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Dive into the research topics where Bongani Kaimila is active.

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Featured researches published by Bongani Kaimila.


British Journal of Haematology | 2016

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

Christopher Stanley; Katherine D. Westmoreland; Brett J. Heimlich; Nader Kim El-Mallawany; Peter Wasswa; Idah Mtete; Mercy Butia; Salama Itimu; Mary Chasela; Mary Mtunda; Mary Chikasema; Victor Makwakwa; Bongani Kaimila; Edwards Kasonkanji; Fred Chimzimu; Coxcilly Kampani; Bal M. Dhungel; Robert Krysiak; Nathan D. Montgomery; Yuri Fedoriw; Nora E. Rosenberg; N. George Liomba; Satish Gopal

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.


Pediatric Blood & Cancer | 2017

Hodgkin lymphoma, HIV, and Epstein–Barr virus in Malawi: Longitudinal results from the Kamuzu Central Hospital Lymphoma study

Katherine D. Westmoreland; Christopher Stanley; Nathan D. Montgomery; Bongani Kaimila; Edwards Kasonkanji; Nader Kim El-Mallawany; Peter Wasswa; Idah Mtete; Mercy Butia; Salama Itimu; Mary Chasela; Mary Mtunda; Maria Chikasema; Victor Makwakwa; Coxcilly Kampani; Bal M. Dhungel; Marcia K. Sanders; Robert Krysiak; Tamiwe Tomoka; N. George Liomba; Dirk P. Dittmer; Yuri Fedoriw; Satish Gopal

Contemporary descriptions of classical Hodgkin lymphoma (cHL) are lacking from sub‐Saharan Africa where human immunodeficiency virus (HIV) and Epstein–Barr virus (EBV) are prevalent.


PLOS ONE | 2016

CHOP Chemotherapy for Aggressive Non-Hodgkin Lymphoma with and without HIV in the Antiretroviral Therapy Era in Malawi.

Satish Gopal; Yuri Fedoriw; Bongani Kaimila; Nathan D. Montgomery; Edwards Kasonkanji; Agnes Moses; Richard Nyasosela; Suzgo Mzumara; Carlos Varela; Maria Chikasema; Victor Makwakwa; Salama Itimu; Tamiwe Tomoka; Steve Kamiza; Bal Mukunda Dhungel; Fred Chimzimu; Coxcilly Kampani; Robert Krysiak; Kristy L. Richards; Thomas C. Shea; N. George Liomba

There are no prospective studies of aggressive non-Hodgkin lymphoma (NHL) treated with CHOP in sub-Saharan Africa. We enrolled adults with aggressive NHL in Malawi between June 2013 and May 2015. Chemotherapy and supportive care were standardized, and HIV+ patients received antiretroviral therapy (ART). Thirty-seven of 58 patients (64%) were HIV+. Median age was 47 years (IQR 39–56), and 35 (60%) were male. Thirty-five patients (60%) had stage III/IV, 43 (74%) B symptoms, and 28 (48%) performance status ≥2. B-cell NHL predominated among HIV+ patients, and all T-cell NHL occurred among HIV- individuals. Thirty-one HIV+ patients (84%) were on ART for a median 9.9 months (IQR 1.1–31.7) before NHL diagnosis, median CD4 was 121 cells/μL (IQR 61–244), and 43% had suppressed HIV RNA. HIV+ patients received a similar number of CHOP cycles compared to HIV- patients, but more frequently developed grade 3/4 neutropenia (84% vs 31%, p = 0.001), resulting in modestly lower cyclophosphamide and doxorubicin doses with longer intervals between cycles. Twelve-month overall survival (OS) was 45% (95% CI 31–57%). T-cell NHL (HR 3.90, p = 0.017), hemoglobin (HR 0.82 per g/dL, p = 0.017), albumin (HR 0.57 per g/dL, p = 0.019), and IPI (HR 2.02 per unit, p<0.001) were associated with mortality. HIV was not associated with mortality, and findings were similar among patients with diffuse large B-cell lymphoma. Twenty-three deaths were from NHL (12 HIV+, 11 HIV-), and 12 from CHOP (9 HIV+, 3 HIV-). CHOP can be safe, effective, and feasible for aggressive NHL in Malawi with and without HIV.


Journal of the International AIDS Society | 2015

Characteristics and survival for HIV-associated multicentric Castleman disease in Malawi

Satish Gopal; N. George Liomba; Nathan D. Montgomery; Agnes Moses; Bongani Kaimila; Richard Nyasosela; Maria Chikasema; Bal M. Dhungel; Coxcilly Kampani; Marcia K. Sanders; Robert Krysiak; Dirk P. Dittmer; Yuri Fedoriw

Clinical reports of multicentric Castleman disease (MCD) from sub‐Saharan Africa (SSA) are scarce despite high prevalence of HIV and Kaposi sarcoma‐associated herpesvirus (KSHV). Our objective is to describe characteristics and survival for HIV‐associated MCD patients in Malawi. To our knowledge, this is the first HIV‐associated MCD case series from the region.


Malawi Medical Journal | 2018

A case of massive splenomegaly due to chronic myeloproliferative neoplasm

Zachary G. Jacobs; Bongani Kaimila; Peter Wasswa; Thuy Bui

A 34-year-old female, HIV non-reactive, presented to Kamuzu Central Hospital (KCH) in Lilongwe, Malawi, complaining of 7 months abdominal pain. She endorsed shortness of breath and early satiety for the same duration, but denied fever, chills, night sweats, and weight loss. The remainder of her review of systems was negative. She had no significant past medical history. There were no identifiable risk factors for myeloproliferative disorders, including family history, known genetic syndromes, chemical exposure, or history of ionizing radiation. On physical exam, she was noted to have a visible spleen (figure 1) which crossed into the right upper quadrant as well as the pelvis, and was non-tender to palpation. There was no cervical or axillary lymphadenopathy. The remainder of her exam was unremarkable.


Journal of Global Oncology | 2018

The African Esophageal Cancer Consortium: A Call to Action

Katherine Van Loon; Michael M. Mwachiro; Christian C. Abnet; Larry Akoko; Mathewos Assefa; Stephen L. Burgert; Steady Chasimpha; Charles Dzamalala; David E. Fleischer; Satish Gopal; Prasad G. Iyer; Bongani Kaimila; Violet Kayamba; Paul Kelly; Maria E. Leon; Christopher G. Mathew; Diana Menya; Daniel Middleton; Yohannie Mlombe; Blandina T. Mmbaga; Elia Mmbaga; Gift Mulima; Gwen Murphy; Beatrice Mushi; Ally Mwanga; Amos O. Mwasamwaja; M. Iqbal Parker; Natalie Pritchett; Joachim Schüz; Mark Topazian

Esophageal cancer is the eighth most common cancer worldwide and the sixth most common cause of cancer-related death; however, worldwide incidence and mortality rates do not reflect the geographic variations in the occurrence of this disease. In recent years, increased attention has been focused on the high incidence of esophageal squamous cell carcinoma (ESCC) throughout the eastern corridor of Africa, extending from Ethiopia to South Africa. Nascent investigations are underway at a number of sites throughout the region in an effort to improve our understanding of the etiology behind the high incidence of ESCC in this region. In 2017, these sites established the African Esophageal Cancer Consortium. Here, we summarize the priorities of this newly established consortium: to implement coordinated multisite investigations into etiology and identify targets for primary prevention; to address the impact of the clinical burden of ESCC via capacity building and shared resources in treatment and palliative care; and to heighten awareness of ESCC among physicians, at-risk populations, policy makers, and funding agencies.


Infectious Agents and Cancer | 2018

Plasmablastic lymphoma in Malawi

Takondwa Zuze; Matthew S. Painschab; Ryan Seguin; Evarista Kudowa; Bongani Kaimila; Edwards Kasonkanji; Tamiwe Tomoka; Bal Mukunda Dhungel; Maurice Mulenga; Maria Chikasema; Blessings Tewete; Asekanadziwa Ntangwanika; Sarah Chiyoyola; Fred Chimzimu; Coxcilly Kampani; Robert Krysiak; Nathan D. Montgomery; Yuri Fedoriw; Satish Gopal

Plasmablastic lymphoma (PBL) clinical descriptions are scarce from sub-Saharan Africa (SSA) where both HIV and EBV are highly endemic. We identified 12 patients with pathologically confirmed PBL from a prospective cohort in Lilongwe, Malawi. Median age was 46 (range 26–71), seven (58%) were male, and six (50%) were HIV-positive. Eight patients were treated with CHOP and four with a modified EPOCH regimen. One-year overall survival was 56% (95% CI 24–79%), without clear differences based on HIV status. PBL occurs in Malawi in HIV-positive and HIV-negative individuals and can be treated successfully with curative intent, even in a low-resource setting in SSA.


Clinical Case Reports | 2018

Rosai-Dorfman disease in Malawi

Edwards Kasonkanji; Ryan Seguin; Bongani Kaimila; Bal M. Dhungel; Matt Painschab; Tamiwe Tomoka; Satish Gopal

Rosai‐Dorfman Disease (RDD) is a rare lymphoproliferative disease with limited cases reported in sub‐Saharan Africa, potentially due to a lack of pathological services throughout the region. RDD diagnosis can be difficult, especially in resource‐limited setting, as symptoms can be nearly identical to more common causes of lymphadenopathy.


Journal of Global Oncology | 2017

Development of an African Esophageal Cancer Consortium

Gwen Murphy; Valerie McCormack; Diana Menya; Blandina T. Mmbaga; Katherine Van Loon; Elia Mmbaga; Satish Gopal; Bongani Kaimila; Gift Mulima; Natalie Pritchett; Michael M. Mwachiro; Russell E. White; Christian C. Abnet; Joachim Schüz; Sanford M. Dawsey

Abstract 44Background:Esophageal cancer is the sixth leading cause of cancer death worldwide. It kills 400,000 people every year, most of whom live in two distinct geographic bands across central Asia and along the eastern Africa corridor that extends from Ethiopia to South Africa. In these high-risk areas, nearly all cases are esophageal squamous cell carcinoma (ESCC). Our group and others have performed many etiologic, genetic, and early detection and treatment studies of ESCC in central Asia, but this disease remains essentially unstudied in eastern Africa. Over the past few years, several groups have begun quality studies of ESCC in Africa, including case-control studies in Dar es Salaam, Tanzania (University of California, San Francisco, and Muhimbili University of Health and Allied Sciences); Eldoret, Kenya (International Agency for Research on Cancer and Moi University); Moshi, Tanzania (International Agency for Research on Cancer and Kilimanjaro Clinical Research Institute); Bomet, Kenya (National...


Journal of Global Oncology | 2017

Leveraging HIV Research and Implementation for Cancer and Noncommunicable Diseases in Malawi

Mwapatsa Mipando; Nyengo Mkandawire; Jones Masiye; Emily Wroe; Luckson Dullie; Ron Mataya; Adamson S. Muula; Victor Mwapatsa; Charles Dzamalala; Leo Masamba; Tamiwe Tomoka; Agnes Moses; Lameck Chinula; Bongani Kaimila; Gift Mulima; Richard Nyasosela; Jonathan Ngoma; Lilian Chunda; Dan Namarika; Steve Kamiza; Moffat Nyirenda; Amelia C. Crampin; Stephen V. Gordon; Michelle Eckerle; Russell Ware; Josh Berman; Joep van Oesterhout; Joe Sclafani; Nader Kim El-Mallawany; Peter Wasswa

Abstract 33Background:Enabled by collaboration and political stability, Malawi is a global leader for HIV research and implementation. We undertook this work to identify ways to leverage successes in HIV treatment and research for cancer and noncommunicable diseases (NCDs).Methods:Over more than two decades, investment from the National Institutes of Health (NIH) and other funders has allowed Malawi participation in international HIV networks. As these sought to address HIV-positive cancer, investment occurred to increase pathology, improve cancer registration, scale up cervical cancer screening, and improve nursing and pharmacy skills for chemotherapy administration. This allowed Malawi to participate in multinational clinical trials for HIV-positive Kaposi sarcoma treatment and cervical cancer prevention. Building on this, Malawi was one of six countries in 2014 to receive an NIH U54 consortium award for HIV-positive malignancies and was one of six countries added to the National Cancer Institute (NCI) ...

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Satish Gopal

University of North Carolina at Chapel Hill

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Yuri Fedoriw

University of North Carolina at Chapel Hill

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Coxcilly Kampani

University of North Carolina at Chapel Hill

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Nathan D. Montgomery

University of North Carolina at Chapel Hill

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Maria Chikasema

University of North Carolina at Chapel Hill

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Christopher Stanley

University of North Carolina at Chapel Hill

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Peter Wasswa

Boston Children's Hospital

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