Table 4.

Clinical characteristics of patients with histologic BOOP and control subjects


Characteristic

BOOP patients, N = 49

Control subjects, N = 161

P*
Mean age at HSC transplantation, y   30.1   30.6   .79  
Men, n (%)   38 (78)   105 (65)   .09  
Diagnosis, n (%)    .08  
Acute lymphocytic leukemia   11 (22)   24 (15)   
Acute nonlymphocytic leukemia (ANL)   20 (41)   40 (25)   
Chronic myelogenous leukemia (CML)   11 (22)   48 (30)   
Lymphoma   3 (6)   10 (6)   
Myelodysplastic syndrome (MDS)   3 (6)   15 (9)   
Aplastic anemia   0 (0)   16 (10)   
Other  1 (3)   8 (5)   
Disease activity, n (%)    .39  
Remission   17 (35)   38 (24)   
Relapse   17 (35)   36 (22)   
Acute-phase CML   2 (4)   11 (7)   
Chronic-phase CML   8 (16)   36 (22)   
De novo  1 (2)   3 (2)   
Unknown   4 (8)   37 (23)   
HLA matching, n (%)    .68  
Matched related   29 (59)   100 (62)   
Mismatched related   5 (10)   21 (13)   
Unrelated   15 (31)   40 (25)   
Stem cell source, n (%)    .91  
Bone marrow   45 (92)   150 (93)   
Peripheral blood   3 (6)   9 (6)   
Cord blood   1 (2)   2 (1)   
Preparative regimen, §n (%)    .004  
Cyclophosphamide   0   5 (3)   
Cyclophosphamide, busulfan   4 (8)   27 (17)   
Cyclophosphamide, buffy coat  0   4 (3)   
Cyclophosphamide, ATG   0   6 (4)   
Cyclophosphamide, TBI   8 (17)   9 (6)   
Cyclophosphamide, F-TBI   12 (26)   53 (34)   
Cyclophosphamide, H-TBI   17 (35)   37 (24)   
Thiotepa-containing regimen   4 (9)   2 (1)   
Busulfan, H-TBI   1 (2)   6 (4)   
VP-16, H-TBI   0 (0)   4 (3)   
Other   1 (2)   2 (1)   
GVHD prophylaxis,n (%)    .81  
Cyclosporin   6 (12)   19 (13)   
Methotrexate   9 (19)   22 (15)   
Cyclosporin, methotrexate   27 (56)   91 (61)   
Other   6 (12)   17 (11)   
Recipient CMV antibody-positive,** n (%)   23 (55)   71 (51)   .71  
Donor CMV antibody-positive,** n (%)   20 (48)   63 (45)   .79  
Survival, n (%)    .05  
1-year survival   27 (55)   95 (59)   
5-year survival
 
15 (31)
 
72 (45)
 

 

Characteristic

BOOP patients, N = 49

Control subjects, N = 161

P*
Mean age at HSC transplantation, y   30.1   30.6   .79  
Men, n (%)   38 (78)   105 (65)   .09  
Diagnosis, n (%)    .08  
Acute lymphocytic leukemia   11 (22)   24 (15)   
Acute nonlymphocytic leukemia (ANL)   20 (41)   40 (25)   
Chronic myelogenous leukemia (CML)   11 (22)   48 (30)   
Lymphoma   3 (6)   10 (6)   
Myelodysplastic syndrome (MDS)   3 (6)   15 (9)   
Aplastic anemia   0 (0)   16 (10)   
Other  1 (3)   8 (5)   
Disease activity, n (%)    .39  
Remission   17 (35)   38 (24)   
Relapse   17 (35)   36 (22)   
Acute-phase CML   2 (4)   11 (7)   
Chronic-phase CML   8 (16)   36 (22)   
De novo  1 (2)   3 (2)   
Unknown   4 (8)   37 (23)   
HLA matching, n (%)    .68  
Matched related   29 (59)   100 (62)   
Mismatched related   5 (10)   21 (13)   
Unrelated   15 (31)   40 (25)   
Stem cell source, n (%)    .91  
Bone marrow   45 (92)   150 (93)   
Peripheral blood   3 (6)   9 (6)   
Cord blood   1 (2)   2 (1)   
Preparative regimen, §n (%)    .004  
Cyclophosphamide   0   5 (3)   
Cyclophosphamide, busulfan   4 (8)   27 (17)   
Cyclophosphamide, buffy coat  0   4 (3)   
Cyclophosphamide, ATG   0   6 (4)   
Cyclophosphamide, TBI   8 (17)   9 (6)   
Cyclophosphamide, F-TBI   12 (26)   53 (34)   
Cyclophosphamide, H-TBI   17 (35)   37 (24)   
Thiotepa-containing regimen   4 (9)   2 (1)   
Busulfan, H-TBI   1 (2)   6 (4)   
VP-16, H-TBI   0 (0)   4 (3)   
Other   1 (2)   2 (1)   
GVHD prophylaxis,n (%)    .81  
Cyclosporin   6 (12)   19 (13)   
Methotrexate   9 (19)   22 (15)   
Cyclosporin, methotrexate   27 (56)   91 (61)   
Other   6 (12)   17 (11)   
Recipient CMV antibody-positive,** n (%)   23 (55)   71 (51)   .71  
Donor CMV antibody-positive,** n (%)   20 (48)   63 (45)   .79  
Survival, n (%)    .05  
1-year survival   27 (55)   95 (59)   
5-year survival
 
15 (31)
 
72 (45)
 

 

HLA indicates human lymphocyte antigen; ATG, antithymocyte globulin; TBI, total body irradiation; F-TBI, fractionated TBI; and H-TBI, hyperfractionated TBI.

*

P value from conditional logistic regression.

Other diagnoses include the following: paroxysmal nocturnal hemoglobinuria, multiple myeloma, Ewing sarcoma.

De novo indicates acute leukemia without prior induction chemotherapy.

§

Missing data for 2 case and 6 control subjects.

Buffy coat indicates administration of nonmobilized peripheral blood cells on days 1 through 4 after bone marrow infusion.

Missing data for 1 case and 12 control patients.

**

Missing data for 7 cases and 22 control patients.

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