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Clinical Outcomes of Patients With Chronic Myeloid Leukemia With Concurrent Core Binding Factor Rearrangement and Philadelphia Chromosome

  • Kiyomi Morita
    ,
  • Elias Jabbour
    ,
  • Farhad Ravandi
    ,
  • Gautam Borthakur
    ,
  • Joseph D. Khoury
    ,
  • Shimin Hu
*Corresponding author for this work
  • University of Texas MD Anderson Cancer Center
    ,
Scholary Output:
Contribution to journal
Article
Research
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Background: Acquisition of additional cytogenetic abnormalities (ACAs) in addition to Philadelphia chromosome is frequently observed in patients with chronic myeloid leukemia (CML) in advanced phase. The presence of core binding factor (CBF) translocations determines the diagnosis of acute myeloid leukemia regardless of blast percentage, and CBF rearrangements are rarely identified as ACAs. Patients and Methods: A retrospective chart review of patients with CML who had CBF rearrangement, t(8;21) or inv(16), in Philadelphia chromosome-positive clones was conducted. Additional cases of CML with CBF rearrangements were identified through literature review. Results: Between August 1997 and December 2014, we identified 11 patients who had Philadelphia chromosome and CBF rearrangement in the same clones: 1 (9%) with t(8;21) and 10 (91%) with inv(16). Nine (82%) patients were in blast phase, and 2 (18%) in second chronic phase. Four (36%) patients received tyrosine kinase inhibitor monotherapy, 2 (18%) received tyrosine kinase inhibitor and chemotherapy, and 5 (45%) received chemotherapy only. Three (27%) patients achieved complete remission with incomplete count recovery, and 4 (36%) had no response after the initial therapy. Three (27%) patients underwent allogeneic stem cell transplantation. The median event-free survival and overall survival for the 11 patients were 2 months and 6 months, respectively. Literature review identified 14 patients with CML with CBF rearrangement with a median overall survival of 14 months. Conclusion: Acquisition of CBF rearrangement in addition to Philadelphia chromosome is a rare phenomenon associated with poor prognosis. CBF rearrangements as ACAs in patients with CML can be considered high-risk features.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Research
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 338-344 (7 pages)

Journal (Volume, Issue Number)

Clinical Lymphoma, Myeloma and Leukemia (Volume 21, Issue 5)

Publication milestones

  • Accepted/In press - 2021
  • Published - 05/2021

Publication status

Published - 05/2021

ISSN

2152-2650

Publication IDs

  • Scopus: 85100960811
  • ORCID: /0000-0002-8636-1071/work/93758088
  • PubMed: 33597098

Publication metrics

Metrics

SciVal
citations
1
Scopus
citations
Fractional count
1
Fractional count
0.06
Fractional count
16
Fractional count
0.94
Fractional count
1
Fractional count
1
SciVal
FWCI
2.57
SciVal
Author count
17
SciVal
Paper percentile
92
SciVal
Top percentile
10

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Citation count
9
Captures
13

Funding Details

E Jabbour reports research support and an advisory role with Adaptive, AbbVie, Amgen, Pfizer, Cyclacel LTD, Takeda, and BMS. F Ravandi reports research support and an advisory role with Macrogeni, Selvita, Cyclacel LTD, Menarini Ricerche, and Xencor. G Garcia-Manero reports research support and an advisory role with Bristol Myers Squibb, Astex, and Helsinn, and research support from Amphivena, Novartis, AbbVie, H3 Biomedicine, Onconova, and Merck. G Issa reports research support and an advisory role with Celegene, Syndax, and Novartis. J Cortes reports research support, consultancy, and an advisory role with Novartis, Pfizer, Takeda, Sun Pharma, BioPath Holdings, Telios, Astellas, Amphivena Therapeutics, Arogs, BiolineRx, BMS, Daiichi-Sankyo, Jazz, Immunogen, Merus, Tolero Pharmaceuticals, and Tovagene. K Sasaki reports an advisory role with Pfizer Japan. The remaining authors have stated that they have no conflicts of interest.This work was supported in part by the University of Texas MD Anderson Cancer Center Support Grant CA016672. This work was supported in part by the University of Texas MD Anderson Cancer Center Support Grant CA016672.
FundersFunding number
Amphivena Therapeutics
-
Amphivena Therapeutics
-
Cyclacel LTD
-
Menarini Ricerche
-
Amgen
-
BMS
-
Pfizer
-
Astellas Pharma
-
Merck
-
Novartis
-
AbbVie
-
University of Texas M.D. Anderson Cancer Center
CA016672
TPUSA
-