Rituximab for children with EBV-positive Burkitt lymphoma in East Africa
The addition of rituximab to the chemotherapy backbone was shown to significantly improve outcomes of children with aggressive high-grade lymphomas in high-income countries. However, data on its safety and efficacy in children with Epstein-Barr virus (EBV)-positive Burkitt lymphoma (BL) are limited. We conducted a prospective nonrandomized observational study in East African patients aged ≤25 years with confirmed BL. Patients received either the International Network for Cancer Treatment and Research (INCTR)-based standard chemotherapy (cyclophosphamide, vincristine, and methotrexate [COM]) or rituximab plus standard chemotherapy (R-COM). The primary end point was safety. The secondary outcomes were event-free and overall survival and cost-effectiveness of incorporating rituximab. Primary analyses were conducted in the intention-to-treat population. The median follow-up was 23 months. Safety analyses included 72 patients: 32 in the COM group and 40 in the R-COM group. Grade ≥3 adverse events occurred in 18% of R-COM patients and 16% of COM patients. With respect to treatment outcomes at 12 months, 5 events were observed in the R-COM group and 14 in the COM group. The 12-month event-free survival was 67% with R-COM and 43% with COM (hazard ratio [HR], 0.49; 95% confidence interval [CI], 0.24-0.98; P = .045). There were 8 deaths in the R-COM group, whereas 16 patients died in the COM group (HR, 0.32; 95% CI, 0.14-0.75; P = .009). R-COM was particularly effective in advanced-stage disease. The addition of rituximab to the INCTR-based protocol (COM) for EBV-positive BL has been observed to be safe and feasible in experienced centers in East Africa and saves lives.
Authors
- Jacqueline Kamanga
- Isaac Omara Otim (ORCID: https://orcid.org/0000-0001-8000-9483)
- Caroline Achola (ORCID: https://orcid.org/0009-0004-4748-5102)
- Liz Morrell (ORCID: https://orcid.org/0000-0001-6382-1795)
- Elifuraha Wilson Mkwizu (ORCID: https://orcid.org/0000-0001-5938-5628)
- Lulu Chirande (ORCID: https://orcid.org/0009-0001-5008-3786)
- Ismail D. Legason (ORCID: https://orcid.org/0000-0002-6118-542X)
- Hadija Mwamtemi (ORCID: https://orcid.org/0009-0007-6501-535X)
- Anna Schuh (ORCID: https://orcid.org/0000-0002-3938-8490)
- William Frank Mawalla (ORCID: https://orcid.org/0000-0002-0016-7551)
- Dimitris V. Vavoulis (ORCID: https://orcid.org/0000-0002-3984-1507)
- Clara C Chamba (ORCID: https://orcid.org/0000-0001-5154-7872)
- Hadijah Nabalende
- Martin Ogwang (ORCID: https://orcid.org/0000-0002-4178-2809)
- Kristin Schroeder (ORCID: https://orcid.org/0000-0002-6433-6174)
- Paul Shadrack Ntemi
- Godlove Sandi (ORCID: https://orcid.org/0000-0001-9068-0991)
- Salama Mahawi
- Pamella Aol (ORCID: https://orcid.org/0009-0001-1979-8396)
- Philomena G Lyamuya
Institutions
- Muhimbili University of Health and Allied Sciences (TZ)
- Duke University (US)
- University of Oxford (GB)
- St. Mary's Hospital Lacor (UG)
- Kilimanjaro Christian Medical Centre (TZ)
- Muhimbili National Hospital (TZ)
- Bugando Medical Centre (TZ)
Publication Details
- Journal
- Blood Advances
- Published
- 2025-02-21
- DOI
- https://doi.org/10.1182/bloodadvances.2024015234
- Citations
- 3
- Primary Topic
- Viral-associated cancers and disorders
- Type
- article
- Field-Weighted Citation Impact
- 3.14