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
調査の概要
状態
条件
詳細な説明
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.
研究の種類
入学 (推定)
段階
- フェーズ2
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Rosa Nadal Rios, MD, PhD
- 電話番号:206-598-3300
- メール:rnadalri@fredhutch.org
研究場所
-
-
Washington
-
Seattle、Washington、アメリカ、98109
- 募集
- Fred Hutch/University of Washington Cancer Consortium
-
主任研究者:
- Rosa Nadal Rios, MD, PhD
-
コンタクト:
- Rosa Nadal Rios, MD, PhD
- 電話番号:206-598-3300
- メール:rnadalri@fredhutch.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:
- 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
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)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的: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.
|
MRIを受ける
他の名前:
与えられた IV
他の名前:
採血を受ける
他の名前:
CTスキャンを受ける
他の名前:
与えられた IV
他の名前:
腫瘍生検を受けます
他の名前:
Given IV
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
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Incidence of treatment related adverse events (Phase Ib)
時間枠:From baseline, up to 21 days after last dose of investigational product
|
As measured by Common Terminology Criteria for Adverse Events version (v) 6.
|
From baseline, up to 21 days after last dose of investigational product
|
|
Overall response rate (ORR) (Phase II)
時間枠: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
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
ORR (Phase Ib)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠:Up to 6 months
|
Will calculate the count and percentage with a 95% CI.
|
Up to 6 months
|
協力者と研究者
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)
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
追加の関連 MeSH 用語
その他の研究ID番号
- RG1125912
- NCI-2026-03972 (レジストリ識別子:CTRP (Clinical Trial Reporting Program))
- FHIRB0021336 (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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