É Possível Evitar a Biópsia do Linfonodo Sentinela em Pacientes com Câncer de Mama e Linfonodo Axilar Positivo com Resposta Patológica Completa à Quimioterapia Neoadjuvante?

Autores

  • Helano de Paula Gonçalves Souza Universidade Federal do Ceará (UFC). Instituto do Câncer do Ceará (ICC). Fortaleza (CE), Brasil. https://orcid.org/0000-0001-9641-0765
  • Francisco das Chagas Medeiros Universidade Federal do Ceará (UFC), Departamento de Saúde da Mulher, da Criança e do Adolescente. Fortaleza (CE), Brasil. https://orcid.org/0000-0003-2716-7807
  • Marcos Venício Alves Lima Instituto Nacional de Câncer (INCA). Rio de Janeiro (RJ), Brasil. https://orcid.org/0000-0002-4944-5022

DOI:

https://doi.org/10.32635/2176-9745.RBC.2023v69n1.2759

Palavras-chave:

neoplasias da mama, biópsia de linfonodo sentinela, terapia neoadjuvante

Resumo

Introdução: O câncer de mama representa 24,5% dos novos casos de neoplasias em mulheres no mundo. A quimioterapia neoadjuvante é uma importante ferramenta no tratamento dessa patologia, possibilita cirurgias menos agressivas na mama e axila, além de minimizar sequelas. Objetivo: Analisar a possibilidade de se evitar a realização da biópsia do linfonodo sentinela em pacientes com câncer de mama submetidas à quimioterapia neoadjuvante que apresentem resposta patológica completa no tumor primário e na axila, tratadas em uma instituição de referência no Nordeste brasileiro. Método: Estudo prospectivo, observacional, de coorte em pacientes com câncer de mama submetidas à quimioterapia neoadjuvante e operadas no Hospital Haroldo Juaçaba, no período de março de 2019 a julho de 2021. Resultados: Foram incluídas no estudo 45 pacientes, com média de idade de 52,6 anos, sendo todas do sexo feminino. Após quimioterapia neoadjuvante, nove pacientes (21,4%) apresentaram resposta patológica completa na mama e 17 (40,5%), resposta patológica completa nos linfonodos. Os pacientes com resposta completa na mama apresentaram uma prevalência de resposta completa em linfonodo 20,44 vezes superior aos pacientes que não tiveram a mesma resposta. Conclusão: A resposta patológica completa na mama à quimioterapia neoadjuvante mostra uma tendência em predizer uma resposta patológica nos linfonodos axilares, reforçando que, com essa condição, a biópsia do linfonodo sentinela poderia ser evitada sem causar prejuízos ao controle local do câncer de mama.

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Referências

Instituto Nacional de Câncer [Internet]. Rio de Janeiro: INCA; [data desconhecida]. Estimativa; 2022 out 12 [atualizado 2022 nov 23; acesso 2023 jan 16]. Disponível em: https://www.gov.br/inca/pt-br/assuntos/cancer/numeros/estimativa

Rastogi P, Anderson SJ, Bear HD, et al. Preoperative chemotherapy: updates of National Surgical Adjuvant Breast and Bowel Project Protocols B-18 and B-27. J Clin Oncol. 2008;26(5):778-85. doi: https://doi.org/10.1200/JCO.2007.15.0235 DOI: https://doi.org/10.1200/JCO.2007.15.0235

Mauri D, Pavlidis N, Ioannidis JP. Neoadjuvant versus adjuvant systemic treatment in breast cancer: a meta-analysis. J Natl Cancer Inst. 2005;97(3):188-94. doi: https://doi.org/10.1093/jnci/dji021 DOI: https://doi.org/10.1093/jnci/dji021

Siso C, Torres J, Esgueva-Colmenarejo A, 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: https://doi.org/10.1245/s10434-017-6270-z DOI: https://doi.org/10.1245/s10434-017-6270-z

Bear HD, Anderson S, Brown A, et al. The effect on tumor response of adding sequential preoperative docetaxel to preoperative doxorubicin and cyclophosphamide: preliminary results from National Surgical Adjuvant Breast and Bowel Project Protocol B-27. J Clin Oncol. 2003;21(22):4165-74. doi: https://doi.org/10.1200/JCO.2003.12.005 DOI: https://doi.org/10.1200/JCO.2003.12.005

Bear HD, Anderson S, Smith RE, et al. Sequential preoperative or postoperative docetaxel added to preoperative doxorubicin plus cyclophosphamide for operable breast cancer: National Surgical Adjuvant Breast and Bowel Project Protocol B-27. J Clin Oncol. 2006;24(13):2019-27. doi: https://doi.org/10.1200/JCO.2005.04.1665 DOI: https://doi.org/10.1200/JCO.2005.04.1665

Giuliano AE, Kirgan DM, Guenther JM, et al. Lymphatic mapping and sentinel lymphadenectomy for breast cancer. Ann Surg. 1994;220(3):391-8. doi: https://doi.org/10.1097/00000658-199409000-00015 DOI: https://doi.org/10.1097/00000658-199409000-00015

Carter CL, Allen C, Henson DE. Relation of tumor size, lymph node status, and survival in 24,740 breast cancer cases. Cancer. 1989;63(1):181-7. doi: https://doi.org/10.1002/1097-0142(19890101)63:1%3C181::AID-CNCR2820630129%3E3.0.CO;2-H DOI: https://doi.org/10.1002/1097-0142(19890101)63:1<181::AID-CNCR2820630129>3.0.CO;2-H

Veronesi U, Paganelli G, Viale G, et al. Sentinel-lymph-node biopsy as a staging procedure in breast cancer: update of a randomised controlled study. Lancet Oncol. 2006;7(12):983-90. doi: https://doi.org/10.1016/S1470-2045(06)70947-0 DOI: https://doi.org/10.1016/S1470-2045(06)70947-0

Krag DN, Anderson SJ, Julian TB, et al. Sentinel-lymph-node resection compared with conventional axillary-lymph-node dissection in clinically node-negative patients with breast cancer: overall survival findings from the NSABP B-32 randomised phase 3 trial. Lancet Oncol. 2010;11(10):927-33. doi: https://doi.org/10.1016/S1470-2045(10)70207-2 DOI: https://doi.org/10.1016/S1470-2045(10)70207-2

Boughey JC, Suman VJ, Mittendorf EA, 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: https://doi.org/10.1001/jama.2013.278932 DOI: https://doi.org/10.1001/jama.2013.278932

Straver ME, Meijnen P, van Tienhoven G, et al. Sentinel node identification rate and nodal involvement in the EORTC 10981-22023 AMAROS trial. Ann Surg Oncol. 2010;17(7):1854-61. doi: https://doi.org/10.1245/s10434-010-0945-z DOI: https://doi.org/10.1245/s10434-010-0945-z

Newman EA, Sabel MS, Nees AV, et al. Sentinel lymph node biopsy performed after neoadjuvant chemotherapy is accurate in patients with documented node-positive breast cancer at presentation. Ann Surg Oncol. 2007;14(10):2946-52. doi: https://doi.org/10.1245/s10434-007-9403-y DOI: https://doi.org/10.1245/s10434-007-9403-y

Lyman GH, Giuliano AE, Somerfield MR, et al. American Society of Clinical Oncology guideline recommendations for sentinel lymph node biopsy in early-stage breast cancer. J Clin Oncol. 2005;23(30):7703-20. doi: https://doi.org/10.1200/JCO.2005.08.001 DOI: https://doi.org/10.1200/JCO.2005.08.001

Fisher B, Anderson S, Bryant J, 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: https://doi.org/10.1056/NEJMoa022152 DOI: https://doi.org/10.1056/NEJMoa022152

Caudle AS, Yang WT, Krishnamurthy S, et al. Improved axillary evaluation following neoadjuvant therapy for patients with node-positive breast cancer using selective evaluation of clipped nodes: implementation of targeted axillary dissection. J Clin Oncol. 2016;34(10):1072-8. doi: https://doi.org/10.1200/JCO.2015.64.0094 DOI: https://doi.org/10.1200/JCO.2015.64.0094

Donker M, Straver ME, Wesseling J, 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: https://doi.org/10.1097/SLA.0000000000000558 DOI: https://doi.org/10.1097/SLA.0000000000000558

Fayanju OM, Ren Y, Thomas SM, et al. The clinical significance of breast-only and node-only Pathologic Complete Response (pCR) After Neoadjuvant Chemotherapy (NACT): a review of 20,000 breast cancer patients in the National Cancer Data Base (NCDB). Ann Surg. 2018;268(4):591-601. doi: https://doi.org/10.1097/SLA.0000000000002953 DOI: https://doi.org/10.1097/SLA.0000000000002953

Conselho Nacional de Saúde (BR). Resolução nº 466, de 12 de dezembro de 2012. Aprova as diretrizes e normas regulamentadoras de pesquisas envolvendo seres humanos [Internet]. Diário Oficial da União, Brasília, DF. 2013 jun 13 [acesso 2021 ago 1]; Seção 1:59. Disponível em: https://bvsms.saude.gov.br/bvs/saudelegis/cns/2013/res0466_12_12_2012.html

Halsted WS. The results of radical operations for the cure of carcinoma of the breast. Ann Surg. 1907;46(1):1-19. doi: https://doi.org/10.1097/00000658-190707000-00001 DOI: https://doi.org/10.1097/00000658-190707000-00001

Halsted WS. The results of operations for the cure of cancer of the breast performed at the Johns Hopkins Hospital from June, 1889, to January, 1894. Ann Surg. 1894;20(5):497-555. doi: https://doi.org/10.1097/00000658-189407000-00075 DOI: https://doi.org/10.1097/00000658-189407000-00075

Patey DH, Dyson WH. The prognosis of carcinoma of the breast in relation to the type of operation performed. Br J Cancer. 1948;2(1):7-13. doi: https://doi.org/10.1038/bjc.1948.2 DOI: https://doi.org/10.1038/bjc.1948.2

Veronesi U, Saccozzi R, Del Vecchio M, et al. Comparing radical mastectomy with quadrantectomy, axillary dissection, and radiotherapy in patients with small cancers of the breast. N Engl J Med. 1981;305(1):6-11. doi: https://doi.org/10.1056/NEJM198107023050102 DOI: https://doi.org/10.1056/NEJM198107023050102

Wilke LG, McCall LM, Posther KE, et al. Surgical complications associated with sentinel lymph node biopsy: results from a prospective international cooperative group trial. Ann Surg Oncol. 2006;13(4):491-500. doi: https://doi.org/10.1245/ASO.2006.05.013 DOI: https://doi.org/10.1245/ASO.2006.05.013

Warmuth MA, Bowen G, Prosnitz LR, et al. Complications of axillary lymph node dissection for carcinoma of the breast: a report based on a patient survey. Cancer. 1998;83(7):1362-8. doi: https://doi.org/10.1002/(sici)1097-0142(19981001)83:7%3C1362::aid-cncr13%3E3.0.co;2-2 DOI: https://doi.org/10.1002/(SICI)1097-0142(19981001)83:7<1362::AID-CNCR13>3.0.CO;2-2

Hartmann S, Reimer T, Gerber B, et al. 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: https://doi.org/10.1016/j.ejso.2018.05.035 DOI: https://doi.org/10.1016/j.ejso.2018.05.035

Balasubramanian R, Morgan C, Shaari E, et al. Wire guided localisation for targeted axillary node dissection is accurate in axillary staging in node positive breast cancer following neoadjuvant chemotherapy. Eur J Surg Oncol. 2020;46(6):1028-33. doi: https://doi.org/10.1016/j.ejso.2019.12.007 DOI: https://doi.org/10.1016/j.ejso.2019.12.007

García-Novoa A, Acea-Nebril B, Díaz Carballada C, et al. Combining wire localization of clipped nodes with sentinel lymph node biopsy after neoadjuvant chemotherapy in node-positive breast cancer: preliminary results from a prospective study. Ann Surg Oncol. 2021;28(2):958-67. doi: https://doi.org/10.1245/s10434-020-08925-5 DOI: https://doi.org/10.1245/s10434-020-08925-5

Kim EY, Byon WS, Lee KH, et al. Feasibility of preoperative axillary lymph node marking with a clip in breast cancer patients before neoadjuvant chemotherapy: a preliminary study. World J Surg. 2018;42(2):582-9. doi: https://doi.org/10.1007/s00268-017-4171-8 DOI: https://doi.org/10.1007/s00268-017-4171-8

Liedtke C, Mazouni C, Hess KR, et al. Response to neoadjuvant therapy and long-term survival in patients with triple-negative breast cancer. J Clin Oncol. 2008;26(8):1275-81. doi: https://doi.org/10.1200/JCO.2007.14.4147 DOI: https://doi.org/10.1200/JCO.2007.14.4147

Buzdar AU, Ibrahim NK, Francis D, et al. Significantly higher pathologic complete remission rate after neoadjuvant therapy with trastuzumab, paclitaxel, and epirubicin chemotherapy: results of a randomized trial in human epidermal growth factor receptor 2-positive operable breast cancer. J Clin Oncol. 2005;23(16):3676-85. doi: https://doi.org/10.1200/JCO.2005.07.032 DOI: https://doi.org/10.1200/JCO.2005.07.032

Green MC, Buzdar AU, Smith T, et al. Weekly paclitaxel improves pathologic complete remission in operable breast cancer when compared with paclitaxel once every 3 weeks. J Clin Oncol. 2005;23(25):5983-92. doi: https://doi.org/10.1200/JCO.2005.06.232 DOI: https://doi.org/10.1200/JCO.2005.06.232

Mariscal Martínez A, Vives Roselló I, Salazar Gómez A, et al. Advantages of preoperative localization and surgical resection of metastatic axillary lymph nodes using magnetic seeds after neoadjuvant chemotherapy in breast cancer. Surg Oncol. 2021;36:28-33. doi: https://doi.org/10.1016/j.suronc.2020.11.013 DOI: https://doi.org/10.1016/j.suronc.2020.11.013

Laws A, Dillon K, Kelly BN, et al. Node-positive patients treated with neoadjuvant chemotherapy can be spared axillary lymph node dissection with wireless non-radioactive localizers. Ann Surg Oncol. 2020;27(12):4819-27. doi: https://doi.org/10.1245/s10434-020-08902-y DOI: https://doi.org/10.1245/s10434-020-08902-y

Publicado

2023-01-25

Como Citar

1.
Souza H de PG, Medeiros F das C, Lima MVA. É Possível Evitar a Biópsia do Linfonodo Sentinela em Pacientes com Câncer de Mama e Linfonodo Axilar Positivo com Resposta Patológica Completa à Quimioterapia Neoadjuvante?. Rev. Bras. Cancerol. [Internet]. 25º de janeiro de 2023 [citado 23º de dezembro de 2024];69(1):e-062759. Disponível em: https://rbc.inca.gov.br/index.php/revista/article/view/2759

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