Evidence map›Paper›PMID 41729399›Full record

ArticleClinical journal of gastroenterology2026

A case of intestinal tumor formation during gilteritinib therapy that resolved without discontinuing the drug.

Koji Oka, Hisaharu Shikata, Masahiko Kaneko, Shoichi Matsukage

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In one paragraph

Article in Clinical journal of gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Koji OkaDepartment of Hematology, Uwajima City Hospital, 1-1 Goten-machi, Uwajima, Ehime, 798- 8510, Japan. oka.koji.ak@ehime-u.ac.jp.ORCID http://orcid.org/0009-0001-9944-6760
Hisaharu ShikataDepartment of Hematology, Uwajima City Hospital, 1-1 Goten-machi, Uwajima, Ehime, 798- 8510, Japan.
Masahiko KanekoDepartment of Hematology, Uwajima City Hospital, 1-1 Goten-machi, Uwajima, Ehime, 798- 8510, Japan.
Shoichi MatsukageDepartment of Pathology, Uwajima City Hospital, Uwajima, Ehime, 798- 8510, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The introduction of FLT3 inhibitors for the treatment of acute myeloid leukemia has demonstrated their efficacy and broadened available treatment options. FLT3 inhibitors have been shown to be safer than conventional chemotherapy; however, numerous adverse effects remain uncharacterized. In this report, we describe the case of a patient who developed bloody stools associated with intestinal tumor formation during gilteritinib therapy. The patient underwent multiple chemotherapy regimens but experienced disease recurrence. Gilteritinib was initiated following confirmation of FLT3-ITD mutation positivity. During gilteritinib therapy, the patient developed bloody stools, and endoscopic examination revealed a tumor with an ulcer located in the sigmoid colon. The tumor resolved without discontinuation of gilteritinib therapy. Based on the clinical course and pathological findings, the event is considered to be gilteritinib-induced. Although gastrointestinal (GI) bleeding has been documented in gilteritinib clinical trials, no prior cases of tumor formation have been reported. Furthermore, only one case has been reported in which endoscopy was performed for GI bleeding in a patient receiving gilteritinib therapy. Thus, this case may provide new insights into drug-induced GI manifestations associated with gilteritinib.

Indexed as

Aniline CompoundsAntineoplastic AgentsLeukemia, Myeloid, AcuteProtein Kinase InhibitorsPyrazinesfms-Like Tyrosine Kinase 3Gastrointestinal HemorrhageHumansAniline CompoundsAntineoplastic AgentsFLT3 protein, humanfms-Like Tyrosine Kinase 3gilteritinibProtein Kinase InhibitorsPyrazinesDrug-induced tumor formationGastrointestinal adverse eventsGilteritinib

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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.