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. Author manuscript; available in PMC: 2022 Oct 5.
Published in final edited form as: Cancer Discov. 2021 Feb 16;11(6):1440–1453. doi: 10.1158/2159-8290.CD-20-1465

Table 1.

Patient demographics and disease characteristics at baseline

Characteristic All patients (N = 47)
Median age (range), y 29 (6–72)

Male sex, n (%)a 29 (61.7)

Race, n (%)a
 White 36 (83.7)
 Black or African American 3 (7.0)
 Other 4 (8.5)
 Missing 4 (8.5)

Type of primary cancer, n (%)a
 ALL 44 (93.6)
 B-ALL 25 (53.2)
 T-ALL 19 (40.4)
 LL 3 (6.4)
 B-LL 1 (2.1)
 T-LL 2 (4.3)

ECOG performance status, n (%)a
 0 4 (13.8)
 1 21 (72.4)
 2 4 (13.8)
 Missing 18 (38.3)

Median prior lines of therapy (range) 4 (1–10)

Key prior treatments, n (%)
 Asparaginase or PEG-asparaginase 28 (59.6)
 Blinatumomab 13 (27.7)
 Inotuzumab ozogamicin 7 (14.9)
 CAR T-cell therapy 6 (12.8)
 Daratumumab 1 (2.1)
 Venetoclax 4 (8.5)

Prior transplant, n (%) 13 (27.7)

Median time from diagnosis to first dose (range), mo 24.7 (1.4–170.3)

Median time since last prior therapy (range), mo 1.5 (0.1–21.2)

Bone marrow blasts
 Median (range), % 51.7 (0.0–99.0)
 Patients with <5%, n (%)b 7 (14.9)
a

Percentages calculated based on total number of patients with available data.

b

Includes all patients (ALL and LL). Patients with relapsed/refractory ALL and LL with measurable disease, as defined as any measurable bone marrow blast percentage or detectable minimal residual disease, were allowed to enroll.

Abbreviations: ALL, acute lymphoblastic leukemia; B-ALL, B-cell acute lymphoblastic leukemia; B-LL, B- cell lymphoblastic lymphoma; CAR, chimeric antigen receptor; ECOG, Eastern Cooperative Oncology Group; LL, lymphoblastic lymphoma; T-ALL, T-cell acute lymphoblastic leukemia; T-LL, T-cell lymphoblastic lymphoma.