Background: The aging marrow stem cell demonstrates more somatic mutations when compared to younger marrow stem cells. These abnormalities have been noted in pts with MDS, as well as in patients with normal peripheral blood counts (Steensma et al, Blood 2015; Jaiswal et al, N Engl J Med 2014). Mutations are rarely detected in people <40 years of age, but increase each decade thereafter (Jaiswal et al, N Engl J Med 2014). Certain mutations (eg, DNMT3A, TET2, ASXL1, and SF3B1) are most prevalent in the oldest pts, and approximately 2% of pts with mutations associated with leukemia or lymphoma have age-related hematopoietic clonal expansion, which increases to 5-6% among patients ≥70 years of age (Xie et al, Nat Med 2014). In another study, 10% of elderly subjects had clonal hematopoiesis with somatic mutations and this number increased with increasing age (Genovese et al, N Engl J Med 2014). In a randomized, Phase III study with intravenous rigosertib (ONTIME) in patients with MDS failing HMA therapy, a much higher proportion of pts with bone marrow mutations was observed. The most frequent mutations were as follows: SRSF2 (28% of pts), TP53 (22%), ASXL1 (19%), SF3B1 (14%), and TET2 (14%) (Mufti et al, Blood 2014). Given that MDS is a disease of the elderly, and the importance of somatic mutations for diagnosis, prognosis, and (potentially) targeted therapy, we explored the correlation between age and type of somatic bone marrow mutation found in pts entered into ONTIME. Methods: We evaluated the bone marrow mutations in patients with MDS who were enrolled in ONTIME after failing to respond to a previous HMA. Bone marrow genomic DNA was isolated from single microscopic slides from 153 pts from ONTIME and subjected to sequence analysis of a "myeloid panel" comprising of 24 selected loci known to be frequently mutated in MDS and AML (Mufti et al, Blood 2014). We investigated these 24 myeloid abnormalities for their frequency in the identified age cohorts prior to study randomization to explore the correlation between age and the somatic mutation identified, specifically looking at pts older or younger than the mean age of pts with MDS in ONTIME (75 years). Results: Approximately 45% of patients had 1 mutation and an equal number had >1 (Figure 1).

Table 1 shows the most frequent clonal myeloid mutations in ONTIME, based on age above and below 75 years (the median age in ONTIME).

Table 3.

Incidence (%) of Patients with Specific Mutations, Age Above and Below 75 Years

Mutation< 75 years
(N=60)		≥ 75 years
(N=51)		Total
(N=111)		Fisher's Exact
Test P-value
SRSF2 27 29 28 0.83 
TP53 25 18 22 0.37 
ASXL1 20 18 19 0.81 
SF3B1 13 16 14 0.79 
U2AF1 12 12 12 1.00 
TET2 12 16 14 0.59 
RUNX1 8 14 11 0.38 
DNMT3A 8 12 10 0.75 
Mutation< 75 years
(N=60)		≥ 75 years
(N=51)		Total
(N=111)		Fisher's Exact
Test P-value
SRSF2 27 29 28 0.83 
TP53 25 18 22 0.37 
ASXL1 20 18 19 0.81 
SF3B1 13 16 14 0.79 
U2AF1 12 12 12 1.00 
TET2 12 16 14 0.59 
RUNX1 8 14 11 0.38 
DNMT3A 8 12 10 0.75 
View Large
In a separate analysis, the number of months from diagnosis of MDS and duration of prior HMA treatment did not appear to influence the pattern of mutations (Table 2).
Table 2.

Mutations by Months Since MDS Diagnosis and Duration of Prior HMA

MutationNMonths from MDS Diagnosis
median (range)		Duration of HMA (mo)
median (range)
All analyzed pts 111 18.5 (0.1-116) 8.9 (1.2-65) 
TP53 24 14.9 (0.7-116) 13.0 (1.2-36) 
SF3B1 16 29.4 (7.5-63) 13.0 (1.2-36) 
TET2 15 22.6 (0.1-63) 11.4 (2.0-36) 
SRSF2 31 17.2 (6.6-116) 6.4 (3.0-35) 
ASXL1 21 15.7 (4.9-66) 8.2 (2.8-44) 
DNMT3A 11 15.1 (7.4-36) 6.5 (4.2-30) 
MutationNMonths from MDS Diagnosis
median (range)		Duration of HMA (mo)
median (range)
All analyzed pts 111 18.5 (0.1-116) 8.9 (1.2-65) 
TP53 24 14.9 (0.7-116) 13.0 (1.2-36) 
SF3B1 16 29.4 (7.5-63) 13.0 (1.2-36) 
TET2 15 22.6 (0.1-63) 11.4 (2.0-36) 
SRSF2 31 17.2 (6.6-116) 6.4 (3.0-35) 
ASXL1 21 15.7 (4.9-66) 8.2 (2.8-44) 
DNMT3A 11 15.1 (7.4-36) 6.5 (4.2-30) 
View Large
Conclusions: Somatic mutations are common in marrow stem cells from patients with HR-MDS. Over 45% of patients had 1 mutational abnormality, and 44% had >1. Of note, patients under and over the median age of pts with MDS had a similar mutational pattern, which was not influenced by either length of time since diagnosis of MDS or prior treatment with an HMA. In this analysis, the mutational genomic abnormalities in the MDS marrow stem cell were similar among younger and older patients with MDS, suggesting the underlying pathogenic mechanisms causing these abnormalities are also similar irrespective of patient age.

Figure 1.
Figure 1. Number of Mutations Per Patient
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Number of Mutations Per Patient

Figure 1.
Figure 1. Number of Mutations Per Patient
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Number of Mutations Per Patient

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Figure 2.
Figure 2. Overall Survival in ONTIME by Number of Marrow Stem Cell Mutations
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Overall Survival in ONTIME by Number of Marrow Stem Cell Mutations

Figure 2.
Figure 2. Overall Survival in ONTIME by Number of Marrow Stem Cell Mutations
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Overall Survival in ONTIME by Number of Marrow Stem Cell Mutations

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Disclosures

Mufti:Onconova Therapeutics Inc: Research Funding. Silverman:Onconova Therapeutics Inc: Honoraria, Patents & Royalties: co-patent holder on combination of rigosertib and azacitdine, Research Funding. Best:Onconova Therapeutics Inc: Research Funding. Fructman:Onconova Therapeutics Inc: Employment. Azarnia:Onconova Therapeutics Inc: Employment. Petrone:Onconova Therapeutics Inc: Employment.

Topics:
brachial plexus neuritis, mutation, myelodysplastic syndrome, protein p53, dna, leukemia, lymphoma, molecular targeted therapy, sequence analysis, age distribution

Author notes

*

Asterisk with author names denotes non-ASH members.

© 2015 by The American Society of Hematology
2015
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