**BCMA CAR-T Therapy Paves New Path for Treating High-Risk Multiple Myeloma** Multiple Myeloma (MM) is a malignant tumor originating from plasma cells, known for its complex biology and treatment resistance, presenting significant challenges to patients’ survival. For high-risk MM, especially in cases of relapse and refractory disease after multiple lines of therapy, treatment options become Read More
Hematological Neoplasms
On April 1, 2024, the US Food and Drug Administration (FDA) granted approval to Kite, a Gilead Sciences subsidiary, for Yescarta (Axicabtagene Ciloleucel), a CAR-T cell therapy, for the treatment of adult patients with large B-cell lymphoma (LBCL) who are refractory to first-line chemotherapy immunotherapy or experience recurrence within 12 months of first-line chemotherapy immunotherapy.
**Uncovering the Hidden Threat: How Serum Protein Electrophoresis Helps Diagnose Multiple Myeloma** #MultipleMyeloma #BloodCancer #SerumProteinElectrophoresis #MM #Mprotein #monoclonalprotein #SPE As we age, it’s common to experience certain health issues—unexplained anemia, bone pain, fractures, nausea, or abnormal urine changes. Many may dismiss these symptoms as a result of aging, poor diet, or even mild illness. However, Read More
On March 5, 2021, Gilead Sciences announced that the U.S. Food and Drug Administration (FDA) has granted accelerated approval to Yescarta (axicabtagene ciloleucel), a groundbreaking treatment for adult patients with relapsed or refractory follicular lymphoma (FL) who have undergone at least two systemic therapies.
On March 5, 2021, the U.S. Food and Drug Administration (FDA) granted accelerated approval to Yescarta (axicabtagene ciloleucel) for the treatment of adult patients with relapsed or refractory follicular lymphoma (FL) who have received at least two prior systemic therapies.
Yescarta (Axicabtagene Ciloleucel), a revolutionary CAR-T cell therapy, has garnered significant attention since its FDA approval in 2017. This article aims to provide a comprehensive overview of Yescarta, including its FDA approval history, indications, efficacy, safety profile, and potential future developments.