B7-H3 Inhibitors in Oncology Clinical Trials: A Review.
Kavanya FeustelJared MartinGerald S FalchookPublished in: Journal of immunotherapy and precision oncology (2024)
B7-H3 is a transmembrane receptor highly prevalent on malignant cells and plays an important role in adaptive immunity that is not fully elucidated. Targeted B7-H3 inhibitors, including antibody-drug conjugates, radioimmunotherapy, and monoclonal antibodies, are a new class of antineoplastic agents showing promising preliminary clinical efficacy, observed with several of these agents against multiple tumor types. Particularly promising treatments are enoblituzumab for prostate cancer, 131 I-omburtamab for central nervous system malignancies, and HS-20093 for small-cell lung cancer but further studies are warranted. There are clinical trials on the horizon that have not yet enrolled patients examining chimeric antigen receptor T-cell therapies, bi- and tri-specific killer engagers, and dual-affinity retargeting proteins. These data will be telling of the efficacy of B7-H3 inhibitors in both hematologic and solid malignancies. This study aimed to compile available results of B7-H3 inhibitors in oncology clinical trials.
Keyphrases
- clinical trial
- prostate cancer
- small cell lung cancer
- end stage renal disease
- palliative care
- newly diagnosed
- chronic kidney disease
- ejection fraction
- induced apoptosis
- phase ii
- radical prostatectomy
- prognostic factors
- randomized controlled trial
- cancer therapy
- cell death
- artificial intelligence
- cell cycle arrest
- electronic health record
- big data
- study protocol
- phase iii
- cell proliferation
- brain metastases
- patient reported outcomes