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. 2022 Mar 31;6(7):2167–2182. doi: 10.1182/bloodadvances.2021006035

Table 1.

Demographic characteristics of 38 patients with non-CNS EMD identifiable by FDG PET/CT imaging at presentation to our institution

Characteristic Value
Age at initial diagnosis, median (range), y 11.5 (2.5-27.4)
Age at presentation to our institution, median (range), y 18.6 (4.7-30.7)
Sex, n (%)
 Male 27 (71.1)
 Female 11 (28.9)
EMD at initial diagnosis, n (%)
 CNS EMD 3 (7.8)
 Non-CNS EMD 5 (13.2)
 Combined CNS/non-CNS EMD 2 (5.3)
 Unknown 28 (68.4)
Prior number of lines of therapy, median (range) 5 (2-9)
Prior HSCT (n = 27), n (%)
 1 22 (60.5)
 >1 5 (13.2)
Prior immunotherapy (n = 23), n (%)
 Prior blinatumomab 16 (42.1)
 Prior inotuzumab 7 (18.4)
Prior CAR T-cell therapy (n = 13), n (%)
 Prior anti–CD19 CAR 12 (31.6)
 Prior anti–CD22 CAR 1 (2.6)
Medullary disease at presentation, n (%) *
 MRD-negative 5 (13.2)
 Low burden 13 (34.2)
 High burden 20 (52.6)
CNS status at presentation, n (%)
 CNS1/CNS2 35 (92.1)
 CNS3 3 (7.9)
Non-CNS EMD at presentation, n (%)
 Single site 12 (31.6)
 Multiple sites 26 (68.4)
Indication for FDG PET/CT imaging, n (%)
 Documented history of non-CNS EMD 23 (60.5)
 Incidental finding on other imaging 8 (21.1)
 Abnormal physical examination 4 (10.5)
 Isolated CNS relapse with suspected non-CNS EMD 3 (7.9)
*

MRD-negative indicates no disease detectable by flow cytometry. Low burden includes M1 marrow (<5% blasts); high burden indicates M2 (5%-25% blasts) and M3 (>25% blasts) marrow.

CNS1 indicates 0 blasts detectable on cytospin; CNS2, white blood cell counts <5/μL, cytospin positive for blasts; and CNS3, white blood cell counts ≥5 μL, cytospin positive for blasts.