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. 2018 Feb 22;67(4):533–540. doi: 10.1093/cid/ciy152

Table 3.

Comparison of Early Versus Late Infections After Chimeric antigen receptor T-cell infusion

Earlya (Day 0–30) (n = 53) Late (Day 31–180) (n = 32)b
Infections, No. Patients, No. (%) Infections, No. Patients, No. (%)
Any infection 26 22 (42)c 15 10 (31)d
Bacterial
 Bloodstreame 8 7 (13) 1 1 (3)
 Bacterial sitef 9 9 (17) 4 4 (13)
Fungal
 Yeastg 1 1 (2) 0 0 (0)
 Moldh 3 3 (6) 1 1 (3)
Viral
 Respiratory virusi 3 3 (6) 8 8 (25)
 Other virusj 2 2 (4) 1 1 (3)

aDay 0 was the day of Chimeric antigen receptor T-cell infusion (CTI).

bPatients with complete remission after CTI.

cTwo patients had >1 infection.

dThree patients had >1 infection.

eEarly bloodstream infections included 3 vancomycin-resistant Enterococcus faecium (VRE) and 2 extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli infections and 1 each of the following infections: Gordonia sputi, Klebsiella pneumoniae, and Stenotrophomonas maltophilia. The single late bloodstream infection was VRE.

fEarly bacterial infections included 4 cases of Clostridium difficile diarrhea, 2 cases of ventilator-associated pneumonia (1 K. pneumoniae, 1 multidrug-resistant Pseudomonas aeruginosa), and 1 case each of acute cholecystitis, pyelonephritis (carbapenemase-producing K. pneumoniae), and chest wall abscess. The late bacterial infections included 1 case each of C. difficile diarrhea, hospital-acquired pneumonia (carbapenemase-producing K. pneumoniae), cystitis (multidrug-resistant P. aeruginosa), and cellulitis.

gThe single yeast infection (early) was Saccharomyces cerevisiae fungemia.

hEarly mold infections included 2 cases of probable pulmonary aspergillosis (1 Aspergillus fumigatus and 1 patient with elevated serum and bronchoalveolar galactomannan levels but no recovered organism) and 1 case of proven pulmonary mucormycosis. The single late mold infection was probable pulmonary aspergillosis (patient had elevated serum galactomannan levels but no recovered organism).

iEarly respiratory virus infections included 2 parainfluenza virus and 1 rhinovirus/enterovirus infection. Late respiratory virus infections included 1 coronavirus, 2 influenza A, 4 rhinovirus/enterovirus, and 1 unknown infection.

jEarly infections with nonrespiratory viruses included 1 herpes simplex virus (orolabial) and 1 varicella zoster virus (shingles) infection. The single late infection was BK virus (hematuria).