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    <timestamp>20260115062231000</timestamp>
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      <email_address>editor.jddt@gmail.com</email_address>
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    <registrant>Universal Journal of Pharmaceutical Research</registrant>
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        <full_title>Universal Journal of Pharmaceutical Research</full_title>
        <abbrev_title>Univ J Pharm Res</abbrev_title>
        <issn media_type="electronic">2456-8058</issn>
        <issn media_type="print">2831-5235</issn>
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        <publication_date media_type="online">
          <month>01</month>
          <day>15</day>
          <year>2026</year>
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          <title>MYELOGENOUS LEUKEMIA: DIAGNOSIS, THERAPEUTIC APPROACH AND FUTURE PERSPECTIVES: A NARRATIVE REVIEW</title>
        </titles>
        <contributors>
          <person_name contributor_role="author" sequence="first">
            <surname>Ibrahim Aliyu Bagudo</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <surname>Ibrahim Kalle Kwaifa</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <surname>Muhammad Khadijah Abubakar</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <surname>Omogboyegun Alaba Ayodeji</surname>
          </person_name>
          <person_name contributor_role="author" sequence="additional">
            <surname>Emmanuel Ifeanyi Obeagu</surname>
          </person_name>
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          <jats:p>Acute myeloid leukaemia (AML) and Chronic myeloid leukaemia (CML) present unique and significant difficulties in the field of blood cancers. They originate from the harmful transformation of myeloid cells and are linked to distinct pathophysiological characteristics that require specialized diagnostic and treatment methods. The diagnosis of CML primarily relies on the detection of the BCR-ABL1 fusion gene, which represents a key feature of the disorder. This genetic marker not only validates the diagnosis but also guides the treatment approach. Nonetheless, AML is characterized by its genetic and clinical diversity, making diagnosis challenging and necessitating a more personalized treatment strategy. Progress in molecular diagnostics has uncovered particular mutations that can be addressed by new therapies, enabling more individualized treatment plans. Studies in both AML and CML seek to determine the shortcomings of current treatments. The main focus of research in CML involves creating next-generation tyrosine kinase inhibitors (TKIs) and methods to eliminate minimal residual disease (MRD), whereas in AML, combining targeted therapies, immunotherapies, and progress in molecular diagnostics offers potential for improved patient results. Trustworthy data was gathered from Tailor and Francis, PubMed, Springer, Nature, Google Scholar, MDPI, BMC, and several other relevant sources. This review explores the molecular mechanisms, diagnostic methods, potential treatment options, and future outlook of myelogenous leukaemia.
                   
Peer Review History: 
Received 20 September 2025;   Reviewed 7 November 2025; Accepted  12 December; Available online 15 January 2026
Academic Editor: Dr. Marwa A. A. Fayed, University of Sadat City, Egypt, maafayed@gmail.com
Reviewers:
Dr. Omid Gholami, Sabzevar University of Medical Sciences, Iran, omidghphd@gmail.com
Dr. O.J Owolabi, University of Benin, Nigeria, owolabi@uniben.edu</jats:p>
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