NIMG-85. RADIOMIC FEATURES PREDICTIVE OF RESPONSE IN HGG-TARGETING CAR-T THERAPY
نویسندگان
چکیده
Abstract SIGNIFICANCE Radiomics may improve precision medicine in CAR-T (Chimeric Antigen Receptor T Cell) therapy patient selection. BACKGROUND High-Grade Glioma (HGG) is a heterogenous primary CNS neoplasm with high recurrence rate and poor outcomes. Many studies are exploring CAR cells to combat HGG. Radiomic models have shown value identifying biomarkers predictive of tumor genetics, response, prognosis. In this study, we explore radiomic features derived from four clinical sequences volumes edema enhancing predict treatment response the first three doses therapy. METHODS IRB-approved phase 1 trial (IRB 13384), patients underwent surgical resection received cell Of 82 accrued, 59 (20 females, median age = 49) completed cycles had 3T field strength MRI scans minimal imaging artifacts. T1 weighted pre-contrast, post-contrast, T2 weighted, FLuid Attenuated Inversion Recovery were used generate 3D 2D radiomics features. total 28,541 generated per using images prior administration. Each patient’s after was determined be either stable disease (29 patients) or progression. The feature set dimensionality reduced Maximum Relevance Minimum Redundancy. 10-fold cross-validation XGBoost determine randomized grid search for hyperparameter tuning. RESULTS Six (four shape-based), SHapley Additive exPlanations (SHAP)-based importance RANO an AUC >0.73. CONCLUSION Despite limited study size, such imaging-based can serve as potential basis optimizing design through more precise screening providing whether will respond HGGs.
منابع مشابه
Design and development of CAR-T cells for cancer therapy
Introduction: Today, treatment with CAR-T cells is accepted as an effective treatment for blood malignancies. CAR-T cells are autologous T cells that are engineered by gene transfer techniques to express a chimeric antigen receptor (CAR). Despite the promising results and the approval of six CAR-T cell products; these products have not yet been approved for solid tumors. In addition, the high c...
متن کاملCAR T-cell Therapy of Hematologic Malignancies: An Update in Targeted Antigens
Immunotherapy with genetically engineered T-cells that express the chimeric antigen receptor (CAR) has raised hopes for the treatment of pediatric malignancies. Although CAR T-cell development is on a fast-moving pace and evolution, the context of exploring novel targetable antigens has been neglected. In this review study, we analyze the prominent hematologic antigens targeted by engineered T-...
متن کاملEfficacy of CAR T-cell therapy in large tumors relies upon stromal targeting by IFNγ.
Adoptive T-cell therapy using chimeric antigen receptor-modified T cells (CAR-T therapy) has shown dramatic efficacy in patients with circulating lymphoma. However, eradication of solid tumors with CAR-T therapy has not been reported yet to be efficacious. In solid tumors, stroma destruction, due to MHC-restricted cross-presentation of tumor antigens to T cells, may be essential. However, CAR-T...
متن کاملNew development in CAR-T cell therapy
Chimeric antigen receptor (CAR)-engineered T cells (CAR-T cells) have yielded unprecedented efficacy in B cell malignancies, most remarkably in anti-CD19 CAR-T cells for B cell acute lymphoblastic leukemia (B-ALL) with up to a 90% complete remission rate. However, tumor antigen escape has emerged as a main challenge for the long-term disease control of this promising immunotherapy in B cell mal...
متن کاملNext frontiers in CAR T-cell therapy
Chimeric antigen receptor (CAR) T-cell therapy is entering a new era, transitioning from an experimental approach being tested in a handful of centers to a more mainstream and broadly investigated therapeutic platform with significant efforts directed towards commercial translation. CARs are synthetic receptors engineered and transduced into T cells to redirect T-cell cytotoxicity by recognitio...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Neuro-oncology
سال: 2022
ISSN: ['1523-5866', '1522-8517']
DOI: https://doi.org/10.1093/neuonc/noac209.703