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E-Poster Display

174P - Genomic testing, biomarkers and treatment patterns in early breast cancer

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Breast Cancer

Presenters

Michael Method

Citation

Annals of Oncology (2020) 31 (suppl_4): S303-S339. 10.1016/annonc/annonc267

Authors

M. Method1, A. Rider2, R. Williams2, J. Brown3

Author affiliations

  • 1 Oncology, Eli Lilly and Company, 46285 - Indianapolis/US
  • 2 Adelphi Real World, Adelphi Group, SK10 5JB - Bollington/GB
  • 3 Gporwe Oncology, Eli Lilly and Company, Windlesham/GB

Resources

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Abstract 174P

Background

For patients with early breast cancer (EBC), genomic testing is increasingly informing the likelihood of benefit from adjuvant (adj) chemotherapy (CT). The objective was to examine, by geographic region, genomic/biomarker testing rates and treatment patterns in HR+, HER2- EBC patients in the adj setting.

Methods

Real-world data from France, Germany, Italy, Spain, United Kingdom (EU5), Japan, and United States (US) were drawn from the Adelphi EBC I Disease Specific Programme, a point in time observational study. 320 physicians completed patient record forms (Jul to Oct 2019) for up to the next 8 eligible HR+, HER2- EBC patients receiving or had received adj therapy in the last 12 months, prior to data collection. Data included demographics, genetic/biomarker testing, and treatment received.

Results

N = 2447 patients (98% female, mean age 59.6 yrs, SD 13.0). The frequency of neo-adjuvant (n-adj) therapy varied by region. Adj treatment patterns differed by region and by the use of n-adj therapy. Breast cancer gene (BRCA) testing was more frequent in patients who received n-adj therapy and more common in the US than EU5 and Japan. EU5 had the highest Ki67 testing rates. OncotypeDx was the most frequent multi-gene assay, more so in the US. Mammaprint was less frequent and Adjuvant! Online more frequent in the EU5 than the US and Japan (Table). Table: 174P

Test* EU5 n=1859 US n=347 Japan n=241
N-adj** n=293 (15.8%) Adj only n=1566 (84.2%) N-adj** n=92 (26.5%) Adj only n=255 (73.5%) N-adj** n=44 (18.3%) Adj only n=197 (81.7%)
BRCA1 100 (34.1%) 236 (15.1%) 42 (45.7%) 96 (37.6%) 8 (18.2%) 13 (6.6%)
BRCA2 91 (31.1%) 209 (13.3%) 31 (33.7%) 87 (34.1%) 2 (4.5%) 3 (1.5%)
Ki67 195 (66.6%) 1121 (71.6%) 31 (33.7%) 73 (28.6%) 9 (20.5%) 85 (43.1%)
OncotypeDx 57 (19.5%) 223 (14.2%) 31 (33.7%) 125 (49.0%) 13 (29.5%) 30 (15.2%)
MammaPrint 16 (5.5%) 74 (4.7%) 10 (10.9%) 15 (5.9%) 10 (22.7%) 9 (4.6%)
Adjuvant! Online 23 (7.8%) 120 (7.7%) 2 (2.2%) 7 (2.7%) 1 (2.3%) 26 (13.2%)

*EndoPredict, Breast Cancer Index, Mammostrat, PAM50 omitted (% use <10%)**Excludes non-Endocrine Therapy

Conclusions

The use of genomic/biomarker testing varied by region. Variation between regions in treatment approach may be driven, in part, by genomic testing/biomarker results as testing is increasingly being used to minimize over and under treatment with CT. Treatment patterns and other factors predicting treatment will be analyzed.

Clinical trial identification

Editorial acknowledgement

Trish Huynh (Eli Lilly and Company, Indianapolis, IN) provided writing assistance.

Legal entity responsible for the study

Eli Lilly and Company.

Funding

Eli Lilly and Company.

Disclosure

M. Method: Shareholder/Stockholder/Stock options, Full/Part-time employment: Eli Lilly and Company. A. Rider: Research grant/Funding (institution): Eli Lilly and Company; Full/Part-time employment: Adelphi Real World. R. Williams: Research grant/Funding (institution): Eli Lilly and Company; Full/Part-time employment: Adelphi Real World. J. Brown: Shareholder/Stockholder/Stock options, Full/Part-time employment: Eli Lilly and Company.

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