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The purpose of this note is to correct both the analysis and typographical errors.
The typos are as follows.
The abstract, line 6: In “in 6 patients (8%)” should read “in 5 patients (6%)”.
Page 4, line 12: In “8% (6) of the samples, being 5 missens” should read “6% (5) of the samples, being 4 missense”.
Page 4, line 19: In “Of the 6 cases” should read “Of the 5 cases”.
Page 4, line 20: In “(5, or 83.3%)” should read “(4, or 80%)”.
Page 4, second column, line 8: In “OS for patients with wild DNMT3A gene was 41.4% and for patients with mutated DNMT3A was 44.4% (
Page 6, line 4: In “found in 8%” should read “found in 6%”.
Page 6, second column, line 13: In “3 of 6 mutations” should read “3 of 5 mutations”.
Page 6, second column, line 16: In “Five, or 80%,” should read “Four, or 80%,”.
Page 6, second column, line 18: In “(
Page 6, second column, line 20: In “(20.7 × 109/L)” should read “(15.6 × 109/L)”.
Table 4, column 2, line 6: In “H896*” should read “P896*”.
Table 4: Entire line 7 was excluded.
Table 5, line 2: In “40.2, 44.8 and 0.56” should read “47.4, 40.4 and 0.42”.
Table 5, line 4: In “50% (3), 59.3% (45) and 0.68” should read “60% (3), 57.9% (44) and 0.92”.
Table 5, line 5: In “50% (3), 40.7% (31)” should read “40% (2), 42.1% (32)”.
Table 5, line 19: In “50% (3), 51.4% (37) and 1.000” should read “40% (2), 52.7% (39) and 0.66”.
Table 5, line 20: In “50% (2), 30.9% (17) and 0.58” should read “40% (2), 29.2% (21) and 0.63”.
We changed Figure 3 as shown above.
Table 4
Description of somatic mutations found in gene DNMT3A.
Patient identification | Mutation | Allelic change | Exon | Type of mutation | FAB subtype | PCR | Risk group | Karyotype |
39 | D748N | G > A | 19 | Missense | M1 | Negative | Intermediate | Normal |
79 | R882H | G > A | 23 | Missense | M1 | Negative | Intermediate | Trisomy (8)(9) |
4 | R882H | G > A | 23 | Missense | M3 | Negative | Intermediate | Normal |
70 | R882H | G > A | 23 | Missense | M2 | Negative | Intermediate | Normal |
41 | P896* | A > G | 23 | Silent | M3 | PML/RARα | Favorable | t(15;17) |
Table 5
Clinical characteristics of patients with Acute Myeloid Leukemia with or without DNMT3A mutations.
Characteristics | Number of pts (%) DNMT3A mutated | Number of pts (%) DNMT3A not mutated |
|
Age (median) | 47.4 | 40.4 | 0.42 |
Sex | |||
Male | 60% |
57.9% |
0.92 |
Female | 40% |
42.1% |
|
Subtype FAB | |||
M0 | 0% | 7.2% |
|
M1 | 60% |
18.8% |
|
M2 | 20% |
30.4% |
0.56 |
M3 | 20% |
20.3% |
|
M4 | 0% | 18.8% |
|
M5 | 0% | 1.4% |
|
Not M3 | 0% | 2.9% |
|
Risk groups | |||
Favorable | 20% |
29.8% |
|
Intermediate | 80% |
59.6% |
1.000 |
Unfavorable | 0% | 10.5% |
|
Leukocytes (×103) (median) | 20.67 | 6.41 | 0.28 |
Death | 40% |
52.7% |
0.66 |
Relapses | 40% |
29.2% |
0.63 |
Refractory | 20% |
19.1% |
0.96 |
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Abstract
Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Patient identification Mutation Allelic change Exon Type of mutation FAB subtype PCR Risk group Karyotype 39 D748N G > A 19 Missense M1 Negative Intermediate Normal 79 R882H G > A 23 Missense M1 Negative Intermediate Trisomy (8)(9) 4 R882H G > A 23 Missense M3 Negative Intermediate Normal 70 R882H G > A 23 Missense M2 Negative Intermediate Normal 41 P896* A > G 23 Silent M3 PML/RARα Favorable t(15;17) Table 5 Clinical characteristics of patients with Acute Myeloid Leukemia with or without DNMT3A mutations. Characteristics Number of pts (%) DNMT3A mutated Number of pts (%) DNMT3A not mutated P Age (median) 47.4 40.4 0.42 Sex Male 60% ( 3 ) 57.9% ( 44 ) 0.92 Female 40% ( 2 ) 42.1% ( 32 ) Subtype FAB M0 0% 7.2% ( 5 ) M1 60% ( 3 ) 18.8% ( 13 ) M2 20% ( 1 ) 30.4% ( 21 ) 0.56 M3 20% ( 1 ) 20.3% ( 14 ) M4 0% 18.8% ( 13 ) M5 0% 1.4% ( 1 ) Not M3 0% 2.9% ( 2 ) Risk groups Favorable 20% ( 1 ) 29.8% ( 17 ) Intermediate 80% ( 4 ) 59.6% ( 34 ) 1.000 Unfavorable 0% 10.5% ( 6 ) Leukocytes (×103) (median) 20.67 6.41 0.28 Death 40% ( 2 ) 52.7% ( 39 ) 0.66 Relapses 40% ( 2 ) 29.2% ( 21 ) 0.63 Refractory 20% ( 1 ) 19.1% ( 13 ) 0.96 [figure omitted; refer to PDF]
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1 Cellular Therapy Center, Center for Experimental Research, Hospital de Clinicas de Porto Alegre, 90035-903 Porto Alegre, RS, Brazil
2 Gene Therapy Center, Center for Experimental Research, Hospital de Clinicas de Porto Alegre, 90035-903 Porto Alegre, RS, Brazil
3 Pediatric Hematology and Oncology Program, Research Center, Instituto Nacional de Câncer, 20230-130 Rio de Janeiro, RJ, Brazil
4 Hematology and Bone Marrow Transplantation, Hospital de Clinicas de Porto Alegre, 90035-903 Porto Alegre, RS, Brazil