PICSTAT Pilot Study for CD8 PET/CT-Guided Lifileucel Treatment in Advanced Melanoma (PICSTAT)
PICSTAT (PET Imaging of CD8 for Selection of Tumors for Autologous TIL): A Pilot Study Assessing the Use of CD8 PET/CT (Zr-89 Crefmirlimab Berdoxam) to Enhance Lifileucel (AMTAGVI) Efficacy in Patients With Treatment Refractory Stage IV Melanoma
This prospective, single-center pilot study is being performed to find out whether Zr-89 crefmirlimab berdoxam "CD8 PET/CT" scans can improve the effectiveness of the tumor-infiltrating lymphocyte (TIL) therapy called lifileucel ("Study Treatment") in treating metastatic melanoma.
Participants must first provide consent to the companion protocol (UPCC 19426, PICSTAT CD8 PET) before being eligible to consent to this protocol.
研究概览
地位
条件
研究类型
注册 (估计的)
阶段
- 第一阶段早期
联系人和位置
学习联系方式
- 姓名:Ravi Amaravadi, MD
- 电话号码:215-796-5159
- 邮箱:Ravi.Amaravadi@pennmedicine.upenn.edu
学习地点
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Pennsylvania
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Philadelphia、Pennsylvania、美国、19104
- Abramson Cancer Center of the University of Pennsylvania
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首席研究员:
- Ravi Amaravadi, MD
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接触:
- Ravi Amaravadi, MD
- 电话号码:215-796-5159
- 邮箱:Ravi.Amaravadi@pennmedicine.upenn.edu
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-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Must have a confirmed diagnosis of unresectable or metastatic melanoma (Stage IV)
- Participants must have progressed following ≥ 1 prior systemic therapy for Stage IV or unresectable Stage III disease including a PD- 1 blocking antibody; and if BRAF V600 mutation-positive, a BRAF inhibitor or BRAF inhibitor in combination with MEK inhibitor.
- At least two resectable previously non-irradiated lesions (or aggregate of lesions resected) of a minimum 1.5 cm in diameter post- resection to generate TIL; surgical removal with minimal morbidity (defined as any procedure for which expected hospitalization is ≤ 3 days)
- Lesions in the spleen should not be selected as resectable lesions, because they are not well evaluated by CD8 PET/CT imaging due to high background signal in that organ
In addition to the two resectable lesions, at least one measurable target lesion, as defined by RECIST v1.1
- Lesions in previously irradiated areas (or other local therapy) should not be selected as target lesions, unless treatment was ≥ 3 months prior to Screening, and there has been demonstrated disease progression in that particular lesion
- If a lesion is partially resected to generate TIL, and remains visible on the Baseline scan after surgery, then the partially resected lesion can be used for RECIST v1.1 response assessment, but only as a non- target lesion
- Participants must be ≥ 18 years of age at the time of consent.
- Participants must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 .
- Participants must have signed informed consent for the PICSTAT companion CD8 PET imaging protocol.
- Participants are eligible for treatment with AMTAGVI per the recommendation of the treating oncologist.
- Participant (or legally authorized representative) is capable of giving signed informed consent form (ICF) which includes compliance with the requirements and restrictions listed in the ICF and in this protocol.
- Participants of childbearing potential or their partners of childbearing potential must be willing to take the appropriate precaution to avoid pregnancy or fathering a child for the duration of the protocol and practice an approved, highly effective method of birth control during treatment and for 12 months after receiving the last protocol-related therapy
- Palliative radiation therapy is permitted so long as it does not involve lesions being selected for TIL, or as target or non-target lesions. Washout is not required if all related toxicities have resolved to ≤ Grade 1 as per CTCAE v 6.0.
Exclusion Criteria:
- Participants who have received an organ allograft or prior cell transfer therapy within the past 20 years that included a non-myeloablative or myeloablative chemotherapy regimen.
- Participant has melanoma of uveal/ocular origin.
- Participants who have a history of hypersensitivity to any component or excipient of lifileucel (AMTAGVI) or other study drugs: a. Hypersensitivity to PET tracer b. LD chemo regimen (cyclophosphamide, mesna, and fludarabine) c. Proleukin®, aldesleukin, IL-2 d. Antibiotics (ABX) of the aminoglycoside group (i.e., streptomycin, gentamicin); (These participants may be eligible if current hypersensitivity has been excluded.) e. Any component of the lifileucel infusion product formulation including dimethyl sulfoxide (DMSO), human serum albumin (HSA), IL-2, and dextran-40.
Participant has symptomatic untreated brain metastases. Participants with brain metastases may be considered for study participation with the following considerations and only after discussion with the Investigator:
- Participants with asymptomatic brain metastases who do not clinically require treatment may be considered for study participation.
- A participant with historically treated brain metastases (i.e., treatment was completed >28 days prior to consenting for study participation) may be considered for study participation if the participant is clinically stable for ≥ 2 weeks, there are no new or worsening brain lesions via screening CT or MRI, and the participant does not require ongoing corticosteroid treatment (>10 mg/day prednisone or equivalent).
- If there are progressive or new brain metastases on the screening CT or MRI, the participant should first receive treatment for them prior to restarting or continuing screening. A participant with recently treated brain metastases (i.e., treatment of brain metastases was completed ≤ 28 days prior to consenting for study participation) may be considered for study participation if the participant is asymptomatic, clinically stable for ≥ 2 weeks, and does not require corticosteroids (>10 mg/day prednisone or equivalent) by the end of the screening period. Repeat brain imaging is not required after treatment.
- Participant requires systemic steroid therapy > 10 mg/day of prednisone or another steroid equivalent dose.
Participants receiving steroids as replacement therapy for adrenocortical insufficiency at ≤ 10 mg/day of prednisone or another steroid equivalent dose may be eligible
- Participant has evidence of any active viral, bacterial, or fungal infection requiring ongoing systemic treatment or identified during screening
- Participants who are pregnant or breastfeeding.
- Participants who have active medical illness(es) that would pose increased risk for study participation, including: active uncontrolled infections requiring systemic ABX, coagulation disorders, or other active major medical illnesses of the cardiovascular, respiratory, or immune systems.
- Participants who have received or will receive a live or attenuated vaccination within 28 days prior to the start of LD chemo regimen.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:CD8 PET/CT imaging for lifileucel therapy
CD8 PET/CT imaging prior to tumor resection (PET0) and after lifileucel treatment.
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Harvest of two tumors to obtain tissue for manufacturing the autologous tumor-infiltrating lymphocyte (TIL) cellular product.
Production of lifileucel (AMTAGVI) for participant infusion) and comparator lifileucel (AMTAGVI) at a centralized Good Manufacturing Practice (GMP)-compliant facility.
Administration of a 7-day lymphodepleting (LD) chemotherapy regimen prior to lifileucel infusion.
Administration of CD8 PET-guided infusion of lifileucel (AMTAGVI) on Day 0 following completion of the lymphodepleting chemotherapy regimen.
Administration of up to six doses of intravenous interleukin-2 (IL-2) following lifileucel (AMTAGVI) infusion.
CD8 PET/CT imaging will be performed before tumor resection and after lifileucel (AMTAGVI) administration (PET1).
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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TILs
大体时间:8-12weeks
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Number of viable TILs (cell count) harvested from resected tumor tissue.
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8-12weeks
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Overall response rate (ORR)
大体时间:4-12 weeks
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ORR as assessed by the Investigator per RECIST 1.1
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4-12 weeks
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Complete Response (CR) rate
大体时间:4-12 months
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CR rate as assessed by the Investigator per RECIST 1.1
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4-12 months
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Treatment-emergent adverse events (TEAEs)
大体时间:3-4 months
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Incidence of Grade ≥ 3 TEAEs
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3-4 months
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Duration of response (DOR)
大体时间:12 months
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DOR as assessed by the Investigator
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12 months
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Progression-free survival (PFS)
大体时间:12 months
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PFS, as assessed by the Investigator
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12 months
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Correlation of T cell
大体时间:12 months
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Correlation of T cell clonotype, T cell phenotype, with CD8 PET measures, response, percent reduction in target lesion sum of diameters, and toxicity following lifileucel (AMTAGVI) therapy.
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12 months
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合作者和调查者
调查人员
- 首席研究员:Ravi Amaravadi, MD、Abramson Cancer Center at Penn Medicine
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- UPCC 05626
- 26-7163 (其他标识符:University of Pennsylvania IRB)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 共享时间框架
IPD 共享访问标准
IPD 共享支持信息类型
- 研究方案
- 树液
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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