Dr Johnson on Treatment Gaps With Immunotherapy in Melanoma

Dr Johnson on Treatment Gaps With Immunotherapy in Melanoma

Publication date: Jun 26, 2025

For example, the PRAME-targeted TCR-T cell therapy IMA203 has shown early response rates near 50% in HLA-A*02:01positive patients, although applicability is limited by HLA restriction, he noted. They can also help simplify treatment logistics through eliminating the need for high-dose interleukin-2, for example, Johnson explained. Emerging T-cell receptor T-cell (TCR-T) therapies represent another novel approach, Johnson continued. Tumor-infiltrating lymphocyte (TIL) therapy, such as lifileucel (Amtagvi), the first FDA-approved TIL product, has demonstrated response rates between 30% to 50% in this setting. “[In melanoma], we’re still seeing a 10% to 30% response rate in the frontline setting. In response, the field is increasingly focused on cellular therapy approaches for immunotherapy-refractory disease, Johnson reported. We’ve come a long way, but [still have] a long way to go. Unlike TILs, these therapies can be derived from peripheral blood, reducing the need for surgical tumor resection.

Concepts Keywords
Hematology Benefit
Nct06743126 Checkpoint
Professor Clinical
Relapse Frontline
Immune
Immunotherapy
Johnson
Limited
Melanoma
Oncology
Response
Setting
Therapy
Treatment

Semantics

Type Source Name
disease MESH Tumor
pathway KEGG Melanoma
disease MESH Melanoma
disease MESH relapse
drug DRUGBANK Spinosad

(Visited 2 times, 1 visits today)

Leave a Comment

Your email address will not be published. Required fields are marked *