Baseline patient characteristics of cohort
Parameter . | n (%) Total cohort = 11 . |
---|---|
Age at initial diagnosis, y | |
<1 | 3 (27) |
1-9.9 | 7 (64) |
≥10 | 1 (9) |
Sex | |
Female | 4 (36) |
Male | 7 (64) |
Ethnicity | |
Not Hispanic or Latino | 5 (45) |
Hispanic or Latino | 6 (55) |
Initial diagnosis | |
Standard-risk ALL | 5 (45) |
High-risk ALL | 5 (45) |
CD19+ MPAL | 1 (9) |
Cytogenetics | |
KMT2A rearranged∗ | 3 (27) |
Philadelphia-chromosome positive | 2 (18) |
Philadelphia-like (CRLF2 fusion) | 2 (18) |
Hyperdiploidy | 2 (18) |
Hypodiploidy | 1 (9) |
iAMP21 | 1 (9) |
Remission status | |
CR1 | 9 (82) |
CR2 | 2 (18) |
MRD status before blinatumomab† | |
Negative | 10 (91) |
Positive | 1 (9) |
Reason for blinatumomab | |
Toxicity precluding chemotherapy | 4 (36) |
Other | 7 (64) |
Therapy before blinatumomab | |
Induction | 6 (55) |
Additional therapy | 5 (45) |
Parameter . | n (%) Total cohort = 11 . |
---|---|
Age at initial diagnosis, y | |
<1 | 3 (27) |
1-9.9 | 7 (64) |
≥10 | 1 (9) |
Sex | |
Female | 4 (36) |
Male | 7 (64) |
Ethnicity | |
Not Hispanic or Latino | 5 (45) |
Hispanic or Latino | 6 (55) |
Initial diagnosis | |
Standard-risk ALL | 5 (45) |
High-risk ALL | 5 (45) |
CD19+ MPAL | 1 (9) |
Cytogenetics | |
KMT2A rearranged∗ | 3 (27) |
Philadelphia-chromosome positive | 2 (18) |
Philadelphia-like (CRLF2 fusion) | 2 (18) |
Hyperdiploidy | 2 (18) |
Hypodiploidy | 1 (9) |
iAMP21 | 1 (9) |
Remission status | |
CR1 | 9 (82) |
CR2 | 2 (18) |
MRD status before blinatumomab† | |
Negative | 10 (91) |
Positive | 1 (9) |
Reason for blinatumomab | |
Toxicity precluding chemotherapy | 4 (36) |
Other | 7 (64) |
Therapy before blinatumomab | |
Induction | 6 (55) |
Additional therapy | 5 (45) |
CR1, first complete remission; CR2, second complete remission; iAMP21, intrachromosomal amplification of chromosome 21; MPAL, mixed phenotypic acute leukemia.
All 3 patients with KMT2A-rearranged disease had infant leukemia; one of these 3 patients had CD19+ MPAL. Among the remaining 8 patients, 3 had National Cancer Institute high-risk B-ALL.
MRD negativity was defined as <0.01% disease by flow cytometry. The patient who was MRD positive (1.1%) achieved MRD negativity after blinatumomab.