Publications by authors named "Bassam F Matti"

Article Synopsis
  • The B cell receptor (BCR) signaling pathway is vital for B cell development and is also involved in the progression of B cell cancers, leading to continuous activation of Bruton tyrosine kinase (BTK), enhancing survival and growth of malignant cells.
  • BTK inhibitors (BTKi), like ibrutinib and acalabrutinib, effectively treat several types of B cell malignancies by permanently blocking BTK, but many patients may relapse due to resistance mechanisms, including mutations at the BTK binding site.
  • Newer approaches, such as non-covalent BTKi (like pirtobrutinib) and proteolysis-targeting chimeras (PROTACs), have shown promise in overcoming
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Chronic lymphocytic leukemia (CLL) is the most common leukemia in adults. Despite its indolent clinical course, therapy refractoriness and disease progression still represent an unmet clinical need. Before the advent of pathway inhibitors, chemoimmunotherapy (CIT) was the commonest option for CLL treatment and is still widely used in areas with limited access to pathway inhibitors.

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The key cell population permits cancer cells to avoid immune-surveillance is regulatory T cells (Tregs). This study evaluates the level of Tregs in chronic myeloid leukemia (CML) patients and the effect of Tyrosine kinase inhibitor (TKI) on Treg levels, as a pathway to understand the immune response and behavior among advance stage and optimal response CML patients using imatinib therapy. Blood samples were collected from 30 CML patients (optimal response to TKI), 30 CML patients (failure response to TKI), and 30 age- and gender-matched controls.

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Chronic myeloid leukemia (CML) is a myeloproliferative disorder characterized by the presence of an acquired mutation which affects the hematopoietic stem cell, leading to a striking overproduction of immature granulocytes. The first important clue to its pathogenesis the Philadelphia chromosome created by a reciprocal translocation between chromosomes 9 and 22 (t [9; 22] [q34; q11]). The development of the BCR-ABL-targeted imatinib mesylate represents a paradigm shift in the treatment of CML.

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Refractory/relapsed acute leukemia has always been a challenging problem for hematologist. Over the past decade emphasis has been made in the development of regimens containing fludarabine, combined with cytosine arabinoside for the treatment of refractory/relapsed acute leukemias. The aim of this study is to evaluate the efficacy and toxicity of the combination of fludarabine, high dose cytarabine, and granulocyte colony stimulating factor in refractory relapsed cases of acute leukaemia, a prospective study is being conducted at the National Center of Hematology and hematology unit/Baghdad teaching hospital from July 2008 to July 2010.

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Imatinib (Glivec(®)/Gleevec(®)) has shown long-term efficacy and safety in randomized trials. No large-scale studies have prospectively assessed the benefit-risk profile of an imatinib copy drug. We prospectively evaluated the response of patients with chronic myeloid leukemia in chronic phase in one institution.

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Article Synopsis
  • Imatinib mesylate is the primary treatment for chronic myeloid leukemia (CML) but can cause various adverse effects during therapy.
  • A study monitored 200 CML patients from December 2007 to October 2009, focusing on the safety and side effects of imatinib treatment, noting common hematological (like anemia and leukopenia) and non-hematological effects (such as edema and weight gain).
  • The findings indicated that imatinib is generally safe and well-tolerated, with manageable side effects that do not require significant dose reductions or result in fatalities.
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