Immunotherapy after surgery shows potential in preventing the spread of aggressive skin cancer
Reports and Proceedings
Updates every hour. Last Updated: 6-Nov-2025 15:11 ET (6-Nov-2025 20:11 GMT/UTC)
A new clinical trials shows that pembrolizumab, a drug that utilizes the body’s immune system to target and eliminate cancer cells, appeared to reduce the risk of distant metastases for an aggressive form of skin cancer when given immediately after surgery, but did not significantly reduce the overall risk of recurrence, which was a co-primary endpoint of the trial. The randomized phase 3 trial called STAMP or EA6174, is the largest clinical study to date evaluating pembrolizumab as adjuvant therapy for Merkel cell carcinoma, an extremely aggressive disease, with fewer than half of patients surviving 5 years after diagnosis.
An international team of researchers has created the most detailed model yet of how cells regulate traffic through the nuclear pore complex—the gateway between a cell’s nucleus and its cytoplasm. The study solves a decades-old puzzle about how these pores can rapidly and selectively transport molecules, revealing that flexible protein chains create a dynamic “entropic barrier” that admits only properly escorted cargo. This computational model not only clarifies how healthy cells maintain precise control but also provides insight into diseases like cancer, Alzheimer’s, and ALS, where this transport system fails. It opens new avenues for medical and biotech innovation, including the design of artificial nanopores for targeted therapies and biosensing.
Patients with cancer who received mRNA-based COVID vaccines within 100 days of starting immune checkpoint therapy were twice as likely to be alive three years after beginning treatment, according to a new study led by researchers at The University of Texas MD Anderson Cancer Center.
Researchers have discovered a protein system that helps explain why some colorectal cancer patients don’t respond to chemotherapy, offering hope for more effective and personalized treatments. The team found that tumors often rely on the cystine/glutamate transporter (Xc-) to survive stress and resist cell death. When this system was blocked in lab models, the cancer became more sensitive to treatment. Importantly, the scientists also identified a unique protein “signature” that could predict which patients are likely to resist standard therapies, paving the way for doctors to tailor treatments more precisely. Beyond colorectal cancer, the findings may also shed light on other cancers and even neurological conditions, making this a promising step toward smarter, more targeted medicine.