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. 2019 Sep 3;3(17):2571–2580. doi: 10.1182/bloodadvances.2019000371

Table 3.

Patient clinical characteristics

Patient ID no. Infused VSTs HLA matching Viral disease Reduction in immuno-suppression Prior antiviral(s) Duration prior antiviral therapy Antiviral drug intolerance CMV resistance Change in antiviral post-VST Response by 6 wk Overall outcome
3910 C6790 2/8 No No Ganciclovir 17 No No No CR Sustained CR
3944 C6798 4/8 No No Leflunomide 94 AKI, cytopenia Yes No CR Sustained CR
3976 C6798 6/8 No Yes, reduction in tacrolimus between wk 4 and 6 Foscarnet, ganciclovir 14 Renal tubulopathy Yes (U97 mutation) No CR Sustained CR after second infusion
3762 C6808 5/8 CMV retinitis No None Unable to tolerate Poor graft function Not done Yes, ganciclovir administered for 1 wk CR Sustained CR
3967 C6823 2/8 CMV colitis (diarrhea) No Foscarnet 211 AKI Yes (U97 mutation) No PR Died of renal failure and AdV infection
4091 C6790 5/8 No No Foscarnet, cidofovir, leflunomide 29 AKI Not done No CR Died of renal failure
4115 C6834 5/8 No No Foscarnet 24 AKI Not done No CR Sustained CR
4170 C6790 3/8 No No Ganciclovir, foscarnet 42 Pancreatitis No No CR Sustained CR
4134 C6798 5/8 CMV colitis (diarrhea) No Foscarnet, ganciclovir 17 No Not done No PR Sustained CR
4201 C6814 3/8 No Yes, tacrolimus taper initiated before VST infusion Foscarnet, ganciclovir 41 No No No PR Sustained CR after third infusion

AdV, adenovirus; AKI, acute kidney injury; PR, partial response.