Search Protocols under revision. Back New search Go to resultsDiseaseMain groupCross-Sectional, Transplantation, Cellular TherapyHematologic NeoplasmsProtocol groupAcute LeukemiasMyeloproliferative neoplasms (MPN) and myelodysplastic neoplasms (MDS)TransplantationDiseaseAcute Myeloid LeukemiaMyelodysplastic NeoplasmsStem Cell Transplantation, AllogeneicSubgroupCD33+FLT3 mutationFLT3-ITDHigh riskIDH1-MutationKMT2A translocationMDS with elevated blasts -2TP53 mutationunfitICD10C92.0-C92.5-C92.6-C92.7-C92.8-C92.9-C93.0-D46.-MeSHLeukemia, Monocytic, AcuteLeukemia, MyeloidLeukemia, Myeloid, AcuteMyelodysplastic SyndromesSequenceALDE16400/HIST0.5, AML, C1-3 (PID2854) -|- C4-10 (PID2856)ALFA-0701, AMLAMLSG 31-19/HOVON 501AZCT75/GILT80/VNTC(100/200/400), AML, C1 (PID2799) -|- C2-24 (PID2800) -|- Z25+ (PID2801)CLAD5/CYTA20/VNTC(100/200/400), AML, Ind, C1 (PID2772) -|- C2 (PID2773) -|- C3-4 (PID2774) -|- C5-6 (PID2773) -|- C7-8 (PID2774) -|- C9-10 (PID2773) -|- C11-12 (PID2774) -|- C13-14 (PID2773) -|- C15-16 (PID2774) -|- C17-18 (PID2773)CLAG-Ida (CLAD5/CYTA2000/IDAR12/FILG300), AML, Ind. (PID2220) -|- CLAG-Ida (CLAD5/CYTA2000/IDAR12/FILG300), Cons. (PID2221)CLAG-M, r/r AML, Polish Adult Leukemia GroupDAUN60/CYTA200, AML ind. (PID1825) -|- HD CYTA 3000, AML cons., below 60, d1,3,5 (PID516)DAUN60/CYTA200/MDST50, AML Ind. (PID1079) -|- Cons. (PID1080) -|- maint. (PID1081)DECI15, AML, C1-4 (PID2321) -|- DECI20, C5+ (PID2322)EORTC-GIMEMA AML-19: GEMOZO(6/3), AML, ind. (PID2590) -|- GEMOZO2, cons. (PID2591)FLAGIDA (FLUD30/CYTA1500/IDAR8)/VNTC400, AML, Ind. (PID2522) -|- Cons. (PID2524)HOVON 132 AML / SAKK 30/13, Arm AHOVON 132 AML / SAKK 30/13, Arm BLDAUN-LCYTA144, AML Ind., C1 (PID1414) -|- C2 (PID1426) -|- cons. (PID1427)QuANTUM-First: DAUN60/CYTA100/QUIZ35.4, AML, Ind. (PID2551) -|- Cons. (PID2553) -|- maint., C1 (PID2554) -|- maint., C2+ (PID2555)QuANTUM-First: IDAR12/CYTA100/QUIZ35.4, AML, Ind. (PID2552) -|- Cons. (PID2553) -|- maint., C1 (PID2554) -|- maint., C2+ (PID2555)SAL Study Group, AMLSORMAIN: SORA400/600, AML, maint., C1 (PID1020) -|- SORA800, C2+ (PID1038)STUDY-AMLSG, Investigational armSTUDY - Dauno DoubleSTUDY AMLSG, Standard armTAD-HAM: TAD (TIOG100/CYTA60/DAUN100), AML ind. below 60 (PID519) -|- HAM (CYTA3000/MXNT10), AML ind. below 60 (PID596)VNTC(100/200/300/400/600)/CYTA20, AML, from 60 y., C1 (PID1260) -|- VNTC600/CYTA20, AML, from 60 y., C2+ (PID1319)VNTC(100/200/400)/AZCT75, AML, C1 (PID1595) -|- VNTC400/AZCT75, AML, C2+ (PID1596)VNTC(100/200/400)/DECI20, AML, C1 (PID1597) -|- VNTC400/DECI20, AML, C2+ (PID1598)VNTC(100/200/400)/GILT120, AML, C1 (PID2148) -|- VNTC400/GILT120, C2+ (PID2149)ChemotherapyChemo-substanceAldesleukinAmsacrineAzacitidineCladribineCytarabineDaunorubicinDaunorubicin-cytarabine liposomalDecitabineDecitabine-CedazuridineEtoposideFludarabineGemtuzumab OzogamicinGilteritinibGlasdegibHistamine DihydrochlorideHydroxyureaIdarubicinIvosidenibLenalidomideMelphalanMidostaurinMitoxantroneQuizartinibRevumenibSorafenibTioguaninVenetoclaxChemo-substanceAldesleukinAmsacrineAzacitidineCladribineCytarabineDaunorubicinDaunorubicin-cytarabine liposomalDecitabineDecitabine-CedazuridineEtoposideFludarabineGemtuzumab OzogamicinGilteritinibGlasdegibHistamine DihydrochlorideHydroxyureaIdarubicinIvosidenibLenalidomideMelphalanMidostaurinMitoxantroneQuizartinibRevumenibSorafenibTioguaninVenetoclaxChemo-substanceAldesleukinAmsacrineAzacitidineCladribineCytarabineDaunorubicinDaunorubicin-cytarabine liposomalDecitabineDecitabine-CedazuridineEtoposideFludarabineGemtuzumab OzogamicinGilteritinibGlasdegibHistamine DihydrochlorideHydroxyureaIdarubicinIvosidenibLenalidomideMelphalanMidostaurinMitoxantroneQuizartinibRevumenibSorafenibTioguaninVenetoclaxChemo-substanceAldesleukinAmsacrineAzacitidineCladribineCytarabineDaunorubicinDaunorubicin-cytarabine liposomalDecitabineDecitabine-CedazuridineEtoposideFludarabineGemtuzumab OzogamicinGilteritinibGlasdegibHistamine DihydrochlorideHydroxyureaIdarubicinIvosidenibLenalidomideMelphalanMidostaurinMitoxantroneQuizartinibRevumenibSorafenibTioguaninVenetoclaxNo. Substances1234 RadiotherapySupportive therapySupportive substanceAcetylsalicylic acidAciclovirAllopurinolBalanced Crystalloid SolutionCiprofloxacinCotrimoxazoleDalteparinDexamethasoneDimetindenFilgrastimFosaprepitantGranisetronPantoprazoleParacetamolPegfilgrastimPosaconazolePrednisoloneSupportive substanceAcetylsalicylic acidAciclovirAllopurinolBalanced Crystalloid SolutionCiprofloxacinCotrimoxazoleDalteparinDexamethasoneDimetindenFilgrastimFosaprepitantGranisetronPantoprazoleParacetamolPegfilgrastimPosaconazolePrednisoloneSupportive substanceAcetylsalicylic acidAciclovirAllopurinolBalanced Crystalloid SolutionCiprofloxacinCotrimoxazoleDalteparinDexamethasoneDimetindenFilgrastimFosaprepitantGranisetronPantoprazoleParacetamolPegfilgrastimPosaconazolePrednisoloneSupportive substanceAcetylsalicylic acidAciclovirAllopurinolBalanced Crystalloid SolutionCiprofloxacinCotrimoxazoleDalteparinDexamethasoneDimetindenFilgrastimFosaprepitantGranisetronPantoprazoleParacetamolPegfilgrastimPosaconazolePrednisoloneNo. Substances123456789Protocol classificationTherapy classificationalternativecurrent standardStudy protocol, currentIntensityhigh doseLow doseStandard doseTherapy indicationFirst lineRelapse therapySecond lineseveral possibleTherapy phaseConsolidationInductionMaintenanceReinductionSalvageTherapy intentioncurativecurative or palliativepalliativeRisksAllergic ReactionAlopeciaAnemia Hb below 8g/dlArthalgiaAstheniaAtrial FibrillationBleedingCardiotoxicityCMV Infection (asympt. + sympt.)CNS ToxicityColitisConstipationDiarrheaDifferentiation syndromeDyspneaEdemaElectrolyte DisturbanceEmetogenicityEmetogenicity (ASCO)Emetogenicity (MASCC/ESMO)FatigueFebrile NeutropeniaGastrointestinal ToxicityHeadacheHemorrhageHepatotoxicityHyperbilirubinemiaHyperglycemiaHyperkalemiaHypertensionHypocalcemiaHypoglycemiaHypokalemiaHyponatremiaHypophosphatemiaHypotensionIncrease AminotransferasesInfectionsLeukopeniaLymphopeniaMucositisMyalgiasNauseaNephrotoxicityNeuropathyNeutropeniaOral MucositisPainPneumoniaPyrexiaQTc Time ExtensionRashRenal FailureSeizuresSepsisThrombocytopenia below 50 000/µlThromboembolic EventTumor Lysis SyndromeUpper Respiratory Tract InfectionVOD/SOS only studiesPublicationAuthorAmadori SB. LöwenbergBraess JBrune MBurchert ABurnett ABurnett AKBüchner TCortes JECraddock CDaver NDiNardo CDDombret HDöhner HErba HPFong CFridle CGaidzik VGeissler KGoldfinger MHolowieki JIssa GCKadia TMKantarjian HMLambert JLancet JELevis MJLöwenberg BLübbert MMayer RJMontesinos PParker JPerl APlatzbecker UPrice SRöllig CSchaich MSchroeder TSeiter KShort NJSperr WRStone RStone RMStratmann JThiel AVellenga EWang ESWei AWei AHWelch JWierzbowska AYates JWDiseaseAkute myeloische Leukämie, Komplettremission, ECOG 0-1Akute myeloische Leukämie, RezidivtherapieAML (Doppel-)InduktionAML, Alter ab 55 J., CR/CRi nach Induktion, nicht für eine HSZT geeignet, ECOG 0-3AML, CD33 positiv, rezidiviertAML, Erstlinie, nicht für eine intensive Therapie geeignetAML, Erstlinie Induktion, ECOG 0-4AML, Erstlinientherapie, für eine Standardtherapie nicht geeignet, ECOG 0-2AML, FLT3-ITD positiv, komplette hämatologische Remission nach allogener SCTAML, FLT3-Mutation (ITD oder TKD), mind. 1 Vortherapie, ECOG 0-2AML, neu diagnostiziertAML, neu diagnostiziert, FLT3-ITD+AML, neu diagnostiziert, rezidiviert oder therapierefraktär, FLT3-MutationAML, nicht geeignet für intensive Chemotherapie, nicht vorbehandeltAML, nicht geeignet für intensive Chemotherapie, nicht vorbehandelt, Alter >65 J.AML, rezidiviert oder therapierefraktärAML, rezidiviert oder therapierefraktär, IDH-1-mutiert, ECOG 0-2AML, rezidiviert oder therapierefraktär, KMT2A TranslokationAML, über 60 J., oder ungeeignet für intensive TherapieAML- oder CMML-Rezidiv nach allogener StammzelltranplantationAML- oder MDS-Rezidiv nach allogener StammzelltranplantationAML > 60 Jahre, rezidivierende AML oder transfusionspflichtiges MDS, ECOG 0-2AML KonsolidierungAML oder Hochrisiko MDS, nicht für eine Standard-Induktionschemotherapie geeignet, ECOG 0-2AML therapierefraktär oder Frührezidivde-novo oder sekundäre AML, mindestens 1 nicht-kurative Vortherapie, über 65 JahreDecitabin für Patienten ab 61 Jahren mit de novo oder sekundärer AML, für intensive Therapie nicht geeignet, ECOG 0-2Decitabin für Patienten ab 65 Jahren mit neudiagnostizierter de novo oder sekundärer AML, ECOG 0-2De novo oder sekundäre AML, Hochrisiko MDS, PS 0-4Drohendes AML- oder MDS-Rezidiv nach allogener Stammzelltranplantation (Spenderchimärismus <80%)FLT3-ITD+ AML nach allogener SCTHochrisiko MDS und AML, Rezidiv oder de novo MDSInduktion AMLneu-diagnostizierte AMLneu-diagnostizierte AML, intermediäres/ungünstiges genetischen Risiko (ELN 2017), ECOG 0-2neudiagnostizierte AML, CD33 positiv, Induktion, Erstlinieneudiagnostizierte AML, CD33 positiv, Induktion, Erstlinie, Leukozytenzahl < 30.000/µlneudiagnostizierte AML, CD33 positiv, Induktion, Erstlinie, Leukozytenzahl ab 30.000/µlneudiagnostizierte AML, CD33 positiv, Induktion, Erstlinie, Leukozytenzahl bis 30.000/µlneudiagnostizierte AML, ECOG 0-2neudiagnostizierte AML, Erhaltung bei Patienten in kompletter Remission, FLT3-Mutation, ErstlinieNeu diagnostizierte AML, FLT3+, nicht für eine intensive Therapie geeignet, ECOG 0-2Neu diagnostizierte AML, IDH-1-mutiert, nicht für eine intensive Therapie geeignet, ECOG 0-2neudiagnostizierte AML, Induktion, FLT3-Mutation, Erstlinieneudiagnostizierte AML, Konsolidierung, FLT3-Mutation, Erstlinieneudiagnostizierte AML, primär oder sekundär, Erstlinie, ECOG 0-2Neu diagnostizierte AML oder MDS mit Blastenüberschuss-2, ECOG 0-2neudiagnostizierte de-novo oder sekundäre AML, ECOG 0-4Neu diagnostizierte de-novo oder sekundäre AML mit Knochenmarkblasten > 30%, Alter > 65 Jahre, ECOG 0-2Neudiagnostizierte oder sekundäre, unbehandelte AMLneu diagnostizierte oder sekundäre AML, Alter ≥60 Jahreprimäre oder sekundäre AML, Erstdiagnose, 18-65, ECOG 0-2primär refraktäre oder rezidivierende AMLRezidivierte oder therapierefraktäre AML, ECOG 0-2Rezidivierte oder therapierefraktäre AML, FLT3 ITD oder TKD D835 oder I836 MutationOriginAbramson Cancer Center, University of Pennsylvania, USA, ADMIRAL StudieCancer and Leukemia Group BCarl Gustav Carus Technical University of Dresden, Dresden, Germany, RELAZA trialDana-Farber Cancer Institute, Boston, USADana-Farber Cancer Institute, Boston MADana-Farber Cancer Institute, Boston MA, RATIFY trialDepartment of Bone Marrow Transplantation, Comprehensive Cancer Center M. Curie- Sklodowska Memorial Institute, Branch Gliwice, PolandDepartment of Clinical Hematology, The Alfred Hospital, Melbourne, AustraliaDepartment of Haematological Medicine, King's College School of Medicine and Dentistry, LondonDepartment of Haematology, Cardiff University School of Medicine, UK, AML15 trialDepartment of Haematology, The Alfred Hospital, MelbourneDepartment of Haematology, Wales School of Medicine, Cardiff University, UK, Leukaemia Research Fund AML14Department of Hematology, University of Groningen and University Medical Center Groningen, HOVON/SAKK AML-29/42Department of Internal Medicine, Washington University School of MedicineDepartment of Leukemia, Division of Cancer Medicine, University of Texas, Houston, USDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, HoustonDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, USADepartment of Oncology and Hematology, Hospital Barmherzige Brüder, Regensburg, Germany, AML-CGDepartment of Pharmacy, H. Lee Moffitt Cancer Center and Research Institute, Tampa, USADepartments of Hematology and Virology, University of Göteborg, SwedenDivision Hematology and Oncology, University of Freiburg Medical Center, Freiburg, GermanyDivision of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA, Augment-101 trialDuke Cancer Institute, Durham, USA, QuANTUM-First trialDutch-Belgian Hemato-Oncology Cooperative Group (HOVON) and Swiss Group for Clinical Cancer Research (SAKK)East German Study Group Hematology/Oncology (OSHO) and the Study Alliance Leukemia (SAL)German AML Cooperative GroupH. Lee Moffitt Cancer Center and Research Institute, Tampa, FLHematology and Oncology, Goethe University, Frankfurt, Frankfurt am Main, GermanyHospital Universitari i Politecnic La Fe, Valencia, AGILE trialHOVON / SAKKHOVON 132 AML / SAKK 30/13Hôpital Saint Louis, Institut Universitaire d´Hématologie, University Paris Diderot, Paris, FranceJohns Hopkins University, Baltimore, MDMedical University of Lodz, Lodz, PolandMedical University of Vienna, AustriaMedizinische Klinik und Poliklinik I, Universitätsklinikum DresdenMonash University, Melbourne, Australia, QUAZAR AML-001 trialMontefiore Einstein Comprehensive Cancer Center, Albert Einstein College of Medicine, Bronx, USANew York Medical College, Valhalla, United StatesOncology and Clinical Immunology, University of Duesseldorf, Medical Faculty, Duesseldorf, GermanyPhilipps University Marburg and University Hospital Gießen and Marburg, Campus Marburg, Marburg, Germany, SORMAIN trialRoswellPark Comprehensive Cancer Center, Buffalo, NY, USA, LACEWING trialSAL - Studienallianz Leukämie Service d Hematologie et Oncologie, Centre Hospitalier de Versailles, ALFA-0701Sigmund Freud PrivatUniversität, Wien, AustriaStudy Alliance Leukemia, SAL, AML 2003 StudieThe University of Texas MD Anderson Cancer Center, Houston, TXThe University of Texas MD Anderson Cancer Center, Houston, TX, USATor Vergata University, EORTC-GIMEMA AML-19 TrialUlm University Hospital, Germany, AMLSG 30-18Ulm University Hospital, Germany, AMLSG 31-19/HOVON 501University Hospital Berne and University of Berne, Berne, SwitzerlandUniversity of Birmingham, Birmingham, United KingdomUniversity of Freiburg Medical Center, Freiburg, GermanyUniversity of Texas, MD Anderson Cancer Center, Houston, USAUniversity of Texas M.D. Anderson Cancer Center, Department of Leukemia, HoustonProtocols in Revision 104 protocols foundAldesleukin 16400 / histamine dihydrochloride 0.5, Acute Myeloid Leukemia, Cycle 1-3 (PID2854 V1.0)Aldesleukin 16400 / histamine dihydrochloride 0.5, Acute Myeloid Leukemia, cycle 4-10 (PID2856 V1.0)Azacitidine 100, Acute Myeloid Leukemia and Myelodysplastic Syndrome after Allogeneic Stem Cell Transplantation (PID2302 V1.0)Azacitidine 100, Acute Myeloid Leukemia and Myelodysplastic Syndrome after Allogeneic Stem Cell Transplantation, Variant 1. (PID2320 V1.0)Azacitidine 300, Acute Myeloid Leukemia (PID1807 V1.0)Azacitidine 75 / Gilteritinib 120, Acute Myeloid Leukemia (PID2430 V1.0)Azacitidine 75 / Gilteritinib 80 / Venetoclax (100/200/400), Acute Myeloid Leukemia, Cycle 1 (PID2799 V1.0)Azacitidine 75 / Gilteritinib 80 / Venetoclax 400, Acute Myeloid Leukemia, Cycle 2-24 (PID2800 V1.0)Azacitidine 75 / Ivosidenib 500, Acute Myeloid Leukemia (PID2368 V1.1)Azacitidine 75 / Lenalidomide 25, Acute Myeloid Leukemia and Myelodysplastic Syndrome after Allogeneic Stem Cell Transplantation (PID827 V1.2)Azacitidine 75 / Venetoclax 400, Acute Myeloid Leukemia, consolidation, cycle 3-4,7-8,11-12,15-16 (PID2774 V1.0)Azacitidine 75, Acute Myeloid Leukemia and Myelodysplastic Syndrome after Allogeneic Stem Cell Transplantation. (PID2327 V1.0)Azacitidine 75, Acute Myeloid Leukemia, over 65 years of age (PID700 V1.2)Cladribine 5 / Cytarabine 20 / Venetoclax (100/200/400), Acute Myeloid Leukemia, Induction, Cycle 1 (PID2772 V1.0)Cladribine 5 / Cytarabine 20 / Venetoclax 400, Acute Myeloid Leukemia, consolidation, cycle 2,5-6,9-10,13-14,17-18 (PID2773 V1.0)Cladribine 5 / Cytarabine 2000 / Idarubicin 12 / Filgrastim 300, Acute Myeloid Leukemia, Induction (PID2220 V1.0)Cladribine 5 / Cytarabine 2000 / Idarubicin 12 / Filgrastim 300, Acute Myeloid Leukemia, consolidation (PID2221 V1.0)Cladribine 5 / Cytarabine 2000 / Idarubicin 8, Acute Myeloid Leukemia (PID2209 V1.1)Cladribine 5 / Cytarabine 2000 / Mitoxantrone 10 / Filgrastim 300, Acute Myeloid Leukemia (PID2203 V1.0)Cladribine 5 / Cytarabine 2000, Acute Myeloid Leukemia (PID2204 V1.0)Cladribine 5 / Daunorubicin 60 / Cytarabine 200, Acute Myeloid Leukemia (PID2436 V1.0)CLAG - Cladribine 5 / Cytarabine 2000 / Filgrastim 300, AML (PID859 V1.2)Cytarabine 1000, Acute Myeloid Leukemia, consolidation, over 60 years of age (PID601 V1.3)Cytarabine 1500 / Mitoxantrone 10, Acute Myeloid Leukemia (PID2208 V1.0)Cytarabine 1500, Acute Myeloid Leukemia, Consolidation (PID2574 V1.0)Cytarabine 20 / Glasdegib 100, Acute Myeloid Leukemia and Myelodysplastic Syndrome (PID1674 V1.0)Cytarabine 20, Acute Myeloid Leukemia (PID833 V1.0)Cytarabine 3000 / Midostaurin 50, Acute Myeloid Leukemia, consolidation (PID1080 V1.4)Cytarabine 3000 / Quizartinib 35.4, Acute Myeloid Leukemia, consolidation (PID2553 V1.0)Cytarabine 3000, Acute Myeloid Leukemia, consolidation, under 60 years, day 1,3,5 (PID516 V1.3)Daunorubicin 60 / Cytarabine 100 / Quizartinib 35.4, Acute Myeloid Leukemia, Induction (PID2551 V1.0)Daunorubicin 60 / Cytarabine 100, Acute Myeloid Leukemia, Induction (PID293 V1.2)Daunorubicin 60 / Cytarabine 200 / Midostaurin 50, Acute Myeloid Leukemia, Induction (PID1079 V1.2)Daunorubicin 60 / Cytarabine 200, Acute Myeloid Leukemia, induction (PID1825 V1.0)Daunorubicin Liposomal - Cytarabine liposomal 144, Acute Myeloid Leukemia, Induction, Cycle 1 (PID1414 V1.1)Daunorubicin Liposomal - Cytarabine liposomal 144, Acute Myeloid Leukemia, Induction, Cycle 2 (PID1426 V1.1)Daunorubicin Liposomal - Cytarabine liposomal 94, Acute Myeloid Leukemia, consolidation (PID1427 V1.0)Decitabine 15, Acute Myeloid Leukemia, cycle 1-4 (PID2321 V1.0)Decitabine 20, Acute Myeloid Leukemia (PID834 V1.2)Decitabine 20, Acute Myeloid Leukemia, First-Line (PID582 V1.2)Decitabine 20, Acute Myeloid Leukemia, cycle 5+ (PID2322 V1.0)Decitabine-Cedazuridine 135, Acute Myeloid Leukemia (PID3044 V1.0)FLAGAMSA (Fludarabine 30 / Cytarabine 2000 / Amsacrine 100), Acute Myeloid Leukemia (PID1710 V1.0)FLAGIDA - Fludarabine 30 / Cytarabine 2000 / Idarubicin 8, Acute Myeloid Leukemia (PID762 V1.2) (PID748 V1.2)FLAGIDA/Venetoclax - Fludarabine 30 / Cytarabine 1500 / Idarubicin 8 / Venetoclax 400, Acute Myeloid Leukemia, Induction (PID2522 V1.0)FLAGIDA/Venetoclax - Fludarabine 30 / Cytarabine 1500 / Idarubicin 8 / Venetoclax 400, Acute Myeloid Leukemia, Consolidation (PID2524 V1.0)Gemtuzumab Ozogamicin (6/3), Acute Myeloid Leukemia, Induction (PID2590 V1.0)Gemtuzumab Ozogamicin / Daunorubicin 35 / Cytarabine 1000, Acute Myeloid Leukemia, Induction, Cycle 2 (PID1 V1.1)Gemtuzumab Ozogamicin 2, Acute Myeloid Leukemia, consolidation (PID2591 V1.0)Gemtuzumab Ozogamicin 3 / Cytarabine 1000 / Daunorubicin 60, Acute Myeloid Leukemia, consolidation, cycle 1 (PID4 V1.0)Gemtuzumab Ozogamicin 3 / Cytarabine 1000 / Daunorubicin 60, Acute Myeloid Leukemia, consolidation, cycle 2 (PID5 V1.0)Gemtuzumab Ozogamicin 3 / Daunorubicin 60 / Cytarabine 200, Acute Myeloid Leukemia, Induction, Leukocyte count from 30,000/µl, Cycle 1 (PID3 V1.2)Gemtuzumab Ozogamicin 3 / Daunorubicin 60 / Cytarabine 200, Acute Myeloid Leukemia, Induction, Leukocyte count up to 30,000/µl, Cycle 1 (PID2 V1.2)Gilteritinib 120, Acute Myeloid Leukemia (PID1505 V1.1)Gilteritinib 120, Acute Myeloid Leukemia after allogeneic stem cell transplantation (PID2589 V1.0)Gilteritinib 120, Acute Myeloid Leukemia, Cycle 25+ (PID2801 V1.0)High-dose Cytarabine 3000 / Mitoxantrone 10, Acute Myeloid Leukemia, induction less than 60 years of age (PID596 V1.2)High-dose Cytarabine 3000 / Mitoxantrone 10, sequential, Acute Myeloid Leukemia, induction, less than 60 years of age (PID603 V1.1)HOVON 132 AML / SAKK 30/13 - B - Idarubicin 12 / Cytarabine 200 / Lenalidomide 20, induction, Acute Myeloid Leukemia, cycle 1 (PID1065 V1.1)HOVON Daunorubicin 60 / Cytarabine 1000, induction, Acute Myeloid Leukemia, cycle 2 (PID1067 V1.1)HOVON Idarubicin 12 / Cytarabine 200, induction, Acute Myeloid Leukemia, cycle 1 (PID1064 V1.1)HOVON Mitoxantrone 10 / Etoposide 100, consolidation, Acute Myeloid Leukemia (PID1069 V1.1)Idarubicin 12 / Cytarabine 100 / Quizartinib 35.4, Acute Myeloid Leukemia, Induction (PID2552 V1.0)Idarubicin 12 / Cytarabine 1000, Acute Myeloid Leukemia, Induction, Cycle 2, salvage therapy (PID1247 V1.1)Ivosidenib 500, acute myeloid leukaemia (PID2369 V1.1)MAMAC - Cytarabine 2000 / Amsacrine 100, Acute Myeloid Leukemia (PID642 V1.0)MEC - Mitoxantrone 8 / Etoposide 100 / Cytarabine 1000, Acute Myeloid Leukemia (PID861 V1.2)Melphalan 2, Acute Myeloid Leukemia, over 65 years of age (PID1735 V1.1)Midostaurin 50, Acute Myeloid Leukemia, maintenance (PID1081 V1.1)Mito-FLAG - Fludarabine 15 / Cytarabine 1000 / Mitoxantrone 7, Acute Myeloid Leukemia (PID2521 V1.0)Quizartinib (26.5/53), Acute Myeloid Leukemia, maintenance, cycle 1 (PID2554 V1.0)Quizartinib 53, Acute Myeloid Leukemia, maintenance, cycle 2+ (PID2555 V1.0)Revumenib 270, Acute Myeloid Leukemia (PID2775 V1.0)Sorafenib 400/600, Acute Myeloid Leukemia, maintenance, cycle 1 (PID1020 V1.0)Sorafenib 800, Acute Myeloid Leukemia, maintenance, cycle 2+ (PID1038 V1.0)Study - DaunoDouble - Daunorubicin 45 / Cytarabine 100, AML Induction II, under 60 years of age (PID626 V1.1)Study - DaunoDouble - Daunorubicin 60 / Cytarabine 100, AML Induction I+II, under 60 years of age (PID627 V1.1)Study - DaunoDouble - Daunorubicin 90 / Cytarabine 100, AML Induction I, under 60 years of age (PID625 V1.1)Study - HOVON 132 AML / SAKK 30/13 - B - Daunorubicin 60 / Cytarabine 1000 / Lenalidomide 20, Induction, Acute Myeloid Leukemia, Cycle 2 (PID1066 V1.1)Study - HOVON 132 AML / SAKK 30/13 - Lenalidomide 10, maintenance, Acute Myeloid Leukemia (PID1068 V1.0)Study-AMLSG - Cytarabine 1000, Acute Myeloid Leukemia, consolidation, over 60 years of age (PID1814 V1.0)Study-AMLSG - Cytarabine 1500, Acute Myeloid Leukemia, consolidation, under 60 years of age (PID1813 V1.0)Study-AMLSG - Daunorubicin 50 / Cytarabine 1000, Acute Myeloid Leukemia, Induction II, under 60 years of age (PID1810 V1.0)Study-AMLSG - Daunorubicin 50 / Cytarabine 500, Acute Myeloid Leukemia, Induction II, over 60 years of age (PID1812 V1.0)Study-AMLSG - Daunorubicin 60 / Cytarabine 200, Acute Myeloid Leukemia, Induction I (PID1811 V1.0)Study-AMLSG - Daunorubicin Liposomal - Cytarabine liposomal 144, Acute Myeloid Leukemia, Induction I (PID1815 V1.0)Study-AMLSG - Daunorubicin Liposomal - Cytarabine liposomal 144, Acute Myeloid Leukemia, Induction II (PID1816 V1.0)Study-AMLSG - Daunorubicin Liposomal - Cytarabine liposomal 94, Acute Myeloid Leukemia, consolidation (PID1817 V1.0)Study-AMLSG 31-19/HOVON 501 - Cytarabine 1000 / Venetoclax 400, Acute Myeloid Leukemia and Myelodysplastic Syndrome, Induction II, over 60 years of age (PID3142 V1.0)Study-AMLSG 31-19/HOVON 501 - Cytarabine 1000 / Venetoclax 400, Acute Myeloid Leukemia and Myelodysplastic Syndrome, consolidation, over 60 years of age (PID3144 V1.0)Study-AMLSG 31-19/HOVON 501 - Cytarabine 1500 / Venetoclax 400, Acute Myeloid Leukemia and Myelodysplastic Syndrome, Consolidation, under 60 years of age (PID3143 V1.0)Study-AMLSG 31-19/HOVON 501 - Daunorubicin 60 / Cytarabine 1000 / Venetoclax 400, Acute Myeloid Leukemia and Myelodysplastic Syndrome, Induction II, under 60 years of age (PID3141 V1.0)Study-AMLSG 31-19/HOVON 501 - Daunorubicin 60 / Cytarabine 200 / Venetoclax (100/200/400), Acute Myeloid Leukemia and Myelodysplastic Syndrome, Induction I (PID3140 V1.0)TAD - Tioguanin 100 / Cytarabine 100 / Daunorubicin 60, AML induction, under 60 years of age (PID519 V1.1)Venetoclax (100/200/300/400/600) / Cytarabine 20, Acute Myeloid Leukemia, 60 years of age and older, Cycle 1 (PID1260 V1.1)Venetoclax (100/200/400) / Azacitidine 75, Acute Myeloid Leukemia, Cycle 1 (PID1595 V1.0)Venetoclax (100/200/400) / Decitabine 20, Acute Myeloid Leukemia, Cycle 1 (PID1597 V1.0)Venetoclax (100/200/400) / Gilteritinib 120, Acute Myeloid Leukemia, Cycle 1 (PID2148 V1.0)Venetoclax 400 / Gilteritinib 120, Acute Myeloid Leukemia, Cycle 2+ (PID2149 V1.0)Venetoclax 400 / Azacitidine 75, Acute Myeloid Leukemia, Cycle 2+ (PID1596 V1.0)Venetoclax 400 / Decitabine 0.2, Acute Myeloid Leukemia (PID2827 V1.0)Venetoclax 400 / Decitabine 20, Acute Myeloid Leukemia, Cycle 2+ (PID1598 V1.0)Venetoclax 600 / Cytarabine 20, Acute Myeloid Leukemia, 60 years and older, cycle 2+ (PID1319 V1.1)
