A significant milestone has been achieved in the fight against melanoma, a highly aggressive form of skin cancer. Researchers at HonorHealth Research Institute have initiated treatment on the first participant in a global clinical trial spanning 50 sites. This innovative therapy focuses on PRAME, a peptide frequently present in melanoma tumors. By harnessing and enhancing the patient's immune system T cells, this cutting-edge approach generates billions of personalized cells to combat melanoma, even when it has metastasized. The potential of this cellular therapy excites medical professionals like Dr. Justin Moser, an associate clinical investigator, who believes it could provide renewed hope for patients with advanced-stage melanoma who have exhausted other treatment options.
The trial, named SUPRAME, involves nearly 360 participants and tests a groundbreaking engineered T cell receptor (TCR) therapy called ACTengine®, developed by Immatics, a biotechnology company based in Houston, Texas. Known as IMA203 TCR-T, this therapy represents the world’s first TCR therapeutic targeting PRAME. In this process, T cells extracted from the patient's blood are genetically modified in a laboratory to specifically target cancer cells containing PRAME. These enhanced cells are then multiplied extensively before being reintroduced into the patient's body to seek out and destroy the cancer. Remarkably, the entire treatment requires only one dose. Initial results from a Phase I trial published in Nature Medicine indicate that the engineered cells are both safe and effective, with minimal side effects, showing a response rate of 54% and a median duration of response exceeding one year.
This revolutionary approach not only demonstrates promising outcomes but also highlights the importance of collaboration among dedicated professionals across continents. Cedrik Britten, Chief Medical Officer of Immatics, expressed gratitude for the support from clinical institutions in the United States and Europe. Their efforts collectively contribute to advancing cancer treatments through the power of T cells. The shortened manufacturing turnaround time of approximately two weeks further underscores the practicality and accessibility of this therapy. As research progresses, the potential impact on melanoma treatment and patient survival rates continues to inspire optimism and innovation in the medical community.