glioblastoma
Conditions
Interventions
Arm A:
(1) 40 Gy in 15 daily fractions with temozolomide
(i) Concomitant phase, temozolomide (75 mg/m2, every day from first day to last day of radiation), radiation (2.67 Gy/day, 5 days/week, 15 tim
Sponsors
ARAKAWA Yoshiki
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: First registration criteria (1) Diagnosed as glioblastoma or Grade III glioma (WHO 2016 edition) in pathological diagnosis during surgery, or histologically proven diagnosis of glioblastoma by WHO 2016 criteria. (2) Tumor specimen is available to analyze MGMT promoter methylation. (3) No history of treatments for glioma except for resection including biopsy and the second resection within 21 days after the first resection (partly resection or biopsy). (4) Within 21 days after surgery. (5) The tumor exists supratentorial region on preoperative head contrast MRI. (6) Preoperative head contrast MRI revealed no dissemination. (7) Presence of measurable lesions is not mandatory. (8) Patient' s age is 71 years or older at registration. Aged 71 to 75 years old with resection of less than 90% of contrast region. (9) ECOG performance status (PS) of 0, 1, 2, or 3 due to neurological signs caused by the tumor. (10) No prior chemotherapy or head radiation therapy for any intracranial tumors. (11) Sufficient organ function. (i) Neutrophil count >= 1,500 /mm3 (ii) Hemoglobin >= 8.0 mg/dl (iii) Platelet count >= 100,000 /mm3 (iv) AST =< 120 U/L (v) ALT =< 120 U/L (vi) Cr =< 1.605 mg/dL (male), =< 1.185 mg/dL (female) (12) Written informed consent. Second registration criteria (1) Within 21 days of the first registration (2) Histologically proven diagnosis of glioblastoma by WHO 2016 edition. (3) Judged as methylation or unmethylation in MGMT promoter region.
Exclusion criteria
Exclusion criteria: (1) Synchronous or metachronous (within 2 years) malignancies. (2) Infections which needs systemic treatment. (3) Body temperature is higher than 38 degrees centigrade at registration. (4) Severe psychological disease. (5) Continuous systemic corticosteroid or immunosuppressant treatment due to the diseases except for brain tumor. (6) Uncontrollable diabetes mellitus. (7) Unstable angina pectoris, or history of myocardial infarction within 6 months. (8) Interstitial pneumonia, pulmonary fibrosis, or severe emphysema on chest X-p. (9) Gadolinium allergy. (10) Positive HIV antibody. (11) Positive HBs antigen.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Overall survival | — |
Secondary
| Measure | Time frame |
|---|---|
| Progression-free survival, Proportion of adverse events, Proportion of Karnofsky Performance Status (KPS) preservation, Proportion of Health-related Quality of Life (QOL) preservation | — |
Contacts
Public ContactYoshiki ARAKAWA
Kyoto University Hospital
Outcome results
None listed