Evidence map›Paper›PMID 40453521›Full record

Trial reportBlood neoplasia2024

KIR3DL1-HLA-Bw status in CML is associated with achievement of TFR: the POKSTIC trial, a multicenter observational study.

Hiroshi Ureshino, Yasunori Ueda, Shin Fujisawa, Kensuke Usuki, Hideo Tanaka, Masaya Okada, Shugo Kowata, Kazunori Murai, Asao Hirose, Motohiro Shindo and 14 more

Abstract readClinical Trial
In one paragraph

Trial report in Blood neoplasia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Road to treatment-free remission in chronic myeloid leukemia.International journal of hematology · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
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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

24 authors.

Hiroshi UreshinoDepartment of Hematology and Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
Yasunori UedaDepartment of Hematology/Oncology, Kurashiki Central Hospital, Kurashiki, Japan.
Shin FujisawaDepartment of Hematology, Yokohama City University Medical Center, Yokohama, Japan.
Kensuke UsukiDepartment of Hematology, NTT Medical Center Tokyo, Tokyo, Japan.
Hideo TanakaDepartment of Hematology, Hiroshima City Asa Hospital, Hiroshima, Japan.
Masaya OkadaFirst Department of Internal Medicine, Kansai Medical University Medical Center, Kansai Medical University, Osaka, Japan.
Shugo KowataDivision of Hematology and Oncology, Department of Internal Medicine, Iwate Medical University, Iwate, Japan.
Kazunori MuraiDepartment of Hematology, Iwate Prefectural Central Hospital, Morioka, Japan.
Asao HiroseDepartment of Hematology, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Japan.
Motohiro ShindoDivision of Metabolism and Biosystemic Science, Gastroenterology and Hematology Oncology, Department of Medicine, Asahikawa Medical University, Asahikawa, Japan.
Takashi KumagaiDepartment of Hematology, Ome Municipal General Hospital, Ome, Japan.
Tomoharu TakeokaDepartment of Hematology and Immunology, Otsu Red Cross Hospital, Otsu, Japan.
Kazuharu KamachiDivision of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Keisuke KidoguchiDivision of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Takero ShindoDepartment of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Satoshi IyamaDepartment of Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Junki InamuraDepartment of Hematology Oncology, Asahikawa Kosei Hospital, Asahikawa, Japan.
Takafumi NakaoDepartment of Hematology, Osaka City General Hospital, Osaka, Japan.
Tsutomu KobayashiDepartment of Hematology and Oncology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Eri KawataDepartment of Hematology, Panasonic Health Insurance Organization, Matsushita Memorial Hospital, Moriguchi, Japan.
Hiroshi OhkawaraDepartment of Hematology, Fukushima Medical University, Fukushima, Japan.
Takayuki IkezoeDepartment of Hematology, Fukushima Medical University, Fukushima, Japan.
Atsushi KawaguchiEducation and Research Center for Community Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Shinya KimuraDivision of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Achievement of treatment-free remission (TFR) after tyrosine kinase inhibitor (TKI) discontinuation in patients who show a durable deep molecular response (DMR) during TKI treatment of chronic myeloid leukemia in chronic phase (CML-CP) is a therapeutic goal; however, the prognostic factors that predict successful achievement of TFR are unclear. Previously, we reported that killer immunoglobulin-like receptor (

Identifiers

PMID40453521
PMCPMC12082104

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Registered trials

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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.