The objective of this project is to reduce the late morbidity and mortality of hematopoietic stem cell transplantation. The major determinants of these late complications include treatment-related toxicities, immunodeficiency and chronic graft-versus-host disease (GVHD). To date, 385 stem cell recipients have been followed annually for up to 25 years after transplantation for aplastic anemia and allied hematologic diseases. Among this cohort (including 105 patients currently more than 10 years posttransplant), late complications included: chronic GVHD (n=179), lung disease (n=67), cataracts (n=47), depression (n=46), bone disease (n=35), lithiasis (n=26), secondary neoplasms (n=10), and major or moderate infections (n-1626 episodes). Accordingly, we propose four interrelated specific aims; 1) Monitor late events and complications after stem cell transplantation and determine the dynamics of psychosocial recovery. In addition, patients will participate in studies of the mechanisms of posttransplant lung disease, pediatric growth and development, and secondary malignancies following transplantation; 2) Reduce infections and mortality after unrelated transplantation in a placebo controlled trial of immunoglobulin prophylaxis. Other studies will evaluate new diagnostic and interventive methods to reduce the morbidity of posttransplant cataract and bone disease; 3) Prevent development of chronic GVHD by novel approaches to long-term immunosuppression and early adjunctive therapy of acute GVHD with ultraviolet radiation; 4) Improve treatment of chronic GVHD by evaluating the efficacy of FK-506, thalidomide, rapamycin and mycophenolate mofetil in an integrated series of pilot and Phase III clinical trials. Concern for the late effects of stem cell transplantation is especially important as new disease indications, preparative regimens and stem cell sources are explored. Although overall survival has improved in recent years, investigation of the late morbidity of transplantation is vital for the well-being of the stem cell recipient.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL036444-19
Application #
6202262
Study Section
Project Start
1999-08-01
Project End
2000-07-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
19
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
075524595
City
Seattle
State
WA
Country
United States
Zip Code
98109
McCune, Jeannine S; Storer, Barry; Thomas, Sushma et al. (2018) Inosine Monophosphate Dehydrogenase Pharmacogenetics in Hematopoietic Cell Transplantation Patients. Biol Blood Marrow Transplant 24:1802-1807
Thakar, M S; Bonfim, C; Walters, M C et al. (2017) Dose-adapted post-transplant cyclophosphamide for HLA-haploidentical transplantation in Fanconi anemia. Bone Marrow Transplant 52:570-573
Burroughs, Lauri M; Shimamura, Akiko; Talano, Julie-An et al. (2017) Allogeneic Hematopoietic Cell Transplantation Using Treosulfan-Based Conditioning for Treatment of Marrow Failure Disorders. Biol Blood Marrow Transplant 23:1669-1677
Vaughn, J E; Anwer, F; Deeg, H J (2016) Treatment of refractory ITP and Evans syndrome by haematopoietic cell transplantation: is it indicated, and for whom? Vox Sang 110:5-11
Aki, S Z; Inamoto, Y; Carpenter, P A et al. (2016) Confounding factors affecting the National Institutes of Health (NIH) chronic Graft-Versus-Host Disease Organ-Specific Score and global severity. Bone Marrow Transplant 51:1350-1353
Khera, Nandita; Gooley, Ted; Flowers, Mary E D et al. (2016) Association of Distance from Transplantation Center and Place of Residence on Outcomes after Allogeneic Hematopoietic Cell Transplantation. Biol Blood Marrow Transplant 22:1319-1323
Karoopongse, Ekapun; Marcondes, A Mario; Yeung, Cecilia et al. (2016) Disruption of Iron Regulation after Radiation and Donor Cell Infusion. Biol Blood Marrow Transplant 22:1173-1181
Hoffmeister, P A; Storer, B E; Syrjala, K L et al. (2016) Physician-diagnosed depression and suicides in pediatric hematopoietic cell transplant survivors with up to 40 years of follow-up. Bone Marrow Transplant 51:153-6
Gallo, S; Woolfrey, A E; Burroughs, L M et al. (2016) Marrow grafts from HLA-identical siblings for severe aplastic anemia: does limiting the number of transplanted marrow cells reduce the risk of chronic GvHD? Bone Marrow Transplant 51:1573-1578
Festuccia, Moreno; Deeg, H Joachim; Gooley, Theodore A et al. (2016) Minimal Identifiable Disease and the Role of Conditioning Intensity in Hematopoietic Cell Transplantation for Myelodysplastic Syndrome and Acute Myelogenous Leukemia Evolving from Myelodysplastic Syndrome. Biol Blood Marrow Transplant 22:1227-1233

Showing the most recent 10 out of 788 publications