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. 2017 Mar 1;31(3):774–775. doi: 10.1038/leu.2016.291

Erratum: Clinical impact of bone marrow morphology for the diagnosis of essential thrombocythemia: comparison between the BCSH and the WHO criteria

H Gisslinger, G Jeryczynski, B Gisslinger, A Wölfler, S Burgstaller, V Buxhofer-Ausch, M Schalling, M-T Krauth, A-I Schiefer, C Kornauth, I Simonitsch-Klupp, C Beham-Schmid, L Müllauer, J Thiele
PMCID: PMC7608183  PMID: 28248312

Correction to: Leukemia (2016) 30, 1126–1132; doi:10.1038/leu.2015.360

Following the publication of this Article, the authors noted that there were errors in Tables 2 and 4. The correct tables are provided below—amended values highlighted in bold and italicised.

Table 2.

Clinical characteristics, molecular analysis and constitutional symptoms of patients with essential thrombocythemia (ET) at presentation and treatment according to applied diagnostic criteria

BCSH-defined ET (criteria A1–A3) 1,2 WHO-defined ET criteria 3 P-value
General characteristics
 n 238 232
 Age at diagnosis (years) 61.3 (18.8–88.8) 57.2 (17.5–88.8) 0.073
 Sex male/female 94/144 93/139 0.925
Clinical characteristics a
 Platelets (G/L) 769 (452–2530) 754 (450–2490) 0.539
 Hemoglobin g/dl 14.2 (8.6–17.3) 14.4 (8.6–17.3) 0.826
 Hematocrit (%) 42.9 (42.9–52.0) 42.7 (29.9–52.6) 0.630
 WBC (G/L) 9.4 (2.21–31.32) 8.82 (2.21–22.3) 0.057
 LDH (U/L) 221 (118–763) 207 (104–763) <0.001
 Palpable splenomegaly (218/238)b 16.4% (39) 11.9% (26) 0.183
 Fibrosis grading ⩾1 8.4% (20) 0.0% (0) <0.001
Molecular characteristics
 Pathogenetic mutation present (238/169)b 100% (238) 72.8% (169)
JAK2 V617F (238/220)b 72.7% (173) 80.5% (136) 0.078
CALR (181/141)b 24.4% (58) 16.0% (27) 0.048
MPL (75/53)b 2.9% (7) 3.5% (6) 0.780
Symptoms at diagnosis
 Constitutional symptoms (200/169)b 16.0% (32) 14.8% (25) 0.774
Weight loss 4.5% (9) 4.1% (7) 1.000
Night sweats 8.5% (17) 8.3% (14) 1.000
Fatigue 5.0% (10) 5.9% (10) 0.818
 Pruritus (202/175)b 2.0% (4) 2.3% (4) 1.000
Cytoreductive therapy (191/164) b
 Hydroxurea 42.9% (82) 42.1% (69) 0.494
 Interferon-alpha 34.6% (66) 30.5% (50) 0.429
 Anagrelide 30.4% (58) 34.1% (56) 0.494
 JAK1/2-Inhibitor 4.7% (9) 3.0% (5) 0.586
 Busulfan 2.6% (5) 2.4% (4) 1.000
 Othersc 4.2% (8) 0.6% (1) 0.042
Antithrombotic therapy with low-dose aspirin (189/160)b 90.5% (171) 88.8% (142) 0.602

Abbreviations: WBC, white blood cell count; LDH, serum lactate dehydrogenase.

aMedian, range.

bNumber evaluable in each cohort.

cPipobroman, P32 and other cytoreductive agents.

Table 4.

Clinical characteristics of patients with WHO-defined essential thrombocythemia (ET) compared with WHO-defined prefibrotic primary myelofibrosis (prePMF) at presentation as derived from the BCSH-confirmed ET cohort

WHO-defined ET 3 WHO-defined prePMF 3 P-value
General characteristics
 n 141 77
 Age at diagnosis (years) 58.9 (18.8–88.8) 64.6 (23.2–88.1) 0.086
 Sex male/female 58/83 27/50 0.486
Clinical characteristics a
 Platelets (G/L) 725 (452–1836) 840 (457–2530) 0.012
 Hemoglobin (g/dl) 14.5 (11.5–17.3) 13.9 (8.6–16.6) 0.007
 Hematocrit (%) 43.0 (33.2–52.0) 41.6 (27.5–48.9) 0.036
 WBC (G/L) 8.8 (2.2–21.1) 10.3 (4.0–31.3) 0.004
 LDH (U/L) 209 (110–763) 270 (136–598) <0.001
 Palpable splenomegaly (141/77)b 9.9% (14) 23.4% (18) 0.009
 Fibrosis grading ⩾1 0.0% (0) 20.8% (16) <0.001
Molecular characteristics
 Pathogenetic mutation present (141/77)b 100% (141) 100% (77)
 JAK2 V617F (141/77)b 78.0% (110) 61.0% (47) 0.011
 CALR (99/65)b 19.2% (27) 35.1% (27) 0.013
 MPL (33/37)b 2.8% (4) 3.9% (3) 0.700
Symptoms at diagnosis
 Constitutional symptoms (111/71)b 15.8% (16) 20.3% (10) 1.000
Weight loss 3.6% (4) 7.0% (5) 0.315
Night sweats 8.1% (9) 4.2% (3) 0.372
Fatigue 5.4% (6) 5.6% (4) 1.000
 Pruritus (111/71)b 1.8% (2) 1.4% (1) 1.000
Cytoreductive therapy (108/63) b
 Hydroxyurea 45.4% (49) 38.1% (24) 0.423
 Interferon-alpha 31.5% (34) 34.9% (22) 0.736
 Anagrelide 33.3% (36) 28.6% (18) 0.610
 JAK1/2-Inhibitor 4.6% (5) 6.3% (4) 0.727
 Busulfan 1.9% (2) 3.2% (2) 0.626
 Othersc 0.9% (1) 6.3% (4) 0.062
Antithrombotic therapy with low-dose aspirin (106/63)b 89.6% (95) 88.9% (56) 1.000

Abbreviations: WBC, white blood cell count; LDH, serum lactate dehydrogenase.

aMedian, range.

bNumber evaluable in each cohort.

cPipobroman, P32 and other cytoreductive agents.

Further the authors confirmed that the last sentence of the third to last paragraph of the methods section should be amended to read ‘Antithrombotic therapy with low-dose aspirin was applied in 142 patients of the WHO-confirmed ET and 171 patients of the BCSH-defined ET cohort.’

The authors wish to apologize for any inconvenience caused.

Footnotes

The online version of the original article can be found at 10.1038/leu.2015.360


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