{"description":"Zero patients enrolled in Ponatinib, Pacritinib, Ruxolitinib, and Idealisib arms.","eventGroups":[{"deathsNumAffected":0,"deathsNumAtRisk":4,"description":"Patients receive dasatinib PO QD on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\nAntitumor Drug Screening Assay: Undergo pre clinical kinase inhibitor activity screening\n\nDasatinib: Given PO\n\nLaboratory Biomarker Analysis: Correlative studies\n\nPharmacological Study: Correlative studies","id":"EG000","otherNumAffected":3,"otherNumAtRisk":4,"seriousNumAffected":2,"seriousNumAtRisk":4,"title":"Group I (Dasatinib)"},{"deathsNumAffected":0,"deathsNumAtRisk":2,"description":"Patients receive sutinib malate PO QD on days 1-28. 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