Vaccination with autologous myeloblasts admixed with GM-K562 cells in patients with advanced MDS or AML after allogeneic HSCT

Author:

Ho Vincent T.12,Kim Haesook T.3,Bavli Natalie12,Mihm Martin45,Pozdnyakova Olga6,Piesche Matthias127,Daley Heather12,Reynolds Carol12,Souders Nicholas C.12,Cutler Corey12,Koreth John12,Alyea Edwin P.12,Antin Joseph H.12,Ritz Jerome12,Dranoff Glenn12,Soiffer Robert J.12

Affiliation:

1. Department of Medical Oncology and Cancer Vaccine Center, Dana-Farber Cancer Institute, Boston, MA;

2. Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA;

3. Department of Biostatistics and Computation Biology, Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA;

4. Department of Dermatology and

5. Department of Pathology, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA;

6. Department of Hematopathology, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA; and

7. Biomedical Research Laboratories, Medicine Faculty, Catholic University of Maule, Talca, Chile

Abstract

Key Points GM-K562 admixed leukemia cell vaccination after allogeneic HSCT has biologic activity in MDS/AML. Postvaccination antibody response to angiopoeitin-2 is associated with improved outcomes.

Publisher

American Society of Hematology

Subject

Hematology

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