Table 1.

Baseline demographics and prior treatment for patients with BRAF V600–mutant LCH

CategoryCDRB436A2102 (dabrafenib monotherapy)
(n = 13)
CTMT212X2101 (dabrafenib + trametinib)
(n = 12)
Age, median (range), y 3 (1-11) 4 (2-13) 
<2 y, n (%) 3 (23.1) 
From 2 to <6 y, n (%) 5 (38.5) 8 (66.7) 
From 6 to <12 y, n (%) 5 (38.5) 3 (25.0) 
≥12 y, n (%) 1 (8.3) 
Male, n (%) 8 (61.5) 8 (66.7) 
Karnofsky/Lansky PS, n (%)   
100 6 (46.2) 8 (66.7) 
90 4 (30.8) 2 (16.7) 
80 1 (7.7) 1 (8.3) 
70 1 (7.7) 
<70 1 (7.7) 1 (8.3) 
Risk organ involvement, n (%)  3 (23.1) N/A 
Time since initial diagnosis, median (range), mo 36.3 (1-116) 33.9 (3.8-137) 
Prior therapy, n (%) 13 (100) 12 (100) 
Chemotherapy 13 (100) 12 (100) 
Biologic therapy  1 (7.7) 
Immunotherapy  1 (7.7) 
Prior radiotherapy, n (%)   
Yes 
No 9 (69.2) 12 (100) 
Missing 4 (30.8) 
Prior lines of chemotherapy   
2 (15.4) 3 (25.0) 
1 (7.7) 2 (16.7) 
≥3 10 (76.9) 7 (58.3) 
CategoryCDRB436A2102 (dabrafenib monotherapy)
(n = 13)
CTMT212X2101 (dabrafenib + trametinib)
(n = 12)
Age, median (range), y 3 (1-11) 4 (2-13) 
<2 y, n (%) 3 (23.1) 
From 2 to <6 y, n (%) 5 (38.5) 8 (66.7) 
From 6 to <12 y, n (%) 5 (38.5) 3 (25.0) 
≥12 y, n (%) 1 (8.3) 
Male, n (%) 8 (61.5) 8 (66.7) 
Karnofsky/Lansky PS, n (%)   
100 6 (46.2) 8 (66.7) 
90 4 (30.8) 2 (16.7) 
80 1 (7.7) 1 (8.3) 
70 1 (7.7) 
<70 1 (7.7) 1 (8.3) 
Risk organ involvement, n (%)  3 (23.1) N/A 
Time since initial diagnosis, median (range), mo 36.3 (1-116) 33.9 (3.8-137) 
Prior therapy, n (%) 13 (100) 12 (100) 
Chemotherapy 13 (100) 12 (100) 
Biologic therapy  1 (7.7) 
Immunotherapy  1 (7.7) 
Prior radiotherapy, n (%)   
Yes 
No 9 (69.2) 12 (100) 
Missing 4 (30.8) 
Prior lines of chemotherapy   
2 (15.4) 3 (25.0) 
1 (7.7) 2 (16.7) 
≥3 10 (76.9) 7 (58.3) 

PS, performance status.

Liver, spleen, and/or bone marrow involvement at baseline; data not available for CTMT212X2101 (dabrafenib + trametinib).

†,‡

The same patient received †prior anti-CD52 monoclonal antibody and ‡prior immunoglobulin.

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