The role of CAR-T cell therapy as second line in diffuse large B-cell lymphoma.
Omar AlbanyanJulio C ChavezJavier MunozPublished in: Therapeutic advances in hematology (2022)
For approximately three decades, autologous hematopoietic cell transplantation (auto-HCT) has been the standard of care for patients with relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) after frontline therapy. This approach is limited due to the intensity of chemotherapy and the proportion of patients who relapse after auto-HCT. Since the approval of anti-CD19 chimeric antigen receptor T-cell (CAR-T) therapy and novel agents, the treatment paradigm for DLBCL has changed remarkably. Anti-CD19 CAR-T therapy was first approved for relapsed DLBCL after two or more previous lines of therapy with long-lasting responses, with over 50% of patients still alive at 5-year follow-up. Here, we discuss recent randomized phase 3 clinical trials using axicabtagene ciloleucel, tisagenlecleucel, and lisocabtagene maraleucel in the second-line therapy setting compared with the standard of care in transplant-eligible patients who have DLBCL R/R within 12 months of completing chemo-immunotherapy, potentially changing the treatment algorithm for DLBCL.
Keyphrases
- diffuse large b cell lymphoma
- epstein barr virus
- cell therapy
- clinical trial
- end stage renal disease
- ejection fraction
- healthcare
- palliative care
- machine learning
- stem cells
- acute myeloid leukemia
- combination therapy
- prognostic factors
- acute lymphoblastic leukemia
- photodynamic therapy
- multiple myeloma
- bone marrow
- squamous cell carcinoma
- signaling pathway
- deep learning
- rectal cancer
- replacement therapy
- smoking cessation
- cell proliferation
- platelet rich plasma