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Sequential Development of JAK2V617F Mutation and BCR-ABL1 Fusion in Individual Patients With Myeloproliferative Neoplasms.

Publication ,  Journal Article
Zhao, Y; Reddi, D; McCracken, J; Iranzad, N; Rehder, C; Neff, J; Wang, E
Published in: Arch Pathol Lab Med
June 1, 2022

CONTEXT.—: Concomitant BCR-ABL1 and JAK2V617F in myeloproliferative neoplasms (MPNs) is rare, and its pathogenesis and clinical significance are unclear. OBJECTIVE.—: To investigate the clonal relationship between the 2 genomic alterations, as well as the clinicopathologic impact. DESIGN.—: Retrospective analysis of MPNs with sequential development of BCR-ABL1 and JAK2V617F. RESULTS.—: Of 6 cases, 5 had JAK2V617F-positive MPN diagnosed before acquiring BCR-ABL1 years later, and 1 had BCR-ABL1+ chronic myeloid leukemia before JAK2V617F-positive myelofibrosis completely replaced the BCR-ABL1+ clone 1 year after tyrosine kinase inhibitor therapy. Among the former group, treatment for the initial MPN involved hydroxyurea, ruxolitinib, and/or supportive care, and the latency to the development of JAK2V617F ranged from 4 to 13 years (median of 9 years). Four cases showed retention of JAK2V617F, whereas BCR-ABL1 emerged as the major clone, including 2 cases that exhibited parallel increases in JAK2V617F and BCR-ABL1 burdens, with both genomic markers exceeding 50%. Three patients received stem cell transplants and demonstrated sustained engraftment, with the genomic markers below detectable levels. CONCLUSIONS.—: Most MPNs with concomitant JAK2V617F and BCR-ABL1 are actually composite MPNs with a "second hit" residing on a different clone. Rare cases demonstrate a subclone harboring a "double-hit" in a background of a JAK2V617F-positive stem line clone. The probability of a "double-hit" with a BCR-ABL1+ stem line clone is probably reduced by effective tyrosine kinase inhibitor treatment. The treatment often involves combined kinase inhibitors and/or hydroxyurea, but the outcome is unpredictable; hematopoietic stem cell transplantation may be the ultimate therapeutic option for this complicated disease.

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Published In

Arch Pathol Lab Med

DOI

EISSN

1543-2165

Publication Date

June 1, 2022

Volume

146

Issue

6

Start / End Page

710 / 717

Location

United States

Related Subject Headings

  • Retrospective Studies
  • Protein Kinase Inhibitors
  • Pathology
  • Myeloproliferative Disorders
  • Mutation
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive
  • Janus Kinase 2
  • Hydroxyurea
  • Humans
  • Fusion Proteins, bcr-abl
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Zhao, Y., Reddi, D., McCracken, J., Iranzad, N., Rehder, C., Neff, J., & Wang, E. (2022). Sequential Development of JAK2V617F Mutation and BCR-ABL1 Fusion in Individual Patients With Myeloproliferative Neoplasms. Arch Pathol Lab Med, 146(6), 710–717. https://doi.org/10.5858/arpa.2021-0096-OA
Zhao, Yue, Deepti Reddi, Jenna McCracken, Natasha Iranzad, Cathrine Rehder, Jadee Neff, and Endi Wang. “Sequential Development of JAK2V617F Mutation and BCR-ABL1 Fusion in Individual Patients With Myeloproliferative Neoplasms.Arch Pathol Lab Med 146, no. 6 (June 1, 2022): 710–17. https://doi.org/10.5858/arpa.2021-0096-OA.
Zhao Y, Reddi D, McCracken J, Iranzad N, Rehder C, Neff J, et al. Sequential Development of JAK2V617F Mutation and BCR-ABL1 Fusion in Individual Patients With Myeloproliferative Neoplasms. Arch Pathol Lab Med. 2022 Jun 1;146(6):710–7.
Zhao, Yue, et al. “Sequential Development of JAK2V617F Mutation and BCR-ABL1 Fusion in Individual Patients With Myeloproliferative Neoplasms.Arch Pathol Lab Med, vol. 146, no. 6, June 2022, pp. 710–17. Pubmed, doi:10.5858/arpa.2021-0096-OA.
Zhao Y, Reddi D, McCracken J, Iranzad N, Rehder C, Neff J, Wang E. Sequential Development of JAK2V617F Mutation and BCR-ABL1 Fusion in Individual Patients With Myeloproliferative Neoplasms. Arch Pathol Lab Med. 2022 Jun 1;146(6):710–717.

Published In

Arch Pathol Lab Med

DOI

EISSN

1543-2165

Publication Date

June 1, 2022

Volume

146

Issue

6

Start / End Page

710 / 717

Location

United States

Related Subject Headings

  • Retrospective Studies
  • Protein Kinase Inhibitors
  • Pathology
  • Myeloproliferative Disorders
  • Mutation
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive
  • Janus Kinase 2
  • Hydroxyurea
  • Humans
  • Fusion Proteins, bcr-abl