New and emerging therapies for the treatment of relapsed/refractory diffuse large B-cell lymphoma

Author:

Moore Donald C.1ORCID,Peery Matthew R.2,Tobon Katherine A.3,Raheem Farah4,Hwang Grace S.5,Alhennawi Lin6,Hughes Mitchell E.7ORCID

Affiliation:

1. Department of Pharmacy, Atrium Health, Levine Cancer Institute, Concord, NC, United States

2. Department of Pharmacy, Virginia Commonwealth University Health, Richmond, VA, United States

3. Malignant Hematology Program, Moffitt Cancer Center, Tampa, FL, United States

4. Mayo Clinic, Phoenix, AZ, United States

5. Baylor St Luke’s Medical Center, Houston, TX, United States

6. University of Cincinnati College of Pharmacy, Cincinnati, OH, United States

7. Lymphoma Program, Hematology/Oncology Division, Perelman Center for Advanced Medicine, University of Pennsylvania, Philadelphia, PA, United States

Abstract

Diffuse large B-cell lymphoma (DLBCL) is the most common form of aggressive non-Hodgkin lymphoma. Approximately 40% of patients with DLBCL will experience disease relapse or will be refractory to first line chemoimmunotherapy, necessitating second-line salvage therapy. This has historically consisted of platinum-based chemotherapy regimens followed by autologous hematopoietic stem cell transplantation with curative intent for transplant-eligible patients or palliative chemotherapy for transplant-ineligible patients. In recent years there have been several new therapeutic agents approved for the treatment of relapsed/refractory DLBCL, thereby expanding the therapeutic landscape. These agents include polatuzumab vedotin, tafasitamab, loncastuximab tesirine, selinexor, and anti-CD19 chimeric antigen receptor T-cell therapies such as axicabtagene ciloleucel, tisagenlecleucel, and lisocabtagene maraleucel. This review summarizes the pharmacology, efficacy, safety, dosing, and administration of new agents recently approved for the treatment of relapsed/refractory DLBCL.

Publisher

SAGE Publications

Subject

Pharmacology (medical),Oncology

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