Global Cancer Drug Development—A Report From the 2022 Accelerating Anticancer Agent Development and Validation Meeting

Author:

Wilson Brooke E.12ORCID,Sullivan Richard34ORCID,Peto Richard5,Abubakar Bello6ORCID,Booth Christopher12ORCID,Werutsky Gustavo7ORCID,Adams Cary8,Saint-Raymond Agnes9ORCID,Fleming Thomas R.10,Lyerly Kim11ORCID,Gralow Julie R.12ORCID

Affiliation:

1. Division of Cancer Care and Epidemiology, Queen's Cancer Research Institute, Kingston, Canada

2. Department of Oncology, Queen's University, Kingston, Canada

3. Institute of Cancer Policy, King's College London, London, United Kingdom

4. Department of Oncology, Guy's & St Thomas' NHS Trust, London, United Kingdom

5. Department of Medical Statistics and Epidemiology, University of Oxford, Oxford, United Kingdom

6. Department of Radiotherapy and Oncology, National Hospital Abuja, Abuja, Nigeria

7. Department of Medical Oncology, Hospital São Lucas, Porto Alegre, Brazil

8. Union for International Cancer Control, Geneva, Switzerland

9. International Affairs Division, European Medicines Agency, Amsterdam, the Netherlands

10. Department of Statistics, University of Washington, Seattle, WA

11. Departments of Surgery, Pathology, and Immunology, Duke University School of Medicine, Durham, NC

12. American Society of Clinical Oncology, Alexandria, VA

Abstract

Rapidly expanding systemic treatment options, combined with improved screening, diagnostic, surgical, and radiotherapy techniques, have led to improved survival outcomes for many cancers over time. However, these overall survival gains have disproportionately benefited patients in high-income countries, whereas patients in low- and middle-income countries (LMICs) continue to experience challenges in accessing timely and guideline concordant care. In September 2022, the Accelerating Anticancer Agent Development and Validation workshop was held, focusing on global cancer drug development. Panelists discussed key barriers such as the lack of diagnostic services and human resources, drug accessibility and affordability, lack of research infrastructure, and regulatory and authorization challenges, with a particular focus on Africa and Latin America. Potential opportunities to improve access and affordability were reviewed, such as the importance of prioritizing investments in diagnostics, investing health infrastructure and work force planning, coordinated drug procurement efforts and streamlined regulatory processing, incentivized pricing through regulatory change, and the importance of developing and promoting clinical trials that can answer relevant clinical questions for patients in LMICs. As a cancer community, we must continue to advocate for and work toward equitable access to high-quality interventions for patients, regardless of their geographical location.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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