Table 4

Patients' characteristics according to KIT sequencing: literature review

No D816V mutation, n = 15§D816V mutations, n = 13
Media age at diagnosis, y (range) 46 (18-66) 58 (52-76) 
Female/Male 10/4 8/5 
Ethnicity, n (%)   
    White 6 (85) 3 (75) 
    Asiatic 1 (15) 1 (25) 
Familial mastocytosis 0 (0) 0 (0) 
Median time from symptoms to diagnosis, mo (range) 5 (0-108) 5 (0-10) 
History of mastocytosis, n (%) 4 (33) 1 (15) 
Aleukemic MCL, n (%) 10 (83) 8 (61) 
Organ involvement, n (%)   
    Skin (UP) 4 (28) 3 (23) 
    Hepatomegaly 8 (57) 8 (66) 
    Splenomegaly 10 (71) 10 (77) 
    Lymph nodes 3 (25) 3 (23) 
    Ascites 2 (15) 5 (38) 
Gastroduodenal ulcer, n (%) 0 (0) 1 (12.5) 
AHNMD, n (%) 0 (0) 3 (43) 
MCAS, n (%) 12 (85) 8 (61) 
KITmutation (%)*   
    D816V KIT mutation  13 (100) 
    WT KIT 2 (25)  
    Exon 9 mutation 3 (37.5)  
    Exon 10 mutation 1 (12.5)  
    Exon 11 mutation 1 (12,5)  
    Exon 13 mutation 1 (12.5)  
    Not available 7 (46)  
Abnormal cytogenetics, n (%) 1 (12.5) 1 (8) 
(t(8;21)(q22;q22))  
Phenotype, n (%)   
    CD2+ 4 (33) 8 (80) 
    CD25+ 4 (36) 11 (92) 
    CD2/CD25+ 1 (8) 1 (8) 
    CD2/CD25 5 (42) 1 (8) 
    CD2+/CD25+ 3 (25) 8 (66) 
    CD2+/CD25 1 (8) 0 (0) 
Biological data, median (range)   
    Tryptase, ng/L 400 (173-742) 200 (111-2357) 
    Hemoglobin, g/dL 10 (5.4-12.5) 10 (7-13.7) 
    Platelets, ×109/L 117.5 (45-318) 74 (5-210) 
    PMN, ×109/L 1.5 (1.1-4) 10.5 (3.5-14) 
    BM mastocytes, % (range) 64 (23-100) 60 (30-90) 
    Blood mastocytes, % (range) 3.5 (1-31) 3.5 (1-20) 
Outcome   
    Death, n (%) 9 (69) 6 (46) 
    Median survival time, mo (range) 5 (0.5-29) 5.5 (2-23) 
No D816V mutation, n = 15§D816V mutations, n = 13
Media age at diagnosis, y (range) 46 (18-66) 58 (52-76) 
Female/Male 10/4 8/5 
Ethnicity, n (%)   
    White 6 (85) 3 (75) 
    Asiatic 1 (15) 1 (25) 
Familial mastocytosis 0 (0) 0 (0) 
Median time from symptoms to diagnosis, mo (range) 5 (0-108) 5 (0-10) 
History of mastocytosis, n (%) 4 (33) 1 (15) 
Aleukemic MCL, n (%) 10 (83) 8 (61) 
Organ involvement, n (%)   
    Skin (UP) 4 (28) 3 (23) 
    Hepatomegaly 8 (57) 8 (66) 
    Splenomegaly 10 (71) 10 (77) 
    Lymph nodes 3 (25) 3 (23) 
    Ascites 2 (15) 5 (38) 
Gastroduodenal ulcer, n (%) 0 (0) 1 (12.5) 
AHNMD, n (%) 0 (0) 3 (43) 
MCAS, n (%) 12 (85) 8 (61) 
KITmutation (%)*   
    D816V KIT mutation  13 (100) 
    WT KIT 2 (25)  
    Exon 9 mutation 3 (37.5)  
    Exon 10 mutation 1 (12.5)  
    Exon 11 mutation 1 (12,5)  
    Exon 13 mutation 1 (12.5)  
    Not available 7 (46)  
Abnormal cytogenetics, n (%) 1 (12.5) 1 (8) 
(t(8;21)(q22;q22))  
Phenotype, n (%)   
    CD2+ 4 (33) 8 (80) 
    CD25+ 4 (36) 11 (92) 
    CD2/CD25+ 1 (8) 1 (8) 
    CD2/CD25 5 (42) 1 (8) 
    CD2+/CD25+ 3 (25) 8 (66) 
    CD2+/CD25 1 (8) 0 (0) 
Biological data, median (range)   
    Tryptase, ng/L 400 (173-742) 200 (111-2357) 
    Hemoglobin, g/dL 10 (5.4-12.5) 10 (7-13.7) 
    Platelets, ×109/L 117.5 (45-318) 74 (5-210) 
    PMN, ×109/L 1.5 (1.1-4) 10.5 (3.5-14) 
    BM mastocytes, % (range) 64 (23-100) 60 (30-90) 
    Blood mastocytes, % (range) 3.5 (1-31) 3.5 (1-20) 
Outcome   
    Death, n (%) 9 (69) 6 (46) 
    Median survival time, mo (range) 5 (0.5-29) 5.5 (2-23) 

MCL indicates mast cell leukemia; UP, urticaria pigmentosa; AHNMD, associated clonal hematologic non–MC-lineage disease; MCAS, mast cell activation syndrome; PMN, polymorphonuclear; and BM, bone marrow.

*

Exon 9 mutation at codons 501-502-503; exon 10 mutation at codon 522, exon 11 mutation at codon 560, exon 13 mutation at codon 654; not available by KIT sequencing.

Abnormal cytogenetics, 5q deletion (2 patients with AHNMD), t(10;16) (q22;q13q22) and t(8;21)(q22;q22) (2 patients).

One missing.

§

Two patients with previous mast cell sarcoma and 2 patients with previous pediatric mastocytosis.

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