[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100275079":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":15,"centralContacts":10,"locations":20,"responsibleParty":39,"collaborators":10,"id":41,"slug":42,"hasResults":43,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":43,"sex":49,"minAge":50,"maxAge":10,"enrollmentInfo":51,"targetDuration":10,"studyType":54,"phases":10,"briefSummary":55,"conditions":56,"keywords":59,"overallStatus":64,"whyStopped":10,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":73},{"fullName":5,"class":6},"Hospices Civils de Lyon","OTHER",[8,12],{"label":9,"type":10,"description":11,"interventionNames":10},"Group 1",null,"Patient with AML de novo or secondary myelodysplasia, in Complete Remission (CR) after induction and \u002F or salvage therapy and candidate to receive a consolidation therapy",{"label":13,"type":10,"description":14,"interventionNames":10},"Group 2","Patient with hematologic malignancies (ALL, AML, chronic lymphocytic leukemia (CLL), non-Hodgkin lymphoma, myeloma, myeloproliferative syndrome (MDS)) and candidate for blood marrow or stem cell or placental blood transplantation.",[16],{"name":17,"affiliation":18,"role":19},"Mauricette Michallet, Prof.","Hematology Department, Hospices Civils de Lyon","STUDY_DIRECTOR",[21],{"facility":22,"status":23,"city":24,"state":10,"zip":10,"country":25,"countryCode":26,"cosmosGeoPoint":27,"geoPoint":32,"contacts":33},"Jeremy MONFRAY","RECRUITING","Pierre-Bénite","France","FR",{"type":28,"coordinates":29},"Point",[30,31],4.82424,45.70359,{"lat":31,"lon":30},[34],{"name":35,"role":36,"phone":37,"phoneExt":10,"email":38},"Jeremy MONFRAY, MD-PHD","CONTACT","+33 4 78 86 22 01","jeremy.monfrey@chu-lyon.fr",{"type":40,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100275079","observatory-of-the-prescription-of-erythropoietin-as-treatment-of-anemia-induced-by-chemotherapy-or-allograft-conditioning-among-the-patients-with-a-haematological-malignancy-100275079",false,"NCT02860598","Observatory of the Prescription of Erythropoietin as Treatment of Anemia Induced by Chemotherapy or Allograft Conditioning Among the Patients With a Haematological Malignancy","Clinical Observatory of the Prescription of Erythropoietin as Treatment of Anemia Induced by Chemotherapy or Allograft Conditioning Among the Patients With a Haematological Malignancy","EPREX\u002FLAM-ALLO","Inclusion Criteria:\n\n* Age ≥ 18 years.\n* Patient with AML de novo or secondary myelodysplasia in Complete Remission (CR) after induction and \u002F or salvage therapy and candidate to receive a consolidation therapy.\n* OR Patient with hematologic malignancies (ALL, AML, chronic lymphocytic leukemia, CLL, non-Hodgkin lymphoma, MDS, myeloma, myeloproliferative syndrome) and candidate for blood marrow or stem cell or placental blood transplantation.\n\nDepending on the hematologic malignancy, pre-transplant status of patients included will be the CR, very good partial or partial response.\n\n* Patient with anemia (Hb blood level ≤ 110g \u002F l) induced by consolidation chemotherapy or allograft conditioning (myeloablative or non-myeloablative).\n* Patient eligible according to the investigator, to treatment with ESA (evaluation by the investigator of the benefice- risk ratio).\n* Written informed consent.\n\nExclusion Criteria:\n\n* Contraindication to epoetin alfa or epoetin zeta.\n* Patient not able to receive adequate antithrombotic prophylaxis.\n* Patients who received ESA therapy within 3 weeks prior to inclusion.\n* non French-speaking patient\n* Patient participating or having participated to a clinical trial evaluating a novel molecule in the 30 days before inclusion.\n* pregnant or nursing, woman or woman of childbearing potential without effective contraception","ALL","18 Years",{"count":52,"type":53},104,"ESTIMATED","OBSERVATIONAL","Anemia concerns a lot of patients with cancer and affects their quality of life (QOL). Numerous studies in oncology have demonstrated the benefit of erythropoiesis-stimulating agents (ESA) in the treatment of anemia. ESAs allow the improvement of QOL,of the hemoglobin level (Hb) and is a validated alternative to transfusion.\n\nHowever, in hematology, if there are some specific recommendations for the use of ESAs in lymphoid pathology, there are none for myeloid disorders and in the context of autografts and allogeneic hematopoietic stem-cell transplantation (HSCT). Thus, the investigators are in particular interested in both indications: treatment of anemia in acute myeloid leukemia (AML) patients treated with chemotherapy, and the in patients receiving a myeloablative or a non-myeloablative conditioning before allogeneic HSCT, whatever type of donor and cell source.",[57,58],"Anemia","Acute Myeloid Leukemia",[60,61,62,63],"ESAs","erythropoietin","AML","HSCT","UNKNOWN","2016-08-04",{"date":67,"type":53},"2016-08-09",{"date":69,"type":10},"2011-12",{"date":71,"type":53},"2019-06",{"name":5,"class":6},1]