Table 1.

Role of CHIP as predisposing factor in t-MNs

Primary disease (PD)nAge at t-MNs
(y, median, range)
CHIP at PD diagnosis (%)Frequently mutated genes*Reference
NHL/HL
MM
Solid tumors 
3/1
2
56 (42-68) 4 of 7 (57) TP53 47  
NHL/HL
APL/AML
ALL 
7/2
4
62 (30-81) 3 of 8 (21) ASXL1 48  
NHL
MM
Solid tumors 
5
1
74 (70-82) 8/13 (62) vs 15/56 (27) controls TP53, TET2 49  
NHL/HL
Solid tumors 
2/1
11 
65 (28-77) 10/14 (71) vs 17/54 (31) controls TP53, TET2, DNMT3A, RUNX1, SRSF2 50  
NHL/HL
MM/amyloidosis 
11/2
61 (41-71) 7/10 (70) in PBSC grafts TP53, DNMT3A 51  
Hematological neoplasms
Solid tumors 
35 NA 19 (54) TP53 26  
Primary disease (PD)nAge at t-MNs
(y, median, range)
CHIP at PD diagnosis (%)Frequently mutated genes*Reference
NHL/HL
MM
Solid tumors 
3/1
2
56 (42-68) 4 of 7 (57) TP53 47  
NHL/HL
APL/AML
ALL 
7/2
4
62 (30-81) 3 of 8 (21) ASXL1 48  
NHL
MM
Solid tumors 
5
1
74 (70-82) 8/13 (62) vs 15/56 (27) controls TP53, TET2 49  
NHL/HL
Solid tumors 
2/1
11 
65 (28-77) 10/14 (71) vs 17/54 (31) controls TP53, TET2, DNMT3A, RUNX1, SRSF2 50  
NHL/HL
MM/amyloidosis 
11/2
61 (41-71) 7/10 (70) in PBSC grafts TP53, DNMT3A 51  
Hematological neoplasms
Solid tumors 
35 NA 19 (54) TP53 26  

HSCT, allogeneic stem cell transplantation; MM, multiple myeloma; NA, not applicable; NHL, non-Hodgkin lymphoma; PBSC, peripheral blood stem cell.

*

More than 1 patient.

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