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EBV Conference 2008 Guangzhou - Baylor College of Medicine

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184 (RegID: 1156)<br />

Beverly Smith Dougall<br />

Imperial <strong>College</strong>, Medical School<br />

E-mail: b.griffin@imperial.ac.uk<br />

<strong>EBV</strong>-ASSOCIATED BURKITT'S LYMPHOMA (BL) IN MALAWI, EAST AFRICA: GENE<br />

EXPRESSION, DIAGNOSIS AND THERAPY<br />

Beverly E. Griffin1, 4, Susan van Noorden2, I.A. Lampert2, S-A Xue3 and J.A. Phillips4. Imperial<br />

<strong>College</strong> School <strong>of</strong> <strong>Medicine</strong> at St. Mary’s1 and at Hammersmith Hospitals2, University <strong>College</strong><br />

Medical School3, London U.K., and the BL unit, Kamuzu Central Hospital, Malawi4<br />

Posterabstract:<br />

A major study on BL in Malawi, East Africa, over the past twenty years, will be presented. Briefly:<br />

this <strong>EBV</strong>-associated malignancy remains the major childhood cancer seen in Malawi, and patient<br />

numbers are high; about 60% <strong>of</strong> confirmed BL cases, whether facial or abdominal, respond to<br />

classical multidose treatment with cyclophosphamide; therapy for the others is generally unsuccessful.<br />

Qualitatively, <strong>EBV</strong> gene expression varies among the tumours. Our chief aims over the past twenty<br />

years have focused on: trying to understand the differences, at a molecular level, between BL patients<br />

that respond to the chemotherapy and those that do not; seeking markers to aid in determining<br />

optimal management <strong>of</strong> patients; and, identifying an alternative therapeutic regiment that can be used<br />

to combat the tumour in non-responding patients. We will present data on all three topics.<br />

Our current focus for alternative treatment <strong>of</strong> the non-responding tumours is based on a small<br />

preliminary pilot study <strong>of</strong> children with gross, cyclophosphamide-resistant multiple lesions. Sodium<br />

phenylbutyrate), a histone deacetylase (HDAC) inhibitor, was added to the treatment protocol for<br />

these patients. This HDAC was chosen for its simple chemistry which suggests that it could<br />

ultimately be made cheaply for Africa, its multiple functions, particularly those associated with<br />

promotion <strong>of</strong> cell differentiation, and its established safety in the treatment <strong>of</strong> another disease (urea<br />

disorder) <strong>of</strong> children. Our data, to be presented, are encouraging, proving positive for half the treated<br />

children. They further highlight differences that exist, moreover, among the tumour populations.<br />

<strong>EBV</strong> <strong>Conference</strong> <strong>2008</strong> <strong>Guangzhou</strong><br />

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