Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Mini Oral session: Breast cancer, early stage

141MO - Pathological response and early survival data according to TNBCtype4 classifier in operable triple-negative breast cancer (TNBC) treated with neoadjuvant carboplatin and docetaxel

Date

12 Sep 2022

Session

Mini Oral session: Breast cancer, early stage

Topics

Molecular Oncology

Tumour Site

Breast Cancer

Presenters

Isabel Echavarria Diaz-Guardamino

Citation

Annals of Oncology (2022) 33 (suppl_7): S55-S84. 10.1016/annonc/annonc1038

Authors

I. Echavarria Diaz-Guardamino1, S. Lopez-Tarruella Cobo2, M. Del Monte-Millan2, E. Alvarez3, Y. Jerez1, F. Moreno Anton4, J.Á. García Saenz4, T. Massarrah2, I. Ocaña1, M. Cebollero5, A.I. Ballesteros Garcia6, U. Bohn Sarmiento7, H. Gomez8, H.A. Fuentes9, B. Herrero Lopez1, S. Gamez Casado1, O. Bueno10, M.J. Jiménez-Santos11, M. Roche-Molina1, M. Martin Jimenez2

Author affiliations

  • 1 Medical Oncology Dept., Hospital General Universitario Gregorio Marañon - Fundación Investigación Biomedica, 28007 - Madrid/ES
  • 2 Medical Oncology Dept., Hospital General Universitario Gregorio Marañon - Fundación Investigación Biomedica, CIBERONC, 28007 - Madrid/ES
  • 3 Medical Oncology Dept., Hospital General Universitario Gregorio Marañon - Fundación Investigación Biomedica, 28009 - Madrid/ES
  • 4 Medical Oncology Dept., Hospital Clinico Universitario San Carlos, CIBERONC, 28040 - Madrid/ES
  • 5 Pathology Dept., Hospital General Universitario Gregorio Maranon, 28007 - Madrid/ES
  • 6 Medical Oncology Dept., Hospital Universitario de la Princesa, 28006 - Madrid/ES
  • 7 Medical Oncology Dept., Hospital Universitario de Gran Canaria Doctor Negrin, 35010 - Las Palmas de Gran Canaria/ES
  • 8 Radioncology Department, Oncosalud SAC, 15036 - Lima/PE
  • 9 Lima, INEN - Instituto Nacional de Enfermedades Neoplasicas, 15038 - Lima/PE
  • 10 Radiology Dept., Hospital General Universitario Gregorio Maranon, 28007 - Madrid/ES
  • 11 ., CNIO - Centro Nacional de Investigaciones Oncologicas, 28029 - Madrid/ES
More

Resources

Login to access the resources on OncologyPRO.

Abstract 141MO

Background

The identification of predictive biomarkers of response to neoadjuvant chemotherapy (NACT) is an unmet need in early-stage TNBC. Transcriptomic classification according to TNBCtype-4 classifier has shown predictive value, and we aimed to validate our previous results (Echavarria I et al, CCR 2018) in terms of response and long-term outcomes in a larger cohort.

Methods

Stage I-III TNBC patients were enrolled across 10 hospitals in a prospective cohort and were treated with neoadjuvant carboplatin and docetaxel for 6 cycles (NCT01560663). RNAseq was performed from FFPE core biopsies and TNBCtype-4 classification was done on the TNBCtype online tool. Response was categorized based on the Symmans residual cancer burden score.

Results

RNAseq and TNCBtype4 classification was available for 235 patients. Median age was 53 years, median tumor size 29.5 mm and 46.0% of the patients were clinically node negative. 14 patients were not evaluable for response due to incomplete axillary evaluation after NACT. Among the 221 remaining patients, the pCR rate was 47.5% (n=105). 71 (30.2%) of the patients were classified as BL1, 48 (20.4%) as BL2, 40 (17.0%) as LAR and 57 (24.3%) as M. 19 additional patients (8.1%) were considered estrogen receptor-positive (ER+) according to the TNBCtype4 classifier. pCR rate differed significantly according to TNBCtype subtyping (p=0.001), with BL1 achieving a pCR rate of 60.6%, followed by BL2 (52.1%), and M and LAR with a pCR rate of 33.3% and 32.5% respectively. Patients classified as ER+ had a pCR rate of 26.3%. This significant association was maintained in the multivariate analysis including clinicopathological factors and TILs. Although different rates of distant relapse were observed across subgroups, they did not reach statistical significance with the current follow-up (p=0.09). With a median follow-up of 53 months, 3 year-distant disease-free survival (dDFS) was 89.4% for BL1, 82.3% for BL2, 83.9% for M and 73.2% for LAR (p=0.13).

Conclusions

TNCBtype-4 classifier significantly predicts pCR rate to NACT in operable TNBC patients. A non-significant trend towards different dDFS was observed, although longer follow-up is needed.

Clinical trial identification

NCT01560663.

Editorial acknowledgement

Legal entity responsible for the study

Hospital General Universitario Gregorio Marañon.

Funding

Instituto de Salud Carlos III PI12/02684, PI15/00117, PI18/01775 Fondo Europeo de Desarrollo Regional.

Disclosure

J.Á. García Saenz: Financial Interests, Personal, Invited Speaker: Novartis, Celgene, Eli Lilly, Eisai; AstraZeneca; Financial Interests, Institutional, Research Grant: AstraZeneca; Financial Interests, Personal, Other, travel support: Novartis, Roche, Pfizer. All other authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.