Literature DB >> 17606446

Repeated infusions of donor-derived cytokine-induced killer cells in patients relapsing after allogeneic stem cell transplantation: a phase I study.

Martino Introna1, Gianmaria Borleri, Elena Conti, Marta Franceschetti, Anna Maria Barbui, Raewyn Broady, Erica Dander, Giuseppe Gaipa, Giovanna D'Amico, Ettore Biagi, Matteo Parma, Enrico M Pogliani, Orietta Spinelli, Donatella Baronciani, Anna Grassi, Josée Golay, Tiziano Barbui, Andrea Biondi, Alessandro Rambaldi.   

Abstract

BACKGROUND AND OBJECTIVES: Cytokine-induced killer (CIK) cells have shown anti-leukemic activity and little graft-versus-host disease (GVHD) in several animal models. The safety of these cells in autologous settings has been shown. We performed a phase I study of allogeneic (donor's) CIK cells in patients relapsing after allogeneic haematopoietic stem cell transplantation (HSCT). DESIGN AND METHODS: Eleven patients with acute myelogenous leukemia (n=4), Hodgkin's disease (n=3), chronic myelomonocytic leukemia, (n=1), pre-B acute lymphoblastic leukemia (n=1) and myelodysplasia (n=2), all of whom had relapsed after sibling (n=6) or matched unrelated donor (n=5) HSCT, entered this study.
RESULTS: Before CIK administration, six patients had received other salvage treatments including chemotherapy (n=5), radiotherapy (n=1) and unmanipulated donor lymphocytes (n=6) without any significant tumor response. The median number of CIK infusions was two (range 1-7) and the median number of total CIK cells was 12.4x106/kg (range 7.2-87.4). The infusions were well tolerated and no acute or late infusion-related reactions were recorded. Acute GVHD (grade I and II) was observed in four patients, 30 days after the last CIK infusion, and progressed into extensive chronic GVHD in two cases. Disease progression and death occurred in six patients. One patient had stable disease, one had hematologic improvement and three achieved complete responses. INTERPRETATION AND
CONCLUSIONS: This study shows that the production of allogeneic CIK cells is feasible under clinical-grade conditions, well tolerated and may contribute to clinical responses.

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Year:  2007        PMID: 17606446     DOI: 10.3324/haematol.11132

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  64 in total

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Authors:  E Todisco; F Ciceri; C Boschini; F Giglio; A Bacigalupo; F Patriarca; I Donnini; E P Alessandrino; W Arcese; A P Iori; P Marenco; I Cavattoni; P Chiusolo; E Terruzzi; L Castagna; A Santoro; A Bosi; E Oldani; B Bruno; F Bonifazi; A Rambaldi
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Review 9.  Adoptive immunotherapy for acute leukemia: New insights in chimeric antigen receptors.

Authors:  Maël Heiblig; Mohamed Elhamri; Mauricette Michallet; Xavier Thomas
Journal:  World J Stem Cells       Date:  2015-08-26       Impact factor: 5.326

10.  Treatment of CD33-directed chimeric antigen receptor-modified T cells in one patient with relapsed and refractory acute myeloid leukemia.

Authors:  Quan-shun Wang; Yao Wang; Hai-yan Lv; Qing-wang Han; Hui Fan; Bo Guo; Li-li Wang; Wei-dong Han
Journal:  Mol Ther       Date:  2014-09-01       Impact factor: 11.454

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