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Lunch and Poster Display session

258P - Real-world (rw) outcomes in patients (pts) with hormone receptor-positive and human epidermal growth factor receptor-2-negative (HR+/HER2-) metastatic breast cancer (mBC) treated with chemotherapy (CT) in France

Date

16 May 2024

Session

Lunch and Poster Display session

Presenters

Verena Kiver

Citation

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

Authors

M. Campone1, J. Frenel1, V.I.I. Kiver2, A. Woeckel3, A.G. Kerscher4, M. Krebs5, C.S. Leal6, V.M. Saglimbene7, M.K. Rehnquist8, N. Sadetsky8, N. Sjekloca9, O. LIBERT10, A. Kaushik8, F. Bocquet11

Author affiliations

  • 1 ICO Institut de Cancerologie de l'Ouest René Gauducheau, Saint-Herblain/FR
  • 2 Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin/DE
  • 3 UKW - University Hospital Würzburg, Würzburg/DE
  • 4 University Hospital Würzburg, Wuerzburg/DE
  • 5 University Hospital Würzburg, Würzburg/DE
  • 6 IQVIA, Porto Salvo/PT
  • 7 IQVIA Italy, Milan/IT
  • 8 Gilead Sciences, Inc, Foster City/US
  • 9 Gilead Sciences Europe Ltd., 81000 - Stockley Park/GB
  • 10 Gilead Sciences SAS, 92100 - Boulogne-Billancourt/FR
  • 11 Institut de Cancérologie de l’Ouest, Saint-Herblain/FR

Resources

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Abstract 258P

Background

Endocrine therapy (ET) combined with CDK4/6 inhibitors (CDK4/6i) is the standard of care for HR+/HER2- mBC pts. However, efficacy is limited due to acquired ET resistance, after which treatment options are limited to CT and, more recently, antibody-drug conjugates. This rw study describes patient characteristics, treatment patterns and survival outcomes in HR+/HER2- mBC pts initiating at least first (1st)CT in France and Germany.

Methods

This is an interim analysis of adults with HR+/HER2- mBC initiating CT (Jan 2016 - Feb 2023) for mBC at the Institut de Cancérologie de l'Ouest in France. Germany data will be assessed in the final analyses. Demographics, clinical characteristics, and treatments were described using descriptive statistics. Kaplan-Meier method was used to describe rw overall survival (OS) for 1st to 4th CT line, separately, from each line start.

Results

339 pts were analysed: 99% were female, 28% had de novo mBC, with median age of 62 years at 1st CT. Prior to 1st CT start, 43% received CDK4/6i and 52% ET for mBC. 61%, 39% and 24% had records of subsequent second, 3rd and 4th CT line, respectively. Most pts received CT as monotherapy: paclitaxel and capecitabine were the most used agents followed by eribulin and cyclophosphamide. Median rwOS was 19.9, 12.3, 8.1 and 7.2 months (mo) from 1st, 2nd, 3rd and 4th CT line, respectively (Table). Table: 258P

rwOS by CT line

1st CT 2nd CT 3rd CT 4th CT
N Pts 339 207 132 83
N Deaths 241 151 102 59
Median rwOS in moInterquartile range 19.9 (8.0-38.7) 12.3 (5.7-24.1) 8.1 (4.3-18.5) 7.2 (2.9-15.1)
6 mo N 268 144 81 39
Survival[95% Confidence interval (CI)] 80% [75-84] 73% [67-79] 66% [58-74] 55% [45-68]
12 mo N 206 92 37 19
Survival[95% CI] 63% [58-68] 50% [44-58] 35% [27-45] 34% [24-47]
18 mo N 164 49 23 -
Survival[95% CI] 54% [49-60] 33% [27-41] 26% [19-35]
24 mo N 112 33 - -
Survival[95% CI] 42% [36-47] 25% [19-33]
32 mo N 53 11 - -
Survival[95% CI] 26% [22-32] 15% [10-23]

Conclusions

HR+/HER2- mBC pts initiating CT in France showed poor survival, decreasing with each subsequent CT line. There is still a high unmet need for improved treatment options in this population.

Legal entity responsible for the study

Gilead Sciences, Inc

Funding

Gilead Sciences, Inc

Disclosure

M. Campone: Financial Interests, Institutional, Advisory Board: AstraZeneca, Novartis, Sanofi, Menarini, Gilead, Seagen; Financial Interests, Personal, Invited Speaker: Novartis, Lilly; Financial Interests, Personal, Advisory Board: Daiichi Sankyo, Lilly. J. Frenel: Financial Interests, Personal, Advisory Board: Pfizer, Novocure, Pierre Fabre, Eisai, Seagen, Gilead; Financial Interests, Personal, Invited Speaker: GSK, Amgen, Eisai; Financial Interests, Institutional, Advisory Board: Exact Science, Lilly, Daiichi Sankyo, AstraZeneca, Clovis Oncology; Financial Interests, Institutional, Invited Speaker: Novartis, MSD; Financial Interests, Invited Speaker: AstraZeneca, Seagen, MSD, Daiichi Sankyo; Non-Financial Interests, Principal Investigator: Novartis, Lilly, AstraZeneca, Pfizer, Daiichi Sankyo, MSD. A.G. Kerscher: Financial Interests, Institutional, Other, IT-Infrastructure: Janssen; Other, Consulting: IQVIA. M. Krebs: Financial Interests, Personal, Advisory Board: Janssen, GSK Oncology; Financial Interests, Personal, Expert Testimony: IQVIA; Financial Interests, Personal, Stocks/Shares: General Electric. C.S. Leal: Financial Interests, Personal, Full or part-time Employment, Epidemiologist: IQVIA. V.M. Saglimbene: Financial Interests, Personal, Full or part-time Employment: IQVIA Solutions. M.K. Rehnquist: Financial Interests, Institutional, Full or part-time Employment: Gilead Sciences; Financial Interests, Institutional, Stocks/Shares: Gilead Sciences. N. Sadetsky: Financial Interests, Personal, Full or part-time Employment: Gilead; Financial Interests, Personal, Stocks/Shares: Gilead, Roche/Genentech. N. Sjekloca: Financial Interests, Personal, Stocks/Shares: Gilead Sciences. O. Libert: Financial Interests, Personal, Full or part-time Employment, Medical Affairs: Gilead Sciences; Financial Interests, Personal, Stocks/Shares: Gilead Sciences. A. Kaushik: Financial Interests, Institutional, Full or part-time Employment: Gilead Sciences; Financial Interests, Institutional, Stocks/Shares: Gilead Sciences. All other authors have declared no conflicts of interest.

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