Alfadel Alshaibani
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:
- Mahmoud Aljurf
King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia
2 shared publications Anna Sureda
Inst Catala Oncol LHosp, Barcelona, Spain
1 shared publicationMahmoud Aljurf
King Faisal Specialist Hosp & Res Ctr, Riyadh 11564, Saudi Arabia
1 shared publication- Mehdi Hamadani
Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI
1 shared publication Mohamed A. Kharfan-Dabaja
Mayo Clin, Div Hematol Oncol, Blood & Marrow Transplantat Program, Jacksonville, FL 32224 USA
1 shared publication- Mohamed Kharfan-Dabaja
Division of Hematology-Oncology, Blood and Marrow Transplantation Program, Mayo Clinic, Jacksonville, USA
1 shared publication
Latest Publications
- 16 July 2025
- Published by Elsevier in Blood Reviews
- Vol. 74, 101321
Programmed death inhibitors in CNS B-cell lymphoma: A literature review
- 16 July 2025
- Published by Elsevier in Blood Reviews
- Vol. 74, 101321
Programmed death inhibitors in CNS B-cell lymphoma: A literature review
- 1 June 2022
- Vol. 20 (6) , 384-390
Follicular Lymphoma Grade 3: A Comprehensive Review
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.
- 1 June 2022
- Vol. 20 (6) , 384-390
Follicular Lymphoma Grade 3: A Comprehensive Review
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
- 23 May 2022
- Published by MDPI AG in Current Oncology
- Vol. 29 (5) , 3759-3769
The Evolution of Our Understanding of Immunoproliferative Small Intestinal Disease (IPSID) over Time
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.
- 23 May 2022
- Published by MDPI AG in Current Oncology
- Vol. 29 (5) , 3759-3769
Open AccessThe Evolution of Our Understanding of Immunoproliferative Small Intestinal Disease (IPSID) over Time
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.