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

Lunch and Poster Display session

221P - Incidence and survival after brain metastases among patients with stage I-III breast cancer: A population-based study

Date

16 May 2024

Session

Lunch and Poster Display session

Presenters

Italo Fernandes

Citation

Annals of Oncology (2024) 9 (suppl_4): 1-47. 10.1016/esmoop/esmoop103200

Authors

R. Chehade1, H. Soliman2, I. Fernandes3, B. Zhang4, R. Saskin5, M.K. Krzyzanowska6, G. Liu6, S. Das7, A. Sahgal3, K.K. Chan3, K. Jerzak3

Author affiliations

  • 1 University of Toronto - St. George Campus, Toronto/CA
  • 2 Sunnybrook Health Sciences Centre, Toronto/CA
  • 3 Sunnybrook Health Sciences Centre - Odette Cancer Centre, Toronto/CA
  • 4 ices institute for clinical evaluative sciences, Toronto/CA
  • 5 ICES - Institute for Clinical Evaluative Sciences, Toronto/CA
  • 6 UHN - University Health Network - Princess Margaret Cancer Center, Toronto/CA
  • 7 St. Michael's Hospital, Toronto/CA

Resources

Login to get immediate access to this content.

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

Abstract 221P

Background

Patients with HER2-positive (HER2+) and triple-negative (TNBC) metastatic breast cancer (BC) have a high propensity to develop brain metastases (BrM), but BrM incidence among patients who present with early-stage BC has not been well studied.

Methods

In this population-based cohort study, we used linked administrative databases in Ontario, Canada to identify adult patients diagnosed with stage I-III BC between 2009-2021. Cumulative incidence of surgery and/or radiotherapy for BrM (surrogate for BrM) accounting for competing risk of death, time from primary BC diagnosis to local BrM therapy, and survival time from BrM diagnosis date as stratified by stage and subtype were analyzed using SAS.

Results

Of 91, 517 BC patients, 1, 858 (2%) received local treatment for BrM. Median [IQR] age at BrM diagnosis was 52.5 [45-62] years and initial stage at BC presentation was as follows: stage I (n=272; 15%), stage II (n=767, 41%), and stage III (n=819, 44%). With a median follow-up of 6.4 years [IQR:3.7-9.6], the incidence proportion of BrM was: 0.6% among patients with stage I; 2.4% with stage II; and 6.9% with stage III BC. Subtypes included 406 (22%) hormone-receptor-positive (HR+)/HER2-negative (HER2-), 161 (9%) HER2+/HR+, 126 (7%) HER2+/HR-, 288 (15%) TNBC; unknown subtype, n=877 (47%). Among stage III patients, the incidence proportion of BrM was 16% (TNBC), 13% (HER2+/HR-), 9% (HER2+/HR+), and 4% (HR+/HER2-); corresponding median time from initial BC diagnosis to local BrM therapy was 1.6, 2.0, 2.9, and 3.7 years, respectively. Among patients with stage I-III BC treated locally for BrM, median (m) OS from date of BrM treatment was 5.8 (2-16) months. Survival by BC subtype was as follows, irrespective of initial stage at diagnosis: HER2+ BC, mOS=13.1 (4.6-28) months; HR+/HER2- BC, mOS=5.1 (1.7-15) months; TNBC, mOS=3.6 (1.5-8.7) months.

Conclusions

A high incidence of BrM among patients with stage III BC was identified particularly among those with TNBC or HER2+ BC. The true incidence is likely higher as screening for asymptomatic BrM is not typically performed. In addition, mOS may be over-estimated because untreated patients were not included in this analysis.

Legal entity responsible for the study

K. Jerzak.

Funding

Has not received any funding.

Disclosure

H. Soliman: Non-Financial Interests, Personal, Other, educational events: Elekta ab. M.K. Krzyzanowska: Financial Interests, Invited Speaker: Eisai, Exelixis, Novartis, Eli Lilly (trial funding), Bayer (grant). G. Liu: Financial Interests, Institutional, Research Grant: AstraZeneca, Takeda, Boehringer Ingelheim, Amgen, EMD Serono, Pfizer, Bayer ; Financial Interests, Personal, Invited Speaker, ;ectures, educational events: AstraZeneca, Pfizer, EMD Serono, Takeda; Financial Interests, Personal, Advisory Board: AstraZeneca, Pfizer, EMD Serono, Merck, AbbVie, Jazz, Takeda, Anheart, Roche, BMS, Novartis, Lilly . S. Das: Non-Financial Interests, Personal, Advisory Board: Subcortical Surgery Group; Financial Interests, Personal, Invited Speaker: Congress of Neurological Surgeons, American Association of Neurological Surgeons and American Board of Neurological Surgery.; Financial Interests, Personal, Royalties: Oxford University Press; Non-Financial Interests, Personal, Other, Provincial lead: CNS Oncology at Ontario Health (Cancer Care Ontario). A. Sahgal: Financial Interests, Personal, Other, consulting: arian, Elekta (Gamma Knife Icon), BrainLAB, Merck, ; Non-Financial Interests, Personal, Leadership Role: International Stereotactic Radiosurgery Society (ISRS), AO Spine Knowledge Forum Tumor; Financial Interests, Personal, Other, educational events: AstraZeneca, Elekta AB, Varian, BrainLAB, Accuray, Seagen; Financial Interests, Institutional, Research Grant: Elekta AB, Varian, Seagen Inc., BrainLAB; Financial Interests, Personal, Other, Travel expenses: Elekta, Varian, BrainLAB; Other, Personal, Other, member: Elekta MR Linac Research Consortium; Other, Personal, Leadership Role: Clinical Steering Committee member, and chairs the Elekta Oligometastases Group and the Elekta Gamma Knife Icon Group. K. Jerzak: Financial Interests, Personal, Advisory Board: Amgen, AstraZeneca, Apo Biologix, Daiichi Sankyo, Eli Lilly, Eisai, Genomic Health, Gilead Sciences, Knight Therapeutics, Merck, Myriad Genetics Inc., Pfizer, Roche, Seagen, Novartis, Viatris; Financial Interests, Institutional, Research Grant: AstraZeneca. Eli Lilly, Seagen. 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.