Evidence map›Paper›PMID 26267232›Full record

Trial reportInternational journal of hematology2015

The longitudinal analysis of large granular lymphocytosis in patients with Philadelphia chromosome-positive leukemia treated with dasatinib.

Yuji Shimura, Shigeo Horiike, Yasuhiko Tsutsumi, Mayumi Hatsuse, Akira Okano, Shin-Ichi Fuchida, Tsutomu Kobayashi, Yosuke Matsumoto, Junya Kuroda, Eri Kawata-Iida and 6 more

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in International journal of hematology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 30% of its field
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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Future Directions in Chronic Phase CML Treatment.Current hematologic malignancy reports · 2021
    Review
  2. 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

16 authors at 3 institutions in 1 country.

Yuji ShimuraDivision of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kajii-cho 465, Kawaramachi-Hirokoji, Kamigyo-Ku, Kyoto, 602-8566, Japan. yshimura@koto.kpu-m.ac.jp.ORCID http://orcid.org/0000-0001-9309-7902
Shigeo HoriikeDivision of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kajii-cho 465, Kawaramachi-Hirokoji, Kamigyo-Ku, Kyoto, 602-8566, Japan.
Yasuhiko TsutsumiDivision of Hematology, Department of Medicine, Kyoto First Red Cross Hospital, Kyoto, Japan.
Mayumi HatsuseDivision of Hematology, Department of Medicine, Kyoto Kuramaguchi Medical Center, Kyoto, Japan.
Akira OkanoDivision of Hematology, Department of Medicine, Kyoto Kuramaguchi Medical Center, Kyoto, Japan.
Shin-Ichi FuchidaDivision of Hematology, Department of Medicine, Kyoto Kuramaguchi Medical Center, Kyoto, Japan.
Tsutomu KobayashiDivision of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kajii-cho 465, Kawaramachi-Hirokoji, Kamigyo-Ku, Kyoto, 602-8566, Japan.
Yosuke MatsumotoDivision of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kajii-cho 465, Kawaramachi-Hirokoji, Kamigyo-Ku, Kyoto, 602-8566, Japan.
Junya KurodaDivision of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kajii-cho 465, Kawaramachi-Hirokoji, Kamigyo-Ku, Kyoto, 602-8566, Japan.
Eri Kawata-IidaDivision of Hematology, Department of Medicine, Kyoto Second Red Cross Hospital, Kyoto, Japan.
Hitoji UchiyamaDivision of Hematology, Department of Medicine, Kyoto Second Red Cross Hospital, Kyoto, Japan.
Nobuhiko UoshimaDivision of Hematology, Department of Medicine, Kyoto Second Red Cross Hospital, Kyoto, Japan.
Chihiro ShimazakiDivision of Hematology, Department of Medicine, Kyoto Kuramaguchi Medical Center, Kyoto, Japan.
Hiroto KanekoDivision of Hematology, Department of Medicine, Kyoto First Red Cross Hospital, Kyoto, Japan.
Yutaka KobayashiDivision of Hematology, Department of Medicine, Kyoto Second Red Cross Hospital, Kyoto, Japan.
Masafumi TaniwakiDivision of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kajii-cho 465, Kawaramachi-Hirokoji, Kamigyo-Ku, Kyoto, 602-8566, Japan.
Kyoto first Red Cross hospital · JPKyoto Prefectural University of Medicine · JPKyoto Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dasatinib, a 2nd-generation tyrosine kinase inhibitor (TKI), can specifically induce large granular lymphocytes (LGL) in some patients with Philadelphia chromosome (Ph)-positive leukemia. To investigate the properties of the induced LGLs, we performed prospective and longitudinal analyses. From Feb 2011 to Jan 2013, a total of 17 patients with Ph-positive leukemia who were previously untreated or refractory to imatinib were enrolled. T cell receptor (TCR)-γ/δ gene rearrangements and phenotypic profiles of lymphocytes were examined before and during administration of dasatinib. LGL lymphocytosis was observed in half of the dasatinib-treated cases (LGL+ group), showing a relation to increased achievement of complete cytogenetic response within 6 months. The phenotypes of the increased lymphocytes were revealed to be mostly natural killer cells. In the LGL+ group, clonal TCR-γ gene rearrangements were frequently detected at diagnosis (six of nine cases) and persisted during therapy, compared with only two of eight in the LGL- group. The proportion of regulatory T cells to CD4+ T cells at diagnosis was lower in the LGL+ compared with the LGL- group (median 4.2 vs. 6.6 %), and this disparity was sustained throughout the therapeutic period. These results demonstrate that immunological condition at diagnosis may affect LGL lymphocytosis in some dasatinib-treated patients.

Indexed as

CD4-Positive T-LymphocytesGene Rearrangement, delta-Chain T-Cell Antigen ReceptorGene Rearrangement, gamma-Chain T-Cell Antigen ReceptorLeukemia, Large Granular LymphocyticPrecursor Cell Lymphoblastic Leukemia-LymphomaReceptors, Antigen, T-Cell, gamma-deltaAdultAgedDasatinibFemaleFollow-Up StudiesHumansKiller Cells, NaturalMaleMiddle AgedDasatinibReceptors, Antigen, T-Cell, gamma-deltaClonalityDasatinibLGLRegulatory T cell

Identifiers

PMID26267232
OpenAlexW1445151278

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.