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DOI: 10.5935/2526-8732.20210026
Analysis on complete pathological response and estimated survival among breast cancer patients undergoing neoadjuvant chemotherapy in a private institution in the state of Rio de Janeiro
Análise da resposta patológica completa e sobrevida estimada em pacientes com câncer de mama em quimioterapia neoadjuvante em instituição privada do estado do Rio de Janeiro Financial support: None to declare.ABSTRACT
Objective: Breast cancer is the most common malignancy among women, both in developed and in developing countries. Indications for neoadjuvant treatment have been expanded so that pathological responses can be evaluated. Diversified therapeutic approaches may thus be indicated in accordance with each residual disease profile. This was a real-life study, in which the aim was to analyze the complete pathological response (CPR) and estimated survival among breast cancer patients undergoing neoadjuvant chemotherapy in a private institution in the state of Rio de Janeiro.
Methods: This was a prospective observational cohort study on patients diagnosed with breast cancer and treated with neoadjuvant chemotherapy, in a private institution. The primary objective of this study was to analyze CPR. As secondary endpoints, we evaluated the disease-free survival (DFS) and overall survival (OS) of these patients and correlated them with clinical-pathological variables.
Results: CPR was achieved in: 12.5% of luminal A cases; 19.5% of luminal B/HER-2-negative cases; 38.5% of luminal B/ HER-2-positive cases; 65% of HER-2-enriched cases; and 37.8% of triple negative cases. There was a significant correlation between CPR and histopathological subtypes (p<0.001). At the end of 36 months, the DFS for patients with CPR was 89.1% vs. 72.4% for the others (p=0.01). OS could not be calculated for patients who achieved CPR, because there was no event.
Conclusion: We confirmed in this study that a correlation exists between CPR and overall survival. In addition, we were able to show that even in developing countries, such as Brazil, appropriate treatments can be offered in accordance with international guidelines, such that our results were consequently similar to those in the worldwide literature.
RESUMO
Objetivo: O câncer de mama é a neoplasia maligna mais comum entre as mulheres, tanto em países desenvolvidos quanto em desenvolvimento. As indicações para o tratamento neoadjuvante foram expandidas para que as respostas patológicas possam ser avaliadas. Abordagens terapêuticas diversificadas podem, portanto, ser indicadas de acordo com o perfil de cada doença residual. Trata-se de um estudo da vida real, cujo objetivo foi analisar a resposta patológica completa (RCP) e a estimativa de sobrevida em pacientes com câncer de mama em quimioterapia neoadjuvante em uma instituição privada do estado do Rio de Janeiro.
Métodos: Estudo de coorte prospectivo observacional em pacientes com diagnóstico de câncer de mama e tratamento com quimioterapia neoadjuvante, em instituição privada. O objetivo principal deste estudo foi analisar a RCP. Como desfechos secundários, avaliamos a sobrevida livre de doença (SLD) e a sobrevida geral (SG) desses pacientes e as correlacionamos com as variáveis clínico-patológicas.
Resultados: A RCP foi alcançada em: 12,5% dos casos luminal A; 19,5% dos casos luminais B/HER-2 negativos; 38,5% dos casos luminais B/HER-2 positivos; 65% dos casos enriquecidos com HER-2; e 37,8% de casos triplo negativos. Houve uma correlação significativa entre a RCP e os subtipos histopatológicos (p<0,001). Ao final de 36 meses, a DFS para pacientes com RCP foi de 89,1% vs. 72,4% para os demais (p=0,01). SG não pôde ser calculado para pacientes que alcançaram RCP, porque não houve nenhum evento.
Conclusão: Confirmamos neste estudo que existe uma correlação entre a RCP e a sobrevida global. Além disso, pudemos mostrar que mesmo em países em desenvolvimento, como o Brasil, tratamentos adequados podem ser oferecidos de acordo com as diretrizes internacionais, de forma que nossos resultados foram, consequentemente, semelhantes aos da literatura mundial.
Publication History
Received: 15 June 2021
Accepted: 19 August 2021
Article published online:
17 September 2021
© 2021. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)
Thieme Revinter Publicações Ltda.
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil
Letícia Morais C. O Sermoud, Maria de Fátima Dias Gaui, Thamirez de Almeida Vieira Ferreira, Lilian Campos Lerner, Gustavo Buscacio, Dante Pagnoncelli, Luiz Henrique Araujo. Analysis on complete pathological response and estimated survival among breast cancer patients undergoing neoadjuvant chemotherapy in a private institution in the state of Rio de Janeiro. Brazilian Journal of Oncology 2021; 17: e-20210026.
DOI: 10.5935/2526-8732.20210026
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REFERENCES
-
1
World Health Organization.
Breast Cancer: prevention and control. Disponível em https://www.who.int/cancer/detection/breastcancer/en/ Acesso em 08/12/2020
- 2 Instituto Nacional do Câncer (INCA). Estimativa 2020 - Incidência do Câncer no Brasil. 2019 Disponível em https://www.inca.gov.br/sites/ufu.sti.inca.local/files//media/document//estimativa-2020-incidencia-de-cancer-no-brasil.pdf . Acesso em 08/12/2020
-
3
AJCC (American Joint Committee on Cancer) Cancer Staging Manual.
8th. 3rd printing, Amin MB, Edge SB, Greene FL, et al (Eds), Springer; Chicago: 2018
- 4 Ikeda T, Jinno H, Matsui A. et al. The role of neoadjuvant chemotherapy for breast cancer treatment. Breast Cancer 2008; 9 (01) 8-14
- 5 Pastorello R.G, Laws A, Grossmith S. et al. Clinico-pathologic predictors of patterns of residual disease following neoadjuvant chemotherapy for breast cancer. Mod Pathol 2020;
- 6 Symmans W.F, Peintinger F, Hatzis C. et al. Measurement of Residual Breast Cancer Burden to Predict Survival After Neoadjuvant Chemotherapy. Journal of Clinical Oncology 2007; 25: 4414-4444
- 7 Kuerer HM, Newman LA, Smith TM. et al. Clinical course of breast cancer patients with complete pathologic primary tumor and axillary lymph node response to doxorubicin-based neoadjuvant chemotherapy. J Clin Oncol 17: 460-469 1999;
- 8 Kaufmann M, Hortobagyi GN, Goldhirsch A. et al. Recommendations from an international expert panel on the use of neoadjuvant (primary) systemic treatment of operable breast cancer: An update. J Clin Oncol 24: 1940-1949 2006;
- 9 Coates AS, Winer EP, Goldhirsch A. et al. Tailoring therapies-improving the management of Early breast cancer: St Gallen International Expert Consensus on the Primary Therapy of Early Breast Cancer 2015. Ann Oncol 2015; 26 (08) 1533-1546
- 10 Goldhirsch A, Winer EP, Coates AS. et al. 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 (09) 2206-2223
-
11
US Department of Health and Human Services Food and Drug Administration, Center for Drug Evaluation and Research (CDER).
Guidance for Industry: Pathological Complete Response in Neoadjuvant Treatment of High-Risk Early-Stage Breast Cancer: Use as an Endpoint to Support Accelerated Approval. Disponível em https://www.fda.gov/media/83507/download . Acesso em 26/01/2021
- 12 Early Breast Cancer Trialists' Group (EBCTCG). Long-term outcomes for neoadjuvant versus adjuvant chemotherapy in early breast cancer: meta-analysis of individual patient data from ten randomised trials. Lancet Oncol 2018; 19: 27-39
- 13 Minckwitz GV, Huang CS, Mano MS. et al. Trastuzumab Emtansine for Residual Invasive HER2-positive Breast Cancer. N Engl J Med 2019; 380: 617-628
- 14 Masuda N, Lee SJ, Ohtani S. et al. Adjuvant Capecitabine for Breast Cancer after Preoperative Chemotherapy. N Engl J Med 2017; 376: 2147-2159
- 15 Spring LM, Fell G, Arfe A. et al. Pathologic complete response after neoadjuvant chemotherapy and impact on breast cancer recurrence and survival: a comprehensive meta- analysis. Clin Cancer Res 2020; 26 (12) 2838-2848
- 16 Petrelli F, Borgonovo K, Cabiddu M. et al. Neoadjuvant chemotherapy and concomitant trastuzumab in breast cancer: a pooled analysis of two randomized trial. Anticancer Drugs 2011; 22 (02) 128
- 17 Gianni L, Pienkowski T, Im Y.-H. et al. 5-year analysis of neoadjuvant pertuzumab and trastuzumab in patients with locally advanced, inflammatory, or early-stage HER2-positive breast cancer (NeoSphere): a multicentre, openlabel, phase 2 randomised trial. The Lancet Oncology 2016; 17 (06) 791-800
- 18 Schneeweiss A, Chia S, Hickish T. et al. Pertuzumab plus trastuzumab in combination with standard neoadjuvant anthracycline-containing and anthracycline-free chemotherapy regimens in patients with HER2-positive early breast cancer: a randomized phase II cardiac safety study (TRYPHAENA). Ann Oncol 2013; Sep; 24 (09) 2278-2284
- 19 Buzatto IPC, Ribeiro-Silva A, Andrade JM. et al. Neoadjuvant chemotherapy with Trastuzumab in HER2-positive breast cancer: pathologic complete response rate, predictive and prognostic factors. Braz J Med Biol Res 2017; 50 (02) e5674
- 20 Amendola LCB, Gaui MFD, Carneiro AHPC. et al. Clinicopathologic profile of breast cancer patients treated with neoadjuvant chemotherapy at HUCFF/UFRJ. Mastology 2021; 31: e20200076
- 21 Bayratar S, Arun B. Dose-dense chemotherapy for breast cancer. 2012; 18 (03) 261-266 https://doi.org/10.1111/j.1524-4741.2012.01236.x
- 22 Sikov WM, Berry DA, Perou CM. et al. Impact of the Addition of Carboplatin and/or Bevacizumab to Neoadjuvant Once-per-Week Paclitaxel Followed by Dose-Dense Doxorubicin and Cyclophosphamide on Pathologic Complete Response Rates in stage II to III Triple-Negative Breast Cancer: CALGB 40603 (Alliance). Journal of Clinical Oncology 2015; 33: 13-21
- 23 Minckwitz GV, Schneeweiss A, Loibl S. et al. Neoadjuvant carboplatin in patients with triplenegative and HER2-positive early breast cancer (GeparSixto;GBG66): a randomised phase 2 trial. The Lancet Oncology 2014; 15 (07) 747-756
- 24 Loibl S, Shaughnessy JO, untch M. et al. Addition of the PARP inhibitor veliparib plus carboplatin or carboplatin alone to standard neoadjuvant chemotherapy in triple-negative breast cancer (BrighTNess): a randomised, phase 3 trial. The Lancet Onclogy 2018; 19 (04) 97-509
- 25 Schmid P, Cortes J, Pusztai L. et al. Pembrolizumab for Early Triple-Negative Breast Cancer. N Engl J Med 2020; 382: 810-821
- 26 Mittendorf EA, Zhang H, Barrios CH. et al. Neoadjuvant atezolizumab in combination with sequential nab-paclitaxel and anthracyclinebased chemotherapy versus placebo and chemotherapy in patients with Early-stage triple-negative breast cancer (IMpassion031): a randomised, double-blind, phase 3 trial. The Lancet 2020; 396 (10257): 1090-1100
- 27 Asaoka M, Gandhi S, Ishikawa T. et al. Neoadjuvant Chemotherapy for Breast Cancer: Past, Present and Future. Breast Cancer: Basic and Clinical Research; 2020. 14. 1-8
- 28 Silva JL, Paula BHR, Small IA. et al. Sociodemographic, Clinical, and Pathological Factors Influencing Outcomes in Locally Advanced Triple Negative Breast Cancer: A Brazilian Cohort. Breast Cancer: Basic and Clinical Research; 2020. 14. 1-12
- 29 Minckwitz G. von, Untch M, Blohmer J. U. et al. “Definition and impact of pathologic complete response on prognosis after neoadjuvant chemotherapy in various intrinsic breast cancer subtypes,”. Journal of Clinical Oncology 2012; 30 (15) 1796-1804
- 30 Catane R, Kaufman B, Zach L. et al. Dose-dense neoadjuvante chemotherapy in breast cancer. Journal of Clinical Oncology 2005; 23 (16) 807-807
- 31 Goto W, Kashiwagi S, Takada K. et al. Significance of intrinsic breast cancer subtypes on the longterm prognosis after neoadjuvant chemotherapy. J Transl Med 2018; 16: 307
- 32 Asaoka M, Narui K, Suganuma N. et al. Clinical and pathological predictors of recurrence in breast cancer patients achieving pathological complete response to neoadjuvant chemotherapy. Eur J Surg Oncol 2019; 45: 2289-2294
- 33 Tao M, Chen S, Zhang X. et al. Ki67 labeling index is a predictive marker for a pathological complete response to neoadjuvant chemotherapy in breast cancer. Medicine 2017; 96: 51