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. 2013 Aug 19;3(3):225–238.

Table 1.

HSC and MSC transplantation characteristics

Diagnoses ALL-10, JMML-2, XLP-2, AML-15; AML/MDS-7, NHL-4, WAS-1, OP-1, SCID-1, CML-2, CLL-2, SAA-1, MM-1, SCD-1
Age Median 19 (1 to 69)
(children-25, adults-25)
Gender M:F 28:22 (56%:44%)
HSC matching (n=50) MFD-12
MUD-25
9/10-7
8/10-2
haplo-2
UCB-2
MSC matching (n=74) 3rd party, full mismatched-62
3rd party, haplo-5
Same donor, haplo-2
Same donor, matched-5
aGVHD development d+9 to d+150
aGVHD severity (maximal) grade IV-42
grade II-III-8
Number of systems involved One-9
Two-18
More-21
Other treatments MP (regular ± high dose)-50, CsA-50, tacrolimus-40, rapamycin-8, MMF-40, ATG-27, anti-CD25 mAb-9, ECP-16
MSC delivery i.v. only-72
i.a. + i.v.-2
Average first MSC dose 1.05 (0.3 to 2.25) x10E6 per kg

Abbreviations: ALL - acute lymphoblastic leukemia; AML - acute myeloid leukemia; ATG - antithymocyte globulin (Fresenius or Thymoglobulin); CLL - chronic lymphocytic leukemia; CML - chronic myeloid leukemia; ECP - extracorporeal photopheresis; i.a. - intra-arterial injection; i.v. - intravenous; JMML - juvenile myelomonocytic leukemia; MDS - myelodysplastic syndrome; MFD - matched family donor; MM - multiple myeloma; MMF - mycophenolate mofetil; MP - methyl prednisolone; MUD - matched unrelated donor; NHL - non-Hodgkin’s lymphoma; OP - osteopetrosis; SAA - severe aplastic anemia; SCD - sickle cell disease; SCID - severe combined immune deficiency; UCB - umbilical cord blood; WAS - Wiscott Aldrich Syndrome; XLP - X-linked lymphoproliferative disease.