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Blast Phase of Myeloproliferative Neoplasm Resembles Acute Myeloid Leukemia, Myelodysplasia-Related, in Clinical Presentation, Cytogenetic Pattern, and Genomic Profile, and Often Undergoes Reversion to Second Chronic Phase Status After Induction Chemotherapy.
- Source :
-
Archives of pathology & laboratory medicine [Arch Pathol Lab Med] 2024 Dec 01; Vol. 148 (12), pp. 1310-1319. - Publication Year :
- 2024
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Abstract
- Context.—: BCR::ABL-negative myeloproliferative neoplasm (MPN) has a prolonged clinical course, and some cases eventually undergo transformation to blast phase; its pathogenesis remains to be elucidated.<br />Objective.—: To evaluate the clinicopathologic characteristics of MPN in blast phase.<br />Design.—: The study aimed to retrospectively analyze the clinical and laboratory data of 24 MPN cases.<br />Results.—: Median latency to blast phase was 48 months (range, 7-384 months). Complex karyotypes were seen in 12 of the 24 cases (50%). Overall, 16 cases (66.7%) exhibited high allele burdens of MPN driver mutations along with increased blasts, consistent with linear clonal evolution, whereas the remainder (8; 33.3%) showed loss or partial loss of the driver mutation, suggestive of a parallel evolution. Additional mutations were noted in 23 cases (100%), including TP53 mutations in 10 of 24 cases (41.7%). Following chemotherapy, 15 of the 24 patients (62.5%) reverted to a second chronic phase while retaining or regaining MPN driver mutations and losing blast-related mutations, although 9 of the 15 patients (60%) later died of disease progression. Median overall survival was 10 months (CI, 4.6-15.4), with those harboring complex karyotypes demonstrating decreased survival (6 versus 29 months; P = .004).<br />Conclusions.—: MPN blast phase resembles acute myeloid leukemia, myelodysplasia-related, in cytogenetic pattern, mutation profile, and clinical outcome. Two patterns of clonal evolution are inferred by dynamic analysis of mutation profiles: linear and parallel evolutions. Although overall survival was dismal, 62.5% of our cases achieved second chronic phase, and they showed better survival than those without second chronic phase.<br />Competing Interests: The authors have no relevant financial interest in the products or companies described in this article.<br /> (© 2024 College of American Pathologists.)
- Subjects :
- Humans
Male
Female
Middle Aged
Aged
Retrospective Studies
Adult
Induction Chemotherapy
Aged, 80 and over
Myelodysplastic Syndromes genetics
Myelodysplastic Syndromes drug therapy
Myelodysplastic Syndromes pathology
Clonal Evolution
Myeloproliferative Disorders genetics
Myeloproliferative Disorders drug therapy
Myeloproliferative Disorders pathology
Myeloproliferative Disorders diagnosis
Leukemia, Myeloid, Acute genetics
Leukemia, Myeloid, Acute drug therapy
Leukemia, Myeloid, Acute pathology
Blast Crisis genetics
Blast Crisis pathology
Blast Crisis drug therapy
Mutation
Subjects
Details
- Language :
- English
- ISSN :
- 1543-2165
- Volume :
- 148
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Archives of pathology & laboratory medicine
- Publication Type :
- Academic Journal
- Accession number :
- 38426696
- Full Text :
- https://doi.org/10.5858/arpa.2023-0363-OA