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. Author manuscript; available in PMC: 2017 Nov 1.
Published in final edited form as: Curr Opin Hematol. 2016 Nov;23(6):524–529. doi: 10.1097/MOH.0000000000000282

Table 2.

Summary of NMA/RIC and non-HLA-identical HSCT for SCD.

Ref. Study period, n, age range (years) Graft failure Mean donor chimerism, myeloid/T cell compartments Acute GVHD, II-IV Chronic GVHD Overall survival Disease-free survival*
Krishnamurti et al[19] ~1999-2006, n=7, 6-18 14.3% M: 78% (range 76-100%) 28.6% 14.3% 100% 85.7%
T: 68.5% (range 50-90%)

Hsieh et al[20] 2004-2013, n=30, 16-65 13.3% M: 86% (95% CI, 70-100% 0% 0% 96.7% at 3 years 87%
T: 48%, (95% CI, 34-62%)

Horan et al [21] 2009-2013, n=14, 4-16 32% M: 67% (95% CI, 55-80%) 14.3% 14.3% 100% 100%
T: 96% (95% CI, 91-101%) (calculated)

Iannone et al [22] 1999-2001, n=7**, 3-20 14% primary graft failure, 86% secondary graft failure Donor chimerism < 10% in long term follow up for all patients 14.3% 0% 100% 0%

Kamani et al [23] ~2008-2011, n=8, 7.4-16.2 62.5% NR 25% 12.5% 87.5% at 2 years 37.5%

Dallas et al (RIC, haplo cohort) [15] ~2000-2012, n=8, 4.2-13.4 38% Not reported 50% 37.5% 75% at 7 years 38%

Bolanos-Meade et al [24] 2006-2011, n=14 (11 haplo and 3 MRD), 21.4% overall, 43% for haplo Unsorted: 80% T: 71% (calculated) 0% 0% 100% 64.7%
*

defined as not requiring treatment for SCD

**

6 patients with SCD, and 1 patient with thalassemia