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Rescooped by Gilbert C FAURE from Cancer Immunotherapy Review and Collection
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Engineered T Cells for Leukemia: A Review of Current Approaches and Applications - Targeted Oncology

Engineered T Cells for Leukemia: A Review of Current Approaches and Applications - Targeted Oncology | Hematology | Scoop.it
This review addresses the basics of CAR T-cell design and reviews data from published clinical studies in leukemia.

 

Abstract

Chimeric antigen receptor T cells (CAR T cells), engineered from individual patients to specifically target tumor-associated antigens, have shown extraordinary promise in the management of B-cell malignancies. Moreover, CAR T cells are being developed for a myriad of other hematologic malignancies. First-generation CAR T cells demonstrated only modest efficacy because of inadequate activation, persistence, and proliferation, but the addition of one (second-generation) or more (third-generation) costimulatory molecules has produced a marked improvement in efficacy. Clinical trials are recruiting patients with leukemia, and CARs are being tested for patients with a large variety of both solid and liquid tumors. It seems likely that CAR T-cell therapy will become an established option in the near future for patients with B-cell malignancies. Significant questions remain about optimal timing for administration, product preparation, and CAR design to optimize response across malignancy types. This review addresses the basics of CAR T-cell design and reviews data from published clinical studies in leukemia. It also contains commentary on the prospects of this promising new therapeutic strategy.

 


Via Krishan Maggon
Gilbert C FAURE's insight:

Targeted Oncology

 

Engineered T Cells for Leukemia: A Review of Current Approaches and Applications

 

Pallawi Torka, MD, and Elizabeth A. Griffiths, MDPublished Online: Jul 27, 2015

 

Krishan Maggon 's curator insight, July 30, 2015 4:02 AM

Targeted Oncology

 

Engineered T Cells for Leukemia: A Review of Current Approaches and Applications

 

Pallawi Torka, MD, and Elizabeth A. Griffiths, MDPublished Online: Jul 27, 2015

 

Rescooped by Gilbert C FAURE from Cancer Vaccines Collection
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Oncogene - The aurora kinases in cell cycle and leukemia

Oncogene - The aurora kinases in cell cycle and leukemia | Hematology | Scoop.it
Oncogene is one of the world’s leading cancer journals. It is published weekly and covers all aspects of the structure and function of Oncogenes.

Via Krishan Maggon
Krishan Maggon 's curator insight, January 29, 2015 11:38 AM

Oncogene (2015) 34, 537–545; doi:10.1038/onc.2014.14; published online 17 March 2014

The aurora kinases in cell cycle and leukemia

B Goldenson1 and J D Crispino1

1Division of Hematology/Oncology, Northwestern University, Chicago, IL, USA

Correspondence: Professor JD Crispino, Division of Hematology/Oncology, Northwestern University, 303 East Superior Street, Lurie 5-113, Chicago, IL 60611, USA. E-mail: j-crispino@northwestern.edu

Received 31 October 2013; Revised 14 January 2014; Accepted 21 January 2014
Advance online publication 17 March 2014

Rescooped by Gilbert C FAURE from Cancer Pathways inhibitors Collection
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Designed to Kill: Novel Menin-MLL Inhibitors Target MLL-Rearranged Leukemia: Cancer Cell

Designed to Kill: Novel Menin-MLL Inhibitors Target MLL-Rearranged Leukemia: Cancer Cell | Hematology | Scoop.it

The interaction between menin and oncogenic mixed lineage leukemia (MLL) fusion proteins is required for leukemic transformation and may represent a therapeutic opportunity. In this issue of Cancer Cell, Borkin and colleagues describe the development of highly potent small-molecule inhibitors of this interaction that reverse the leukemic phenotype and prolong survival in murine models of MLL-rearranged leukemia.


Via Krishan Maggon
Krishan Maggon 's curator insight, May 9, 2015 10:47 AM

Cancer cell  Volume 27, Issue 4, p431–433, 13 April 2015


Designed to Kill: Novel Menin-MLL Inhibitors Target MLL-Rearranged LeukemiaMichael W.M. Kühn, Scott A. Armstrong DOI: http://dx.doi.org/10.1016/j.ccell.2015.03.012 | Article Info