AAAlfadel Alshaibani

Alfadel Alshaibani

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Alfadel Alshaibani has a total of 12 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Programmed death inhibitors in CNS B-cell lymphoma: A literature review

    by Mostafa Mohammed Saleh, Walid Rasheed, Saud Alhayli, Alfadel Alshaibani, Mahmoud Aljurf, Riad El Fakih


    • 1 June 2022
      • Vol. 20  (6) , 384-390

    Follicular Lymphoma Grade 3: A Comprehensive Review

    by Alfadel Alshaibani, Riad El Fakih, Anna Sureda, Mohamed A. Kharfan-Dabaja, Mahmoud Aljurf

    Follicular lymphoma (FL) is a heterogeneous entity with disparate outcomes based on clinical and pathologic char-acteristics. An increasingly detailed understanding of high-grade FL (grade 3) has led to the identification of separate categories of FL3A and FL3B. Recently, genomic studies have made much progress in delineating the genetic differences between FL3A and FL3B. Although a general consensus exists that FL3B follows an aggressive course matching that of diffuse large B-cell lymphoma, there is less certainty regarding the course of FL3A. Uncertainty also exists regarding the management of high-grade FL. Given that a majority of the prospective landmark trials in FL have exclud-ed patients with high-grade FL, most of the available evidence is retrospective. This review summarizes the recent advances in the management of high-grade FL.


  • Open Access

    The Evolution of Our Understanding of Immunoproliferative Small Intestinal Disease (IPSID) over Time

    by Ruah AlYamany, Mohamed A. Kharfan-Dabaja, Mehdi Hamadani, Alfadel Alshaibani, Mahmoud Aljurf

    Immunoproliferative small intestinal disease (IPSID) is an uncommon disease with a higher prevalence in the developing world. IPSID diagnosis relies mainly on a tissue biopsy and a high index of suspicion. Treatment options are variable; however, they mainly include anthracycline-based chemotherapy with or without antibiotics in advanced stages. Because of the paucity of IPSID, our perception of the disease remains narrow, and investigating the optimal lines of therapy and prevention without a complete comprehension of the disease is challenging. In our review, we explore the expansion of knowledge about IPSID, which has been developing over the years, to help increase the detection of IPISD cases and further research the most appropriate lines of therapy and prevention.