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Society for Immunotherapy of Cancer Publishes Clinical Practice Guideline on Immune Effector Cell-related Adverse Events Share Article The Society for Immunotherapy of Cancer (SITC), the world’s leading member-driven organization dedicated solely to cancer immunotherapy, is pleased to announce the publication of a clinical practice guideline for the management of cell therapy adverse events. Immune effector cell therapies include the three U.S. Food and Drug Administration (FDA)-approved chimeric antigen receptor (CAR) T cell products for treatment of blood-based cancers. “This is the tenth manuscript published in SITC’s Cancer Immunotherapy Guidelines series, a critically important effort to educate physicians and other health care providers, and improve outcomes for cancer patients receiving FDA-approved immunotherapies, said SITC President Mario Sznol, MD.

United statesMarcela mausMario sznolStephan gruppEmily whitehead foundationFoundation for the accreditation of cellular therapySociety for immunotherapy of cancerUniversity of nebraska medical centerAdverse events expert panelDrug administrationAmerican society for transplantationAmerican society of hematologyEffector adverse events expert panelEffector cell related adverse events expertAmerican societyCellular therapy