Publications by authors named "Nawar Maher"

The mutational status of immunoglobulin (IG) light chain genes in chronic lymphocytic leukemia (CLL) and its clinical impact have not been extensively studied. To assess their prognostic significance, the IG light chain gene repertoire in CLL patients has been evaluated using a training-validation approach. In the training cohort (N = 573 CLL), 92.

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The treatment landscape of chronic lymphocytic leukemia (CLL), the most frequent leukemia in adults, is constantly changing. CLL patients can be divided into three risk categories, based on their IGHV mutational status and the occurrence of disruption and/or complex karyotype. For the first-line treatment of low- and intermediate-risk CLL, both the BCL2 inhibitor venetoclax plus obinutuzumab and the second generation BTK inhibitors (BTKi), namely acalabrutinib and zanubrutinib, are valuable and effective options.

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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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