? CORE B Core B, Pharmaceutical Production, is responsible for the production of the monoclonal antibodies (MAbs), the antibody conjugates, the alpha-emitting radionuclide astatine-211 (211At) and the 211At-labeled antibody conjugates. The Core will produce anti-CD45 and anti-CD38 MAbs used in preclinical studies (Projects 1, 2 and 3) and produce clinical grade anti-human CD45 BC8 MAb and anti-human CD38 OKT10 MAb used in clinical trials (Projects 2 and 3). The MAbs will be conjugated with a novel reagent (B10-NCS) to produce MAb-B10 conjugates for radiolabeling with astatine-211 (211At). All MAbs and clinical grade reagents will be produced, purified and vialed in the Biologics Production Facility (BPF) of the Fred Hutch. The B10-NCS reagent and MAb-B10 conjugates used for preclinical studies will be produced in appropriate chemical laboratories at the University of Washington. Clinical grade BC8-B10 conjugate and OKT10-B10 will be produced, purified and vialed under current good manufacturing practice (cGMP) conditions in the Fred Hutch BPF. Production, isolation and purification of the 211At will be done in the UW Medical Cyclotron Facility and UW Radionuclide Production Laboratory. The 211At-MAb-B10 for preclinical studies will be conducted in UW radiochemistry laboratory, and 211At-BC8-B10 and 211At-OKT10-B10 used in the clinical trials will be produced in a cGMP facility at UW. Testing of the materials produced will be conducted at UW or Fred Hutch, depending on the assay. Patient samples obtained from Projects 2 and 3 will be collected, processed and stored at the Fred Hutch for use in Project 1.

Public Health Relevance

- Core B The radiolabeled antibodies produced under federally approved methods in Core B are critical for use in key clinical trials in patients, which will ultimately lead to development of minimally toxic hematopoietic cell transplant regimens for the treatment of patients with blood-based cancers. Production of these antibodies is made possible through the use of unique facilities at the Fred Hutch and the University of Washington.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA078902-22
Application #
10025204
Study Section
Special Emphasis Panel (ZCA1)
Project Start
1999-04-12
Project End
2025-06-30
Budget Start
2020-09-10
Budget End
2021-06-30
Support Year
22
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
078200995
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
Maffini, Enrico; Anderson Jr, Larry D; Sandmaier, Brenda M et al. (2018) Non-myeloablative allogeneic hematopoietic cell transplantation for relapsed or refractory Waldenström macroglobulinemia: evidence for a graft-versus-lymphoma effect. Haematologica 103:e252-e255
Li, Yawen; Hamlin, Donald K; Chyan, Ming-Kuan et al. (2018) cGMP production of astatine-211-labeled anti-CD45 antibodies for use in allogeneic hematopoietic cell transplantation for treatment of advanced hematopoietic malignancies. PLoS One 13:e0205135
Bar, Merav; Flowers, Mary E D; Storer, Barry E et al. (2018) Reversal of Low Donor Chimerism after Hematopoietic Cell Transplantation Using Pentostatin and Donor Lymphocyte Infusion: A Prospective Phase II Multicenter Trial. Biol Blood Marrow Transplant 24:308-313
Graves, Scott S; Parker, Maura H; Stone, Diane et al. (2018) Anti-Inducible Costimulator Monoclonal Antibody Treatment of Canine Chronic Graft-versus-Host Disease. Biol Blood Marrow Transplant 24:50-54
Hill, Joshua A; Mayer, Bryan T; Xie, Hu et al. (2017) The cumulative burden of double-stranded DNA virus detection after allogeneic HCT is associated with increased mortality. Blood 129:2316-2325
Venkataraman, G M; Kennedy, L J; Little, M-T E et al. (2017) Thirteen novel canine dog leukocyte antigen-88 alleles identified by sequence-based typing. HLA 90:165-170
McDonald, George B; Tabellini, Laura; Storer, Barry E et al. (2017) Predictive Value of Clinical Findings and Plasma Biomarkers after Fourteen Days of Prednisone Treatment for Acute Graft-versus-host Disease. Biol Blood Marrow Transplant 23:1257-1263
Hill, Joshua A; Magaret, Amalia S; Hall-Sedlak, Ruth et al. (2017) Outcomes of hematopoietic cell transplantation using donors or recipients with inherited chromosomally integrated HHV-6. Blood 130:1062-1069
Green, Damian J; Maloney, David G; Storer, Barry E et al. (2017) Tandem autologous/allogeneic hematopoietic cell transplantation with bortezomib maintenance therapy for high-risk myeloma. Blood Adv 1:2247-2256

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