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ePoster Display

623P - Real-world treatment patterns in metastatic hormone-sensitive prostate cancer (mHSPC) patients in the US, Germany, France, China and Japan

Date

16 Sep 2021

Session

ePoster Display

Topics

Tumour Site

Prostate Cancer

Presenters

Peter Goebell

Citation

Annals of Oncology (2021) 32 (suppl_5): S626-S677. 10.1016/annonc/annonc702

Authors

P.J. Goebell1, R. Shah2, R. Raina3, S. Rege4, S.L. Chen5, V.E. Lee6, R. Waldeck7

Author affiliations

  • 1 Division Of Urology, University Hospital Erlangen, D-91054 - Erlangen/DE
  • 2 Real World Evidence & Patient Centered Outcomes, OPEN Health, 20814 - Bethesda/US
  • 3 Real World Evidence, OPEN Health, 02458 - Newton/US
  • 4 Real World Evidence, OPEN Health, 20814 - Bethesda/US
  • 5 Global Access Marketing Oncology, Bayer Pharmaceuticals, 07981 - Whippany/US
  • 6 Oncology Diagnostic Accounts, Bayer Pharmaceuticals, 07981 - Whippany/US
  • 7 Global Market Access, Oncology, Bayer Pharmaceuticals, 07981 - Whippany/US

Resources

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Abstract 623P

Background

The mHSPC treatment landscape is rapidly evolving, most recently with the entry of second-generation anti-androgen receptor inhibitors (SGARIs). This study describes mHSPC patients’ demographic, clinical, physician characteristics, and current treatment patterns.

Methods

This cross-sectional, retrospective, chart review study included mHSPC patients (aged ≥ 18 years) in the US, Germany, France, Japan, and China from the IPSOS Global Oncology Monitor Database (2018-2020). Descriptive analyses were conducted for all study objectives.

Results

6,198 mHSPC patients were included; US (N=3893), Germany, (N=867), France, (N=513), Japan, (N=641), and China, (N=284). Patients were generally aged ≥70 years (69.5%), well-functioning (ECOG score 0-1: 83.3%), and most patients were treated by urologists (59.8%) without oncologist co-management. Patients in Europe (Germany, 69.4%; France, 76.6%) and the US (82.6%) were primarily treated with luteinizing hormone releasing hormone (LHRH) agonists, and in Asia, with a combination of LHRH agonist(s) (China, 71.8%; Japan, 82.6%) and first-generation (FG) ARIs (China, 74.6%; Japan, 70.8%). With the exception of France (38.6%), the majority of patients were treated with combination therapy (57.4%) across the remaining four markets. Across the five countries, use of androgen synthesis inhibitor (ASI) (14.3%) and SGARIs (5.6%) was relatively infrequent, but increasing over the study period, as measured in successive cross-sectional data cuts. Chemotherapy was used consistently across the study period, with more use in Europe and China (Germany, 17.0%; France, 15.0%; 13.4%) than in the US (8.5%) or Japan (0.2%).

Conclusions

LHRH agonists and FGARIs were used most commonly, while use of ASIs and SGARIs was in the single digits yet increasing. Differences in guideline evolution, regulatory approval and reimbursement during the study period likely explains some of the cross-country differences. In addition, the differences of disciplines involved in treatment may have an impact.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

OPEN Health.

Funding

Bayer Pharmaceuticals.

Disclosure

P.J. Goebell: Other, Institutional, Other, Honoraria: Astellas; Other, Institutional, Other, Honoraria: AstraZeneca; Other, Institutional, Other, Honoraria: Bayer; Other, Institutional, Other, Honoraria: BMS; Other, Institutional, Other, Honoraria: Eisai; Other, Institutional, Other, Honoraria: Ipsen; Other, Institutional, Other, Honoraria: Janssen; Other, Institutional, Other, Honoraria: Novartis; Other, Institutional, Other, Honoraria: Pfizer; Other, Institutional, Other, Honoraria: Roche; Other, Institutional, Other, Honoraria: Sanofi; Other, Institutional, Other, Travel, Accommodations, Expenses: Astellas; Other, Institutional, Other, Travel, Accommodations, Expenses: AstraZeneca; Other, Institutional, Other, Travel, Accommodations, Expenses: Bayer; Other, Institutional, Other, Travel, Accommodations, Expenses: BMS; Other, Institutional, Other, Travel, Accommodations, Expenses: Eisai; Other, Institutional, Other, Travel, Accommodations, Expenses: Ipsen; Other, Institutional, Other, Travel, Accommodations, Expenses: Janssen; Other, Institutional, Other, Travel, Accommodations, Expenses: Novartis; Other, Institutional, Other, Travel, Accommodations, Expenses: Pfizer; Other, Institutional, Other, Travel, Accommodations, Expenses: Roche; Other, Institutional, Other, Travel, Accommodations, Expenses: Sanofi; Other, Institutional, Advisory Role, Clinical and scientific advisor for the present study: Bayer. R. Shah: Financial Interests, Institutional, Funding, Ruchit Shah is an employee of OPEN Health Evidence and Access. OPEN Health Evidence and Access received funding from Merck and Co, Inc for conducting this study: Merck and Co, Inc. R. Raina: Financial Interests, Institutional, Full or part-time Employment: OPEN Health. S. Rege: Financial Interests, Institutional, Full or part-time Employment: OPEN Health Evidence and Access. S.L. Chen: Financial Interests, Personal, Full or part-time Employment: Bayer Healthcare Pharmaceuticals; Financial Interests, Institutional, Stocks/Shares: Bayer Healthcare Pharmaceuticals; Financial Interests, Institutional, Funding: Bayer Healthcare Pharmaceuticals. V.E. Lee: Financial Interests, Personal, Full or part-time Employment: Bayer Pharmaceuticals; Financial Interests, Personal, Stocks/Shares, Employee Shares: Bayer Pharmaceuticals. R. Waldeck: Financial Interests, Institutional, Full or part-time Employment: Bayer Pharmaceuticals; Financial Interests, Institutional, Stocks/Shares: Bayer Pharmaceuticals; Financial Interests, Institutional, Funding: Bayer Pharmaceuticals; Non-Financial Interests, Personal, Sponsor/Funding: European Cancer Organization.

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