Table 2

Postinfusion progress of patients receiving CMV-specific T cells

Patient no.Day of infusionDose,107/m2Infusional adverse events, Y/NLast day of follow-upCMV reactivation*
GVHD†
Non-CMV infection‡Y/NRelapse
Other§Y/N
Y/NDayTreatmentY/NDayGradeY/NDay
06213 45 419 46 146 Nil 90, 201 III  
0702 31 239 38 Val    
06205 101 453   220 II  
0735 38 359     174 
0743 38 335 45 Nil 171 II  
0775 59 311     166 
0786 61 288      
07110 68 239      
07141 50 201      
07143 45 214 50 101 Val 87 II  
07138 73 213     137 
07169 61 155      
Patient no.Day of infusionDose,107/m2Infusional adverse events, Y/NLast day of follow-upCMV reactivation*
GVHD†
Non-CMV infection‡Y/NRelapse
Other§Y/N
Y/NDayTreatmentY/NDayGradeY/NDay
06213 45 419 46 146 Nil 90, 201 III  
0702 31 239 38 Val    
06205 101 453   220 II  
0735 38 359     174 
0743 38 335 45 Nil 171 II  
0775 59 311     166 
0786 61 288      
07110 68 239      
07141 50 201      
07143 45 214 50 101 Val 87 II  
07138 73 213     137 
07169 61 155      

Day indicates day after HSCT; and Val, valciclovir.

*

Any positive peripheral blood CMV PCR.

Episodes of acute GVHD after T-cell infusion.

Infectious events not associated with any evidence of CMV reactivation.

§

Includes bone marrow failure day 125 in patient 0702, likely secondary to trimethoprim/sulphamethoxazole, necessitating a second transplantation with death from uncontrolled GVHD on day 239, death from relapse in patient 0735 on day 359, and an episode of hypoxia with uncertain etiology in patient 0743 on day 281.

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