Adult Glioblastoma
Conditions
Keywords
newly diagnosed glioblastoma, p38 MAPK inhibitor, temozolomide, radiotherapy
Brief summary
Glioblastomas are extremely resistant to treatment, including radiotherapy and/or chemotherapy. Mitogen-activated protein kinase (MAPK) cascades are key signaling pathways involved in the regulation of normal cell proliferation, survival and differentiation. Activation of p38 MAPK has been associated with a poor prognosis among patients with glioblastoma during the temozolomide (TMZ) era and represents a compensatory response by tumor cell to environmental stress such as radiation or chemotherapy. LY2228820 is a potent and selective inhibitor of p38 MAPK, and reduces phosphorylation of its cellular target, MAPK-activated protein kinase 2 (MAPKAPK-2) . LY2228820 is a good candidate to target malignant glioma resistance to the gold standard treatment combining radiation and TMZ by acting on both tumor and stromal cells. The primary objectives of this study were to determine the recommended dose of LY2228820 in combination with TMZ and radiotherapy during chemoradiotherapy period (phase I) and to estimate the 6-month progression free survival (PFS) rate of patients treated with LY2228820 when administered at the recommended dose in combination with radiotherapy and concomitant TMZ (phase II)
Interventions
Sponsors
National Cancer Institute, France
ARC Foundation for Cancer Research
Centre Jean Perrin
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
* Newly diagnosed and histologically confirmed glioblastoma * Recursive partitioning analysis (RPA) class III or IV * Age \> or = 18 years and \< 75 years of age * Life expectancy \> or = 6 months * Patient must have at least 1 formalin fixed paraffin embedded tumor tissue block representative of glioblastoma available for pathology central review and biomarker exploration * Adequate hematologic (absolute neutrophil count (ANC) \> or = 1.5 x 109/L, platelet count \> or = 100 x 109/L, hemoglobin \> or = 10 g/dL ), renal (creatinine \> or = 1.25 x ULN ), and hepatic function (total bilirubin \< or = 1.5 x ULN, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) \< or = 2.5 x ULN) * Patients who were receiving corticosteroids had to receive a stable or decreasing dose for at least 14 days before enrollment * Patients must be able to swallow and retain oral medication * Women must have a negative serum pregnancy test less than 7 days prior to the first dose of study drug * Both men and women of reproductive potential agree to use approved contraception during the study and for 6 months after discontinuation of study treatment. * Willing and able to comply with the protocol as judged by the investigator * Patients must provide written consent
Exclusion criteria
* Any prior chemotherapy (including carmustine-containing wafers) or immunotherapy (including vaccine therapy ) * Any prior radiotherapy to the brain * Any contraindication to temozolomide listed in the local label * Have had, in the judgment of the investigator, a major bowel resection that would alter oral drug absorption * Have a diagnosis of inflammatory bowel disease (Crohn's disease or ulcerative colitis) * Have previously completed or withdrawn from this study or any other study investigating LY2228820 * Are receiving, in the judgment of the investigator, concurrent administration of immunosuppressive therapy * Diarrhea of any cause CTCAE \> or = grade 2 * Current or recent (within 30 days of enrollment) treatment with another investigational drug or participation in another investigational study * History of other malignancy within 5 years prior enrollment except for basal cell carcinoma of the skin or carcinoma in situ of the cervix * Pregnant or nursing (lactating) woman, or fertile women unwilling or unable to use effective means of contraception * Psychiatric illness / social situations that would compromise patient safety or limit compliance with study requirements including maintenance of a compliance / pill diary
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| maximum tolerated dose (MTD) (phase I) of LY2228820 in combination with TMZ and radiotherapy during chemoradiotherapy period | from D1 Week 0 (first dose of LY2228820) to D63 Week 8. | defined as the highest dose tested in which a dose limiting toxicity (DLT) is experienced by no more than 33% of patients during chemoradiotherapy period. |
| 6-month Progression Free Survival (PFS) rate (phase II) defined as the rate of patients who not presented a progression at 6 months from the first dose of LY2228820 | 6 months from the first dose of LY2228820 | — |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| PFS | from the first dose of LY2228820 to disease progression or death for any reason, up to 24 months | disease progression assessed per Response Assessment in Neuro-Oncology (RANO) criteria |
| Overall Survival | from the first dose of LY2228820 to death, up to 24 months | — |
| 12-month PFS rate defined as the rate of patients who not presented a progression at 12 months from the first dose of LY2228820 | 12 months from the first dose of LY2228820 | — |
| MAPKAPK-2 activation | baseline (tumor) D1 D7 week 0, D28 Week 3, D35 Week 4 (PBMCs) | in tumor and stromal cells and Peripheral Blood Mononucleated Cells (PBMCs) |
| The neurologic status evaluated by clinical assessment and Mini-Mental State Examination (MMSE) and evaluation of corticosteroid dosage | from baseline to progression, up to 24 months | — |
| Pharmacokinetic of LY2228820 and TMZ (AUC0-12h) | D7 Week 0, D28 Week 3, D35 Week 4 | — |
| Validated biomarker of glioblastoma (MGMT, IDH1 (isocitrate dehydrogenase 1), pTEN (phosphatase and tensin homolog), p53) | baseline | on tumor |
| Objective response rate according to RANO criteria for patients with incomplete resection or only biopsy | from the first dose of LY2228820 to treatment completion | — |
| Safety profile according to NCI Common Toxicity Criteria for Adverse Effect (CTCAE) criteria version 4.03. | from baseline to 30 days after treatment (concomitant and adjuvant treatment) (week 35) | — |
Countries
France
Outcome results
None listed