Table 1.

Clinical characteristics of the patients

Patient numberDiagnosisAgeConditioning*Rejection prophylaxisGVHD prophylaxis
CyA (months)
GVHD a/c1-153
ALL 17 Cy-TBI  (12) TLI, MP 0/0 
ALL 17 Cy-TBI  (12) TLI, MP — 0/0 
AML 20 Cy-TBI  (13.5) TLI, MP 0/0 
AML 29 Cy-TBI  (13.5) TLI, MP 0/0 
AML 35 Cy-TBI  (12) MP 0/0 
AML 44 Cy-TBI  (12) — 0/0 
AML 44 Bu-Cy MP 19 1/+ 
MM 45 Cy-TBI  (12) MP 1/0 
AML 48 Cy-TBI  (12) MP 0/0 
10 AML 52 Cy-TBI  (12) MP 0/0 
Patient numberDiagnosisAgeConditioning*Rejection prophylaxisGVHD prophylaxis
CyA (months)
GVHD a/c1-153
ALL 17 Cy-TBI  (12) TLI, MP 0/0 
ALL 17 Cy-TBI  (12) TLI, MP — 0/0 
AML 20 Cy-TBI  (13.5) TLI, MP 0/0 
AML 29 Cy-TBI  (13.5) TLI, MP 0/0 
AML 35 Cy-TBI  (12) MP 0/0 
AML 44 Cy-TBI  (12) — 0/0 
AML 44 Bu-Cy MP 19 1/+ 
MM 45 Cy-TBI  (12) MP 1/0 
AML 48 Cy-TBI  (12) MP 0/0 
10 AML 52 Cy-TBI  (12) MP 0/0 

ALL indicates acute lymphocytic leukemia; AML, acute myelogenous leukemia; MM, multiple myeloma.

*

Cy indicates cyclophosphamide (120 mg/kg or 200 mg/kg in combination with busulfan (Bu) (4 daily doses of 4 mg/kg body weight, Mesna was used systematically). TBI indicates total body irradiation (Gy given in 6 doses).

TLI indicates total lymphoid irradiation (6 Gy at day −5 and −4); MP indicates methyl prednisolone (4 × 1 g/m2).

GVHD prophylaxis consisted of in vitro T-cell depletion with Campath 1M and Cyclosporin A (CyA) with a trough at 200 ng/mL.

F1-153

a/c indicates acute/chronic.

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