Enfortumab Vedotin, Pembrolizumab and Quemliclustat for the Treatment of Unresectable Locally Advanced and Metastatic Urothelial Cancer
A Phase Ib/II Study to Evaluate the Safety and Efficacy of Enfortumab Vedotin Plus Pembrolizumab in Combination With Quemliclustat in Unresectable Locally Advanced and Metastatic Urothelial Carcinoma
研究概览
地位
条件
详细说明
OUTLINE:
Patients receive quemliclustat intravenously (IV) on day 1, enfortumab vedotin IV on days 1 and 8 and pembrolizumab IV on day 1 of each cycle. Cycles repeat every 21 days for 2 years in the absence of disease progression or unacceptable toxicity. Patients may undergo tumor biopsy during screening and optionally undergo throughout the study. Patients also undergo computed tomography (CT)/magnetic resonance imaging (MRI) and blood sample collection throughout the study.
After completion of study treatment, patients are followed up within 30 days and then every 12 weeks for 3 years.
研究类型
注册 (估计的)
阶段
- 阶段2
- 阶段1
联系人和位置
学习联系方式
- 姓名:Rosa Nadal Rios, MD, PhD
- 电话号码:206-598-3300
- 邮箱:rnadalri@fredhutch.org
学习地点
-
-
Washington
-
Seattle、Washington、美国、98109
- 招聘中
- Fred Hutch/University of Washington Cancer Consortium
-
首席研究员:
- Rosa Nadal Rios, MD, PhD
-
接触:
- Rosa Nadal Rios, MD, PhD
- 电话号码:206-598-3300
- 邮箱:rnadalri@fredhutch.org
-
-
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:
- Participants must be at least 18 years of age on the day of signing informed consent. Participant (or legally authorized representative if applicable) provides written informed consent for trial
- Participants must have previously untreated locally advanced or metastatic bladder cancer including bladder cancer [stage IIIB: T1-T4N2-3M0, stage IVa: T4bAnyNM0 or AnyTAnyNM1a, and stage IVB: AnyTAnyNM1b clinical stage per American Joint Commission on Cancer (AJCC)] or renal pelvis or ureter cancer [stage IV: T4Nx-0M0, AnyTN1-2M0, AnyTAnyNM1 clinical stage per AJCC]. Lymph node with ≥ 15 mm short axis or biopsy-positive for carcinoma will be considered pathologically enlarged and measurable
Participants must have either conventional urothelial carcinoma or urothelial carcinoma variants. A review of pathology by a local expert genitourinary (GU) pathologist is required to confirm the diagnosis. Any component (%) of non-conventional urothelial noted on tumor specimen is allowed for only histologic subtypes listed below in up to 20% of participants enrolled in this study.
- Urothelial carcinoma with squamous differentiation
- Urothelial carcinoma with glandular differentiation
- Urothelial carcinoma with trophoblastic differentiation
- Nested urothelial carcinoma
- Tubular and microcystic urothelial carcinoma
- Micropapillary urothelial carcinoma
- Lymphoepithelioma-like urothelial carcinoma
- Plasmacytoid urothelial carcinoma
- Sarcomatoid urothelial carcinoma
- Giant cell urothelial carcinoma
- Lipid-rich urothelial carcinoma
- Clear cell (glycogen rich) urothelial carcinoma
- Poorly differentiated urothelial carcinoma
- Squamous cell neoplasms including pure squamous cell carcinomas, verrucous carcinomas and squamous cell papilloma
- Measurable disease by RECIST v 1.1
- Participants must have an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-2
- Available baseline fresh biopsy tissue sample obtained in the protocol RG1712006 though clinically indicated procedures or participants must be willing to undergo a baseline research biopsy when safe and feasible
- Participant must have an estimated life expectancy of at least 3 months
- Hemoglobin ≥ 9 gr/dl
- Absolute neutrophil count: ≥ 1500/ µL
- White blood cell count: ≥ 3000/µL
- Absolute lymphocyte count: ≥ 1000/µL
- Platelet count: ≥ 100.000/µL (without transfusion support)
- Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT): ≤ 2.5 x upper limit of normal (ULN)
- Total bilirubin: ≤ 1.5 mg/dl except for patients with Gilbert's syndrome who must have a total bilirubin ≤ 3 mg/dl
- Creatinine clearance: ≥ 30 ml/min/1.73m^2 by the method of Chronic Kidney Disease Epidemiology Collaboration (CKI-EPI) or ≥ 30 ml/min by the method of 24 hour (h) clearance of creatinine calculation
- International Normalized Ratio (INR): < 1.5
Exclusion Criteria:
- Participants who are receiving any other investigational agents or concurrent anticancer treatment. Participants must have adequate treatment washout period before treatment, defined as: Major surgery (≥ 4 weeks), palliative radiation therapy (≥ 1 weeks from completion of treatment if they have recovered from the acute toxic effect of radiotherapy), prior adjuvant immunotherapy (≥ 4 weeks)
- Participants whose tumors have any % neuroendocrine or small cell histology, glandular neoplasms, urachal carcinomas, tumor of mullerian type, mesenchymal tumors or urothelial tract hematopoietic and lymphoid tumors
- Participants considered to be medically unfit for EV-P regimen as per Investigator discretion
- Participants with concurrent use of systemic steroids (within 10 days of enrollment), except for physiologic doses of systemic steroid replacement or local (topical, nasal, intraarticular or inhaled) steroid use
- Participants who have experienced disease progression following neoadjuvant or adjuvant systemic therapy within 12 months prior to enrollment will not be eligible
Patients with Fridericia's corrected QT interval (QTcF) interval at screening of > 480 milliseconds.
- Note: For any QTcF > 480 milliseconds on initial electrocardiogram (ECG), a follow-up ECG will be performed to confirm QTcF interval prolongation and exclude the patient from this study
- Participants with active systemic autoimmune disease (e.g., lupus erythematosus, rheumatoid arthritis, Addison's disease, autoimmune disease associated with lymphoma, inflammatory bowel disease). Participants with autoimmune endocrine disorders controlled by medical management (e.g. thyroid disorders, type 1 diabetes, or adrenal insufficiency) will not be excluded
- Participants who are known to be serologically positive for human immunodeficiency virus (HIV) and a CD4 count < 350 cells/microliter
- Participants with known active hepatitis (i.e. Hepatitis B or C). Prior hepatitis (Hep) C infection is allowed as long as polymerase chain reaction (PCR) test is negative
- Participants with clinically inactive brain metastases may be included. Participants with treated brain metastases that are no longer symptomatic and who require no treatment with corticosteroids or anticonvulsants may be included in the study if they have recovered from the acute toxic effect of radiotherapy. A minimum of 2 weeks must have elapsed between the end of whole-brain radiation therapy and study treatment
- Participants with new or progressive brain metastases (less or equal of 1 cm of larger diameter) are eligible if the treating physician determines that immediate central nervous system (CNS) specific treatment is not required and is unlikely to be required for at least 4 weeks (or scheduled assessment after the first cycle of treatment), and a risk-benefit analysis (discussion) by the participant and the investigator favors participation in the clinical trial. Patients with leptomeningeal disease will be excluded
- History or current evidence of any condition, therapy, or laboratory abnormality that might confound the results, interfere with the participant's participation for the full duration of the trial, or is not in the best interest of the participant to participate, in the opinion of the treating investigator
- Participants with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy of assessment of the investigational regimen are eligible for this trial
- Woman of childbearing potential with positive serum pregnancy test within 72 hours prior to enrollment. Active lactation is an exclusion criterion
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 |
|---|---|
|
实验性的:Treatment (enfortumab vedotin, pembrolizumab, quemliclustat)
Patients receive quemliclustat IV on day 1, enfortumab vedotin IV on days 1 and 8 and pembrolizumab IV on day 1 of each cycle.
Cycles repeat every 21 days for 2 years in the absence of disease progression or unacceptable toxicity.
Patients may undergo tumor biopsy during screening and optionally undergo throughout the study.
Patients also undergo CT/MRI and blood sample collection throughout the study.
|
进行核磁共振
其他名称:
鉴于IV
其他名称:
进行血液样本采集
其他名称:
接受CT扫描
其他名称:
鉴于IV
其他名称:
进行肿瘤活检
其他名称:
Given IV
其他名称:
|
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 |
|---|---|---|
|
Incidence of treatment related adverse events (Phase Ib)
大体时间:From baseline, up to 21 days after last dose of investigational product
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As measured by Common Terminology Criteria for Adverse Events version (v) 6.
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From baseline, up to 21 days after last dose of investigational product
|
|
Overall response rate (ORR) (Phase II)
大体时间:From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
|
Assessed by Response Evaluation Criteria in Solid Tumors (RECIST) v 1.1.
Will calculate the count and percentage with a 95% confidence interval (CI).
|
From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
ORR (Phase Ib)
大体时间:From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
|
Assessed by RECIST v 1.1.
Will calculate the count and percentage with a 95% CI.
|
From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
|
|
Complete response rate (Phase II)
大体时间:From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
|
Assessed by RECIST v 1.1.
Will calculate the count and percentage with a 95% CI.
|
From baseline, up to disease progression or unacceptable side effects, up to 3 years after completion of study treatment
|
|
Duration of response (Phase II)
大体时间:From response (ORR) until disease progression or unacceptable side effects or death which occurs earlier, up to 3 years after completion of study treatment
|
Will use Kaplan Meier method to estimate the survival curve, median and its corresponding 95% CI.
|
From response (ORR) until disease progression or unacceptable side effects or death which occurs earlier, up to 3 years after completion of study treatment
|
|
Progression free survival (Phase II)
大体时间:From date of registration to date of first documentation of progression assessed by local review or symptomatic deterioration, or death due to any cause, up to 3 years after completion of study treatment
|
Will use Kaplan Meier method to estimate the survival curve, median and its corresponding 95% CI.
|
From date of registration to date of first documentation of progression assessed by local review or symptomatic deterioration, or death due to any cause, up to 3 years after completion of study treatment
|
|
Rate of consolidative therapy with cystectomy or chemoradiation with stage 3b (Phase II)
大体时间:Up to 6 months
|
Will calculate the count and percentage with a 95% CI.
|
Up to 6 months
|
合作者和调查者
调查人员
- 首席研究员:Rosa Nadal Rios, MD, PhD、Fred Hutch/University of Washington Cancer Consortium
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
- RG1125912
- NCI-2026-03972 (注册表标识符:CTRP (Clinical Trial Reporting Program))
- FHIRB0021336 (其他标识符:Fred Hutch/University of Washington Cancer Consortium)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
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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