Evidence map›Paper›PMID 40799021›Full record

ArticleBritish journal of haematology2025

Treatment-free remission in chronic myeloid leukaemia patients with accelerated phase or tyrosine kinase inhibitor therapy failure.

Mengyao Yuan, Yanli Zhang, Bingcheng Liu, Li Zhou, Yu Zhu, Zhenling Li, Shaolei Zang, Zhenfang Liu, Weiming Li, Qian Jiang

Abstract read
In one paragraph

Article in British journal of haematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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

10 authors.

Mengyao YuanBeijing Key Laboratory of Cell and Gene Therapy for Haematologic Malignancies, National Clinical Research Center for Haematologic Disease, Peking University People's Hospital, Peking University Institute of Haematology, Peking University, Beijing, China.
Yanli ZhangDepartment of Haematology, Henan Cancer Hospital, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Bingcheng LiuNational Clinical Research Center for Blood Diseases, Institute of Haematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjing, China.
Li ZhouState Key Laboratory of Medical Genomics, National Research Center for Translational Medicine at Shanghai, Shanghai Institute of Haematology, Ruijin Hospital Affiliated with Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yu ZhuThe First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Nanjing, China.ORCID https://orcid.org/0000-0002-6928-4027
Zhenling LiDepartment of Haematology, China-Japan Friendship Hospital, Beijing, China.
Shaolei ZangDepartment of Haematology, Qilu Hospital, Shandong University, Jinan, China.
Zhenfang LiuDepartment of Haematopathology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Weiming LiDepartment of Haematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID https://orcid.org/0000-0001-6276-1989
Qian JiangBeijing Key Laboratory of Cell and Gene Therapy for Haematologic Malignancies, National Clinical Research Center for Haematologic Disease, Peking University People's Hospital, Peking University Institute of Haematology, Peking University, Beijing, China.ORCID https://orcid.org/0000-0001-7131-0522

Funding

National Natural Science Foundation of China 81970140National Natural Science Foundation of China 82370161
6 · The paper itself

Abstract

We studied 60 chronic myeloid leukaemia (CML) patients with a prior history of accelerated phase (AP) including de novo AP (n = 19) and transformation to AP (n = 4), or tyrosine kinase inhibitor (TKI) therapy failure in the chronic phase (CP, n = 37), who discontinued TKI therapy. Median interval from diagnosis with AP or TKI therapy failure to achieving a deep molecular response (DMR) was 19 months (interquartile range [IQR], 9-30 months). Median TKI treatment and DMR duration were 108 months (IQR, 72-137 months) and 59 months (IQR, 39-87 months) respectively. At a median follow-up of 21 months (IQR, 11-36 months) after TKI discontinuation, 19 (31%) patients lost the major molecular response (MMR). The 3-year probability of a sustained MMR was 59% (95% confidence interval [CI], [45%, 78%]). In the multivariable analyses, age at discontinuation <32 years (hazard ratio [HR] = 4.1 [1.3, 12.7], p = 0.014) and BCR::ABL1 >0.1% at 12 months on TKI therapy (reference, ≤0.1%; HR = 3.9 [1.4, 11.5], p = 0.011) were significantly associated with a higher probability of MMR loss after TKI discontinuation. CML patients with a history of AP or TKI therapy failure may achieve successful treatment-free remission after an adequate TKI therapy duration and a sustained DMR.

Indexed as

Leukemia, Myelogenous, Chronic, BCR-ABL PositiveLeukemia, Myeloid, Accelerated PhaseProtein Kinase InhibitorsAdultAgedFemaleFollow-Up StudiesHumansMaleMiddle AgedRemission InductionRetrospective StudiesTreatment FailureTyrosine Kinase InhibitorsProtein Kinase InhibitorsTyrosine Kinase Inhibitorsaccelerated phasechronic myeloid leukaemiatherapy failuretreatment‐free remissiontyrosine kinase inhibitor

Identifiers

PMID40799021
PMCPMC12512077

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.