Table 1

Long-term follow-up for RIC allogeneic SCT in CLL

Sorror et al*Dreger et alBrown et alKhouri et al§
No. of patients 82 (n = 64 with 5-y follow-up) 90 76 86 
Median follow-up 5 y 72 mo 5.1 y 37.2 mo 
Time period 1997-2006 2001-2007 1998-2009 1996-2007 
Purine analog refractory disease, % 87 47 55 83 
Cytogenetics n = 7 (del17p), n = 7 (del11q), n = 9 (complex karyotype) 18% del17p, 36% del11q 17% del17p, 8% del11q Not reported 
Disease status SCT 55% refractory disease 21% refractory disease 43% SD/PD 17% refractory disease 
Bulky disease SCT 24% Not reported 21% Not reported 
Conditioning regimen 2-Gy TBI ± fludarabine (URD) Fludarabine + cyclophosphamide ± ATG (URD) Fludarabine + busulphan Fludarabine + cyclophosphamide+ rituximab 
Donor status 37% URD 45% URD 63% URD Not reported 
Relapse rate 38% (5 y) 46% (6 y) 40% (5 y) 39% (3 y) 
PFS 39% (5 y) 38% (6-y EFS) 43% (5 y) 36% (5 y) 
OS 50% (5 y) 58% (6 y) 63% (5 y) 51% (5 y) 
Chronic extensive GVHD 49% sib donor, 53% URD 53% (35/66) 65% (limited + extensive) at 2 y 56% (5 y) 
NRM 23% (5 y) 23% (6 y) 16% (5 y) 17.4% (1 y) 
Reported use of MRD monitoring/DLI No Yes No Yes 
Impact of pre-SCT cytogenetics on SCT outcomes No impact No impact No impact Not assessed 
Prognostic factors that influenced outcome Model to predict 3-y inferior OS: LN size ≥5 cm, HCT CI score ≥1 Model to predict inferior EFS, OS, NRM: refractory disease at SCT, use of alemtuzumab prior to SCT Model to predict inferior PFS: disease status at SCT, LDH, comorbidity, ALC Model to predict inferior OS: hypogammaglobulinemia, CD4 <100/mm3 
Sorror et al*Dreger et alBrown et alKhouri et al§
No. of patients 82 (n = 64 with 5-y follow-up) 90 76 86 
Median follow-up 5 y 72 mo 5.1 y 37.2 mo 
Time period 1997-2006 2001-2007 1998-2009 1996-2007 
Purine analog refractory disease, % 87 47 55 83 
Cytogenetics n = 7 (del17p), n = 7 (del11q), n = 9 (complex karyotype) 18% del17p, 36% del11q 17% del17p, 8% del11q Not reported 
Disease status SCT 55% refractory disease 21% refractory disease 43% SD/PD 17% refractory disease 
Bulky disease SCT 24% Not reported 21% Not reported 
Conditioning regimen 2-Gy TBI ± fludarabine (URD) Fludarabine + cyclophosphamide ± ATG (URD) Fludarabine + busulphan Fludarabine + cyclophosphamide+ rituximab 
Donor status 37% URD 45% URD 63% URD Not reported 
Relapse rate 38% (5 y) 46% (6 y) 40% (5 y) 39% (3 y) 
PFS 39% (5 y) 38% (6-y EFS) 43% (5 y) 36% (5 y) 
OS 50% (5 y) 58% (6 y) 63% (5 y) 51% (5 y) 
Chronic extensive GVHD 49% sib donor, 53% URD 53% (35/66) 65% (limited + extensive) at 2 y 56% (5 y) 
NRM 23% (5 y) 23% (6 y) 16% (5 y) 17.4% (1 y) 
Reported use of MRD monitoring/DLI No Yes No Yes 
Impact of pre-SCT cytogenetics on SCT outcomes No impact No impact No impact Not assessed 
Prognostic factors that influenced outcome Model to predict 3-y inferior OS: LN size ≥5 cm, HCT CI score ≥1 Model to predict inferior EFS, OS, NRM: refractory disease at SCT, use of alemtuzumab prior to SCT Model to predict inferior PFS: disease status at SCT, LDH, comorbidity, ALC Model to predict inferior OS: hypogammaglobulinemia, CD4 <100/mm3 

ALC, absolute lymphocyte count; ATG, anti-thymocyte globulin; CLL, chronic lymphocytic leukemia; DLI, donor lymphocyte infusion; EFS, event-free survival; GVHD, graft-versus-host disease; HCT CI, hematopoietic cell transplant comorbidity index; LDH, lactate dehydrogenase; LN, lymph node; MRD, minimal residual disease; NRM, nonrelapse mortality; OS, overall survival; PD, progressive disease; PFS, progression-free survival; RIC, reduced-intensity conditioning; SCT, stem cell transplantation; SD, stable disease; TBI, total body irradiation; URD, unrelated donor.

*

Please see Sorror et al.35 

Please see Dreger et al.36,50 

Please see Brown et al.47 

§

Please see Khouri et al.52 

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