The landscape of oncology clinical trials in Africa over the last three decades (1995-2025).
Abstract
e23236 Background: Africa is home not only to 20% of the world’s population but also to the highest human genetic diversity. Genomics increasingly drives cancer drug discovery, biomarker development, and dose optimization. This study reviews Africa’s representation in high-impact oncology clinical trials. Methods: We identified all oncology clinical trials published in The Lancet and The New England Journal of Medicine (NEJM) between 1995 and 2025, and retrieved full-text PDFs from the journals' websites. Using an LLM (Gemini-2.5-Flash), structured variables, including trial phase, cancer type, enrollment countries, and participant race and/or ethnicity, were automatically extracted from texts, tables, and figures. Trials were stratified by decade (1995–2005, 2006–2015, and 2016–2025) to evaluate temporal trends. Results: Among the 1,385 global oncology trials reviewed, only 66 (4.8%) were conducted in African countries: 16 in 1995–2005, 30 in 2006–2015, and 20 in 2016–2025. The trials occurred in just 11 African countries, with South Africa alone accounting for 56 (84.8%) of these 66 trials. Egypt contributed 6 trials (9.1%), and Mauritius 5 trials (7.6%). Early-phase trials were rare: only 1 Phase 0 (1.5%) and 1 Phase 2 (1.5%) trial were identified, while the majority were Phase 3 (64 trials, 97.0%). Across all periods, Phase 3 studies dominated. The trials covered 58 distinct cancer types, but the most frequent were squamous cell carcinoma of the head and neck (n = 3), non-small cell lung cancer (n = 2), colorectal adenomas (n = 2), and chronic lymphocytic leukemia (n = 2). The number of African trials increased from 16 (24.2%) in 1995–2005 to 30 (45.5%) in 2006–2015, before declining to 20 (30.3%) in 2016–2025. Geographic diversity improved modestly: 5 countries participated in the first two periods, compared with 7 in the most recent period. Conclusions: This study shows that cancer research continues to overlook Africa and its genetic diversity. This omission demands deliberate investment in clinical trial infrastructure, regulatory harmonization, diaspora-academic partnerships, and early-phase trial capacity in Africa to ensure the development of globally representative, biologically robust cancer therapeutics. Characteristic Overall (N=66) 1995–2005 (n=16) 2006–2015 (n=30) 2016–2025 (n=20) Global trials, n 1,385 – – – Trials with African sites, n (%) 66 (4.8) 16 (24) 30 (46) 20 (30) African countries, n 11 5 5 7 Trial phases 0, 2, 3 3 2, 3 0, 3 0, n (%) 1 (1.5) 0 0 1 (5.0) 2, n (%) 1 (1.5) 0 1 (3.3) 0 3, n (%) 64 (97.0) 16 (100) 29 (96.7) 19 (95.0) Cancer types, n 58 14 29 18 Most frequent cancers HNSCC, NSCLC, CLL, CRC, Prostate NSCLC, CLL HNSCC, CRC, Breast NSCLC, Prostate, TNBC Trials by country, n (%) South Africa 56 (84.8) 14 (87.5) 28 (93.3) 14 (70.0) Egypt 6 (9.1) 2 (12.5) 4 (13.3) 0 Mauritius 5 (7.6) 0 1 (3.3) 4 (20.0) CAR 3 (4.5) 0 1 (3.3) 2 (10.0) Tunisia 2 (3.0) 1 (6.2) 1 (3.3) 0 Algeria 2 (3.0) 2 (12.5) 0 0 Other countries ≤1 each – – –
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (3)
Rahman Adesoji Olusoji
The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, Columbus, OH
Edmund Folefac
Ohio State University, Columbus, OH
Jiasheng Wang
Dr. Li Dak Sum and Yip Yio Chin Center for Stem Cells and Regenerative Medicine, Zhejiang University School of Medicine