Finding studies
Finding studies
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Saves the questions and what to expect into your notes, next to the visit they belong to.
Sarah Hamidi, MD
CONTACT
Lead
M.D. Anderson Cancer Center
Primary Objective: The study's primary objective is to determine the overall survival (OS) of zanzalintinib plus cemiplimab in treatment-naïve BRAF wild type ATC patients. Secondary Objectives: * Determine the 6-month OS rate with zanzalintinib plus cemiplimab in treatment-naïve BRAF wild type ATC patients * Determine the objective response rate (ORR) and progression-free survival (PFS) in patients treated with zanzalintinib plus cemiplimab, per RECIST v1.1 * Determine the metabolic response rate (MRR) to zanzalintinib plus cemiplimab, per PERCIST 1.0 in patients undergoing serial 18F-FDG PET/CT imaging * Establish safety for concurrent administration of zanzalintinib plus cemiplimab * Evaluate the Quality of Life (QoL) of patients with ATC treated with zanzalintinib plus cemiplimab Exploratory Objectives: * Assess response of locoregional disease to zanzalintinib plus cemiplimab in the subgroup of patients who underwent palliative neck RT prior to or within the first month of trial enrollment. This will be determined by the ORR of the neck disease per modified neck RECIST and PERCIST. * Determine whether features of the tumor genomic landscape and tumor immune microenvironment are associated with response and survival outcomes with zanzalintinib plus cemiplimab * Determine whether baseline PD-L1 expression and NLR correlate with response to zanzalintinib plus cemiplimab and survival outcomes. * Evaluate if ctDNA changes and presence of MRD correlate with response to zanzalintinib plus cemiplimab and survival outcomes. * Investigate the immunomodulatory effects of palliative-dose radiation in ATC * Determine whether systemic immune dynamics predict response to zanzalintinib plus cemiplimab
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
