Evidence map›Paper›PMID 41423591›Full record

ArticleBlood research2025

Insights into Treatment-Free Remission (TFR) outcomes in Chronic Myeloid Leukaemia (CML) - a tertiary centre experience in Malaysia.

Christopher Chin Keong Liam, Yang Liang Boo, Li Min Lim, Siew Lian Chong, Azizan Sharif, Yih Seong Wong, Veena Selvaratnam, Sen Mui Tan, Soo Min Lim

Abstract read
In one paragraph

Article in Blood research, 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. Review
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

9 authors.

Christopher Chin Keong LiamHaematology Unit, Department of Medicine, Hospital Sultanah Aminah, Jalan Persiaran Abu Bakar Sultan, Johor Bahru, Johor, 80100, Malaysia. liamck85@hotmail.com.
Yang Liang BooHaematology Unit, Department of Medicine, Hospital Sultanah Aminah, Jalan Persiaran Abu Bakar Sultan, Johor Bahru, Johor, 80100, Malaysia.
Li Min LimHaematology Unit, Department of Medicine, Hospital Sultanah Aminah, Jalan Persiaran Abu Bakar Sultan, Johor Bahru, Johor, 80100, Malaysia.
Siew Lian ChongDepartment of Haematology, Hospital Ampang, Selangor, Malaysia.
Azizan SharifHaematology Unit, Department of Medicine, Hospital Sultanah Aminah, Jalan Persiaran Abu Bakar Sultan, Johor Bahru, Johor, 80100, Malaysia.
Yih Seong WongHaematology Unit, Department of Medicine, Hospital Sultanah Aminah, Jalan Persiaran Abu Bakar Sultan, Johor Bahru, Johor, 80100, Malaysia.
Veena SelvaratnamDepartment of Haematology, Hospital Ampang, Selangor, Malaysia.
Sen Mui TanDepartment of Haematology, Hospital Ampang, Selangor, Malaysia.
Soo Min LimHaematology Unit, Department of Medicine, Hospital Sultanah Aminah, Jalan Persiaran Abu Bakar Sultan, Johor Bahru, Johor, 80100, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTyrosine kinase inhibitors (TKIs) have improved the prognosis of chronic myeloid leukaemia (CML), allowing patients with favourable disease profiles and molecular responses to attempt treatment-free remission (TFR). We aim to establish the relapse-free survival (RFS) outcomes and identify prognostic factors for successful remission maintenance among those who attempt TFR.

methodsAdult CML patients who had undergone TFR from January 1, 2016, to June 30, 2024, were included. Upon TKI discontinuation, real-time quantitative polymerase chain reaction (RQ-PCR) was monitored monthly for the first 12 months, then every 3 months, with TKI reinitiated upon a transcript level above 0.1% (IS). Data analysis was performed using SPSS version 29.0 (SPSS Inc., Chicago, IL, USA).

resultsFifty-seven patients (27 males and 30 females) with a median age of 46 years (range 16 - 70) were analysed. The majority had a low EUTOS long-term survival (ELTS) score (61.4%, n = 35) and received imatinib (87.7%, n = 50). The median treatment duration was 8.8 years (range 4.2 - 18.8), and the median duration for sustained deep molecular remission (DMR) was 4.6 years (range 2.1 - 11.1). RFS was 70.2% at 6 months, 62.5% at 12 months and 56.8% at 2 years after a median follow-up of 34 months (range 9 - 101). The MR5 level was identified as an independent factor associated with sustained remission. All relapsed patients achieved DMR upon treatment reinitiation.

conclusionTreatment discontinuation can be safely performed, with many achieving long-term treatment-free remission. A deeper molecular response (MR5) is associated with an improved likelihood of remission maintenance.

Indexed as

Chronic Myeloid LeukaemiaTreatment Free Remission

Identifiers

PMID41423591
PMCPMC12738440

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