CAR-T Therapy, short for Chimeric Antigen Receptor T-Cell Immunotherapy, is an advanced gene therapy method that involves genetically modifying a patient’s own T cells to target and destroy cancer cells. Unlike traditional medications, CAR-T therapy is tailored to each patient and requires collecting T cells from the patient’s blood before reinfusing them back into the body after genetic engineering.
Scientists then change these T cells in the laboratory to add a special new receptor called a chimeric antigen receptor (CAR). This receptor acts like a “homing device” that helps T cells find and attach to cancer cells. The modified T cells, now called CAR T cells, are grown in large numbers until there are enough to fight the cancer effectively.
Once ready, the CAR T cells are infused back into the patient’s bloodstream, where they seek out and destroy cancer cells. This therapy is often called a “living drug” because the CAR T cells continue to multiply and stay active in the body, providing ongoing protection against cancer.
One month CR rate | One month PR rate | One month OR rate | CRS≥3 | CRES≥3 |
71.95%(59/82) | 25.6(21/82) | 97.55(80/82) | 12.19%(10/82) | 0 |
One month CR rate | One month PR rate | One month OR rate | CRS≥3 | CRES≥3 |
92.1%(35/38) | 7.9%(3/38) | 100%(38/38) | 15.79%(6/38) | 0 |
One month CR rate | One month PR rate | One month OR rate | CRS≥3 | CRES≥3 |
72.41%(21/29) | 27.59%(8/29) | 100%(29/29) | 6.9%(2/29) | 0 |
At Immuno Vector, we are committed to pushing the boundaries of CAR-T research and delivering treatments that improve and save lives. Together, we can change the future of cancer care.