Project 1 will serve to translate concepts developed in other Projects to the clinic and build upon our priorwork on developing novel strategies to improve outcomes in patients undergoing allogeneic hematopoieticcell transplantation (HCT). The concepts developed will likely benefit patients with serious hematologicalmalignancies but could also provide novel treatment strategies for patients with severe autoimmunedisorders and those undergoing solid organ transplantation. Therefore, the concepts developed are broadand have significant implications for a number of fields. We will build upon our successful translation of thestudies developed in Project 4 where the novel non-myeloablative regimen of total lymphoid irradiation (TLI)and anti-thymocyte globulin (ATG) has been explored with marked reduction in acute graft vs host disease(GVHD) risk with retained graft vs tumor (GVT) responses, The TLI/ATG regimen will be tested as comparedto standard chemotherapy in older (ages 50-75) patients with AML in first CR in a multi-institutional phase IIItrial with those patients with HLA matched sibling donors receiving allogeneic HCT and those without treatedwith standard chemotherapy (Specific Aim #1). We will attempt to augment the TLI/ATG regimen in twoimportant ways by utilizing prophylactic administration of cytokine induced killer (CIK) cells developed inProject 3 in an effort to reduce relapse risk in patients with high risk myeloid malignancies (Specific Aim #2).A second approach will be to utilize the anti-CD20 monoclonal antibody rituximab in combination withTLI/ATG in patients with mantle cell lymphoma and chronic lymphocytic leukemia to explore whether thiscombined approach will reduce chronic GVHD and disease relapse (Specific Aim #3). Finally we willtranslate basic observations in regulatory T cell biology where we have observed that cyclosporine A has amajor impact on Treg function whereas rapamycin and MMF do not. We will test the combination ofRAPA/MMF following myeloablative HCT in patients with high risk malignancies in an effort to reduce GVHDrisk. This Project interacts with all of the other Projects and utilizes all four of the Cores.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA049605-19
Application #
7212894
Study Section
Special Emphasis Panel (ZCA1-RPRB-7 (O5))
Project Start
2007-03-01
Project End
2012-02-29
Budget Start
2007-04-05
Budget End
2008-03-31
Support Year
19
Fiscal Year
2007
Total Cost
$213,006
Indirect Cost
Name
Stanford University
Department
Type
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
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