Table 1.

Clinical and demographic characteristics of pediatric Langerhans cell Histiocytosis samples

Characteristicsn (%)
Total 217 (100) 
Sex  
 Male 128 (59.0) 
 Female 89 (41.0) 
Age at diagnosis, years; median [range] 3.1 [0.07-13.6] 
Mutation status  
 Plasma cell-free  
  BRAFV600E(+) 63 (29.0) 
  BRAFV600E (−) 154 (71.0) 
 Lesion sequence  
  BRAFV600E (+) 95 (43.8) 
  BRAFV600E (−) 79 (36.4) 
  NA 43 (19.8) 
Clinical classification  
 MS-high risk 33 (15.2) 
 MS-low risk 65 (30.0) 
 SS-low risk 119 (54.8) 
Treatment  
 First-line therapy 153 (70.5) 
 Second-line therapy 11 (5.1) 
 Targeted therapy 7 (3.2) 
 First-line + Second-line therapy 22 (10.1) 
 Second-line + Targeted therapy 3 (1.4) 
 First-line + Targeted therapy 10 (4.6) 
 First-line + Second-line +  Targeted therapy 4 (1.9) 
 Without treatment 7 (3.2) 
Characteristicsn (%)
Total 217 (100) 
Sex  
 Male 128 (59.0) 
 Female 89 (41.0) 
Age at diagnosis, years; median [range] 3.1 [0.07-13.6] 
Mutation status  
 Plasma cell-free  
  BRAFV600E(+) 63 (29.0) 
  BRAFV600E (−) 154 (71.0) 
 Lesion sequence  
  BRAFV600E (+) 95 (43.8) 
  BRAFV600E (−) 79 (36.4) 
  NA 43 (19.8) 
Clinical classification  
 MS-high risk 33 (15.2) 
 MS-low risk 65 (30.0) 
 SS-low risk 119 (54.8) 
Treatment  
 First-line therapy 153 (70.5) 
 Second-line therapy 11 (5.1) 
 Targeted therapy 7 (3.2) 
 First-line + Second-line therapy 22 (10.1) 
 Second-line + Targeted therapy 3 (1.4) 
 First-line + Targeted therapy 10 (4.6) 
 First-line + Second-line +  Targeted therapy 4 (1.9) 
 Without treatment 7 (3.2) 

NA: Not available; SS: single-system; MS: multiple system.

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