Table 2

Clinical predictors of IL-2 response

No response (MR/SD/PD)Response (PR)P
NMedianMinimumMaximumNMedianMinimumMaximum
Age, y 13 61 29 70 20 50 22 72 .044 
No. of prior therapies 13 20 .6 
Prednisone start dose, mg 13 25 40 20 20 50 .9 
No. of cGVHD sites 13 20 .27 
Time from HSCT to start of IL-2, d 13 917 348 2145 20 508 270 1065 .005 
Time from cGVHD to start of IL-2, d 13 461 119 1880 20 249 28 847 .03 
Time from HSCT to cGVHD, d 13 265 153 996 20 266 46 433 .35 
Prednisone dose reduction, week 12, % 13 50 20 25 75 .15 
No response (MR/SD/PD)Response (PR)P
NMedianMinimumMaximumNMedianMinimumMaximum
Age, y 13 61 29 70 20 50 22 72 .044 
No. of prior therapies 13 20 .6 
Prednisone start dose, mg 13 25 40 20 20 50 .9 
No. of cGVHD sites 13 20 .27 
Time from HSCT to start of IL-2, d 13 917 348 2145 20 508 270 1065 .005 
Time from cGVHD to start of IL-2, d 13 461 119 1880 20 249 28 847 .03 
Time from HSCT to cGVHD, d 13 265 153 996 20 266 46 433 .35 
Prednisone dose reduction, week 12, % 13 50 20 25 75 .15 

Additional nonsignificant variables: patient sex, conditioning regimen intensity (MAC, RIC), HLA match (HLA-matched related donor, HLA-matched unrelated donor, mismatched), prior hematologic malignancy (lymphoid, myeloid), specific cGVHD agents (eg, sirolimus, mycophenolate mofetil). Note: Other baseline patient and transplant characteristics listed in Table 1 are not included in this table and none of them was different between PR and no PR at the 0.05 level.

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