Literature DB >> 26914979

Outcomes for paediatric Burkitt lymphoma treated with anthracycline-based therapy in Malawi.

Christopher C Stanley1, Kate D Westmoreland1, Brett J Heimlich1, Nader K El-Mallawany2, Peter Wasswa3, Idah Mtete4, Mercy Butia4, Salama Itimu1, Mary Chasela4, Mary Mtunda4, Mary Chikasema1, Victor Makwakwa1, Bongani Kaimila1, Edwards Kasonkanji1, Fred Chimzimu1, Coxcilly Kampani1, Bal M Dhungel1, Robert Krysiak1, Nathan D Montgomery5, Yuri Fedoriw5, Nora E Rosenberg1,5, N George Liomba1, Satish Gopal1,5,6.   

Abstract

Burkitt lymphoma (BL) is the most common paediatric cancer in sub-Saharan Africa (SSA). Anthracyline-based treatment is standard in resource-rich settings, but has not been described in SSA. Children ≤18 years of age with newly diagnosed BL were prospectively enrolled from June 2013 to May 2015 in Malawi. Staging and supportive care were standardized, as was treatment with CHOP (cyclophosphamide, doxorubicin, vincristine, prednisone) for six cycles. Among 73 children with BL, median age was 9·2 years (interquartile range 7·7-11·8), 48 (66%) were male and two were positive for human immunodeficiency virus. Twelve (16%) had stage I/II disease, 36 (49%) stage III and 25 (34%) stage IV. Grade 3/4 neutropenia occurred in 17 (25%), and grade 3/4 anaemia in 29 (42%) of 69 evaluable children. Eighteen-month overall survival was 29% (95% confidence interval [CI] 18-41%) overall. Mortality was associated with age >9 years [hazard ratio [HR] 2·13, 95% CI 1·15-3·94], female gender (HR 2·12, 95% CI 1·12-4·03), stage (HR 1·52 per unit, 95% CI 1·07-2·17), lactate dehydrogenase (HR 1·03 per 100 iu/l, 95% CI 1·01-1·05), albumin (HR 0·96 per g/l, 95% CI 0·93-0·99) and performance status (HR 0·78 per 10-point increase, 95% CI 0·69-0·89). CHOP did not improve outcomes in paediatric BL compared to less intensive regimens in Malawi.
© 2016 John Wiley & Sons Ltd.

Entities:  

Keywords:  Burkitt lymphoma; Epstein-Barr virus; Malawi; paediatric cancer; sub-Saharan Africa

Mesh:

Substances:

Year:  2016        PMID: 26914979      PMCID: PMC4884132          DOI: 10.1111/bjh.13986

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


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