Table 1.

Demographics, baseline disease characteristics, and previous therapies for the overall population and group I patients who received RO7283420 IV

Overall population (N = 62)Group I, IV administration (n = 51)
Age, median (range), y 65.5 (35-84) 66 (35-84) 
≥65 years, n (%) 36 (58.1) 30 (58.8) 
Male sex, n (%) 34 (54.8) 30 (58.8) 
Race, n (%)   
Asian 10 (16.1) 8 (15.7) 
White 50 (80.6) 41 (80.4) 
Unknown 2 (3.2) 2 (3.9) 
ECOG PS, n (%)   
36 (58.1) 29 (56.9) 
23 (37.1) 19 (37.3) 
3 (4.8) 3 (5.9) 
Primary refractory, n (%) 23 (37.1) 21 (41.2) 
Relapsed, n (%) 34 (54.8) 30 (58.8) 
ELN risk category, n (%)   
Favorable 6 (9.7) 5 (9.8) 
Intermediate 22 (35.5) 19 (37.3) 
Adverse 32 (51.6) 25 (49) 
Missing 2 (3.2) 2 (3.9) 
BM blast count category, n (%)   
<30% 28 (45.2) 20 (39.2) 
≥30 to <50% 13 (21) 13 (25.5) 
≥50% 19 (30.6) 17 (33.3) 
Missing 2 (3.2) 1 (2) 
Number of previous AML therapies   
Median (range) 2 (1-5) 2 (1-5) 
1, n (%) 14 (22.6) 7 (13.7) 
2, n (%) 28 (45.2) 25 (49) 
>2, n (%) 20 (32.3) 19 (37.3) 
Previous HSCT, n (%) 18 (29) 15 (29.4) 
Previous AML therapy, induction/re-induction, n (%)  58 (93.5) 48 (94.1) 
Cytarabine 48 (77.4) 39 (76.5) 
Idarubicin 29 (46.8) 24 (47.1) 
Fludarabine 22 (35.5) 18 (35.3) 
Azacitidine 18 (29.0) 15 (29.4) 
Daunorubicin 17 (27.4) 15 (29.4) 
Venetoclax 16 (25.8) 15 (29.4) 
Gemtuzumab 6 (9.7) 6 (11.8) 
Previous AML therapy,
consolidation/conditioning/maintenance/other, n (%)  
40 (64.5) 34 (66.7) 
Cytarabine 25 (40.3) 21 (41.2) 
Azacitidine 22 (35.5) 18 (35.3) 
Venetoclax 13 (21.0) 12 (23.5) 
Fludarabine 10 (16.1) 8 (15.7) 
Overall population (N = 62)Group I, IV administration (n = 51)
Age, median (range), y 65.5 (35-84) 66 (35-84) 
≥65 years, n (%) 36 (58.1) 30 (58.8) 
Male sex, n (%) 34 (54.8) 30 (58.8) 
Race, n (%)   
Asian 10 (16.1) 8 (15.7) 
White 50 (80.6) 41 (80.4) 
Unknown 2 (3.2) 2 (3.9) 
ECOG PS, n (%)   
36 (58.1) 29 (56.9) 
23 (37.1) 19 (37.3) 
3 (4.8) 3 (5.9) 
Primary refractory, n (%) 23 (37.1) 21 (41.2) 
Relapsed, n (%) 34 (54.8) 30 (58.8) 
ELN risk category, n (%)   
Favorable 6 (9.7) 5 (9.8) 
Intermediate 22 (35.5) 19 (37.3) 
Adverse 32 (51.6) 25 (49) 
Missing 2 (3.2) 2 (3.9) 
BM blast count category, n (%)   
<30% 28 (45.2) 20 (39.2) 
≥30 to <50% 13 (21) 13 (25.5) 
≥50% 19 (30.6) 17 (33.3) 
Missing 2 (3.2) 1 (2) 
Number of previous AML therapies   
Median (range) 2 (1-5) 2 (1-5) 
1, n (%) 14 (22.6) 7 (13.7) 
2, n (%) 28 (45.2) 25 (49) 
>2, n (%) 20 (32.3) 19 (37.3) 
Previous HSCT, n (%) 18 (29) 15 (29.4) 
Previous AML therapy, induction/re-induction, n (%)  58 (93.5) 48 (94.1) 
Cytarabine 48 (77.4) 39 (76.5) 
Idarubicin 29 (46.8) 24 (47.1) 
Fludarabine 22 (35.5) 18 (35.3) 
Azacitidine 18 (29.0) 15 (29.4) 
Daunorubicin 17 (27.4) 15 (29.4) 
Venetoclax 16 (25.8) 15 (29.4) 
Gemtuzumab 6 (9.7) 6 (11.8) 
Previous AML therapy,
consolidation/conditioning/maintenance/other, n (%)  
40 (64.5) 34 (66.7) 
Cytarabine 25 (40.3) 21 (41.2) 
Azacitidine 22 (35.5) 18 (35.3) 
Venetoclax 13 (21.0) 12 (23.5) 
Fludarabine 10 (16.1) 8 (15.7) 

AML, acute myeloid leukemia; BM, bone marrow; ECOG, Eastern Cooperative Oncology Group; ELN, European LeukemiaNet; HSCT, hematopoietic stem cell transplantation; IV, intravenous; PS, performance status.

Data are displayed for the therapies that were received by ≥10% of patients in group I who received IV RO7283420.

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