Bispecific Antibodies in Hematological Malignancies: A Scoping Review.
Mohamed H OmerAreez ShafqatOmar AhmadKhaled Manae AlKattanAhmed YaqinuddinMoussab DamlajPublished in: Cancers (2023)
Bispecific T-cell engagers (BiTEs) and bispecific antibodies (BiAbs) have revolutionized the treatment landscape of hematological malignancies. By directing T cells towards specific tumor antigens, BiTEs and BiAbs facilitate the T-cell-mediated lysis of neoplastic cells. The success of blinatumomab, a CD19xCD3 BiTE, in acute lymphoblastic leukemia spearheaded the expansive development of BiTEs/BiAbs in the context of hematological neoplasms. Nearly a decade later, numerous BiTEs/BiAbs targeting a range of tumor-associated antigens have transpired in the treatment of multiple myeloma, non-Hodgkin's lymphoma, acute myelogenous leukemia, and acute lymphoblastic leukemia. However, despite their generally favorable safety profiles, particular toxicities such as infections, cytokine release syndrome, myelosuppression, and neurotoxicity after BiAb/BiTE therapy raise valid concerns. Moreover, target antigen loss and the immunosuppressive microenvironment of hematological neoplasms facilitate resistance towards BiTEs/BiAbs. This review aims to highlight the most recent evidence from clinical trials evaluating the safety and efficacy of BiAbs/BiTEs. Additionally, the review will provide mechanistic insights into the limitations of BiAbs whilst outlining practical applications and strategies to overcome these limitations.
Keyphrases
- acute lymphoblastic leukemia
- clinical trial
- allogeneic hematopoietic stem cell transplantation
- multiple myeloma
- stem cells
- induced apoptosis
- dendritic cells
- acute myeloid leukemia
- randomized controlled trial
- liver failure
- immune response
- single cell
- drug delivery
- cell cycle arrest
- respiratory failure
- combination therapy
- oxidative stress
- replacement therapy
- hodgkin lymphoma
- cell therapy
- acute respiratory distress syndrome
- double blind
- pi k akt
- placebo controlled