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. Author manuscript; available in PMC: 2016 Mar 1.
Published in final edited form as: Transfusion. 2014 Oct 14;55(3):674–679. doi: 10.1111/trf.12881

Table 3. Summary of efficacy, safety, and clinical response outcome data collected at Month 3.

Each row represents cell product data collected from a unique PACT approved project or clinical trial having the unique attributes of cell product type, administration of fresh or cryopreserved cells, and route of administration unless as otherwise footnoted below. A form data entry field without a response was included in the ‘unknown’ category for this analysis. The product source is indicated in parentheses.

Cell Product Type Indication Product Administrations (2010-2014) Efficacy Safety Clinical Response
BM-MNCs (auto, BM-derived)a Cardiovascular 26 Unknown 26 Unknown 26 Unknown 26
CTLs (allo, PB-derived)b Other disease indication 8 Achieved 6 No toxicity 6 Complete 2
Unknown 1 Mild toxicity 1 Unknown 1
Not Applicable 1 Unknown 1 Partial 3
-- -- -- -- None 2
CTLs (allo, BM-derived) Other disease indication 1 Achieved 1 No toxicity 1 Complete 1
HSCs (allo, UCB-derived) Hematology 29 Unknown 29 Unknown 29 Unknown 29
MSCs (allo, BM-derived) Hematology 10 Unknown 10 Unknown 10 Unknown 10
NK cells (auto and allo, leukapheresis) Other disease indication 7 Achieved 1 No toxicity 5 None 5
Not Achieved 5 Unknown 2 Complete 1
Not Applicable 1 -- -- Unknown 1
NK cells (allo, apheresis) BMT 6 Unknown 6 Unknown 6 Unknown 6
Tregs (allo, UCB-derived) BMT 3 Unknown 3 Unknown 3 Unknown 3
Total product administrations with outcome data 90

Source: auto = autologous; allo = allogeneic; BM-derived = bone marrow-derived; PB-derived = peripheral blood-derived; UCB-derived = umbilical cord blood-derived. BM-MNCs = bone marrow mononuclear cells; CTLs = cytotoxic T lymphocytes; DCs = dendritic cells; MSCs = mesenchymal stem/stromal cells; NK = natural killer cells; Tregs = T regulatory cells; UCB-derived HSCs = umbilical cord blood-derived hematopoietic stem cells.

a

Data collected from 2 single-site trials.

b

Data collected from 2 single-site trials, 1 multi-site trial, and from third party use under compassionate use INDs.