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Hematopoietic and Immune Cancer Biology Research Program

$80,004P30FY2022CANIH

Case Western Reserve University, Cleveland OH

Investigators

Linked publications, trials & patents

Trial NCT05340673Trial NCT05198830Trial NCT02590107Trial NCT02535325Trial NCT02451124Trial NCT02419846Trial NCT02417948Trial NCT02392377Trial NCT02388932Trial NCT02383433Trial NCT02375477Trial NCT02354326Trial NCT02345460Trial NCT02342730Trial NCT02337465Trial NCT02327390Trial NCT02319889Trial NCT02307474Trial NCT02287636Trial NCT02252393Trial NCT02181478Trial NCT02179762Trial NCT02163317Trial NCT02158767Trial NCT02153450Trial NCT02135562Trial NCT02131207Trial NCT02129582Trial NCT02129569Trial NCT02129517Trial NCT02129218Trial NCT02128373Trial NCT02108587Trial NCT02100423Trial NCT02084147Trial NCT02082405Trial NCT02081794Trial NCT02079155Trial NCT02073097Trial NCT02073045Trial NCT02071901Trial NCT02070458Trial NCT02070419Trial NCT02055586Trial NCT02037048Trial NCT01973062Trial NCT01959490Trial NCT01959477Trial NCT01954784Trial NCT01954732Trial NCT01951885Trial NCT01939028Trial NCT01928485Trial NCT01894061Trial NCT01408043Trial NCT00991991Trial NCT00970684Trial NCT00961220Trial NCT00956475Trial NCT00952939Trial NCT00949247Trial NCT00945061Trial NCT00941720Trial NCT00941070Trial NCT00939510Trial NCT00918892Trial NCT00918788Trial NCT00918658Trial NCT00918216Trial NCT00910039Trial NCT00909662Trial NCT00908739Trial NCT00908141Trial NCT00907699Trial NCT00905086Trial NCT00900133Trial NCT00899158Trial NCT00899132Trial NCT00898573Trial NCT00898274Trial NCT00897143Trial NCT00892385Trial NCT00873600Trial NCT00873002Trial NCT00866320Trial NCT00856115Trial NCT00853021Trial NCT00842452Trial NCT00809185Trial NCT00796978Trial NCT00795678Trial NCT00769951Trial NCT00769249Trial NCT00752323Trial NCT00740961Trial NCT00736216Trial NCT00735514Trial NCT00733252Trial NCT00732745Trial NCT00732173

Abstract

HEMATOPOIETIC AND IMMUNE CANCER BIOLOGY (HICB) REASEARCH PROGRAM PROJECT SUMMARY/ABSTRACT The objectives of the Hematopoietic and Immune Cancer Biology (HICB) Program are to improve cancer diagnosis, care and cure rates through better understanding of molecular pathogenesis of blood neoplasms and optimizing the efficacy of cellular immunotherapy and stem cell transplantation (SCT). Program members investigate the roles of hematopoietic processes in health and disease, including the evolution of hematologic neoplasms from normal hematopoiesis and the roles of cellular immunity in cancer immune responses, especially toward developing new treatments for hematological malignancies. The program is organized around 3 scientific aims: (1) Discover novel molecular features of hematologic neoplasms to improve diagnosis, prognostication, and develop a new generation of rationally-targeted therapeutic approaches, (2) Interrogate mechanisms of tumor immune surveillance and evasion to develop and apply new anti-tumor cell- based immune therapies, and (3) Develop and administer an innovative portfolio of clinical trials based on rationally-targeted molecular, cellular and immune cancer therapeutics. These aims reflect major working groups and initiatives that coalesces program members with other Cancer Center investigators through inter- programmatic collaborations that result in preclinical and clinical research efforts, grants, and trial protocols. Extensive use of an array of shared resources, in particular, Genomics, Hematopoietic, Cytometry, Athymic, Biostatistics, Transgenic, Tissue, and Translational Research facilitate all aspects of member discoveries. Under the leadership of Jaroslaw Maciejewski (Co-Leader), Marcos de Lima (Co-Leader) and Alex Huang (Co-Leader) the HICB Program has 59 members including 32 full, 7 associate, and 20 clinical members representing 18 different departments across all 3 consortium institutions. Members are funded with a total of $13.4M in grant funding (annual direct costs), of which $8.9M is peer-reviewed and $2.2M is NCI-funded. Between 2012 and 2016, HICB program members published 1,264 publications. Cancer and program related publications included 17% inter-programmatic, 24% intra-programmatic, 5% inter- and intra-programmatic and 6% that involved collaborations with another Cancer Center. This highly effective program has made major practice-changing contributions benefiting cancer patients. Examples include: the discovery of novel driver genes in the evolution of MDS leading to improved disease classification and molecular prognostication; new and effective strategies for MDS treatment emerged using demethylating agents; and members have led a SWOG study identifying significant survival advantage for Inotuzumab ozogamicin in relapsed/refractory ALL. Â

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