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<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Academy of Medical Sciences of I.R. Iran</PublisherName>
      <JournalTitle>Archives of Iranian Medicine</JournalTitle>
      <Issn>1029-2977</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2011</Year>
        <Month>05</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>The Influence of Bcl-2 and Myeloid Antigen Expression on Response to Therapy in Childhood Acute Lymphoblastic Leukemia</ArticleTitle>
    <FirstPage>170</FirstPage>
    <LastPage>174</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Zahra</FirstName>
        <LastName>Amirghofran</LastName>
      </Author>
      <Author>
        <FirstName>Yahya</FirstName>
        <LastName>Daneshbod</LastName>
      </Author>
      <Author>
        <FirstName>Naser</FirstName>
        <LastName>Gholijani</LastName>
      </Author>
      <Author>
        <FirstName>Maryam</FirstName>
        <LastName>Esmaeilbeig</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">
      </ArticleId>
    </ArticleIdList>
    <History>
    </History>
    <Abstract>BACKGROUND: The possible prognostic significance of the expression of a variety of markers has been investigated in acute lymphoblastic leukemia (ALL).  METHODS: In the present study we investigated the prognostic significance of CD13 and CD33 myeloid antigens (MY) aberrantly expressed on the blasts of ALL patients and Bcl-2 anti- apoptotic molecule expression in childhood ALL.  RESULTS: Aberrant expression of MY occurred in 8.8&amp;percnt; of cases. Variant levels of Bcl-2 were expressed in patients (44.2&amp;plusmn;25.5&amp;percnt;), with more than 20&amp;percnt; positivity for Bcl-2 in 64.7&amp;percnt; of patients. Bcl-2+ patients survived 959&amp;plusmn;242 days compared to 1059+230 days for Bcl-2- patients (P=0.2). Corresponding data for complete remission duration was 682&amp;plusmn;170 and 716&amp;plusmn;173 days (P=0.3), respectively, indicating no significant association between survival and complete remission duration of patients with expression of the Bcl-2 molecule. Analysis of clinical response according to MY expression, however, showed significant association with survival and complete remission duration. MY+ patients had shorter complete remission duration (383&amp;plusmn;58 days) and survival (473&amp;plusmn;68 days) than MY- patients (complete remission duration, 724&amp;plusmn;144 days; survival, 1045&amp;plusmn;186 days; P&amp;lt;0.001). Expression of Bcl-2 along with MY was not associated with a significant decrease in survival or complete remission duration  CONCLUSION: Results of this study indicated that expression of MY was a poor prognostic factor in childhood ALL. Bcl-2 expression in MY+ patients could not influence the response to therapy. </Abstract>
  </Article>
</ArticleSet>