The Cameroon 2008 burkitt lymphoma protocol: Improved event-free survival with treatment adapted to disease stage and the response to induction therapy
dc.contributor.author | Hesseling, P. B. | |
dc.contributor.author | Njume, E. | |
dc.contributor.author | Kouya, F. | |
dc.contributor.author | Katayi, T. | |
dc.contributor.author | Wharin, P. | |
dc.contributor.author | Tamannai, M. | |
dc.contributor.author | Achu, P. | |
dc.contributor.author | Kidd, M. | |
dc.contributor.author | McCormick, P. | |
dc.date.accessioned | 2012-04-12T08:21:53Z | |
dc.date.available | 2012-04-12T08:21:53Z | |
dc.date.issued | 2012 | |
dc.description.abstract | Treatment of endemic Burkitt lymphoma (BL) with cyclophosphamide (CPM) and intrathecal methotrexate (IT MTX) can cure 50% of patients. In this study, induction therapy with CPM and IT MTX was followed by consolidation chemotherapy adapted for stage, clinical response, and abdominal ultrasound findings. One hundred and twenty-nine consecutive patients with BL, 77 male and 52 female with a median age of 7.9 years, were treated in mission hospitals in Cameroon. The diagnosis rested on fine-needle aspirate (79%), biopsy, bone marrow, cerebrospinal fluid, abdominal ultrasound, and clinical examination. Six percent had St Jude stage I, 13% stage II, 72% stage III, and 12% stage IV disease. The abdomen (76%) and face (50%) were mainly involved. Induction chemotherapy was CPM 40 mg/kg and IT MTX 12.5 mg and IT hydrocortisone 12.5 mg on days 1, 8, and 15. Stage I and II patients received CPM 60 mg/kg on day 29, and stage III patients CPM 60 mg/kg on days 29 and 43 if in remission on day 28. Stage IV patients and patients not in remission received CPM 60 mg/kg on days 29, 43, and 57 and 1.0 g/m 2 MTX intravenous (IV) and vincristine 1.5 mg/m 2 IV on day 29. Event-free survival (EFS) at mean 365 days was 61% (n = 79) and 100% in stage I, 85% in stage II, 60% in stage III, and 27% in stage IV patients. Deaths (n = 24) were disease or treatment related and 26 patients relapsed (mean 135 days). Risk-adapted treatment achieved 61% 1-year EFS. © 2012 Informa Healthcare USA, Inc. | |
dc.identifier.citation | Pediatric Hematology and Oncology | |
dc.identifier.citation | 29 | |
dc.identifier.citation | 2 | |
dc.identifier.citation | 119 | |
dc.identifier.citation | 129 | |
dc.identifier.issn | 8880018 | |
dc.identifier.other | 10.3109/08880018.2011.644881 | |
dc.identifier.uri | http://hdl.handle.net/10019.1/20600 | |
dc.subject | Cameroon | |
dc.subject | Endemic Burkitt lymphoma | |
dc.subject | Treatment | |
dc.title | The Cameroon 2008 burkitt lymphoma protocol: Improved event-free survival with treatment adapted to disease stage and the response to induction therapy | |
dc.type | Article |