDFS.
REFERENCES
-
1 Mamounas EP, Brown A, Anderson S, Smith R, Julian T, Miller B, et al. Sentinel node biopsy after neoadjuvant chemotherapy in breast cancer: Results from National Surgical Adjuvant Breast and Bowel Project protocol B-27. J Clin Oncol. 2005;23(12):2694-702. doi: 10.1200/JCO.2005.05.188.
» https://doi.org/10.1200/JCO.2005.05.188 -
2 van Deurzen CHM, Vriens BEPJ, Tjan-Heijnen VCG, van der Wall E, Albregts M, van Hilligersberg R, et al. Accuracy of sentinel node biopsy after neoadjuvant chemotherapy in breast cancer patients: A systematic review. Eur J Cancer. 2009;45(18):3124-30. doi: 10.1016/j.ejca.2009.08.001.
» https://doi.org/10.1016/j.ejca.2009.08.001 -
3 Xing Y, Foy M, Cox DD, Kuerer HM, Hunt KK, Cormier JN. Meta-analysis of sentinel lymph node biopsy after preoperative chemotherapy in patients with breast cancer. Br J Surg. 2006;93(5):539-46. doi: 10.1002/bjs.5209.
» https://doi.org/10.1002/bjs.5209 -
4 Yagata H, Yamauchi H, Tsugawa K, Hayashi N, Yoshida A, Kajiura Y, et al. Sentinel node biopsy after neoadjuvant chemotherapy in cytologically proven node-positive breast cancer. Clin Breast Cancer. 2013;13(6):471-7. doi: 10.1016/j.clbc.2013.08.014.
» https://doi.org/10.1016/j.clbc.2013.08.014 -
5 Shen J, Gilcrease MZ, Babiera GV, Ross MI, Meric-Bernstam F, Feig BW, et al. Feasibility and accuracy of sentinel lymph node biopsy after preoperative chemotherapy in breast cancer patients with documented axillary metastases. Cancer. 2007;109(7):1255-63. doi: 10.1002/cncr.22540.
» https://doi.org/10.1002/cncr.22540 -
6 Boughey JC, Suman VJ, Mittendorf EA, Ahrendt GM, Wilke LG, Taback B, et al. Sentinel lymph node surgery after neoadjuvant chemotherapy in patients with node-positive breast cancer: The ACOSOG Z1071 (alliance) clinical trial. JAMA. 2013;310(14):1455-61. doi: 10.1001/jama.2013.278932.
» https://doi.org/10.1001/jama.2013.278932 -
7 Kuehn T, Bauerfeind I, Fehm T, Fleige B, Hausschild M, Helms G, et al. Sentinel-lymph-node biopsy in patients with breast cancer before and after neoadjuvant chemotherapy (SENTINA): A prospective, multicentre cohort study. Lancet Oncol. 2013;14(7):609-18. doi: 10.1016/S1470-2045(13)70166-9.
» https://doi.org/10.1016/S1470-2045(13)70166-9 -
8 Boileau J-F, Poirier B, Basik M, Holloway CMB, Gaboury L, Sideris L, et al. Sentinel node biopsy after neoadjuvant chemotherapy in biopsy-proven node-positive breast cancer: the SN FNAC study. J Clin Oncol. 2015;33(3):258-64. doi: 10.1200/JCO.2014.55.7827.
» https://doi.org/10.1200/JCO.2014.55.7827 -
9 Kahler-Ribeiro-Fontana S, Pagan E, Magnoni F, Vicini E, Morigi C, Corso G, et al. Long-term standard sentinel node biopsy after neoadjuvant treatment in breast cancer: a single institution ten-year follow-up. Eur J Surg Oncol. 2021;47(4):804-12. doi: 10.1016/j.ejso.2020.10.014.
» https://doi.org/10.1016/j.ejso.2020.10.014 -
10 Damin AP, Zancan M, Melo MP, Biazus JV, Classe JM, Loaec C, et al. Sentinel lymph node biopsy after neoadjuvant chemotherapy in patients with node-positive breast cancer: guiding a more selective axillary approach. Breast Cancer Res Treat. 2019;173(2):527-34. doi: 10.1245/s10434-020-08900-0.
» https://doi.org/10.1245/s10434-020-08900-0 -
11 Masuda N, Lee S-J, Ohtani S, Im Y-H, Lee E-S, Yokota I, et al. Adjuvant T-DM1 versus trastuzumab in patients with residual invasive disease after neoadjuvant therapy for HER2-positive breast cancer: subgroup analyses from KATHERINE. Ann Oncol. 2021;32(22):2147-59.doi: 10.1016/j.annonc.2021.04.011.
» https://doi.org/10.1016/j.annonc.2021.04.011 -
12 Masuda N, Lee S-J, Ohtani S, Im Y-H, Lee E-S, Yokota I, et al. Adjuvant Capecitabine for Breast Cancer after Preoperative Chemotherapy. N Engl J Med. 2017;376(22):2147-59. doi: 10.1056/NEJMoa1612645.
» https://doi.org/10.1056/NEJMoa1612645 -
13 Mamounas EP, Untch M, Mano MS, Huang CS, Geyer CE, von Minckwitz G, et al. Adjuvant abemaciclib combined with endocrine therapy for high-risk early breast cancer: updated efficacy and Ki-67 analysis from the monarchE study. Ann Oncol. 2021;32(12):1005-14. doi: 10.1016/j.annonc.2021.04.011.
» https://doi.org/10.1016/j.annonc.2021.04.011 -
14 Siso C, de Torres J, Esgueva-Colmenarejo A, Espinosa-Bravo M, Rus N, Cordoba O, et al. Intraoperative Ultrasound-Guided Excision of Axillary Clip in Patients with Node-Positive Breast Cancer Treated with Neoadjuvant Therapy (ILINA Trial): A New Tool to Guide the Excision of the Clipped Node After Neoadjuvant Treatment. Ann Surg Oncol. 2018;25(3):784-91. doi: 10.1245/s10434-017-6270-z.
» https://doi.org/10.1245/s10434-017-6270-z -
15 Caudle AS, Yang WT, Krishnamurthy S, Mittendorf EA, Black DM, Gilcrease MZ, et al. Improved axillary evaluation following neoadjuvant therapy for patientswith node-positive breast cancer using selective evaluation of clipped nodes: Implementation of targeted axillary dissection. J Clin Oncol. 2016;34(10):1072-8. doi: 10.1200/JCO.2015.64.0094.
» https://doi.org/10.1200/JCO.2015.64.0094 -
16 Donker M, Straver ME, Wesseling J, Loo CE, Schot M, Drukker CA, et al. Marking axillary lymph nodes with radioactive iodine seeds for axillary staging after neoadjuvant systemic treatment in breast cancer patients the mari procedure. Ann Surg. 2015;261(2):378-82. doi: 10.1097/SLA.0000000000000558.
» https://doi.org/10.1097/SLA.0000000000000558 -
17 Swarnkar PK, Tayeh S, Michell MJ, Mokbel K. The evolving role of marked lymph node biopsy (Mlnb) and targeted axillary dissection (tad) after neoadjuvant chemotherapy (nact) for node-positive breast cancer: Systematic review and pooled analysis. Cancers (Basel). 2021;13(7):1539. doi: 10.3390/cancers13071539.
» https://doi.org/10.3390/cancers13071539 -
18 Woods RW, Camp MS, Durr NJ, Harvey SC. A Review of Options for Localization of Axillary Lymph Nodes in the Treatment of Invasive Breast Cancer. Acad Radiol. 2019;26(6):805-19. doi: 10.1016/j.acra.2018.07.002.
» https://doi.org/10.1016/j.acra.2018.07.002 -
19 Hartmann S, Reimer T, Gerber B, Stubert J, Stengel B, Stachs A. Wire localization of clip-marked axillary lymph nodes in breast cancer patients treated with primary systemic therapy. Eur J Surg Oncol. 2018;44(9):1307-11. doi: 10.1016/j.ejso.2018.05.035.
» https://doi.org/10.1016/j.ejso.2018.05.035 -
20 Flores-Funes D, Aguilar-Jiménez J, Martínez-Gálvez M, Ibáñez-Ibáñez MJ, Carrasco-González L, Gil-Izquierdo JI, et al. The problem of axillary staging in breast cancer after neoadjuvant chemotherapy. Role of targeted axillary dissection and types of lymph node markers. Cir Esp (Engl Ed). 2020;98(9):510-515. doi: 10.1016/j.ciresp.2020.03.012.
» https://doi.org/10.1016/j.ciresp.2020.03.012 -
21 Harvey JR, Lim Y, Murphy J, Howe M, Morris J, Goyal A, et al. Safety and feasibility of breast lesion localization using magnetic seeds (Magseed): a multi-centre, open-label cohort study. Breast Cancer Res Treat. 2018;169(3):531-6. doi: 10.1007/s10549-018-4709-y.
» https://doi.org/10.1007/s10549-018-4709-y -
22 Tayeh S, Muktar S, Heeney J, Michell MJ, Perry N, Suaris T, et al. Reflector-guided localization of non-palpable breast lesions: The first reported european evaluation of the SAVI SCOUT(r) system. Anticancer Res. 2020;40(7):3915-24. doi: 10.21873/anticanres.14382.
» https://doi.org/10.21873/anticanres.14382 -
23 Spautz CC, Schunemann Junior E, Budel LR, Cavalcanti TCS, Louveira MH, Junior PG, et al. Marking axillary nodes with 4% carbon microparticle suspension before neoadjuvant chemotherapy improves sentinel node identification rate and axillary staging. J Surg Oncol. 2020;122(2):164-9. doi: 10.1002/jso.25928.
» https://doi.org/10.1002/jso.25928 -
24 Patel R, MacKerricher W, Tsai J, Choy N, Lipson J, Ikeda D, et al. Pretreatment Tattoo Marking of Suspicious Axillary Lymph Nodes: Reliability and Correlation with Sentinel Lymph Node. Ann Surg Oncol. 2019;26(8):2452-8. doi: 10.1245/s10434-019-07419-3.
» https://doi.org/10.1245/s10434-019-07419-3 -
25 Park S, Koo JS, Kim GM, Sohn J, Kim S Il, Cho YU, et al. Feasibility of charcoal tattooing of cytology-proven metastatic axillary lymph node at diagnosis and sentinel lymph node biopsy after neoadjuvant chemotherapy in breast cancer patients. Cancer Res Treat. 2018;50(3):801-12. doi: 10.4143/crt.2017.210.
» https://doi.org/10.4143/crt.2017.210 -
26 Canavese G, Catturich A, Vecchio C, Tomei D, Estienne M, Moresco L, et al. Pre-operative localization of non-palpable lesions in breast cancer by charcoal suspension. Eur J Surg Oncol. 1995;21(1):47-9. doi: 10.1016/s0748-7983(05)80067-8.
» https://doi.org/10.1016/s0748-7983(05)80067-8 -
27 Svane G. A stereotaxic technique for preoperative marking of non-palpable breast lesions. Acta Radiol Diagn (Stockh). 1983;24(2):145-51. doi: 10.1177/028418518302400207.
» https://doi.org/10.1177/028418518302400207 - 28 Hortobagyi GN, Connolly JL, Orsi CJD, Edge SB, Mittendorf EA, Rugo HS, et al. AJCC Cancer Staging Manual 8th Edition. Definitions. 2020.
-
29 Cavalcanti TCS, Malafaia O, Nassif PAN, Skare TL, Ogata DC, Miguel MT, et al. Lesões impalpáveis da mama marcadas com suspensão de carvão: Non-palpable breast lesions marked with coal suspension: evaluation of anatomopathological aspects, viability of interpretation and inflammatory response. Rev. Col. Bras. Cir. 2012;39(6):469-75. doi: 10.1590/S0100-69912012000600005.
» https://doi.org/10.1590/S0100-69912012000600005 -
30 Rose A, Collins JP, Neerhut P, Bishop CV, Mann GB. Carbon localisation of impalpable breast lesions. Breast. 2003;12(4):264-9. doi: 10.1016/s0960-9776(03)00105-x.
» https://doi.org/10.1016/s0960-9776(03)00105-x -
31 Gobardhan PD, Gavilá P, De Wall LL, van der Laan L, Ten Tije F, van der Meer DCH, et al. The role of radioactive iodine-125 seed localization in breast-conserving therapy following neoadjuvant chemotherapy. Ann Oncol. 2013;24(3):668-73. doi: 10.1093/annonc/mds475.
» https://doi.org/10.1093/annonc/mds475 -
32 Houssami N, MacAskill P, Marinovich ML, Dixon JM, Irwig L, Brennan ME, et al. Meta-analysis of the impact of surgical margins on local recurrence in women with early-stage invasive breast cancer treated with breast-conserving therapy. Eur J Cancer. 2010;46(18):3219-32. doi: 10.1016/j.ejca.2010.07.043.
» https://doi.org/10.1016/j.ejca.2010.07.043 -
33 Barentsz MW, Van Den Bosch MAAJ, Veldhuis WB, Van Diest PJ, Pijnappel RM, Witkamp AJ, et al. Radioactive seed localization for non-palpable breast cancer. Br J Surg. 2013;100(5):582-8. doi: 10.1002/bjs.9068.
» https://doi.org/10.1002/bjs.9068 -
34 Kass R, Kumar G, Klimberg VS, Kass L, Henry-Tillman R, Johnson A, et al. Clip migration in stereotactic biopsy. Am J Surg. 2002;184(4):325-31. doi: 10.1016/s0002-9610(02)00952-2.
» https://doi.org/10.1016/s0002-9610(02)00952-2 -
35 Calhoun K, Giuliano A, Brenner RJ. Intraoperative loss of core biopsy clips: clinical implications. AJR Am J Roentgenol. 2008;190(3):196-200. doi: 10.2214/AJR.07.2569.
» https://doi.org/10.2214/AJR.07.2569 -
36 Langer I, Marti WR, Guller U, Moch H, Harder F, Oertli D, et al. Axillary recurrence rate in breast cancer patients with negative sentinel lymph node (SLN) or SLN micrometastases: Prospective analysis of 150 patients after SLN biopsy. Ann Surg. 2005;241(1):152-8. doi: 10.1097/01.sla.0000149305.23322.3c.
» https://doi.org/10.1097/01.sla.0000149305.23322.3c -
37 Fisher B, Anderson S, Bryant J, Margolese RG, Deutsch M, Fisher ER, et al. Twenty-Year Follow-up of a Randomized Trial Comparing Total Mastectomy, Lumpectomy, and Lumpectomy plus Irradiation for the Treatment of Invasive Breast Cancer. N Engl J Med. 2002;347(16):1233-41. doi: 10.1056/NEJMoa022152.
» https://doi.org/10.1056/NEJMoa022152 -
38 Fredriksson I, Liljegren G, Arnesson LG, Emdin SO, Palm-Sjövall M, Fornander T, et al. Consequences of axillary recurrence after conservative breast surgery. Br J Surg. 2002;89(7):902-8. doi: 10.1046/j.1365-2168.2002.02117.x.
» https://doi.org/10.1046/j.1365-2168.2002.02117.x -
39 Fisher B, Redmond C, Fisher ER, Bauer M, Wolmark N, Wickerham DL, et al. Ten-Year Results of a Randomized Clinical Trial Comparing Radical Mastectomy and Total Mastectomy with or without Radiation. N Engl J Med. 1985;312(11):674-81. doi: 10.1056/NEJM198503143121102.
» https://doi.org/10.1056/NEJM198503143121102 -
40 Arvold ND, Taghian AG, Niemierko A, Abi Raad RF, Sreedhara M, Nguyen PL, et al. Age, breast cancer subtype approximation, and local recurrence after breast-conserving therapy. J Clin Oncol. 2011;29(29):3885-91. doi: 10.1200/JCO.2011.36.1105.
» https://doi.org/10.1200/JCO.2011.36.1105 -
41 Andreis D, Bonardi S, Allevi G, Aguggini S, Gussago F, Milani M, et al. Sentinel lymph node surgery after neoadjuvant chemotherapy in patients with T2 to T4, N0 and N1 breast cancer. Breast. 2016;29:55-61. doi: 10.1016/j.breast.2016.07.003.
» https://doi.org/10.1016/j.breast.2016.07.003 -
42 Laot L, Laas E, Girard N, Dumas E, Daoud E, Grandal B, et al. The prognostic value of lymph node involvement after neoadjuvant chemotherapy is different among breast cancer subtypes. Cancers (Basel). 2021;13(2):1-20. doi: 10.3390/cancers13020171.
» https://doi.org/10.3390/cancers13020171 -
43 Yau C, Osdoit M, van der Noordaa M, Shad S, Wei J, de Croze D, et al. Measurement of residual breast cancer burden to predict survival after neoadjuvant chemotherapy. Lancet Oncol. 2007;25(28):4414-22. doi: 10.1200/JCO.2007.10.6823.
» https://doi.org/10.1200/JCO.2007.10.6823 -
44 Yau C, Osdoit M, van der Noordaa M, Shad S, Wei J, de Croze D, et al. Residual cancer burden after neoadjuvant chemotherapy and long-term survival outcomes in breast cancer: a multicentre pooled analysis of 5161 patients. Lancet Oncol. 2022;23(1):149-60. doi: 10.1016/S1470-2045(21)00589-1.
» https://doi.org/10.1016/S1470-2045(21)00589-1 -
45 Tutt ANJ, Garber JE, Kaufman B, Viale G, Fumagalli D, Rastogi P, et al. Adjuvant Olaparib for Patients with BRCA1 - or BRCA2 -Mutated Breast Cancer . N Engl J Med. 2021;384(25):2394-405. doi: 10.1056/NEJMoa2105215.
» https://doi.org/10.1056/NEJMoa2105215




