Evidence map›Paper›PMID 38146352›Full record

ArticleBlood cell therapy2023

Gilteritinib in peritransplant period for relapsed or refractory FLT3-mutated acute myeloid leukemia: A case report of three patients.

Fuka Mima, Shigeo Fuji, Kumi Shibata, Shuhei Kida, Kazuhito Tsutsumi, Yuma Tada, Yasuhiro Shingai, Sayako Yuda, Takafumi Yokota, Jun Ishikawa

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Blood cell therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 1 institution in 1 country.

Fuka MimaDepartment of Hematology, Osaka International Cancer Institute, Osaka, Japan.
Shigeo FujiDepartment of Hematology, Osaka International Cancer Institute, Osaka, Japan.
Kumi ShibataDepartment of Hematology, Osaka International Cancer Institute, Osaka, Japan.
Shuhei KidaDepartment of Hematology, Osaka International Cancer Institute, Osaka, Japan.
Kazuhito TsutsumiDepartment of Hematology, Osaka International Cancer Institute, Osaka, Japan.
Yuma TadaDepartment of Hematology, Osaka International Cancer Institute, Osaka, Japan.
Yasuhiro ShingaiDepartment of Hematology, Osaka International Cancer Institute, Osaka, Japan.
Sayako YudaDepartment of Hematology, Osaka International Cancer Institute, Osaka, Japan.
Takafumi YokotaDepartment of Hematology, Osaka International Cancer Institute, Osaka, Japan.
Jun IshikawaDepartment of Hematology, Osaka International Cancer Institute, Osaka, Japan.
Osaka International Cancer Institute · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with relapsed or refractory acute myeloid leukemia (RR-AML) with mutations of FMS-like tyrosine kinase 3 (FLT3) have a poor prognosis even after allogeneic hematopoietic cell transplantation (allo-HCT). Multiple FLT3 inhibitors, including gilteritinib, have been developed and serve as treatment options for RR-AML. Here, we describe three cases of FLT3 mutated RR-AML that were successfully treated with gilteritinib administration before and after allo-HCT. Gilteritinib treatment before HCT was helpful in achieving remission. However, HCT often resulted in mild liver damage, and careful introduction of gilteritinib after HCT at a lower dose may be helpful for its safe usage. The three cases discussed had a successful clinical outcome in terms of disease control as well as the management of side effects associated with gilteritinib treatment.

Indexed as

acute myeloid leukemiaallogeneic hematopoietic cell transplantationFLT3gilteritinib

Identifiers

PMID38146352
PMCPMC10749211
OpenAlexW4386642160

What OpenQuestion holds

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LicenceCC BY-NC
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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.