A Biopsy of Sentinel Lymph Nodes in Patients with Clinically Positive Lymph Nodes Following Neoadjuvant Therapy: A Comparison of Distant Results of SLNB and ALND in Patients with ycN0 Status
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Keywords

breast cancer
sentinel lymph node biopsy
axillary lymph node dissection

How to Cite

Tabagua, T. T., Krivorotko, P. V., Amirov, N. S., Levchenko, V. E., Emelyanov, A. S., Vychegzhanina, E. P., Semiglazov, V. F., Novikov, S. S., & Krzhivitskiy, P. I. (2025). A Biopsy of Sentinel Lymph Nodes in Patients with Clinically Positive Lymph Nodes Following Neoadjuvant Therapy: A Comparison of Distant Results of SLNB and ALND in Patients with ycN0 Status. Voprosy Onkologii, 71(3), OF–2315. https://doi.org/10.37469/0507-3758-2025-71-3-OF-2315

Abstract

Aim. To evaluate the long-term treatment outcomes of SLNB and ALND in patients who received NACT and achieved complete clinical regression in lymph nodes.

Materials and Methods. A retrospective cohort study was conducted which included data from 288 patients with no clinical lymph node involvement on the background of NACT between 2016 and 2023. 189 patients who underwent ALND were included in the control group. The experimental group comprised 99 patients who underwent ALND only. Patient characteristics were categorized according to the type of axillary surgery, with numeric variables presented as medians and ranges, and categorical data presented as frequencies (number and percentage). All statistical tests were two-sided and p-values below 0.05 were considered to be statistically significant.

Results. At a median follow-up of 60 months, locoregional recurrence was observed in three patients across different treatment groups. One patient in the ALD group (1/146, 0.6 %) had stage ypN1a and received adjuvant radiation therapy. In the BSLU group, followed by ALD, recurrence occurred in one patient (1/43, 2.3 %), who had a similar stage and received further adjuvant radiation therapy. One patient who underwent BSLU alone (1/99, 1 %) had ypN0 status and received adjuvant radiation therapy. Two cases of recurrence were accompanied by skin manifestations in patients who underwent mastectomy, and in one case recurrence was limited to the axillary region. During the entire follow-up period, 52 patients (18 %) died, including 42 (42/146, 28.8 %) from the ALD group and 10 (10/142, 7 %) from the BSLU group. To evaluate the long-term outcomes, patients were categorized according to the method of axillary surgery (BSLU or ALD). The overall survival (OS) in the BSLU group was 96.3 and 93.3 % after 3 and 5 years, respectively. In the ALD group, the rates were 86.3 and 80.8 % (p = 0.001). The recurrence-free survival (RFS) at 3 and 5 years was significantly higher in the BSLU group, at 90.1 and 85.2 % respectively, compared to 77.4 and 73.3 % in the ALD group (p = 0.005). The survival rate without distant metastases was also higher in the BSLU group, at 93.7 and 89.4 %, vs. 79.5 and 75.3 % in the ALD group (p = 0.001). The breast cancer-specific survival was higher in the BSLU group, reaching 97.9 and 95.7 % at 3 and 5 years, respectively, compared to 89.7 and 84.9 % in the ALD group (p = 0.002).

Conclusion. The difference in OS between the control and experimental groups suggests that these results are probably influenced by factors unrelated to the surgical approach. The choice of surgical approach has a significant impact on patients' quality of life.

https://doi.org/10.37469/0507-3758-2025-71-3-OF-2315
##article.numberofdownloads## 9
##article.numberofviews## 29
pdf (Русский)

References

Giuliano A.E., Hunt K.K., Ballman K.V., et al. Axillary dissection vs no axillary dissection in women with invasive breast cancer and sentinel node metastasis: a randomized clinical trial. JAMA. 2011; 305(6): 569-575.-DOI: 10.1001/jama.2011.90.

Veronesi U., Paganelli G., Viale G., et al. A randomized comparison of sentinel-node biopsy with routine axillary dissection in breast cancer. N Engl J Med. 2003; 349(6): 546-553.-DOI: 10.1056/NEJMoa012782.

Tinterri C., Barbieri E., Sagona A., et al. De-Escalation surgery in cT3-4 breast cancer patients after neoadjuvant therapy: predictors of breast conservation and comparison of long-term oncological outcomes with mastectomy. Cancers (Basel). 2024; 16(6): 1169.-DOI: 10.3390/cancers16061169.

Montagna G., Mamtani A., Knezevic A., et al. Selecting node-positive patients for axillary downstaging with neoadjuvant chemotherapy. Ann Surg Oncol. 2020; 27(11): 4515-4522.-DOI: 10.1245/s10434-020-08650-z.

Boughey J.C., Suman V.J., Mittendorf E.A., 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): 1455-1461.-DOI: 10.1001/jama.2013.278932.

Aragon-Sanchez S., Oliver-Perez M.R., Madariaga A., et al. Accuracy and limitations of sentinel lymph node biopsy after neoadjuvant chemotherapy in breast cancer patients with positive nodes. Breast J. 2022; 2022: 1507881.-DOI: 10.1155/2022/1507881.

Vanni G., Pellicciaro M., Materazzo M., et al. Neoadjuvant treatment as a risk factor for variation of upper limb lymph node drainage during axillary reverse mapping in breast cancer: a prospective observational study. Anticancer Res. 2022; 42(8): 3879-3888.-DOI: 10.21873/anticanres.15881.

Jain U., Stewart-Parker E., Shaari E., et al. Feasibility study to identify changes in lymphatic drainage pathway post neo-adjuvant chemotherapy (NACT) in breast cancer patients with cN1 axilla –– FILNAC trial. Eur J Surg Oncol. 2023; 49(2): e23.-DOI: 10.1016/j.ejso.2022.11.114.

Tan V.K., Goh B.K., Fook-Chong S., et al. The feasibility and accuracy of sentinel lymph node biopsy in clinically node-negative patients after neoadjuvant chemotherapy for breast cancer--a systematic review and meta-analysis. J Surg Oncol. 2011; 104(1): 97-103.-DOI: 10.1002/jso.21911.

Sanchez A.M., Terribile D., Franco A., et al. Sentinel node biopsy after neoadjuvant chemotherapy for breast cancer: preliminary experience with clinically node negative patients after systemic treatment. J Pers Med. 2021; 11(3): 172.-DOI: 10.3390/jpm11030172.

Murphy B.L., Day C.N., Hoskin T.L., et al. Neoadjuvant chemotherapy use in breast cancer is greatest in excellent responders: triple-negative and HER2+ subtypes. Ann Surg Oncol. 2018; 25(8): 2241-2248.-DOI: 10.1245/s10434-018-6531-5.

van der Voort A., Liefaard M.C., van Ramshorst M.S., et al. Efficacy of neoadjuvant treatment with or without pertuzumab in patients with stage II and III HER2-positive breast cancer: a nationwide cohort analysis of pathologic response and 5-year survival. Breast. 2022; 65: 110-115.-DOI: 10.1016/j.breast.2022.07.005.

Zhou M., Wang S, Wan N., et al. Efficacy and safety of neoadjuvant pertuzumab plus trastuzumab in combination with chemotherapy regimen in Chinese patients with HER2-positive early breast cancer: a real-world retrospective multi-center cohort study. Ann Transl Med. 2022; 10(24): 1387.-DOI: 10.21037/atm-22-6054.

Simons J.M., van Nijnatten T.J.A., van der Pol C.C., et al. Diagnostic accuracy of different surgical procedures for axillary staging after neoadjuvant systemic therapy in node-positive breast cancer: a systematic review and meta-analysis. Ann Surg. 2019; 269(3): 432-442.-DOI: 10.1097/SLA.0000000000003075.

Kuehn T., Bauerfeind I., Fehm T., 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): 609-618.-DOI: 10.1016/S1470-2045(13)70166-9.

Semiglazov V.F., Krivorotko P.V., Zhiltsova E.K., et al. Twenty-year experience of examining biopsies of signal lymph nodes in breast cancer. Tumors of Female Reproductive System. 2020; 16(1): 12-20.-DOI: 10.17650/1994-4098-2020-16-1-12-20.

Kuemmel S., Heil J., Rueland A., et al. A prospective, multicenter registry study to evaluate the clinical feasibility of targeted axillary dissection (TAD) in node-positive breast cancer patients. Ann Surg. 2022; 276(5): e553-e562.-DOI: 10.1097/SLA.0000000000004572.

Krivorotko P.V., Novikov S.N., Tabagua T.T., et al. Method of determination of signaling lymph nodes in breast cancer using radioisotope and/or fluorescent methods. Educational and methodological manual. St. Petersburg: N.N. Petrov NMRC of oncology. 2024.

Swarnkar P.K., Tayeh S., Michell M.J., 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.

Volkova Yu.I., Zikiryakhodzhaev A.D., Volchenko N.N., et al. Diagnosis of the sentinel lymph node during neoadjuvant chemotherapy. P.A. Herzen Journal of Oncology. 2021; 10(6): 100-105.-DOI: 10.17116/onkolog202110061100.

van Nijnatten T.J., Schipper R.J., Lobbes M.B., et al. The diagnostic performance of sentinel lymph node biopsy in pathologically confirmed node positive breast cancer patients after neoadjuvant systemic therapy: A systematic review and meta-analysis. Eur J Surg Oncol. 2015; 41(10): 1278-1287.-DOI: 10.1016/j.ejso.2015.07.020.

Keelan S., Boland M.R., Ryan É.J., et al. Long-term survival in patients with node-positive breast cancer who undergo sentinel lymph node biopsy alone after neoadjuvant chemotherapy: meta-analysis. Br J Surg. 2023; 110(3): 324-332.-DOI: 10.1093/bjs/znac413.

Semiglazov V.F., Topuzov E.E., Bavli J.L., et al. Neoadjuvant chemotherapy in the complex treatment of breast cancer. Voprosy Onkologii = Problems in Oncology. 1992; 38(8).

Lim S.Z., Yoo T.K., Lee S.B., et al. Long-term outcome in patients with nodal-positive breast cancer treated with sentinel lymph node biopsy alone after neoadjuvant chemotherapy. Breast Cancer Res Treat. 2024; 203(1): 95-102.-DOI: 10.1007/s10549-023-07104-w.

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