Literature DB >> 26841014

The Promise of Chimeric Antigen Receptor Engineered T Cells in the Treatment of Hematologic Malignancies.

Sarah J Nagle1, Alfred L Garfall, Edward A Stadtmauer.   

Abstract

Relapsed and refractory hematologic malignancies have a very poor prognosis. Chimeric antigen receptor T cells are emerging as a powerful therapy in this setting. Early clinical trials of genetically modified T cells for the treatment of non-Hodgkin lymphoma, chronic lymphocytic leukemia, and acute lymphoblastic leukemia have shown high complete response rates in patients with few therapeutic options. Exploration is ongoing for other hematologic malignancies including multiple myeloma, acute myeloid leukemia, and Hodgkin lymphoma (HL). At the same time, the design and production of chimeric antigen receptor T cells are being advanced so that this therapy can be more widely utilized. Cytokine release syndrome and neurotoxicity are common, but they are treatable and fully reversible. This review will review available data as well as future developments and challenges in the field.

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Year:  2016        PMID: 26841014      PMCID: PMC4742356          DOI: 10.1097/PPO.0000000000000166

Source DB:  PubMed          Journal:  Cancer J        ISSN: 1528-9117            Impact factor:   3.360


  68 in total

1.  Case report of a serious adverse event following the administration of T cells transduced with a chimeric antigen receptor recognizing ERBB2.

Authors:  Richard A Morgan; James C Yang; Mio Kitano; Mark E Dudley; Carolyn M Laurencot; Steven A Rosenberg
Journal:  Mol Ther       Date:  2010-02-23       Impact factor: 11.454

2.  Insertional transformation of hematopoietic cells by self-inactivating lentiviral and gammaretroviral vectors.

Authors:  Ute Modlich; Susana Navarro; Daniela Zychlinski; Tobias Maetzig; Sabine Knoess; Martijn H Brugman; Axel Schambach; Sabine Charrier; Anne Galy; Adrian J Thrasher; Juan Bueren; Christopher Baum
Journal:  Mol Ther       Date:  2009-08-11       Impact factor: 11.454

3.  Adoptive immunotherapy with genetically engineered T cells: modification of the IgG1 Fc 'spacer' domain in the extracellular moiety of chimeric antigen receptors avoids 'off-target' activation and unintended initiation of an innate immune response.

Authors:  A Hombach; A A Hombach; H Abken
Journal:  Gene Ther       Date:  2010-06-17       Impact factor: 5.250

4.  Antitransgene rejection responses contribute to attenuated persistence of adoptively transferred CD20/CD19-specific chimeric antigen receptor redirected T cells in humans.

Authors:  Michael C Jensen; Leslie Popplewell; Laurence J Cooper; David DiGiusto; Michael Kalos; Julie R Ostberg; Stephen J Forman
Journal:  Biol Blood Marrow Transplant       Date:  2010-03-19       Impact factor: 5.742

5.  Adoptive transfer of syngeneic T cells transduced with a chimeric antigen receptor that recognizes murine CD19 can eradicate lymphoma and normal B cells.

Authors:  James N Kochenderfer; Zhiya Yu; Dorina Frasheri; Nicholas P Restifo; Steven A Rosenberg
Journal:  Blood       Date:  2010-07-14       Impact factor: 22.113

6.  Manufacturing validation of biologically functional T cells targeted to CD19 antigen for autologous adoptive cell therapy.

Authors:  Daniel Hollyman; Jolanta Stefanski; Mark Przybylowski; Shirley Bartido; Oriana Borquez-Ojeda; Clare Taylor; Raymond Yeh; Vanessa Capacio; Malgorzata Olszewska; James Hosey; Michel Sadelain; Renier J Brentjens; Isabelle Rivière
Journal:  J Immunother       Date:  2009 Feb-Mar       Impact factor: 4.456

7.  CS1, a potential new therapeutic antibody target for the treatment of multiple myeloma.

Authors:  Eric D Hsi; Roxanne Steinle; Balaji Balasa; Susann Szmania; Aparna Draksharapu; Benny P Shum; Mahrukh Huseni; David Powers; Amulya Nanisetti; Yin Zhang; Audie G Rice; Anne van Abbema; Melanie Wong; Gao Liu; Fenghuang Zhan; Myles Dillon; Shihao Chen; Susan Rhodes; Franklin Fuh; Naoya Tsurushita; Shankar Kumar; Vladimir Vexler; John D Shaughnessy; Bart Barlogie; Frits van Rhee; Mohamad Hussein; Daniel E H Afar; Marna B Williams
Journal:  Clin Cancer Res       Date:  2008-05-01       Impact factor: 12.531

8.  IL-2 and IL-21 confer opposing differentiation programs to CD8+ T cells for adoptive immunotherapy.

Authors:  Christian S Hinrichs; Rosanne Spolski; Chrystal M Paulos; Luca Gattinoni; Keith W Kerstann; Douglas C Palmer; Christopher A Klebanoff; Steven A Rosenberg; Warren J Leonard; Nicholas P Restifo
Journal:  Blood       Date:  2008-02-14       Impact factor: 22.113

9.  Chimeric NKG2D receptor-expressing T cells as an immunotherapy for multiple myeloma.

Authors:  Amorette Barber; Tong Zhang; Christina J Megli; Jillian Wu; Kenneth R Meehan; Charles L Sentman
Journal:  Exp Hematol       Date:  2008-07-02       Impact factor: 3.084

Review 10.  A transposon and transposase system for human application.

Authors:  Perry B Hackett; David A Largaespada; Laurence J N Cooper
Journal:  Mol Ther       Date:  2010-01-26       Impact factor: 11.454

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  4 in total

Review 1.  Building upon the success of CART19: chimeric antigen receptor T cells for hematologic malignancies.

Authors:  Antonia Rotolo; Anastasios Karadimitris; Marco Ruella
Journal:  Leuk Lymphoma       Date:  2017-11-22

Review 2.  Dendritic Cell Therapies for Hematologic Malignancies.

Authors:  Matthew Weinstock; Jacalyn Rosenblatt; David Avigan
Journal:  Mol Ther Methods Clin Dev       Date:  2017-03-18       Impact factor: 6.698

Review 3.  Cell-based immunotherapy approaches for multiple myeloma.

Authors:  Katharina Kriegsmann; Mark Kriegsmann; Martin Cremer; Michael Schmitt; Peter Dreger; Hartmut Goldschmidt; Carsten Müller-Tidow; Michael Hundemer
Journal:  Br J Cancer       Date:  2018-12-06       Impact factor: 7.640

Review 4.  Neurotoxicity of Tumor Immunotherapy: The Emergence of Clinical Attention.

Authors:  Benxia Zhang; Xue Li; Tao Yin; Diyuan Qin; Yue Chen; Qizhi Ma; Pei Shu; Yongsheng Wang
Journal:  J Oncol       Date:  2022-01-18       Impact factor: 4.375

  4 in total

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