IL-18 Armored STEAP1 CAR T Cells for the Treatment of Metastatic Castration Resistant Prostate Cancer
Phase 1 Dose-Escalation and Expansion Study of IL-18 Armored STEAP1 CAR T in Participants With mCRPC
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
OUTLINE:
Patients undergo leukapheresis. Patients receive cyclophosphamide intravenously (IV) and fludarabine IV on days -5 to -3. Patients receive FH-STEAP1 IL-18 CAR T cell IV on day 0. Patients may continue to receive androgen deprivation therapy per standard of care, throughout the study. Patients undergo nuclear medicine bone scan, computed tomography (CT) scan, magnetic resonance imaging (MRI) and/or positron emission tomography (PET) scan, tumor biopsy and blood sample collection throughout the study. Patients may also undergo multigated acquisition (MUGA) scan or echocardiography during screening.
After completion of study treatment, patients are followed up on day +1, +3, +7, +10, +14, +21, + 28, months 2-6, month 9, month 12, then every 6 months until year 5 then yearly until year 15.
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- フェーズ 1
連絡先と場所
研究連絡先
研究連絡先
- 名前:Fred Hutch Intake
- 電話番号:206-606-1024
- メール:hutchdoc@fredhutch.org
研究場所
-
-
Washington
-
Seattle、Washington、アメリカ、98109
- Fred Hutch/University of Washington Cancer Consortium
-
コンタクト:
- Fred Hutch Intake
- 電話番号:206-606-1024
- メール:hutchdoc@fredhutch.org
-
主任研究者:
- Rosa Nadal Rios, MD, PhD
-
-
参加基準
適格基準
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:
- Documented, histologically confirmed adenocarcinoma of the prostate
- Measurable disease by RECIST 1.1 criteria or bone only metastases with measurable PSA (≥ 1ng/mL)
- Must have mCRPC with progressive disease (PD), stable disease (SD), lack of clinical benefit or intolerance to ≥ 1 line of systemic therapy, after becoming castration resistant
Have received the following for metastatic prostate cancer:
- At least two lines of Food and Drug Administration (FDA)-approved therapies with at least one being a second-generation androgen receptor signaling inhibitor.
- Targeted therapies for which they are eligible in the metastatic setting unless the patient has contraindications to receiving those medications, the agents are not available to the patient or the patient declines to receive these drugs due to personal preference
- Castrate levels of testosterone (< 50 ng/dL) with or without the use of androgen deprivation therapy
- 18 years or older at the time of enrollment
- Capable of understanding and providing written informed consent
- Fertile male participants and their female partners must be willing to use an effective contraceptive method before, during, and for at least 4 months after the FH-STEAP1 IL-18 CAR T cell infusion
- Participants will be permitted to receive radiation therapy for palliative purposes throughout the study period, except during the 2-week period prior to undergoing leukapheresis
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
- Serum creatinine ≤ 1.5 x upper limit of normal (ULN) or estimated creatinine clearance > 50 mL/min as calculated using the Cockcroft-Gault formula and not dialysis dependent
- Total bilirubin ≤ 1.5 x ULN. Participants with suspected Gilbert syndrome may be included if total bilirubin (bili) > 3 mg/dL but no other evidence of hepatic dysfunction
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 5 x ULN
- ≤ grade 1 dyspnea and oxygen saturation (SaO2) ≥ 92% on ambient air. If pulmonary function tests (PFTs) are performed based on the clinical judgement of the treating physician, participants with forced expiratory volume at 1 second (FEVI) ≥ 50% of predicted and carbon monoxide diffusing capability (DLCO) (adjusted for lung volume) of ≥ 40% of predicted will be eligible
- All participants ≥ 60 years of age are required to have left ventricular ejection fraction (LVEF) evaluation performed within 1 year prior to lymphodepletion chemotherapy. LVEF may be established with an echocardiogram or MUGA scan, and left ejection fraction must be ≥ 45%
- Absolute neutrophil count (ANC) > 1500 cells/ mm^3
- Hemoglobin ≥ 9g g/dL
- Platelets > 100,000 per mm^3
Exclusion Criteria:
- Expecting to conceive or father children for the duration of the trial through 4 months after T cell infusion
- Patients that require immediate therapy due to mass effect or spinal cord compression
- Active autoimmune disease: Participants with active autoimmune disease requiring chronic immunosuppressive therapy are excluded. Case by case exemptions are possible with approval by principal investigator (PI)
- Corticosteroid therapy at a dose equivalent of > 10 mg of prednisone per day (or equivalent). Pulsed corticosteroid use for disease control is acceptable
- Concurrent use of other investigational anti-cancer agents except for androgen deprivation therapy
Uncontrolled concurrent illness: Participants may not have uncontrolled respiratory, endocrine, renal, gastrointestinal, genitourinary or systemic infection. There are exceptions to this criterion:
- HIV positive participants on highly active antiretroviral therapy (HAART) with a CD4 count > 500 cells/mm^3 are considered controlled, as are individuals with a history of hepatitis C who have successfully completed antiviral therapy with an undetectable viral load, and those with hepatitis B who have hepatitis well controlled on medication;
- Patients who have recent history of cerebrovascular accident, transient ischemic attack should be cleared by the neurology service before enrolling this study
- Patients who have recent history of coronary artery disease or cardiac arrhythmia should be cleared by the cardiology service before enrolling this study. Case by case exemptions are possible with approval by PI
- Participants with brain metastasis
- Active treatment for prior immune related adverse event to any immunotherapy: Participants receiving ongoing treatment for prior serious immune-related adverse events are excluded, with exception of hormone supplementation or corticosteroid therapy at equivalent of > 10 mg prednisone (or equivalent) per day, unless otherwise approved by PI
- Patients with a second malignancy in addition to their prostate cancer are not eligible if the second malignancy has required systemic treatment within the past 4 years or is not in complete remission. There are exceptions to this criterion: successfully treated non-metastatic basal cell and squamous cell skin carcinoma
- Other medical, social, or psychiatric factor that interferes with medical appropriateness and/or ability to comply with study, as determined by the PI
- Known allergic reactions to any of the components of study treatments
- Participants who do not have a reasonable standard-of-care bridging therapy option available, as determined by the treating medical oncologist, to maintain disease control should clinically significant disease progression or worsening symptoms occur during the screening and T-cell manufacturing period
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:なし
- 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)
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
実験的:Treatment (chemotherapy, FH-STEAP1 IL-18 CAR T cells)
Patients undergo leukapheresis.
Patients receive cyclophosphamide intravenously (IV) and fludarabine IV on days -5 to -3.
Patients receive FH-STEAP1 IL-18 CAR T cell IV on day 0. Patients may continue to receive androgen deprivation therapy per standard of care, throughout the study.
Patients undergo nuclear medicine bone scan, CT scan, MRI and/or PET scan, tumor biopsy and blood sample collection throughout the study.
Patients may also undergo MUGA scan or echocardiography during screening.
|
MRIを受ける
他の名前:
採血を受ける
他の名前:
与えられた IV
他の名前:
与えられた IV
他の名前:
白血球除去療法を受ける
他の名前:
PETスキャンを受ける
他の名前:
CTスキャンを受ける
他の名前:
MUGAスキャンを受ける
他の名前:
腫瘍生検を受けます
他の名前:
心エコー検査を受けます
他の名前:
Given FH-STEAP1 IL-18 CAR T cells IV
他の名前:
Receive standard of care androgen deprivation therapy
他の名前:
Undergo nuclear medicine bone scan
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Treatment-related unexpected grade 3 or higher toxicity
時間枠:Up to 28 days post infusion
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Up to 28 days post infusion
|
|
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Incidence of adverse events
時間枠:Up to 28 days post infusion
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Up to 28 days post infusion
|
|
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Prostate cancer response
時間枠:Up to 1 year post infusion
|
Assessed by Prostate Cancer Working Group 3 (PCWG3) criteria.
|
Up to 1 year post infusion
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Progression free survival
時間枠:From initiation of protocol treatment to disease progression or death of any cause, up to 1 year post infusion
|
Will be analyzed using Kaplan-Meier method and the results will be summarized by the median with a 95% confidence interval if appropriate.
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From initiation of protocol treatment to disease progression or death of any cause, up to 1 year post infusion
|
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Overall survival
時間枠:From initiation of protocol treatment to death of any cause, up to 1 year post infusion
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Will be analyzed using Kaplan-Meier method and the results will be summarized by the median with a 95% confidence interval if appropriate.
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From initiation of protocol treatment to death of any cause, up to 1 year post infusion
|
|
Objective response rate
時間枠:Up to 1 year post infusion
|
Defined as complete response or partial response by Response Evaluation Criteria in Solid Tumors 1.1 criteria and PCWG 3.
|
Up to 1 year post infusion
|
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Stable disease
時間枠:Up to 1 year post infusion
|
Assessed by RECIST 1.1 criteria and PCWG3.
|
Up to 1 year post infusion
|
|
Clinical benefit
時間枠:Up to 1 year post infusion
|
Defined as overall response and stable disease assessed by RECIST 1.1 criteria and PCWG3.
|
Up to 1 year post infusion
|
|
Overall response
時間枠:Up to 1 year post infusion
|
Assessed by immune RECIST criteria.
|
Up to 1 year post infusion
|
|
Prostate specific antigen (PSA) response
時間枠:From baseline, up to 15 years
|
Defined as ≥ 50% reductions in PSA.
The estimation with an exact 95% confidence interval will be provided.
|
From baseline, up to 15 years
|
協力者と研究者
協力者
協力者
捜査官
捜査官
- 主任研究者:Rosa Nadal Rios, MD, PhD、Fred Hutch/University of Washington Cancer Consortium
研究記録日
主要日程の研究
研究開始 (推定)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
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
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
- 泌尿生殖器疾患
- 生殖器疾患
- 性器腫瘍、男性
- 泌尿生殖器腫瘍
- 部位別新生物
- 新生物
- 生殖器疾患、男性
- 前立腺疾患
- 男性の泌尿生殖器疾患
- 前立腺腫瘍
- 薬物の生理学的影響
- ホルモン、ホルモン代替品、ホルモン拮抗薬
- ホルモン拮抗薬
- 有機化学物質
- 調査手法
- 治療
- 臨床検査技術
- 診断技術と手順
- 診断
- 外科的処置、手術
- 細胞学的技術
- 細胞診断
- 薬理学的行動
- 化学作用と用途
- 炭化水素
- 診断技術、外科的
- 化学技術、分析
- スペクトル分析
- ホスホルアミドマスタード
- 窒素マスタード化合物
- マスタード化合物
- 炭化水素、ハロゲン化
- ホスホラミド
- 有機リン化合物
- 生物療法
- 細胞質
- 血液成分の除去
- 白血球減少手順
- 細胞分離
- シクロホスファミド
- アンドロゲン拮抗薬
- 生検
- 標本処理
- 磁気共鳴分光法
- フルダラビン
- 薬物療法
- 白血球
その他の研究ID番号
その他の研究ID番号
- RG1126433
- NCI-2026-06012 (レジストリ識別子:CTRP (Clinical Trial Reporting Program))
- FH21226 (その他の識別子:Fred Hutch/University of Washington Cancer Consortium)
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?
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
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