Table 1.

Survival after allo-HCT in patients with MDS/AML with TP53 loss of function and concurrent high-risk cytogenetics

AuthorStudy typeDiseasePts with TP53 LOF receiving allo-HCTSubset with high-risk cytogeneticsDFS from time of HCTOS from time of HCT
MDS  
Lindsley et al25  Registry MDS TP53 mut: 289 pts Not listed Not listed 3-y OS: ∼15% (complex) 
Yoshizato et al26  Registry MDS including subset with sAML TP53 mut: 98 pts Complex: 86 pts Not listed Median OS: 4.3 mo
3-y OS: ∼10% (complex) 
AML 
Middeke et al23  Registry AML 17p abnl: 201 pts Monosomal: 77 pts
Complex: 180 pts 
3-y EFS: 9% (monosomal)
3-y EFS: 9% (complex) 
3-y OS: 11% (monosomal)
3-y OS: 11% (complex) 
Middeke et al22  3 multicenter clinical trials AML TP53 mut: 40 pts Adverse: 40 pts 3-y PFS: 7.5% (adverse) 3-y OS: 10% (adverse) 
Luskin et al27  Single center AML TP53 mut: 9 pts Adverse: 6 pts All relapsed (adverse; range, 1.6-18.6 mo after HCT) Not listed 
Poire et al24  Registry AML 17p abnl: 125 pts Monosomal: 86 pts
−5/5q-: 58 pts 
2-y: 17% (monosomal)
2-y: 11% (−5/5q-) 
2-y OS: 19% (monosomal)
2-y OS: 16% (−5/5q-) 
Najima et al28  Single center AML (nonremission) TP53 mut: 23 pts Monosomal: 11 pts Not listed All died within 12 mo post allo-HCT (monosomal) 
Grob et al18  4 multicenter clinical trials MDS-EB
AML 
TP53 mut: 59 pts Complex: 48 pts Not listed 3-y OS: ∼10% (complex) 
Loke et al21  Registry AML TP53 mut: 179 pts 17p loss and/or complex: 126 pts 2-y PFS: 15.2% (17p loss and/or complex) 2-y OS: 24.6% (17p loss and/or complex) 
AuthorStudy typeDiseasePts with TP53 LOF receiving allo-HCTSubset with high-risk cytogeneticsDFS from time of HCTOS from time of HCT
MDS  
Lindsley et al25  Registry MDS TP53 mut: 289 pts Not listed Not listed 3-y OS: ∼15% (complex) 
Yoshizato et al26  Registry MDS including subset with sAML TP53 mut: 98 pts Complex: 86 pts Not listed Median OS: 4.3 mo
3-y OS: ∼10% (complex) 
AML 
Middeke et al23  Registry AML 17p abnl: 201 pts Monosomal: 77 pts
Complex: 180 pts 
3-y EFS: 9% (monosomal)
3-y EFS: 9% (complex) 
3-y OS: 11% (monosomal)
3-y OS: 11% (complex) 
Middeke et al22  3 multicenter clinical trials AML TP53 mut: 40 pts Adverse: 40 pts 3-y PFS: 7.5% (adverse) 3-y OS: 10% (adverse) 
Luskin et al27  Single center AML TP53 mut: 9 pts Adverse: 6 pts All relapsed (adverse; range, 1.6-18.6 mo after HCT) Not listed 
Poire et al24  Registry AML 17p abnl: 125 pts Monosomal: 86 pts
−5/5q-: 58 pts 
2-y: 17% (monosomal)
2-y: 11% (−5/5q-) 
2-y OS: 19% (monosomal)
2-y OS: 16% (−5/5q-) 
Najima et al28  Single center AML (nonremission) TP53 mut: 23 pts Monosomal: 11 pts Not listed All died within 12 mo post allo-HCT (monosomal) 
Grob et al18  4 multicenter clinical trials MDS-EB
AML 
TP53 mut: 59 pts Complex: 48 pts Not listed 3-y OS: ∼10% (complex) 
Loke et al21  Registry AML TP53 mut: 179 pts 17p loss and/or complex: 126 pts 2-y PFS: 15.2% (17p loss and/or complex) 2-y OS: 24.6% (17p loss and/or complex) 

abnl, abnormality; DFS, disease-free survival; EB, excess blasts; EFS, event-free survival; mut, mutation; LOF, loss-of-function; PFS, progression-free survival; pts, patients; sAML, secondary AML.

Included MDS-EB so long as <20% blasts.

Defined as (1) complex karyotype, (2) monosomy of chromosome 7, (3) monosomy and/or deletion of the long arm of chromosome 5, and (4) abnormalities of chromosome 17p.

Defined as 4 or more abnormalities.

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