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Response to upfront azacitidine in juvenile myelomonocytic leukemia in the AZA-JMML-001 trial.
Niemeyer, Charlotte M; Flotho, Christian; Lipka, Daniel B; Starý, Jan; Rössig, Claudia; Baruchel, André; Klingebiel, Thomas; Micalizzi, Concetta; Michel, Gérard; Nysom, Karsten; Rives, Susana; Schmugge Liner, Markus; Zecca, Marco; Schönung, Maximilian; Baumann, Irith; Nöllke, Peter; Benettaib, Bouchra; Biserna, Noha; Poon, Jennifer; Simcock, Mathew; Patturajan, Meera; Menezes, Daniel; Gaudy, Allison; van den Heuvel-Eibrink, Marry M; Locatelli, Franco.
Afiliación
  • Niemeyer CM; Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical Center, University of Freiburg, Freiburg, Germany.
  • Flotho C; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Lipka DB; Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical Center, University of Freiburg, Freiburg, Germany.
  • Starý J; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Rössig C; Translational Cancer Epigenomics Section, Division of Translational Medical Oncology, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany.
  • Baruchel A; Department of Paediatric Hematology and Oncology, Charles University and University Hospital Motol, Prague, Czech Republic.
  • Klingebiel T; Department of Pediatric Hematology and Oncology, Münster University Children's Hospital, Münster, Germany.
  • Micalizzi C; Department of Pediatric Hematology and Immunology, Centre Hospitalier Universitaire (CHU) Paris-Hôpital Universitaire Robert-Debré (Assistance Publique-Hôpitaux de Paris [AP-HP]), Paris, France.
  • Michel G; German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Nysom K; Department of Pediatrics, Universitätsklinikum Frankfurt, Frankfurt, Germany.
  • Rives S; German Cancer Consortium (DKTK), Site Frankfurt, Frankfurt, Germany.
  • Schmugge Liner M; Department of Pediatric Sciences, Istituto Giannina Gaslini, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Genoa, Italy.
  • Zecca M; Pediatrics and Pediatric Oncology, Hôpital de la Timone, Marseilles, France.
  • Schönung M; Department of Paediatrics and Adolescent Medicine, Rigshospitalet, Copenhagen, Denmark.
  • Baumann I; Pediatric Hematology and Oncology, Institut de Recerca, Hospital Sant Joan de Deu de Barcelona, Barcelona, Spain.
  • Nöllke P; Division of Haematology, Kinderspital Zürich, Zürich, Switzerland.
  • Benettaib B; Pediatric Hematology/Oncology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Biserna N; Translational Cancer Epigenomics Section, Division of Translational Medical Oncology, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany.
  • Poon J; Faculty of Biosciences, Heidelberg University, Heidelberg, Germany.
  • Simcock M; Department of Pathology, Böblingen Hospital, Sindelfingen, Germany.
  • Patturajan M; Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical Center, University of Freiburg, Freiburg, Germany.
  • Menezes D; Formerly Bristol Myers Squibb, Princeton, NJ.
  • Gaudy A; Formerly Bristol Myers Squibb, Princeton, NJ.
  • van den Heuvel-Eibrink MM; Bristol Myers Squibb, Princeton, NJ.
  • Locatelli F; Celgene Corporation, a Bristol Myers Squibb company, Uxbridge, United Kingdom.
Blood Adv ; 5(14): 2901-2908, 2021 07 27.
Article en En | MEDLINE | ID: mdl-34297046
Allogeneic hematopoietic stem cell transplantation (HSCT) is the only curative therapy for most children with juvenile myelomonocytic leukemia (JMML). Novel therapies controlling the disorder prior to HSCT are needed. We conducted a phase 2, multicenter, open-label study to evaluate the safety and antileukemic activity of azacitidine monotherapy prior to HSCT in newly diagnosed JMML patients. Eighteen patients enrolled from September 2015 to November 2017 were treated with azacitidine (75 mg/m2) administered IV once daily on days 1 to 7 of a 28-day cycle. The primary end point was the number of patients with clinical complete remission (cCR) or clinical partial remission (cPR) after 3 cycles of therapy. Pharmacokinetics, genome-wide DNA-methylation levels, and variant allele frequencies of leukemia-specific index mutations were also analyzed. Sixteen patients completed 3 cycles and 5 patients completed 6 cycles. After 3 cycles, 11 patients (61%) were in cPR and 7 (39%) had progressive disease. Six of 16 patients (38%) who needed platelet transfusions were transfusion-free after 3 cycles. All 7 patients with intermediate- or low-methylation signatures in genome-wide DNA-methylation studies achieved cPR. Seventeen patients received HSCT; 14 (82%) were leukemia-free at a median follow-up of 23.8 months (range, 7.0-39.3 months) after HSCT. Azacitidine was well tolerated and plasma concentration--time profiles were similar to observed profiles in adults. In conclusion, azacitidine monotherapy is a suitable option for children with newly diagnosed JMML. Although long-term safety and efficacy remain to be fully elucidated in this population, these data demonstrate that azacitidine provides valuable clinical benefit to JMML patients prior to HSCT. This trial was registered at www.clinicaltrials.gov as #NCT02447666.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Leucemia Mielomonocítica Juvenil Tipo de estudio: Clinical_trials Límite: Adult / Child / Humans Idioma: En Revista: Blood Adv Año: 2021 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Leucemia Mielomonocítica Juvenil Tipo de estudio: Clinical_trials Límite: Adult / Child / Humans Idioma: En Revista: Blood Adv Año: 2021 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos