Table 1.

Characteristics and outcomes of patients with cancer and chemotherapy associated TMA

PatientAge/ sexType of cancerChemotherapy duration (mo)ADAMTS 13 activity (%)Platelet count (G/L)Hemoglobin (g/dL)LDHSerum creatinineHematological responseRenal responseSerum creatinine at end of follow-upTreated with eculizumab (duration)Eculizumab continued/ stoppedChemotherapy restartedStatus (duration of follow-up)Genetics
61/M Pancreatic 21 87 5.9 547 2.0 2.2 Y/13 mo Continued Alive/24 mo No variants 
73/F Pancreatic 12 96 21 7.7 742 2.5 1.4 Y/13 wk Stopped Unknown Alive/3 mo No variants 
55/M SCC of Nasal Cavity 17 56 29 6.8 695 4.5 Y/2 wk Stopped Deceased/6 mo No variants 
67/F Ovarian 79 199 5.9 797 4.2 2.1 Y/41 mo Continued Alive/41 mo N/A 
53/F Germ cell tumor <1 42 43 6.3 3459 4.8 Y/Unknown Continued Unknown No rare pathogenic variant  
54/M Prostate N/A 100 11 7.4 5280 13.5 1.33 Y/12 mo Stopped Alive/32 mo No variants 
69/M DLBCL N/A 15 17 6.5 676 2.3 1.4 Y/6 wk Continued Deceased/65 mo No variants 
PatientAge/ sexType of cancerChemotherapy duration (mo)ADAMTS 13 activity (%)Platelet count (G/L)Hemoglobin (g/dL)LDHSerum creatinineHematological responseRenal responseSerum creatinine at end of follow-upTreated with eculizumab (duration)Eculizumab continued/ stoppedChemotherapy restartedStatus (duration of follow-up)Genetics
61/M Pancreatic 21 87 5.9 547 2.0 2.2 Y/13 mo Continued Alive/24 mo No variants 
73/F Pancreatic 12 96 21 7.7 742 2.5 1.4 Y/13 wk Stopped Unknown Alive/3 mo No variants 
55/M SCC of Nasal Cavity 17 56 29 6.8 695 4.5 Y/2 wk Stopped Deceased/6 mo No variants 
67/F Ovarian 79 199 5.9 797 4.2 2.1 Y/41 mo Continued Alive/41 mo N/A 
53/F Germ cell tumor <1 42 43 6.3 3459 4.8 Y/Unknown Continued Unknown No rare pathogenic variant  
54/M Prostate N/A 100 11 7.4 5280 13.5 1.33 Y/12 mo Stopped Alive/32 mo No variants 
69/M DLBCL N/A 15 17 6.5 676 2.3 1.4 Y/6 wk Continued Deceased/65 mo No variants 

F, female; M, male; N, no; N/A, not applicable; Y, yes.

Patient 4 had a variant of uncertain significance in CFI (c.1246A>C, p.Ile416Leu, heterozygous) reported on clinical sequencing completed at Cincinnati Children’s Hospital. This was also detected on research sequencing but not considered positive for a rate variant in our analysis because the minor allege frequency was not <0.005 in any ethnic population, our threshold for calling a rare germline variant.

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