EXALT-2 is a prospective, randomized, three arm study for treatment decision guided either by either comprehensive genomic profiling, next generation drug screening or physician's choice
Study Type
OBSERVATIONAL
Enrollment
150
High-throughput image based in-vitro drug screening on primary patient tumor cells
Comprehensive targeted profiling of genetic aberrations on primary patient tumor material
Medical University of Vienna
Vienna, Austria
RECRUITINGPercentage of patients with a ratio ≥1.3 of progression free survival (PFS) compared to most recent treatment
The study aims to identify if next-generation functional drug screening (ngFDS) and/or comprehensive genomic profiling (CGP; FoundationOne®Heme) compared to physicians' choice guided treatment will have an increased percentage of patients with a ratio ≥1.3 of progression free survival (PFS)/PFS of most recent treatment in patients with aggressive haematological malignancies
Time frame: Through study completion, an average of 8 month
Average Ratio of PFS/PFS of most prior treatment
Average Ratio of PFS/PFS of most prior treatment
Time frame: Through study completion, an average of 8 months
Overall response rate (ORR)
Overall response rate (ORR)
Time frame: Through study completion, an average of 8 months
Number of treatable targets identified
Number of treatable targets identified
Time frame: Through study completion, an average of 8 months
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