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Microtransplantation in older patients with AML: A pilot study of safety, efficacy and immunologic effects.
Sung, Anthony D; Jauhari, Shekeab; Siamakpour-Reihani, Sharareh; Rao, Arati V; Staats, Janet; Chan, Cliburn; Meyer, Everett; Gadi, Vijayakrishna K; Nixon, Andrew B; Lyu, Jing; Xie, Jichun; Bohannon, Lauren; Li, Zhiguo; Hourigan, Christopher S; Dillon, Laura W; Wong, Hong Yuen; Shelby, Rebecca; Diehl, Louis; de Castro, Carlos; LeBlanc, Thomas; Brander, Danielle; Erba, Harry; Galal, Ahmed; Stefanovic, Alexandra; Chao, Nelson; Rizzieri, David A.
Afiliação
  • Sung AD; Duke University School of Medicine, Durham, North Carolina, USA.
  • Jauhari S; Duke University School of Medicine, Durham, North Carolina, USA.
  • Siamakpour-Reihani S; Duke University School of Medicine, Durham, North Carolina, USA.
  • Rao AV; Kite Pharma, San Francisco, California, USA.
  • Staats J; Duke University School of Medicine, Durham, North Carolina, USA.
  • Chan C; Duke University School of Medicine, Durham, North Carolina, USA.
  • Meyer E; Stanford University Medical School, Palo Alto, California, USA.
  • Gadi VK; Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
  • Nixon AB; Duke University School of Medicine, Durham, North Carolina, USA.
  • Lyu J; Duke University School of Medicine, Durham, North Carolina, USA.
  • Xie J; Duke University School of Medicine, Durham, North Carolina, USA.
  • Bohannon L; Duke University School of Medicine, Durham, North Carolina, USA.
  • Li Z; Duke University School of Medicine, Durham, North Carolina, USA.
  • Hourigan CS; Laboratory of Myeloid Malignancies, Hematology Branch, National Heart, Lung and Blood Institute, Bethesda, Maryland, USA.
  • Dillon LW; Laboratory of Myeloid Malignancies, Hematology Branch, National Heart, Lung and Blood Institute, Bethesda, Maryland, USA.
  • Wong HY; Laboratory of Myeloid Malignancies, Hematology Branch, National Heart, Lung and Blood Institute, Bethesda, Maryland, USA.
  • Shelby R; Duke University School of Medicine, Durham, North Carolina, USA.
  • Diehl L; Duke University School of Medicine, Durham, North Carolina, USA.
  • de Castro C; Duke University School of Medicine, Durham, North Carolina, USA.
  • LeBlanc T; Duke University School of Medicine, Durham, North Carolina, USA.
  • Brander D; Duke University School of Medicine, Durham, North Carolina, USA.
  • Erba H; Duke University School of Medicine, Durham, North Carolina, USA.
  • Galal A; Duke University School of Medicine, Durham, North Carolina, USA.
  • Stefanovic A; Duke University School of Medicine, Durham, North Carolina, USA.
  • Chao N; Duke University School of Medicine, Durham, North Carolina, USA.
  • Rizzieri DA; Duke University School of Medicine, Durham, North Carolina, USA.
Am J Hematol ; 95(6): 662-671, 2020 06.
Article em En | MEDLINE | ID: mdl-32162718
ABSTRACT
Older AML patients have low remission rates and poor survival outcomes with standard chemotherapy. Microtransplantation (MST) refers to infusion of allogeneic hematopoietic stem cells without substantial engraftment. MST has been shown to improve clinical outcomes compared with chemotherapy alone. This is the first trial reporting on broad correlative studies to define immunologic mechanisms of action of MST in older AML patients. Older patients with newly diagnosed AML were eligible for enrollment, receiving induction chemotherapy with cytarabine (100 mg/m2) on days 1-7 and idarubicin (12 mg/m2) on days 1-3 (7 + 3). MST was administered 24 hours later. Patients with complete response (CR) were eligible for consolidation with high dose cytarabine (HiDAC) and a second cycle of MST. Responses were evaluated according to standard criteria per NCCN. Immune correlative studies were performed. Sixteen patients were enrolled and received 7 + 3 and MST (median age 73 years). Nine (56%) had high-risk and seven (44%) had standard-risk cytogenetics. Ten episodes of CRS were observed. No cases of GVHD or treatment-related mortality were reported. Event-free survival (EFS) was 50% at 6 months and 19% at 1 year. Overall survival (OS) was 63% at 6 months and 44% at 1 year. Donor microchimerism was not detected. Longitudinal changes were noted in NGS, TCR sequencing, and cytokine assays. Addition of MST to induction and consolidation chemotherapy was well tolerated in older AML patients. Inferior survival outcomes in our study may be attributed to a higher proportion of very elderly patients with high-risk features. Potential immunologic mechanisms of activity of MST include attenuation of inflammatory cytokines and emergence of tumor-specific T cell clones.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Idarubicina / Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas / Citarabina / Quimioterapia de Indução Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Hematol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Idarubicina / Leucemia Mieloide Aguda / Transplante de Células-Tronco Hematopoéticas / Citarabina / Quimioterapia de Indução Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Hematol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos