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ePoster Display

180P - Relapse pattern after neoadjuvant treatment in early breast cancer

Date

16 Sep 2021

Session

ePoster Display

Topics

Tumour Site

Breast Cancer

Presenters

Ariadna Gasol Cudos

Citation

Annals of Oncology (2021) 32 (suppl_5): S407-S446. 10.1016/annonc/annonc687

Authors

A. Gasol Cudos1, S. Morales Murillo2, O. Pallisé Subirats1, F. Vilardell Villellas1, D.R. Sánchez Guzman3, C. Canosa Morales1, J. Melé Olivé1, A. Velasco Sánchez1, J.F. Cordoba Ortega4

Author affiliations

  • 1 Breast Cancer Unit, Hospital Universitario Arnau de Vilanova, 25198 - Lleida/ES
  • 2 Medical Oncology Department, Hospital Arnau de Vilanova - Lleida, 25198 - Lleida/ES
  • 3 Breast Cancer Unit, Hospital Universitario Arnau de Vilanova, 25110 - SPAIN/ES
  • 4 Medical Oncology Department, Hospital Universitario Arnau de Vilanova, 25198 - Lleida/ES

Resources

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Abstract 180P

Background

Neoadjuvant treatment is becoming established in early breast cancer due to its impact in overall survival. Although it is the Her2 and triple-negative phenotypes where the greatest impact has been seen, the luminal has also seen it, so it is interesting to find the patterns of recurrence after neoadjuvant treatment.

Methods

624 patients with early breast cancer treated with neoadjuvant therapy (2004-2018) were analyzed to determine factors associated with relapse.

Results

Median age was 55 (28-89), median tumor size 38 mm (12-100), 325 (50%) had nodal involvement, phenotypes according to immunohistochemistry were: luminal 224 (35%) HER2+ 227 (35%) and triple-negative 191 (30%). With median follow-up of 72 months (4-331) a total of 32% of pathologic complete response (pCR) was detected and 26% relapsed. We found a significant association in relapse in the global series for pCR (OR 0.245, p=0.000), tumor size (OR 1.01, p=0.000) and nodal involvement (OR 2.431, p=0.000). The pCR and recurrence according to subtypes is represented in the table, luminal with pCR is the group with least recurrence (4,5%) and HER2 + non luminal and triple-negative without pCR is the group with most recurrence (46%). Table: 180P

Luminal HER2+Luminal HER2+ No luminal Triple-negative Total
pCR 9.8% 34.1% 58.7% 42.9% 32.0%
Rec in pCR 4.5% 7.1% 18.0% 9.8% 11.1%
Rec in non pCR 30,0% 18.0% 46,0% 45.9% 33.8%

The median disease-free survival (DFS) and overall survival (OS) was 242 and 240 months for the global series. pCR was associated with better DFS and OS (Cox model: HR 0,30 p:0.000 and HR 0,32 p:0.000) than non pCR and was more significant associated with less recurrence or death in triple-negative (Cox model: HR 0.16 p:0.000) and less significant in HER2 + luminal ( Cox model: HR 0.39 p:0.14 and HR 0.81 p:0.764).

Conclusions

pCR is the most robust factor associated with better survival with only a 11% of relapse. All subtypes benefited from pCR except the HER2 luminal, with a recurrence rate of only 14%. Achieving a pCR has a great impact on survival, specially in the HER2 + and triple-negative. The luminal subtype, despite only achieving 9% of pCR, also has an impact on survival with only 4.5% relapses compared to 30% in those who fail to achieve a pCR.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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