The new WHO and ICC classification systems for myelodysplastic syndromes and their impact on the clinical laboratory
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作者:
Bruehl, Frido K.
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Mayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN 55902 USAMayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN 55902 USA
Bruehl, Frido K.
[1
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Osman, Mazen M.
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Mayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN 55902 USAMayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN 55902 USA
Osman, Mazen M.
[1
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Chen, Dong
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Mayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN 55902 USAMayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN 55902 USA
Chen, Dong
[1
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Dalland, Joanna C.
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Mayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN 55902 USAMayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN 55902 USA
Dalland, Joanna C.
[1
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机构:
[1] Mayo Clin, Dept Lab Med & Pathol, Div Hematopathol, Rochester, MN 55902 USA
The International Consensus Classification (ICC) and World Health Organization (WHO) proposed significant changes to the diagnostic criteria of myelodysplastic syndromes (MDS) in 2022. The impact of these criteria on hematopathology practice is uncertain. This study aims to evaluate the impact of the 2022 ICC and WHO 5th edition classifications on the diagnosis of cytopenias and MDS. Cases from 2021 performed for primary diagnosis of cytopenia(s)/MDS and their clinical, laboratory, and pathologic findings were reviewed and classified according to the new classification systems. The rate of major changes to the diagnosis was determined and potential pitfalls in the diagnostic approach, laboratory workflow, and clinical communication challenges were investigated. A total of 49 cases were recruited. Major changes to the diagnostic entities were made in 18/49 (37%) cases according to the WHO 5th edition, and 23/49 (47%) cases classified according to the ICC. The difference was accounted for by five cases of MDS-EB2 (revised WHO 4th edition) classified as MDS/AML (major change) in the ICC in contrast to no significant change (MDS-IB2) in the WHO 5th edition. MDS-SLD cases were not subject to major reclassification according to either system. The new molecularly defined categories of CCUS/CHIP, MDS-SF3B1, and MDS with biallelic TP53 mutations were almost identically represented in both systems in our cohort. A case of MDS-MLD was reclassified as CMML by both classification systems. There are few but important differences between the new MDS classification systems. A preimplementation assessment is helpful to identify diagnostic and potential clinical impacts of their adoption.
机构:
Ist Sci San Raffaele, Pathol Unit, I-20132 Milan, Italy
Ist Sci San Raffaele, Unit Lymphoid Malignancies, I-20132 Milan, ItalyPoliclin San Matteo, Fdn IRCCS, Dept Hematol Oncol, I-27100 Pavia, Italy
机构:
Ist Sci San Raffaele, Pathol Unit, I-20132 Milan, Italy
Ist Sci San Raffaele, Unit Lymphoid Malignancies, I-20132 Milan, ItalyPoliclin San Matteo, Fdn IRCCS, Dept Hematol Oncol, I-27100 Pavia, Italy
机构:
Univ Rochester, Med Ctr, Dept Pathol, Pathol & Lab Med,James P Wilmot Canc Inst, Rochester, NY 14642 USA
Univ Rochester, Med Ctr, Dept Med, Pathol & Lab Med,James P Wilmot Canc Inst, Rochester, NY 14642 USAUniv Rochester, Med Ctr, Dept Pathol, Pathol & Lab Med,James P Wilmot Canc Inst, Rochester, NY 14642 USA
机构:
Saitama Med Univ, Saitama Int Med Ctr, Dept Hematooncol, Hidaka, Saitama 3501298, JapanSaitama Med Univ, Saitama Int Med Ctr, Dept Hematooncol, Hidaka, Saitama 3501298, Japan
Matsuda, Akira
Germing, Ulrich
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Univ Dusseldorf, Dept Hematol Oncol & Clin Immunol, D-40225 Dusseldorf, GermanySaitama Med Univ, Saitama Int Med Ctr, Dept Hematooncol, Hidaka, Saitama 3501298, Japan
Germing, Ulrich
Miyazaki, Yasushi
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机构:
Nagasaki Univ, Grad Sch Biomed Sci, Atom Bomb Dis Inst, Dept Hematol,Mol Med Unit, Nagasaki 852, JapanSaitama Med Univ, Saitama Int Med Ctr, Dept Hematooncol, Hidaka, Saitama 3501298, Japan