Study of Disulfiram to Reduce Myeloid Immunosuppression and Steroid Dependence in Resectable High Grade Glioma
A Window-of-Opportunity Study of Disulfiram to Reduce Myeloid Immunosuppression and Steroid Dependence in Resectable High-Grade Glioma
調査の概要
詳細な説明
Glioblastoma is one of the most common brain cancers that affect adults and is very hard to treat. This is due to myeloid cells, which are special immune cells in the body that prevent the body from recognizing and attacking the tumor. Because of this, immunotherapies have not worked well in treating glioblastoma.
Disulfiram may also reduce brain swelling, which may decrease or delay the need for subjects to be treated with steroids.
The purpose of this study is to find out if disulfiram can help reduce immunosuppression and help prevent edema symptoms when taken 3-14 days before planned surgery.
研究の種類
入学 (推定)
段階
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Tiffany Hodges, MD
- 電話番号:216-286-7122
- メール:tiffany.hodges@uhhospitals.org
研究場所
-
-
Ohio
-
Cleveland、Ohio、アメリカ、44106
- University Hospitals Cleveland Medical Center
-
コンタクト:
- Tiffany Hodges, MD
- 電話番号:216-286-7122
- メール:tiffany.hodges@uhhospitals.org
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Age ≥18 years.
- Radiographically suspected or confirmed high-grade glioma planned for surgical resection as part of standard clinical care.
- Able to start disulfiram at least 3 days prior to planned surgery (treatment window 3-14 days pre-op).
- In-patient status for the duration of study.
- Karnofsky Performance Status (KPS) ≥70%.
Adequate organ function within 14 days prior to first dose:
- ANC ≥1.5 x 10^9/L
- Platelets ≥100 x 10^9/L
- Hemoglobin ≥9 g/dL
- AST/ALT ≤2.5 x ULN
- Total bilirubin ≤1.5 x ULN (unless Gilbert syndrome, in which case <5 x ULN).
- Total bilirubin ≤1.5 x ULN (unless Gilbert syndrome, in which case <5 x ULN).
- Ability to understand and willingness to sign written informed consent.
- Willingness to avoid alcohol and alcohol-containing products during treatment and for 14 days after last dose.
Exclusion Criteria:
- Any dexamethasone (or other systemic glucocorticoid for cerebral edema) administered prior to enrollment/first dose (including outpatient or ED administration). This does not include inhalers or topical steroids.
- Imaging features that are atypical for high-grade glioma that have reasonable concern for competing differential diagnoses (e.g. PCNSL, tumefactive MS, etc.)
- Known hypersensitivity to disulfiram or thiuram derivatives.
- Active or severe hepatic disease (e.g. hepatitis, cirrhosis, known liver disease that may be exacerbated by disulfiram), or baseline liver tests above inclusion thresholds.
- Current use of metronidazole or other contraindicated interacting medications. See section 6.0; medication reconciliation for the list of medications/foods.
- Pregnant or breastfeeding. Pregnant women are excluded from the trial because the safety in pregnancy has not been established. Women who are breastfeeding are excluded from the trial because it is not known if disulfiram is present in breast milk.
- Clinically unstable neurologic status requiring immediate steroid initiation, where delaying dexamethasone for a disulfiram trial would be unsafe (investigator judgment).
- Any condition that would limit compliance with alcohol avoidance or study procedures, or that would make participation unsafe in investigator judgment.
- Subjects receiving any other investigational agents.
- Subjects with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, uncontrolled or unstable cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:非ランダム化
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Disulfiram
description here
|
250 milligrams (mg) disulfiram will be given daily for 3-14 prior to operation.
Participants can have the option to be treated at 500mg after initial evaluation.
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Reduction in Complement Immunosuppressive program
時間枠:day 0, up to 14 days
|
Evaluate whether disulfiram given pre-operation reduces the Complement Immunosuppressive myeloid program scores vs historical controls, which will be compared using a two-sample Wilcoxon rank-sum test (primary) and a two-sample t-test on the participant-level program scores (sensitivity).
Measured using scRNA-sequence data.
|
day 0, up to 14 days
|
|
Reduction in Scavenger Immunosuppressive program
時間枠:day 0, up to 14 days
|
Evaluate whether disulfiram given pre-operation reduces the Scavenger Immunosuppressive myeloid program scores vs historical controls, which will be compared using a two-sample Wilcoxon rank-sum test (primary) and a two-sample t-test on the participant-level program scores (sensitivity).
Measured using scRNA-sequence data.
|
day 0, up to 14 days
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Proportion of participants needing dexamethasone within 48 hour window
時間枠:48 hours
|
Change in investigator-rated edema symptom composite score from baseline to Day 2 on therapy.
|
48 hours
|
|
Safety of disulfiram
時間枠:14 days
|
Safety is defined as the rates of adverse events experienced by participants.
Adverse event severity is graded according to the NCI Common Terminology for Adverse Events (CTCAE) Version 5.0
|
14 days
|
|
Change in Edema Symptom Composite Score (ESCS)
時間枠:day 0, up to 14 days
|
Change in ESCS is analyzed using a Wilcoxon signed-rank test
|
day 0, up to 14 days
|
|
Tolerability of disulfiram
時間枠:14 days
|
Tolerability as measured by participant toxicity rates.
|
14 days
|
|
Change in Microglial Inflammatory program scores
時間枠:day 0, up to 14 days
|
Evaluate the change in microglial inflammatory program scores vs historical controls, which will be compared using a two-sample Wilcoxon rank-sum test (primary) and a two-sample t-test on the participant-level program scores (sensitivity).
Measured using scRNA-sequence data.
|
day 0, up to 14 days
|
|
Change in Systemic Inflammatory Program Scores
時間枠:day 0, up to 14 days
|
Evaluate the change in systemic inflammatory program scores vs historical controls, which will be compared using a two-sample Wilcoxon rank-sum test (primary) and a two-sample t-test on the participant-level program scores (sensitivity).
Measured using scRNA-sequence data.
|
day 0, up to 14 days
|
協力者と研究者
捜査官
- 主任研究者:Tiffany Hodges, MD、University Hospitals Cleveland Medical Center
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- CASE7326
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
IPD 共有時間枠
IPD 共有アクセス基準
IPD 共有サポート情報タイプ
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
米国で製造され、米国から輸出された製品。
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。