A groundbreaking discovery in cancer immunotherapy sheds light on immune checkpoint blockade (ICB) therapy resistance, offering promising solutions.
Research led by Dr. Shoba Amarnath at Newcastle University reveals mechanisms behind ICB therapy failure in metastatic skin cancers.
The study, to be published in Nature Immunology, proposes a novel combination strategy to enhance immunotherapy efficacy.
Immune checkpoint blockade targets PD-1 to activate T cells against cancer, but over 60% of patients do not benefit from this therapy.
The study focuses on the role of regulatory T cells (Tregs) in tumor resistance to ICB, uncovering a paradoxical effect of PD-1 inhibition.
By targeting CD30, an emerging immunosuppressive axis in solid tumors, researchers reversed resistance and suppressed melanoma growth in preclinical models.
A Phase II trial combining anti-PD1 ICB with anti-CD30 therapy showed a 24% survival advantage in refractory metastatic melanoma patients.
The research's implications extend to various solid tumors, offering a promising approach to overcoming immune evasion in cancer.
Insights into Treg behavior in ICB resistance and identification of targetable molecules aim to broaden clinical responses and reduce treatment resistance.
Newcastle University's research, supported by prestigious bodies, aims to optimize cancer immunotherapy outcomes through innovative solutions.