Evidence map›Paper›PMID 40488811›Full record

SynthesisInternational journal of clinical oncology2025

Different outcomes by sex in metastatic gastrointestinal stromal tumor patients receiving imatinib: a trial-level analysis.

Antonella Venturino, Giuseppe Antonio Colloca

Abstract readMeta-AnalysisSystematic Review
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In one paragraph

Synthesis in International journal of clinical oncology, 2025. 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

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

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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.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Antonella VenturinoOncologia Medica & Innovation, Via Aicardi n. 37, I-18100, Imperia, Italy. vent.ant.470@gmail.com.ORCID http://orcid.org/0000-0001-8793-8138
Giuseppe Antonio CollocaOncologia Medica & Innovation, Via Aicardi n. 37, I-18100, Imperia, Italy.ORCID http://orcid.org/0000-0002-0903-6793

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmong gastrointestinal stromal tumors patients, many authors have reported longer overall survival for female sex regardless of stage. Other studies showed more favourable prognosis for young women, while others found no effect of sex on outcome. Few data about survival differences by sex are available on patients with unresectable/metastatic gastrointestinal stromal tumors (mGIST) receiving imatinib. The study aims to perform a trial-level analysis of metastatic gastrointestinal stromal tumors patients treated with imatinib to define the effect of sex on overall survival.

methodsAfter a systematic literature review, studies enrolling mGIST patients receiving upfront imatinib and reporting hazard ratios and confidence intervals of the relationship of sex with overall survival (OS) were selected. A meta-analysis was performed, calculating a global effect size. Finally, the study explored the effect on the relationship of other baseline variables, such as age, sex, tumor location, and patient origin.

resultsFifteen articles were selected, including 3612 patients. The meta-analysis documented longer OS among women, with significant overall effect size (HR 0.77, CI 0.71-0.84). Furthermore, there was no significant heterogeneity among studies (Q=9.13, p-value=0.8229; I

conclusionsThe analysis documented better prognosis for female sex after upfront imatinib. The absence of heterogeneity between studies suggests that sex may condition a different response to imatinib. However, other factors, such as second malignancies and mutation patterns, may also contribute to the observed differences.

Indexed as

Antineoplastic AgentsGastrointestinal NeoplasmsGastrointestinal Stromal TumorsImatinib MesylateFemaleHumansMaleNeoplasm MetastasisPrognosisSex FactorsTreatment OutcomeAntineoplastic AgentsImatinib MesylateFemale sexGastrointestinal stromal tumorsImatinibPrognosisSurvival

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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.