Lifileucel (TIL) Therapy After PD-1 Blockade Failure in Kidney Cancer
A Phase II Trial of Autologous Ex Vivo Expanded Tumor-Infiltrating Lymphocyte (TIL) Therapy With Lifileucel After Failure of PD-1 Blockade in Kidney Cancer.
This study aims to evaluate autologous ex vivo expanded tumor-infiltrating lymphocyte therapy (lifileucel/LN-145) for kidney cancer after failure of PD-1 blockade.
研究概览
地位
详细说明
This is a Phase II single-arm trial of tumor-infiltrating lymphocyte (TIL) therapy in kidney cancer. Briefly, participants who meet eligibility criteria undergo surgical removal of a metastasis or primary tumor to provide material for generation of the TIL product in a lab, which involves growing and expanding the immune cells contained in the tumor before infusing the TIL product into the patient.
Baseline evaluations occur before tumor harvest, and participants who proceed on study undergo tumor resection so tissue can be shipped to a manufacturing facility to create the autologous TIL product LN-145/lifileucel. The treatment plan includes 5 days of lymphodepleting chemotherapy before TIL infusion, using cyclophosphamide and fludarabine, followed by LN-145 infusion on Day 0 and IL-2 (aldesleukin) afterward. The study calendar includes post-treatment visits around Day 14, Day 28, Weeks 8, 12, and 18, then every 3 months starting at Month 6, with long-term follow-up by telephone continuing until study end or withdrawal, up to Month 36. Participants undergo screening and tumor resection to obtain tissue for manufacture of the TIL product. If treatment proceeds, participants receive lymphodepleting chemotherapy with cyclophosphamide and fludarabine, followed by LN-145 infusion and IL-2 (aldesleukin). Participants complete scheduled clinic-based assessments and longer-term follow-up, including telephone follow-up approximately every 3 months for up to about 3 years
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:David Einstein, MD
- 电话号码:(617) 667-2100
- 邮箱:Deinstei@bidmc.harvard.edu
学习地点
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Massachusetts
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Boston、Massachusetts、美国、02115
- Dana-Farber Cancer Institute
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接触:
- David Einstein, MD
- 电话号码:(617) 667-2100
- 邮箱:Deinstei@bidmc.harvard.edu
-
接触:
- Wenxin Xu, MD
- 电话号码:617-632-3000
- 邮箱:Wenxin_Xu1@dfci.harvard.edu
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Boston、Massachusetts、美国、02115
- Brigham and Women's Hospital
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接触:
- David Einstein, MD
- 电话号码:(617) 667-2100
- 邮箱:Deinstei@bidmc.harvard.edu
-
接触:
- Wenxin (Vincent) Xu, MD
- 电话号码:(617) 632-3000
- 邮箱:Wenxin_Xu1@dfci.harvard.edu
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Boston、Massachusetts、美国、02115
- Beth Israel Deaconess Medical Center (BIDMC)
-
接触:
- David Einstein, MD
- 电话号码:(617) 667-2100
- 邮箱:Deinstei@bidmc.harvard.edu
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
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Histologically or cytologically confirmed, advanced or metastatic renal cell carcinoma with clear cell, papillary, sarcomatoid (with or without other subtypes present), or unclassified histology. Other non-clear cell subtypes are also eligible if the patient has had a prior documented response to immune checkpoint inhibitor therapy.
- Participants must have measurable disease with at least two malignant lesions, one for disease monitoring as response to therapy and one for TIL harvest.
- Age ≥18 years
- Received one of the following regimens:
- Anti-PD-(L)1 immune checkpoint inhibitor (ICI) with or without an anti-CTLA-4 ICI or VEGF tyrosine kinase inhibitor (TKI) for treatment of advanced/metastatic disease, and experienced either (1) radiographic progression of disease while on treatment or (2) best response of stable disease after at least 6 months
- Adjuvant anti-PD-(L)1 ICI after nephrectomy for localized disease and had either (1) disease recurrence while receiving adjuvant ICI or (2) disease recurrence within 6 months of the final dose of any amount of adjuvant ICI
- Prior HIF2α inhibitor exposure in the adjuvant or advanced/metastatic setting is allowed but not required
- Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 and an estimated life expectancy of ≥ 3 months in the opinion of the Investigator.
- Participants must have adequate organ and marrow function as defined in the protocol.
- Patients with definitively treated brain metastases may be considered for enrollment if the patient is clinically stable for ≥ 14 days, with no lesions on follow-up imaging and no requirement for ongoing steroid treatment.
- Participants must have a washout period from any anticancer therapy prior to tumor harvest. The protocol contains provisions for optional use of "bridging" TKI between tumor harvest and lymphodepleting chemotherapy.
- Palliative radiation therapy is permitted as long as it does not involve lesions being selected for resection for TIL manufacturing, or being assessed radiographically as target lesions.
- Participants must have recovered from all prior anti-cancer therapy-related adverse events (AEs), as defined in the protocol.
- Participants of childbearing potential or those with partners of childbearing potential must be willing to practice an approved method of highly effective birth control.
- Previous surgical procedure(s) is/are permitted provided that wound healing has occurred, all complications have resolved, and at least 14 days have elapsed (for major operative procedures) prior to the tumor resection.
Exclusion Criteria:
- Patients 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.
- Patients who have a history of hypersensitivity to any component of the study intervention.
- Patients with rapidly progressive disease or symptomatic disease requiring urgent treatment per investigator discretion.
- Patients with symptomatic and/or untreated brain metastases.
- Patients who are on chronic systemic steroid therapy except for those requiring steroid therapy for management of adrenal insufficiency.
- Patients who are pregnant or breastfeeding.
- Patients who have any form of primary immunodeficiency (such as severe combined immunodeficiency disease [SCID] and acquired immunodeficiency syndrome [AIDS]).
- Patients with any other primary malignancy that is radiographically visible or is expected to require treatment within the next three years.
- Patients who are hypoxemic (oxygen saturation <90%) on room air at baseline or who require supplemental oxygen.
Other protocol-defined inclusion/exclusion criteria may apply.
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:Lifileucel (LN-145) TIL regimen
Participants undergo tumor resection for TIL manufacturing, then receive lymphodepleting cyclophosphamide and fludarabine, followed byLN-145/lifileucel infusion and IL-2 (aldesleukin), with scheduled post-treatment clinic visits and long-term follow-up |
Part of the lymphodepleting chemotherapy given before LN-145 infusion Part of the lymphodepleting chemotherapy given before LN-145 infusion. Administered after LN-145 infusion as part of the treatment regimen. Surgical removal of tumor tissue for TIL production/manufacture |
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 |
|---|---|---|
|
Radiographic Objective Response Rate
大体时间:Participants will be followed thought out the course of the trial for 3 years
|
HCC-centrally assessed Objective Response Rate per RECIST 1.1 of the efficacy evaluable population Primary analysis is performed on patients who receive TIL. |
Participants will be followed thought out the course of the trial for 3 years
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Radiographic change in target lesions
大体时间:Participants will be followed thought out the course of the trial for 3 years
|
Longitudinal and best change in target lesion measurements. Target lesions are measured at baseline and followed per RECIST 1.1 |
Participants will be followed thought out the course of the trial for 3 years
|
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Radiographic Disease Control Rate (SD + PR + CR)
大体时间:Participants will be followed thought out the course of the trial for 3 years
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Disease control rate is listed as a secondary endpoint and will be summarized in the efficacy cohort. |
Participants will be followed thought out the course of the trial for 3 years
|
|
Duration of response
大体时间:Participants will be followed thought out the course of the trial for 3 years
|
Duration of overall response is measured from the first time CR or PR criteria are met until the first date recurrent or progressive disease is objectively documented, or death due to any cause |
Participants will be followed thought out the course of the trial for 3 years
|
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Progression-free survival
大体时间:Participants will be followed thought out the course of the trial for 3 years
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Progression-free survival is a listed secondary endpoint for both the efficacy evaluable population and the total population. Time-to-event variables are calculated from TIL infusion; PFS is also calculated for the total population from trial enrollment. |
Participants will be followed thought out the course of the trial for 3 years
|
|
Toxicity per CTCAE v6.0
大体时间:Participants will be followed thought out the course of the trial for 3 years
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Adverse events are graded using NCI Common Terminology Criteria for Adverse Events version 6.0. |
Participants will be followed thought out the course of the trial for 3 years
|
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Feasibility
大体时间:Assessed at time of TIL infusion (D0)
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Feasibility is defined as the proportion of patients who successfully undergo tumor harvest, ex vivo TIL expansion, lymphodepletion, and TIL infusion, regardless of number of IL-2 doses given post-TIL. |
Assessed at time of TIL infusion (D0)
|
合作者和调查者
调查人员
- 首席研究员:David Einstein, MD、Beth Israel Deaconess Medical Center
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
- 26-686
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
The Harvard Cancer Consortium encourages and supports the responsible and ethical sharing of data from clinical trials. De-identified participant data from the final research dataset used in the published manuscript may only be shared under the terms of a Data Use Agreement. Requests may be directed to: [contact information for Sponsor Investigator or designee]. The protocol and statistical analysis plan will be made available on Clinicaltrials.gov only as required by federal regulation or as a condition of awards and agreements supporting the research.
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
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