Glioblastoma Clinical Trial
— TIGREOfficial title:
Early Diagnosis of Pseudoprogression Using 11C-Methionine PET-MRI After Concomitant Radiochemotherapy Treatment for Glioblastoma.
Pseudoprogression is a phenomenon related to post-treatment rearrangements (including
radiation necrosis). It appears early in the first year after treatment and accounts for 30
to 50% of patients followed with glioblastoma. On MRI (current gold standard with
international therapeutic response evaluation criteria RANO 2010), pseudoprogression is
manifested by a progression of morphological abnormalities (contrast enhancement, FLAIR
hypersignal) and can simulate tumor recurrence, even though the corticosteroid improved or
kept clinical symptoms stabilized. In view of prognosis, the current diagnostic tools have
not enough diagnosis accuracy for differentiation between pseudo-progression and early tumor
recurrence, and are based on MRI retrospective analysis (2-3 months after). Recurrence of
glioblastoma, is characterized by a higher amino acid metabolism than pseudoprogression, also
11C-Methionine (11C-MET), positron emitting radiotracer, showed promising results to
differentiate these two entities. To date, hybrid 11C-MET PET-MRI studies remains limited to
small sample size (a few dozen patients), and none focuses exclusively on glioblastoma.
Hypothesis of our study is that 11C-MET PET-MRI may be performed as a first-line MRI for
suspected pseudoprogression and may changes therapeutic decision making and also patient
prognosis.
The main objective is to evaluate the performance of hybrid PET-MRI imaging with 11C-MET to
differentiate pseudoprogression from glioblastoma recurrence in patients treated with surgery
and radiochemotherapy, compared to multimodality MRI).
Status | Recruiting |
Enrollment | 40 |
Est. completion date | January 26, 2025 |
Est. primary completion date | February 26, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients aged 18 or over, - Patient with glioblastoma treated by radiochemotherapy with temozolomide, - Patient with suspicion of pseudoprogression between the 1st and 12th month after the end of concomitant chemoradiotherapy, - Patient receiving a social security scheme, - Patient for whom informed and written consent to participate has been obtained, Exclusion Criteria: - Subject under safeguard of justice (tutelage, curatorship), - Minor patient, - Patient without signs of progression MRI (stable disease or good response to treatment according to the RANO 2010 criteria), - Clinical or radiological progression justifying a change of treatment, - Patient not able to decide and with refusal of the family entitled to continue research. - Pregnant woman, breastfeeding or old enough to have children but without effective contraception, - Contraindication to performing an MRI: permanently fixed metal parts (pacemaker, cerebral clip, cochlear implant, pin or screw for recent bone fracture, dental equipment, metal splinters), claustrophobia, - Contraindication to gadolinium according to ANSM 2017 recommendations |
Country | Name | City | State |
---|---|---|---|
France | Hopices Civils de Lyon | Bron |
Lead Sponsor | Collaborator |
---|---|
Hospices Civils de Lyon |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | false negatives and false positives description (diagnosis accuracy) of 11C-Methionine PET-MRI | diagnosis accuracy of 11C-MET PET-MRI to differentiated pseudoprogression from tumor recurrence, compared to MRI. The gold-standard being retrospective MRI analysis. | within 1 months and 12 months post-treatment | |
Secondary | ROC curves for comparison of two diagnostic tests: MRI and PET-MRI | use of area under the curve for each tests to identify the best | within 1 months and 24 months after inclusion | |
Secondary | The proportion of pseudoprogression identified by PET-MRI to 11C-MET according to the genetic data | The proportion of pseudoprogression identified by PET-MRI to 11C-MET according to the methylation status of the O6-methylguanine-DNA- methyltransferase (MGMT) promoter, the level of expression of isocitrate dehydrogenase (IDH) mutation, ki67 and 1p19q mutation. | during 24 months after inclusion | |
Secondary | Overall survival analysis | Patients will be followed regularly for 2 years to assess overall survival at 12 months and at 24 months. | during 24 months after inclusion |
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