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临床试验/JPRN-jRCTs051220019
JPRN-jRCTs051220019招募中2 期

Exploratory study of PET to detect early local response of boron neutron capture therapy for recurrent malignant glioma - PET detection of early local response of BNCT for malignant glioma

ihei Keiji0 个研究点目标入组 21 人开始时间: 2022年4月28日最近更新:

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
21

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 <= 79age old(—)
性别
All

入选标准

  • 1. A histopathological diagnosis of malignant glioma has been obtained.
  • 2.Receiving bevacizumab treatment for recurrence after standard treatment.
  • 3. Having an evaluable lesion, which obviously recurred by MRI after bevacizumab administration.
  • Recurrence is defined as progression disease (PD) in RANO criteria by MRI.
  • 4. Surgical treatment is difficult.
  • 5. The age at the time of obtaining consent is between 20 and 79 years old.
  • 6. Written consent has been obtained from the patient or the legal representative for participation in
  • the research.
  • 7. Karnofsky performance status is 60 percent or higher.
  • 8. No obvious tumor growth is observed on the contralateral cerebral hemisphere or infratentorial area by MRI (no contrast-enhanced/contrast-enhanced).
  • 9. Expected to survive for 3 months or more, and to visit outpatient clinic 3 months after BNCT.
  • 10. The functions of major organs are maintained, and the clinical laboratory test values meet the following conditions at the time of obtaining consent.
  • White blood cell count >= 3,000/microL
  • Neutrophil count >= 1,500/maicroL
  • Hemoglobin >= 8.0 g/dL
  • Platelet count >= 100,000/microL
  • AST =< 100 IU/L
  • ALT =< 100 IU/L
  • Total bilirubin =< 1.5 mg/dL
  • Serum creatinine =< 1.5 mg/dL
  • Proteinuria =< +

排除标准

  • Patients with the following medical conditions or circumstances are excluded.
  • 1. Medullary cavity dissemination.
  • 2. Infections that require intravenous administration of antibiotics, antiviral drugs, antifungal drugs, etc.
  • 3. Serious complications (heart disease, pulmonary fibrosis / interstitial pneumonia, bleeding tendency, uncontrolled hypertension, diabetes, etc.).
  • 4. Phenylketonuria.
  • 5. Currently bleeding (intracranial bleeding, gastrointestinal bleeding, urinary tract bleeding, retroperitoneal bleeding, hemoptysis, etc.).
  • 6. Even with oral anticoagulants, poor control or PT-INR is over 2.5.
  • 7. History of severe hypersensitivity to MRI contrast medium, ingredients of Steboronine or 18F-FBPA.
  • 8. Pregnant women or lactating women.
  • 9. Participating in other clinical trials.
  • 10. In addition, the patient judged by the principal investigator or the doctor in charge to be inappropriate for conducting this research safely.

研究者

发起方
ihei Keiji

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