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

Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

4722 - Evaluation of Human epidermal growth factor receptor 2 overexpression (HER2+) after administration of neoadjuvant treatment (NAT) and prognostic impact in breast cancer (BC)

Date

22 Oct 2018

Session

Poster display session: Breast cancer - early stage, locally advanced & metastatic, CNS tumours, Developmental therapeutics, Genitourinary tumours - prostate & non-prostate, Palliative care, Psycho-oncology, Public health policy, Sarcoma, Supportive care

Topics

Clinical Research

Tumour Site

Breast Cancer

Presenters

Duarte Machado

Citation

Annals of Oncology (2018) 29 (suppl_8): viii58-viii86. 10.1093/annonc/mdy270

Authors

D.H.R. Machado1, F. Branco2, F.F. Silva3, S. André4, M. Brito5, M. Casanova6, M. Nave7, A. Moreira1, J.L.C. Passos-Coelho7

Author affiliations

  • 1 Medical Oncology, Instituto Portuguès de Oncologia de Lisboa Francisco Gentil, E.P.E. (IPOLFG EPE), 1099-023 - Lisbon/PT
  • 2 Medical Oncology, Hospital Beatriz Angelo-Loures, 2674-514 - Loures/PT
  • 3 Medical Oncology, Hospital da Luz, 1500-650 - Lisboa/PT
  • 4 Department Of Pathology And Laboratory Medicine, Instituto Portuguès de Oncologia de Lisboa Francisco Gentil, E.P.E. (IPOLFG EPE), 1099-023 - Lisbon/PT
  • 5 Francisco Gentil De Lisboa, Instituto Portugues de Oncologia, Lisboa/PT
  • 6 Medical Oncology, Hospital Beatriz Ângelo, 26744-514 - Loures/PT
  • 7 Oncology, Hospital da Luz, 1500-650 - Lisbon/PT

Resources

Login to access the resources on OncologyPRO.

If you do not have an ESMO account, please create one for free.

Abstract 4722

Background

HER2+ occurs in 15-20% of BC and is associated with worse prognosis. While previous studies reported that NAT-associated changes in HER2 status adversely affect patients (pts) prognosis (Guarneri et al), others did not (Yoshida et al). To assess the efficacy of NAT in pts with HER2+ BC and its influence on HER2 status and associated prognostic impact. HER2 status was determined by immunohistochemically (IHC) or Silver in situ hybridization (SISH).

Methods

Retrospective chart review and pathologic evaluation of all consecutive pts with HER2+ BC (defined as IHC 3+ or IHC 2+ confirmed by SISH) submitted to NAT between Jan2010 and Oct2015 in 3 Portuguese Hospitals. All diagnostic tumor biopsies and surgical specimens were assessed for IHC.

Results

108 female pts were included (median age 52yo, range 30-82; TNM stage was III in 68, II in 40. Hormone receptor (HR) were positive (ER and/or PR) in 68. HER2 status at diagnosis was IHC 3+ in 100 pts and IHC 2+ SISH amplified in 8. NAT included chemotherapy (CT) in all pts (anthracyclines (AC)/ taxanes (Tax) 102, AC/non-Tax 3, non-AC regimen 3), trastuzumab (T) in 87 and T and pertuzumab (P) in 3. Pathological complete response (pCR) (ypT0/isN0) was achieved in 48 pts (44.4%): 28 of 70 HR+ and 20 of 38 HR neg (p = 0.2), 27 of 40 with stage II and 21 of 68 with stage III (p < 0.001). pCR rate was 46% after CT+T/P and 39% with CT alone (p = 0.6). With a median follow-up of 55 months, there were 5 disease free survival (DFS) events (4 relapses and 1 non-BC death) among pCR pts and 19 among non-pCR (16 relapses and 3 non-BC deaths) (p = 0.02, log rank test). Of the 60 pts with residual invasive tumor at surgery, 52 remained HER2+ and 8 (13.3%) lost Her2+. 5y-DFS and 5-OS is 70% and 84%, respectively, for pts whose tumors remained HER2 + (14 DFS events; 8 deaths), and 21% and 50% for pts whose residual tumors became HER2 negative (5 DFS events; 4 deaths) (p = 0.02 and <0,001, log-rank test).

Conclusions

We confirmed the negative prognostic impact of NAT-induced HER2 loss on residual tumor leading to worse DFS. Despite the retrospective design and small sample size, these results suggest the importance of retesting HER2 after NAT, to better refine pts prognosis.

Clinical trial identification

Legal entity responsible for the study

José Luís Passos Coelho.

Funding

Has not received any funding.

Editorial Acknowledgement

Disclosure

All 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.