Brain tumor study reveals hidden toll of chemo on daily life
NCT ID NCT03257618
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study followed 26 adults with low-grade glioma who were receiving chemotherapy (temozolomide) for the first time after surgery. Researchers measured how the treatment affected patients' quality of life, thinking skills, and emotional well-being over one year. The goal was to better understand the full impact of the disease and its treatment, since preserving quality of life is a key priority when a cure is not available.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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26 people
The number who actually took part.
- Started
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Jul 2017
- Finished
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Dec 2021
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patient aged ≥ 18, no age limit; * Histologically-proven DLGG; * Patient receiving TMZ as a first line treatment after surgery, whatever the delay between the surgery and the introduction of TMZ; * No previous oncologic treatment (except for surgery) for the DLGG; * Performance status (PS) score ≤ 2; * Absolute neutrophil count (ANC) ≥ 1500 cells/µL and platelet count ≥ 100 000 cells/µL; * Total serum bilirubin concentration ≤ 1.5 x the upper limit of normal (ULN); * Aspartate aminotransferase (AST), alanine aminotransferase (ALT) and alkaline phosphatase ≤ 2.5 x the ULN; * Serum creatine concentration ≤ 1.5 x the ULN; * Negative pregnancy test in women of childbearing potential; * A signed informed consent obtained before any study specific procedures; * Patient fluent in French ; * Patient affiliated to a French social security system Exclusion Criteria: * Anaplastic glioma (WHO grade III glioma); * Impaired neurocognitive functioning defined by a score \< 22 at the MoCA evaluation; * Visual or auditory deficit ; * Previous chemotherapy for the DLGG; * Previous RT for the DLGG; * Known hypersensitivity to any of the study drugs, or excipients in the formulation; * Hypersensitivity to dacarbazine (DTIC); * Severe myelosuppression; * Problems of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption; * Legal incapacity or physical, psychological social or geographical status interfering with the patient's ability to sign the informed consent or to terminate the study; * Pregnant or breastfeeding women; * Men or women of childbearing potential who are unwilling to employ adequate contraception, from the beginning of the study until 6 months after administration of the last treatment dose; * Participation in another clinical trial with 30 prior to study entry.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Institut regional du Cancer - Val d Aurelle
Montpellier, 34298, France
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Other studies related to the condition(s) this trial covers.
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