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New Therapeutic Strategies for Lymphoma

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Pathology, Diagnostics, and Therapeutics".

Deadline for manuscript submissions: closed (31 March 2024) | Viewed by 399

Special Issue Editor


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Guest Editor
Division of Lymphoma, Department of Hematology and HCT, City of Hope National Medical Center, 1500 E. Duarte Rd., Duarte, CA 91010, USA
Interests: cellular immunotherapy for lymphoma; non-Hodgkin lymphoma

Special Issue Information

Dear Colleagues, 

Lymphoma treatment has seen a revolution over the past 5 years with the development and approval of novel therapeutic strategies including chimeric antigen receptor T-cell therapy, bispecific antibodies, antibody–drug conjugates, monoclonal antibodies, immune checkpoint inhibitors, and molecular targeted therapies. Novel approaches to the timing and potential combinations of these therapies are areas of active study. The optimal strategies appear to be disease- and disease-subtype-specific and benefits appear to vary based on disease-specific characteristics. For example, large B cell lymphoma and follicular lymphoma have been inundated with novel CAR T therapies and bispecific antibody treatment options, while mantle cell lymphoma has seen both CAR T and molecular targeted therapies showing benefits. Despite these advances, diseases including peripheral T cell lymphomas have only had modest advancement with efficacy seen with targeted therapy and epigenetic modifying agents. In addition, although these advances have drastically changed the therapeutic landscape of lymphoma in general, there is still significant room for improvement.  Novel therapies in this setting would be considered those beyond the recent advancements that have become standard practice. These would include novel cellular therapeutics beyond CD19-targeted CAR T including novel targeting CAR T product and novel cellular products such as CAR NK as well as novel monoclonal and bispecific and trispecific antibodies and combinations beyond the well-described CD20 monoclonal and bispecific antibodies that are well known. Novel molecular targets beyond the well-known Bruton's tyrosine kinase, phosphoinositide-3-kinase, BCL2 inhibitors, or novel combinations of these agents would also be of interest. 

Original research and review articles on new therapeutic strategies for Lymphoma are welcome to this special issue.

Dr. Geoffrey Shouse
Guest Editor

Manuscript Submission Information

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Keywords

  • chimeric antigen receptor
  • immunotherapy
  • bispecific antibody
  • trispecific antibody
  • antibody–drug conjugate
  • immune checkpoint
  • molecular targeted therapy
  • epigenetic modifiers

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Published Papers

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