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. Author manuscript; available in PMC: 2014 Sep 1.
Published in final edited form as: Leukemia. 2013 Aug 30;28(3):658–665. doi: 10.1038/leu.2013.253

Table 1.

Characteristics of adults with Ph+ ALL who received reduced intensity conditioning (RIC) allogeneic donor HCT in CR1 between 2000–2009 and a matched cohort receiving myeloablative (MAC) allogeneic HCT

Variable RIC MAC P-value
Number of patients 67 130
Number of centers 30 66
Age, median (range) 54 (19–69) 50 (19–66) 0.02
Sex 0.94
  Male 37 (55) 71 (55)
  Female 30 (45) 59 (45)
Karnofsky score 0.36
  < 80% 8 (12) 8 (6)
  80 – 100% 54 (81) 113 (87)
  Missing 5 (7) 9 (7)
HCT Comorbidity Index 0.03
  0 54 (81) 119 (92)
  ≥1 13 (19) 11 (8)
Fungal infection prior to HCT 0.006
  No 57 (85) 126 (97)
  Yes 8 (12) 4 (3)
  Missing 2 (3) 0
WBC at diagnosis, ×10^9/L 0.23
  < 30 41 (61) 70 (54)
  30 – 100 14 (21) 23 (18)
  > 100 5 (7) 24 (18)
  Missing 7 (10) 13 (10)
Cytogenetic abnormalities 0.34
  t(9:22) only 32 (48) 48 (37)
  t(9:22) and other 25 (37) 58 (45)
  Other 4 (6) 5 (4)
  Missing 6 (9) 19 (15)
Time from diagnosis to 1st complete remission 0.76
  Median (interquartile range) in days 42 (34–82) 52 (31–111)
  Missing 1 (1) 7 (5)
Time from diagnosis to transplant 0.02
  ≤ 5 months 20 (30) 64 (49)
  > 5 months 46 (69) 66 (51)
  Missing 1 (1) 0
Minimal residual disease pre-HCT
  FISH tested 59 (88) 113 (87) 0.75
    FISH neg/tested for MRD 36/59 (54) 63/113 (48)
    FISH pos/tested for MRD 23/59 (34) 50/113 (38)
  FISH not performed or unknown 8 (12) 17 (13)
  BCR/ABL PCR tested 42 (63) 82 (63) 0.73
    PCR neg/tested for MRD 21/42 (50) 46/82 (35)
    PCR pos/tested for MRD 21/42 (50) 36/82 (28)
    PCR not performed or unknown 24 (36) 48 (37)
  MRDneg** 26 (39) 58 (49) 0.79
  MRDpos* 39 (58) 62 (47)
TKI use prior to HCT 0.71
     No 16 (24) 28 (22)
     Yes 51 (76) 102 (78)
Duration of TKI pre HCT, months 0.41
     Median (range) 7 (1–12) 6 (1–54)
     <6 month 28 (42) 66 (51)
     ≥6 month 15 (22) 18 (14)
     TKI not given or unknown 24 (36) 48 (36)
Conditioning regimen N/A
  MAC
     TBI>500 cGy single dose or > 800cGy 0 108 (83)
     Busulfan > 9 mg/kg + other 0 22 (17)
  RIC (includes non-myeloablative)
     Melphalan ≤ 150 mg/m2 24 (36) 0
     Busulfan ≤ 9 mg/kg 20 (30) 0
     TBI ≤ 200 cGy dose# 18 (26) 0
     Fludarabine + other 5 (7) 0
Total body irradiation N/A
     No 45 (67) 22 (17)
     Yes 21 (31) 108 (83)
     Missing 1 (1) 0
Type of donor 0.10
     HLA - identical sibling 26 (39) 50 (38)
     Well - matched URD 28 (42) 54 (42)
     Partially – matched/ mismatched URD 5 (7) 21 (16)
     URD (matching unknown) 8 (12) 5 (4)
Donor –Recipient sex match 0.79
     Male-Male 22 (33) 47 (36)
     Male-Female 18 (27) 40 (31)
     Female-Male 15 (22) 24 (18)
     Female-Female 12 (18) 18 (14)
     Missing 0 1 (<1)
Donor-Recipient CMV match 0.55
     Donor positive/Recipient positive 27 (40) 39 (30)
     Donor positive/Recipient negative 9 (13) 15 (12)
     Donor negative/Recipient positive 14 (21) 35 (27)
     Donor negative/Recipient negative 15 (22) 38 (29)
     Missing 2 (3) 3 (2)
Graft type 0.12
     Bone marrow 15 (22) 43 (33)
     Peripheral blood 52 (78) 87 (67)
Year of transplant 0.53
     2001–2004 40 (59) 70 (54)
     2005–2009 27 (41) 60 (46)
GVHD prophylaxis 0.36
     Tacrolimus ± other 61 (46) 72 (58)
     Cyclosporine ± other 30 (45) 47 (36)
     ATG/alemtuzumab 25 (37) 23 (17) 0.032
     Other 6 (8) 9 (7)
Median follow-up of survivors: months (range) 49 (3–108) 61 (3–119)
Post-transplant therapy
Any TKI given as maintenance post-HCT 0.02
     No 46 (69) 108 (83)
     Yes 21 (31) 22 (17)
Duration of TKI given for maintenance post-HCT 0.05
     < 3 months 7 (10) 4 (3)
     3–12 months 9 (13) 9 (7)
     ≤ 12 months 4 (6) 9 (7)
*

Includes both FISH and/or BCR/ABL PCR positive,

**

Includes FISH negative and BCR/ABL PCR negative or missing,

#

one patient received TBI <500 cGy single dose

Abbreviations: ALL acute lymphoblastic leukemia, RIC reduced intensity conditioning, MAC myeloablative conditioning, HCT hematopoietic cell transplantation, MRD minimal residual disease, TKI tyrosine kinase inhibitor, CMV cytomegalovirus, TBI total body irradiation, GVHD graft versus host disease,