Sirolimus, Docetaxel, and Carboplatin in Treating Patients With Metastatic Castration-Resistant Prostate Cancer
A Phase 1-2 Study of Sirolimus, Docetaxel and Carboplatin for Treatment of Patients With Metastatic, Castration Resistant Prostate Cancer: (Rapamycin Inhibition of DDSP [RID])
研究概览
详细说明
PRIMARY OBJECTIVES:
I. To define the recommended phase 2 dose (RP2D) of sirolimus combined with docetaxel and carboplatin in the treatment of metastatic castration resistant prostate cancer (CRPC). (Phase I)
II. To assess the effectiveness of sirolimus in suppressing the induction of the deoxyribonucleic acid (DNA) damage secretory component WNT16B in tumor stroma following docetaxel and carboplatin. (Phase II)
EXPLORATORY OBJECTIVES:
I. To assess maximal prostate-specific antigen (PSA) response to sirolimus combined with docetaxel and carboplatin. (Phase I)
II. To assess PSA response duration to sirolimus combined with docetaxel and carboplatin. (Phase I)
III. To assess response of measurable disease. (Phase I)
IV. To assess time to progression of bone lesions or measurable disease (Response Evaluation Criteria in Solid Tumors [RECIST] 1.1). (Phase I)
V. To assess effect of sirolimus with docetaxel and carboplatin on DNA damage surrogates in cancer associated stroma compared to untreated and docetaxel and carboplatin treated stroma. (Phase I)
VI. To assess maximal PSA response to sirolimus combined with docetaxel and carboplatin. (Phase II)
VII. To assess PSA response duration to sirolimus combined with docetaxel and carboplatin. (Phase II)
VIII. To assess response of measurable disease (RECIST 1.1). (Phase II)
IX. To assess time to progression of bone lesions or measurable disease (RECIST 1.1). (Phase II)
X. To assess toxicity of the RP2D dose of sirolimus with docetaxel and carboplatin. (Phase II)
XI. To determine the effect of docetaxel and carboplatin therapy on the DNA damage secretory program (DDSP) in serum. (Phase II)
XII. To determine response to sirolimus, docetaxel and carboplatin in tumors with mutation of DNA repair pathway genes (breast cancer gene 2 [BRCA2], ataxia telangiectasia mutated [ATM] and other Fanconi anemia complementation groups [FANC] pathway members). (Phase II)
XIII. To correlate the presence of DNA repair pathway mutations in circulating tumor cells (CTC) and circulating tumor DNA (ctDNA) with tumor biopsy and correlate changes in CTC number and ctDNA mutation levels with clinical responses. (Phase II)
OUTLINE: This is a phase I, dose de-escalation study of sirolimus followed by a phase II study.
PHASE I: Patients receive sirolimus orally (PO) on day -2*. Patients also receive docetaxel intravenously (IV) over 30-60 minutes and carboplatin IV over 30-60 minutes on day 1. Treatment repeats every 21 days for 10 cycles in the absence of disease progression or unacceptable toxicity.
PHASE II: Patients are randomized to 1 of 2 treatment arms.
ARM I: Patients receive docetaxel IV over 30-60 minutes and carboplatin IV over 30 minutes on day 1. Beginning in cycle 2 and continuing in subsequent cycles, patients also receive sirolimus PO on day -2. Treatment repeats every 21 days for 10 cycles in the absence of disease progression or unacceptable toxicity.
ARM II: Patients receive sirolimus PO on day -2. Patients also receive docetaxel IV over 30-60 minutes and carboplatin IV over 30-60 minutes on day 1. Treatment repeats every 21 days for 10 cycles in the absence of disease progression or unacceptable toxicity.
* NOTE: Patients receive sirolimus 2 days prior to chemotherapy day 1 (there is no day 0).
研究类型
注册 (实际的)
阶段
- 阶段2
- 阶段1
联系人和位置
学习地点
-
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Washington
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Seattle、Washington、美国、98109
- Fred Hutch/University of Washington Cancer Consortium
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-
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:
- Signed informed consent form (ICF) providing agreement to adhere to the dosing schedule, report for all trial visits and authorization, use and release of health and research trial information
- Histologically or cytologically confirmed carcinoma of the prostate (excluding neuroendocrine differentiation or squamous cell histology)
- Ongoing gonadal androgen deprivation therapy with gonadotropin-releasing hormone (GnRH) analogues, antagonists or orchiectomy; patients who have not had an orchiectomy must be maintained on effective GnRH analogue/antagonist therapy
Castration resistant prostate cancer as defined by serum testosterone < 50 ng/ml and at least one of the following:
- PSA level of at least 2 ng/ml that has risen on at least 2 successive occasions at least 1 week apart
- Evaluable disease progression by modified RECIST 1.1
- Progression of metastatic bone disease on bone scan with > 2 new lesions
- Prior therapy with abiraterone, enzalutamide and/or docetaxel; if a patient has not received docetaxel or cabazitaxel chemotherapy, the patient must be informed of this treatment choice as an alternative; if the patient has received docetaxel or cabazitaxel chemotherapy or refuses one of both of these therapies, this rationale must be documented and the patient is then eligible; patient must be offered and made aware of all Food and Drug Administration (FDA)-approved treatment options; patients with bone only disease may not have received radium-223
- The presence of metastatic disease amenable to computed tomography (CT) or ultrasound guided biopsy; this may include thoracolumbar vertebral bodies, pelvis, femur or humerus or soft tissue or nodal metastasis amenable to biopsy (excluding lung or pleural lesions)
- Agree to participate in biopsy of metastatic lesion during the study at day 21
- Eastern Cooperative Oncology Group (ECOG) performance status of =< 1
- Life expectancy >= 12 weeks
No prior malignancy is allowed except:
- Adequately treated basal cell or squamous cell skin cancer or
- In situ carcinoma of any site or
- Other adequately treated malignancy for which the patient is currently disease free for at least one year
- Patients with any prior chemotherapy regimens are eligible
- Patients with disease only in the bone may not have received Xofigo/radium 223 to avoid ongoing DNA damage in bone marrow
- Patients who are or are not receiving bisphosphonates or denosumab are eligible; bisphosphonates or denosumab should not be initiated after registration and during active treatment
- Absolute neutrophil count >= 1.5 x 10^9 cells/L (within 14 days prior to registration)
- Hemoglobin (Hgb) >= 9.0 g/dL (within 14 days prior to registration)
- Platelets >= 100,000 x 10^9/L (within 14 days prior to registration)
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =< 1.5 x upper limit of normal (ULN) (within 14 days prior to registration)
- Total bilirubin =< 1.5 x ULN (within 14 days prior to registration)
- Serum creatinine < 1.5 X institutional ULN mg/dL OR estimated glomerular filtration rate (eGFR) >= 50 mL/min (within 14 days prior to registration)
Exclusion Criteria:
- Patients currently receiving active therapy for other neoplastic disorders
- Patients with histologic evidence of small cell carcinoma of the prostate will not be eligible
- Patients with disease only in the bone previously treated with radium-223 will not be eligible
- Known parenchymal brain metastasis
- Active or symptomatic viral hepatitis or chronic liver disease
- Estimated creatinine clearance less than 50 ml/minute
- Clinically significant heart disease as evidenced by myocardial infarction, or arterial thrombotic events in the past 6 months, severe or unstable angina, or New York Heart Association (NYHA) class II-IV heart disease
- Atrial fibrillation, or other cardiac arrhythmia requiring medical therapy
- Administration of an investigational therapeutic within 30 days of cycle 1, day -2
- Patients with dementia/psychiatric illness/social situations that would limit compliance with study requirements or would prohibit the understanding and/or giving of informed consent
- Patients with medical conditions, which, in the opinion of the investigators, would jeopardize either the patient or the integrity of the data obtained will not be eligible
- Any condition which, in the opinion of the investigator, would preclude participation in this trial
- Patients on anticoagulation therapy which cannot be held for metastatic biopsies
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 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:Arm I (sirolimus, docetaxel, carboplatin)
Patients receive docetaxel IV over 30-60 minutes and carboplatin IV over 30 minutes on day 1.
Beginning in cycle 2 and continuing in subsequent cycles, patients also receive sirolimus PO on day -2.
Treatment repeats every 21 days for 10 cycles in the absence of disease progression or unacceptable toxicity.
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相关研究
鉴于IV
其他名称:
鉴于IV
其他名称:
给定采购订单
其他名称:
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实验性的:Arm II (sirolimus, docetaxel, carboplatin)
Patients receive sirolimus PO on day -2.
Patients also receive docetaxel IV over 30-60 minutes and carboplatin IV over 30-60 minutes on day 1.
Treatment repeats every 21 days for 10 cycles in the absence of disease progression or unacceptable toxicity.
|
相关研究
鉴于IV
其他名称:
鉴于IV
其他名称:
给定采购订单
其他名称:
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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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Percentage Change in Deoxyribonucleic Acid (DNA) Damage Secretory Program Induction (DDSP) (Phase II)
大体时间:Baseline up to day 21 after starting treatment
|
Will be determined by the level of genetic expression of WNT16, IL6, or SFRP2 in tissue after chemotherapy (carboplatin/docetaxel) compared to background/baseline measurement.
The primary metric of DDSP induction will be quantitative reverse transcription-polymerase chain reaction, which is quantitative, but in the event of ribonucleic acid degradation in sample processing, the alternative measure will be immunohistochemistry (0-2 scale of expression).
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Baseline up to day 21 after starting treatment
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Incidence of Adverse Events Graded According to the National Cancer Institute Common Terminology Criteria for Adverse Events Version 4.0 (Phases I and II)
大体时间:Up to 3 years
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Safety will be assessed through summaries of adverse events, vital signs, physical examinations, and clinical laboratory test data.
Adverse events will then be quantified via CTCAE 4.0.
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Up to 3 years
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Percentage of Patients With Reduction in Prostate Specific Antigen According to the Prostate Cancer Working Group 2 (PCWG2) Criteria (Phases I and II)
大体时间:Baseline to up to 3 years
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PSA decline from the level at registration will be quantified for each patient and proportion of patients with PSA decline divided by the total number of patients enrolled in study will be described.
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Baseline to up to 3 years
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合作者和调查者
调查人员
- 首席研究员:Robert Montgomery、Fred Hutch/University of Washington Cancer Consortium
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
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
- 9388 (其他标识符:Fred Hutch/University of Washington Cancer Consortium)
- P30CA015704 (美国 NIH 拨款/合同)
- P50CA097186 (美国 NIH 拨款/合同)
- NCI-2015-01478 (注册表标识符:CTRP (Clinical Trial Reporting Program))
- RG1715104 (其他标识符:Fred Hutch/University of Washington Cancer Consortium)
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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