TY - JOUR
T1 - WHO-histological criteria for myeloproliferative neoplasms: Reproducibility, diagnostic accuracy and correlation with gene mutations and clinical outcomes
AU - Alvarez-Larrán, Alberto
AU - Ancochea, Agueda
AU - García, Mar
AU - Climent, Fina
AU - García-Pallarols, Francesc
AU - Angona, Anna
AU - Senín, Alicia
AU - Barranco, Carlos
AU - Martínez-Avilés, Luz
AU - Serrano, Sergio
AU - Bellosillo, Beatriz
AU - Besses, Carlos
PY - 2014/1/1
Y1 - 2014/1/1
N2 - Bone marrow histology is included in the diagnostic criteria of myeloproliferative neoplasms (MPNs). However, some concerns have emerged about its reproducibility. To evaluate the diagnostic accuracy of histology and to assess its correlation with presence of mutations and clinical outcomes, two pathologists reviewed the bone marrow biopsies corresponding to 211 patients with MPN. Despite the low agreement in the evaluation of individual histopathological characteristics, the concordance among pathologists when establishing the diagnosis was good (Kappa index 0·67). The specificity of histology was 100%, 98·5% and 98% in polycythaemia vera (PV), essential thrombocythaemia (ET) and primary myelofibrosis (PMF), respectively, whereas the sensitivity of histological diagnosis was low in PV and ET (32·5% and 54% respectively) and acceptable in PMF (75%). Thirteen out of 146 (9%) patients with clinical ET were diagnosed as prefibrotic PMF. No histological agreement or MPN otherwise unspecified was more frequently observed in JAK2 V617F-positive ET than in CALR-mutated cases, whereas megakaryocytic abnormalities and prefibrotic PMF were more frequently observed in CALR-mutated ET. In conclusion, histological criteria of MPN have a limited diagnostic accuracy due to low sensitivity. Patients with JAK2 V617F-positive MPN have a heterogeneous histology while CALR-positive ET is associated with megakaryocyte abnormalities and prefibrotic PMF. © 2014 John Wiley & Sons Ltd.
AB - Bone marrow histology is included in the diagnostic criteria of myeloproliferative neoplasms (MPNs). However, some concerns have emerged about its reproducibility. To evaluate the diagnostic accuracy of histology and to assess its correlation with presence of mutations and clinical outcomes, two pathologists reviewed the bone marrow biopsies corresponding to 211 patients with MPN. Despite the low agreement in the evaluation of individual histopathological characteristics, the concordance among pathologists when establishing the diagnosis was good (Kappa index 0·67). The specificity of histology was 100%, 98·5% and 98% in polycythaemia vera (PV), essential thrombocythaemia (ET) and primary myelofibrosis (PMF), respectively, whereas the sensitivity of histological diagnosis was low in PV and ET (32·5% and 54% respectively) and acceptable in PMF (75%). Thirteen out of 146 (9%) patients with clinical ET were diagnosed as prefibrotic PMF. No histological agreement or MPN otherwise unspecified was more frequently observed in JAK2 V617F-positive ET than in CALR-mutated cases, whereas megakaryocytic abnormalities and prefibrotic PMF were more frequently observed in CALR-mutated ET. In conclusion, histological criteria of MPN have a limited diagnostic accuracy due to low sensitivity. Patients with JAK2 V617F-positive MPN have a heterogeneous histology while CALR-positive ET is associated with megakaryocyte abnormalities and prefibrotic PMF. © 2014 John Wiley & Sons Ltd.
KW - Bone marrow histology
KW - CALR
KW - JAK2 V617F
KW - Myelopoliferative neoplasms
KW - Prefibrotic myelofibrosis
U2 - 10.1111/bjh.12990
DO - 10.1111/bjh.12990
M3 - Article
SN - 0007-1048
VL - 166
SP - 911
EP - 919
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 6
ER -