Table 3.

Adverse events of special interest

Acute GVHD
DLOrganEnrollees, n (%)Onset in relation to infusionMax overall gradeSystemic steroidsOutcome
DL2 and DL5 Skin 2 of 24 (8) 7 d after infusion for both No Resolved in 1 wk for both 
DL2 Upper GI 1 of 24 (4) 14 d after infusion Yes Resolved in 2 wk, steroid treatment discontinued 
Acute GVHD
DLOrganEnrollees, n (%)Onset in relation to infusionMax overall gradeSystemic steroidsOutcome
DL2 and DL5 Skin 2 of 24 (8) 7 d after infusion for both No Resolved in 1 wk for both 
DL2 Upper GI 1 of 24 (4) 14 d after infusion Yes Resolved in 2 wk, steroid treatment discontinued 
Chronic GVHD
DLOrganEnrollees, n (%)Onset in relation to infusionMax overall severitySystemic treatmentOutcome
DL1 Vaginal 1 of 24 (4) 1 y after infusion Mild No Ongoing 
DL3 Skin 1 of 24 (4) 9 mo after infusion Mild No Ongoing 
DL3 Joint 1 of 24 (4) 9 mo after infusion Mild No Ongoing 
DL3 Eyes 1 of 24 (4) 9 mo after infusion Mild No Ongoing 
CRS None at any dose level 
Neurotoxicity None at any dose level 
Myelotoxicity (cytopenias persisting >28 d) None at any dose level 
Chronic GVHD
DLOrganEnrollees, n (%)Onset in relation to infusionMax overall severitySystemic treatmentOutcome
DL1 Vaginal 1 of 24 (4) 1 y after infusion Mild No Ongoing 
DL3 Skin 1 of 24 (4) 9 mo after infusion Mild No Ongoing 
DL3 Joint 1 of 24 (4) 9 mo after infusion Mild No Ongoing 
DL3 Eyes 1 of 24 (4) 9 mo after infusion Mild No Ongoing 
CRS None at any dose level 
Neurotoxicity None at any dose level 
Myelotoxicity (cytopenias persisting >28 d) None at any dose level 

CRS, cytokine release syndrome; Max, maximum grade seen in any of the patients at the indicated dose level.

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