{"eventGroups":[{"deathsNumAffected":3,"deathsNumAtRisk":7,"description":"Patients receive liposome-encapsulated daunorubicin-cytarabine IV over 90 minutes on days 1, 3, and 5 and then pomalidomide PO QD beginning between days 21-30 for 14 days in the absence of disease progression or unacceptable toxicity. Patients who do not respond, may receive a second cycle of liposome-encapsulated daunorubicin-cytarabine IV over 90 minutes on days 1 and 3 in the absence of disease progression or unacceptable toxicity.\n\nCONSOLIDATION: Patients who achieve CR/CRi receive liposome-encapsulated daunorubicin-cytarabine IV over 90 minutes on days 1 and 3. Treatment repeats every 21 days for 2 cycles in the absence of disease progression and unacceptable toxicity. Patients also undergo bone marrow aspirate and biopsy and collection of blood samples throughout all phases of the trial.\n\nBiospecimen Collection: Undergo collection of blood samples Bone Marrow Aspiration and Biopsy: Undergo bone marrow aspirate and biopsy Liposome-encapsulated Daunorubicin-Cytarabine: Given IV Pomalidomide: Given PO","id":"EG000","otherNumAffected":7,"otherNumAtRisk":7,"seriousNumAffected":7,"seriousNumAtRisk":7,"title":"Safety Run In DL1 (14 Days Pomalidomide)"},{"deathsNumAffected":2,"deathsNumAtRisk":3,"description":"Patients receive liposome-encapsulated daunorubicin-cytarabine IV over 90 minutes on days 1, 3, and 5 and then pomalidomide PO QD beginning between days 21-30 for 10 days in the absence of disease progression or unacceptable toxicity. Patients who do not respond, may receive a second cycle of liposome-encapsulated daunorubicin-cytarabine IV over 90 minutes on days 1 and 3 in the absence of disease progression or unacceptable toxicity.\n\nCONSOLIDATION: Patients who achieve CR/CRi receive liposome-encapsulated daunorubicin-cytarabine IV over 90 minutes on days 1 and 3. Treatment repeats every 21 days for 2 cycles in the absence of disease progression and unacceptable toxicity. Patients also undergo bone marrow aspirate and biopsy and collection of blood samples throughout all phases of the trial.\n\nBiospecimen Collection: Undergo collection of blood samples Bone Marrow Aspiration and Biopsy: Undergo bone marrow aspirate and biopsy Liposome-encapsulated Daunorubicin-Cytarabine: Given IV Pomalidomide: Given PO","id":"EG001","otherNumAffected":3,"otherNumAtRisk":3,"seriousNumAffected":3,"seriousNumAtRisk":3,"title":"Safety Run In DL-1 (10 Days Pomalidomide)"},{"deathsNumAffected":11,"deathsNumAtRisk":20,"description":"INDUCTION: Patients receive liposome-encapsulated daunorubicin-cytarabine IV over 90 minutes on days 1, 3, and 5 and then pomalidomide PO QD beginning between days 21-30 for 14 days in the absence of disease progression or unacceptable toxicity. Patients who do not respond, may receive a second cycle of liposome-encapsulated daunorubicin-cytarabine IV over 90 minutes on days 1 and 3 in the absence of disease progression or unacceptable toxicity.\n\nCONSOLIDATION: Patients who achieve CR/CRi receive liposome-encapsulated daunorubicin-cytarabine IV over 90 minutes on days 1 and 3. Treatment repeats every 21 days for 2 cycles in the absence of disease progression and unacceptable toxicity. Patients also undergo bone marrow aspirate and biopsy and collection of blood samples throughout all phases of the trial.\n\nBiospecimen Collection: Undergo collection of blood samples\n\nBone Marrow Aspiration and Biopsy: Undergo bone marrow aspirate and biopsy\n\nLiposome-encapsulated Daunorubicin-Cytarabine: Given IV\n\nPomalidomide: Given PO","id":"EG002","otherNumAffected":20,"otherNumAtRisk":20,"seriousNumAffected":19,"seriousNumAtRisk":20,"title":"Arm A (Daunorubicin and Cytarabine Liposome, Pomalidomide)"},{"deathsNumAffected":7,"deathsNumAtRisk":19,"description":"INDUCTION: Patients receive liposome-encapsulated daunorubicin-cytarabine IV over 90 minutes on days 1, 3, and 5 in the absence of disease progression or unacceptable toxicity. Patients who do not respond, may receive a second cycle of liposome-encapsulated daunorubicin-cytarabine IV over 90 minutes on days 1 and 3 in the absence of disease progression or unacceptable toxicity.\n\nCONSOLIDATION: Patients who achieve CR/CRi receive liposome-encapsulated daunorubicin-cytarabine IV over 90 minutes on days 1 and 3. Treatment repeats every 21 days for 2 cycles in the absence of disease progression and unacceptable toxicity. Patients also undergo bone marrow aspirate and biopsy and collection of blood samples throughout all phases of the trial.\n\nBiospecimen Collection: Undergo collection of blood samples\n\nBone Marrow Aspiration and Biopsy: Undergo bone marrow aspirate and biopsy\n\nLiposome-encapsulated Daunorubicin-Cytarabine: Given IV","id":"EG003","otherNumAffected":18,"otherNumAtRisk":19,"seriousNumAffected":19,"seriousNumAtRisk":19,"title":"Arm B (Daunorubicin and Cytarabine Liposome)"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"CTCAE v.5.0","stats":[{"groupId":"EG000","numAffected":4,"numAtRisk":7,"numEvents":17},{"groupId":"EG001","numAffected":2,"numAtRisk":3,"numEvents":10},{"groupId":"EG002","numAffected":8,"numAtRisk":20,"numEvents":24},{"groupId":"EG003","numAffected":8,"numAtRisk":19,"numEvents":27}],"term":"Alanine Aminotransferase Increased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"CTCAE v.5.0","stats":[{"groupId":"EG000","numAffected":6,"numAtRisk":7,"numEvents":25},{"groupId":"EG001","numAffected":2,"numAtRisk":3,"numEvents":16},{"groupId":"EG002","numAffected":8,"numAtRisk":20,"numEvents":34},{"groupId":"EG003","numAffected":8,"numAtRisk":19,"numEvents":36}],"term":"Aspartate Aminotransferase Increased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"CTCAE v.5.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7,"numEvents":0},{"groupId":"EG001","numAffected":0,"numAtRisk":3,"numEvents":0},{"groupId":"EG002","numAffected":1,"numAtRisk":20,"numEvents":1},{"groupId":"EG003","numAffected":0,"numAtRisk":19,"numEvents":0}],"term":"Abdominal distension"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"CTCAE v.5.0","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":7,"numEvents":1},{"groupId":"EG001","numAffected":1,"numAtRisk":3,"numEvents":2},{"groupId":"EG002","numAffected":6,"numAtRisk":20,"numEvents":12},{"groupId":"EG003","numAffected":1,"numAtRisk":19,"numEvents":1}],"term":"Abdominal Pain"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"CTCAE v.5.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7,"numEvents":0},{"groupId":"EG001","numAffected":0,"numAtRisk":3,"numEvents":0},{"groupId":"EG002","numAffected":2,"numAtRisk":20,"numEvents":2},{"groupId":"EG003","numAffected":0,"numAtRisk":19,"numEvents":0}],"term":"Activated Partial Thromboplastin Time Prolonged"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Renal and urinary disorders","sourceVocabulary":"CTCAE v.5.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7,"numEvents":0},{"groupId":"EG001","numAffected":0,"numAtRisk":3,"numEvents":0},{"groupId":"EG002","numAffected":1,"numAtRisk":20,"numEvents":1},{"groupId":"EG003","numAffected":0,"numAtRisk":19,"numEvents":0}],"term":"Acute Kidney Injury"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"CTCAE v.5.0","stats":[{"groupId":"EG000","numAffected":4,"numAtRisk":7,"numEvents":10},{"groupId":"EG001","numAffected":2,"numAtRisk":3,"numEvents":15},{"groupId":"EG002","numAffected":7,"numAtRisk":20,"numEvents":18},{"groupId":"EG003","numAffected":4,"numAtRisk":19,"numEvents":9}],"term":"Alkaline Phosphatase Increased"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Metabolism and nutrition disorders","sourceVocabulary":"CTCAE 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