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Outcomes following hematopoietic stem cell transplantation in patients treated with standard chemotherapy with or without gemtuzumab ozogamicin for acute myeloid leukemia.
Pautas, Cécile; Raffoux, Emmanuel; Lambert, Juliette; Legrand, Ollivier; Chantepie, Sylvain; Gastaud, Lauris; Marolleau, Jean-Pierre; Thomas, Xavier; Turlure, Pascal; Benner, Rebecca J; Vandendries, Erik; Gogat, Karïn; Dombret, Hervé; Castaigne, Sylvie.
Afiliación
  • Pautas C; Service d'Hématologie et de thérapie cellulaire, Hôpital Henri Mondor, Créteil, France. cecile.pautas@aphp.fr.
  • Raffoux E; Hôpital Saint-Louis (AP-HP), EA 3518, Université de Paris, Paris, France.
  • Lambert J; Service d'Hématologie et Oncologie, Centre Hospitalier de Versailles, Le Chesnay, France.
  • Legrand O; Service d'hématologie clinique et de thérapie cellulaire, Hôpital Saint-Antoine (AP-HP), Université Paris Pierre et Marie Curie, Paris, France.
  • Chantepie S; Institut d'Hématologie de Basse-Normandie, Caen, France.
  • Gastaud L; Service hématologie, Centre Lacassagne, Nice, France.
  • Marolleau JP; Service hématologie, CHU Amiens, Amiens, France.
  • Thomas X; Service hématologie, Centre Hospitalier Lyon Sud, Lyon, France.
  • Turlure P; Service hématologie et de thérapie cellulaire, CHU de Limoges, Limoges, France.
  • Benner RJ; Global Product Development, Pfizer Inc, Groton, CT, USA.
  • Vandendries E; Pfizer Inc, Cambridge, MA, USA.
  • Gogat K; Global Clinical Development, Pfizer Inc, Paris, France.
  • Dombret H; Hôpital Saint-Louis (AP-HP), EA 3518, Université de Paris, Paris, France.
  • Castaigne S; Service d'Hématologie et Oncologie, Centre Hospitalier de Versailles, Université de Versailles Saint Quentin, Le Chesnay, France.
Bone Marrow Transplant ; 56(6): 1474-1477, 2021 06.
Article en En | MEDLINE | ID: mdl-33564120
The phase 3 ALFA-0701 trial demonstrated improved outcomes with fractionated-dose gemtuzumab ozogamicin (GO) combined with standard chemotherapy vs. standard chemotherapy alone in adults with de novo acute myeloid leukemia (AML). We examined post-transplant outcomes and occurrence of hepatic veno-occlusive disease/sinusoidal obstruction syndrome (VOD/SOS) in patients who received hematopoietic stem cell transplantation (HSCT) as follow-up therapy in ALFA-0701. Patients aged 50-70 years were randomized to standard chemotherapy with or without GO (3 mg/m2 on days 1, 4, and 7 of induction and day 1 on each of two consolidation courses). Allogeneic HSCT was recommended for patients in first complete remission with matched (related or unrelated) donor, except those with core-binding factor AML or normal karyotype and either NPM1+/FLT3-ITDwt or CEBPA+ AML. Eighty-five patients (GO: n = 32; control: n = 53) received HSCT in first complete remission or after relapse/primary induction failure. Three patients (GO: n = 2; control: n = 1 [received GO as follow-up therapy]) developed VOD/SOS after HSCT or conditioning. Post-transplant survival, non-relapse mortality, and relapse were not different between arms. Results indicate fractionated-dose GO as part of induction and consolidation chemotherapy for AML does not induce excess post-transplant VOD/SOS or mortality and thus does not preclude the use of HSCT as consolidation treatment.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad Veno-Oclusiva Hepática / Leucemia Mieloide Aguda / Trasplante de Células Madre Hematopoyéticas Tipo de estudio: Clinical_trials Límite: Adult / Humans Idioma: En Revista: Bone Marrow Transplant Asunto de la revista: TRANSPLANTE Año: 2021 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad Veno-Oclusiva Hepática / Leucemia Mieloide Aguda / Trasplante de Células Madre Hematopoyéticas Tipo de estudio: Clinical_trials Límite: Adult / Humans Idioma: En Revista: Bone Marrow Transplant Asunto de la revista: TRANSPLANTE Año: 2021 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido