Update on Burkitt Lymphoma

Because of its rarity and high curability, progress in advancing therapeutics in Burkitt lymphoma (BL) has been difficult. Over recent years, several new mutations that cooperate with MYC have been identified, and this has paved the way for testing novel agents in the disease. One of the challenges...

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Published inHematology/oncology clinics of North America Vol. 30; no. 6; p. 1333
Main Authors Dunleavy, Kieron, Little, Richard F, Wilson, Wyndham H
Format Journal Article
LanguageEnglish
Published United States 01.12.2016
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Abstract Because of its rarity and high curability, progress in advancing therapeutics in Burkitt lymphoma (BL) has been difficult. Over recent years, several new mutations that cooperate with MYC have been identified, and this has paved the way for testing novel agents in the disease. One of the challenges of most standard approaches typically used is severe treatment-related toxicity that often leads to discontinuation of therapy. To that point, there has been recent success developing intermediate intensity approaches that are well tolerated in all patient groups and maintain high cure rates in a multicenter setting.
AbstractList Because of its rarity and high curability, progress in advancing therapeutics in Burkitt lymphoma (BL) has been difficult. Over recent years, several new mutations that cooperate with MYC have been identified, and this has paved the way for testing novel agents in the disease. One of the challenges of most standard approaches typically used is severe treatment-related toxicity that often leads to discontinuation of therapy. To that point, there has been recent success developing intermediate intensity approaches that are well tolerated in all patient groups and maintain high cure rates in a multicenter setting.
Author Dunleavy, Kieron
Little, Richard F
Wilson, Wyndham H
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  organization: Lymphoid Malignancies Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USA. Electronic address: dunleavk@mail.nih.gov
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  givenname: Richard F
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  givenname: Wyndham H
  surname: Wilson
  fullname: Wilson, Wyndham H
  organization: Lymphoid Malignancies Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USA
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Keywords CCND3
Sporadic
MYC
Burkitt lymphoma
ID3
TCF3
Risk-adapted
Endemic
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Snippet Because of its rarity and high curability, progress in advancing therapeutics in Burkitt lymphoma (BL) has been difficult. Over recent years, several new...
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StartPage 1333
SubjectTerms Burkitt Lymphoma - genetics
Burkitt Lymphoma - metabolism
Burkitt Lymphoma - therapy
Humans
Mutation
Proto-Oncogene Proteins c-myc - genetics
Proto-Oncogene Proteins c-myc - metabolism
Title Update on Burkitt Lymphoma
URI https://www.ncbi.nlm.nih.gov/pubmed/27888884
Volume 30
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