Evidence map›Paper›PMID 40932956›Full record

ArticleCureus2025

A Long-Term Survival Case of Acute Myeloid Leukemia With MYC-Positive Double Minute Chromosomes.

Ryo Yoshimaru, Ayumi Kuzume, Hirotaka Nakamura, Yon-Mei Guo, SungGi Chi, Saki Nakamura, Michiko Iida, Kimihiko Kawamura, Kenta Akie, Yosuke Minami and 1 more

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Ryo YoshimaruDepartment of Hematology and Oncology, National Cancer Center Hospital East, Kashiwa, JPN.
Ayumi KuzumeDepartment of Hematology and Oncology, National Cancer Center Hospital East, Kashiwa, JPN.
Hirotaka NakamuraDepartment of Hematology and Oncology, National Cancer Center Hospital East, Kashiwa, JPN.
Yon-Mei GuoDepartment of Hematology and Oncology, National Cancer Center Hospital East, Kashiwa, JPN.
SungGi ChiDepartment of Hematology and Oncology, National Cancer Center Hospital East, Kashiwa, JPN.
Saki NakamuraDepartment of Clinical Laboratory, National Cancer Center Hospital East, Kashiwa, JPN.
Michiko IidaDepartment of Clinical Laboratory, National Cancer Center Hospital East, Kashiwa, JPN.
Kimihiko KawamuraDepartment of Clinical Laboratory, National Cancer Center Hospital East, Kashiwa, JPN.
Kenta AkieDepartment of Clinical Laboratory, National Cancer Center Hospital East, Kashiwa, JPN.
Yosuke MinamiDepartment of Hematology and Oncology, National Cancer Center Hospital East, Kashiwa, JPN.
Junichiro YudaDepartment of Hematology and Oncology, National Cancer Center Hospital East, Kashiwa, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) with double minute chromosomes (dmin) is a rare complication and has been reported to be refractory to chemotherapy, with a poor prognosis. A 65-year-old woman presented to a local hospital with chronic thyroiditis and sarcoidosis. She underwent a routine blood test that indicated 13% blasts in her peripheral blood. Bone marrow examination revealed 51% myeloblasts with Auer bodies, leading to the diagnosis of AML (French-American-British classification: M2; WHO classification: AML, NOS; AML with maturation). Chromosome examination (G-banding) showed the following karyotypes: 46,XX,2-11 dmin(4/20); 47,idem,+4(5/20); and 46,XX(11/20). Fluorescence in situ hybridization analysis demonstrated amplification of MYC. Genetic testing via leukemia chimeric screening was negative. The patient achieved complete remission (CR) with reduced-dose induction therapy (daunorubicin 50 mg/m² × 3 days; cytarabine 100 mg/m² × 7 days). After three courses of reduced-dose consolidation therapy (high-dose cytarabine 1,500 mg/m²), the patient remained in CR for 5 years and showed long-term survival. AML with amplification of MYC on dmin, combined with complex karyotypes, can acquire resistance to treatment due to the activity of other oncogenes in addition to MYC amplification. In cases with dmin, evaluation of other chromosomes and genetic abnormalities associated with poor prognosis is key to predicting outcome and determining the treatment plan.

Indexed as

acute myeloid leukemia (aml)double minute chromosomeslong-term survivalmyctrisomy 4

Identifiers

PMID40932956
PMCPMC12418050

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