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Ipilimumab and GMCSF Immunotherapy for Prostate Cancer

2015年10月1日 更新者:Lawrence Fong

Anti-CTLA4 Blockade Alone or Combined With Systemic GM-CSF for Prostate Cancer Immunotherapy

This is an open-label randomized phase II study. Patients are randomized so as to achieve uniform patient cohorts treated on each regimen. Twenty-seven patients will be required per treatment arm, and a total of 54 prostate cancer patients will be required to complete this study. The study will assess for clinical activity by Prostate Specific Antigen (PSA) response, of both single agent ipilimumab and the combination of GM-CSF and ipilimumab in chemotherapy-naïve patients with metastatic castrate resistant prostate cancer.

研究概览

地位

撤销

条件

详细说明

Ipilimumab is an antibody (proteins that can find and destroy foreign molecules such as those on bacteria and viruses) against CTLA-4 (a molecule that controls a part of the immune system by shutting it down). It is approved by the U.S. Food and Drug Administration (FDA) to treat patients with late-stage melanoma, skin cancer. The use of ipilimumab in patients with CRPC has not been approved by the FDA.

Some patients in this study will receive GM-CSF along with ipilimumab. In clinical trials, GM-CSF has been safely given to prostate cancer patients in combination with ipilimumab. GM-CSF is not approved by the FDA for use as treatment for prostate cancer. Studies in patients with prostate cancer suggest that GM-CSF may activate the immune system. Since ipilimumab can help keep the immune system from turning off and allow an immune reaction to occur, and GM-CSF can increase the activity of the immune system, it is possible that they may work together to increase the immune response to cancer. The use of ipilimumab in combination with GM-CSF in patients with CRPC has not been approved by the FDA.

It is theorized that if antigen presentation could be improved, the immunostimulatory effects of CTLA-4 blockade could be augmented with improvements in clinical response. To that end, UCSF conducted a phase I clinical trial of ipilimumab in combination with GM-CSF, a cytokine that has been demonstrated to enhance the functional activities of effector cells, including dendritic cells (DC), neutrophils, and monocytes, in chemotherapy-naïve men with CRPC (Protocol 6032).32 Exposure to GM-CSF increases class II MHC expression on dendritic cells and is thought to lead to increased antigen presentation to T cells, stimulating T cell responses, although this mechanism has not been confirmed. We have extensively studied the effects of treatment demonstrating a dose-response relationship in the activation of CD4 and CD8 T cells. Moreover, the expansion of activated (CD25+CD69+) CD4 and CD8 T cells seen with this GM-CSF/ipilimumab combination trial was higher than that seen with GM-CSF or ipilimumab monotherapy seen in our other trials in prostate cancer patients.

We are proposing to conduct a non-comparative randomized phase II study of repetitive dosing of ipilimumab either alone or in combination with GM-CSF in patients with metastatic CRPC. The dosing interval for ipilimumab is based on the prior study which demonstrated drug levels ≥ 10 mg/mL (a minimum level required for CTLA-4 blockade in pre-clinical models) for greater than 28 days. Six doses of ipilimumab were chosen because six doses have been given safely in other trials. Maintenance dosing every three months is empirical, but this dosing frequency is based on discussions with Medarex, Inc. and Bristol-Meyers Squibb and is based on reports indicating the safety and potential efficacy of this maintenance regimen.

This study will use ipilimumab given every 28 days for six cycles (induction) followed by administration once every three months for patients who are not progressing (maintenance). A dosage of 10 mg/kg has been chosen based on the results to date of the phase I study. GM-CSF 250 mcg/m2 SQ will be administered on days 1-14 in Cycles 1-6 and then every 3 months for 14 days beginning on the day of ipilimumab administration during the maintenance therapy phase.

研究类型

介入性

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • California
      • San Francisco、California、美国、94115
        • University of California

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

男性

描述

Inclusion Criteria:

  1. Histologically confirmed, metastatic prostate cancer (positive bone scan and/or measurable disease on CT scan and/or MRI of the abdomen and pelvis).
  2. Progressive disease after androgen deprivation, as defined by PSA Working Group 237 and/or RECIST criteria.38 Patients must have disease progression by one or both of the following:

    • For patients with measurable disease, progression is defined as at least a 20% increase in the sum of the longest diameter (LD) of target lesions or the appearance of one or more new lesions, as per RECIST criteria version 1.1
    • For patients with no measurable disease, a positive bone scan and elevated PSA will be required. PSA evidence for progressive prostate cancer consists of a PSA level of at least 2 ng/ml, which has risen on at least 2 successive occasions, at least 1 week apart. If the confirmatory PSA (#3) value is not greater (i.e., #3b) than the screening PSA (#2) value, then an additional test for rising PSA (#4) will be required to document progression
    • If no prior orchiectomy has been performed, patients must remain on LHRH agonist or antagonist therapy. Patients who are receiving an antiandrogen as part of primary androgen ablation must demonstrate disease progression following discontinuation of the antiandrogen, defined as two consecutive rising PSA values, obtained at least two weeks apart, or documented osseous or soft tissue progression. At least one of the PSA values must be obtained at least four weeks (flutamide) or six weeks (bicalutamide or nilutamide) after discontinuation
  3. Laboratory requirements:

    • Absolute neutrophil count (ANC) ≥ 1500/μL
    • Bilirubin < 1.5 x ULN
    • Hemoglobin ≥ 8 g/dL
    • PSA ≥ 2 ng/mL
    • Platelets > 100,000/μL
    • AST and ALT < 2.5 x ULN
    • Creatinine clearance ≥ 60mL/min by the Cockcroft Gault equation Testosterone < 50 ng/dL
  4. Eastern Cooperative Oncology Group (ECOG) performance status 0 - 2 and life expectancy > 12 weeks.
  5. At least 18 years of age or older.
  6. Patients receiving any other hormonal therapy, including any dose of megestrol acetate (Megace), Proscar (finasteride), any herbal product known to decrease PSA levels (e.g. Saw Palmetto, PC-SPES), or any systemic corticosteroid, must discontinue the agent for at least four weeks prior to study treatment. Progressive disease as defined above must be documented after discontinuation of any hormonal therapy (with the exception of a LHRH agonist or antagonist).
  7. Prior radiation therapy must be completed > 4 weeks prior to enrollment and the patient must be recovered from all toxicity. Prior radiopharmaceuticals (strontium, samarium) must be completed ≥ 8 weeks prior to enrollment.
  8. Because of the unknown potential risk to a gamete and/or developing embryo from this investigational therapy, patients must agree to use adequate contraception (barrier method for males) for the duration of study participation, and for three months after discontinuing therapy.

Exclusion Criteria:

  1. Prior chemotherapy for prostate cancer, with the exception of neoadjuvant chemotherapy, because of the potential effect of chemotherapy on the immune system.
  2. Prior investigational immunotherapy. Prior sipuleucel-T treatment is allowed but must be completed at least 4 weeks prior to initiating treatment on this protocol.
  3. Current treatment with systemic steroid therapy (inhaled/topical steroids are acceptable). Systemic corticosteroids must be discontinued for at least 4 weeks prior to first treatment.
  4. History of autoimmune disease including, but not limited to:

    • Systemic lupus erythematosis (SLE), scleroderma, CREST syndrome, rheumatoid arthritis
    • Inflammatory bowel disease, celiac disease, primary biliary cirrhosis, autoimmune hepatitis
    • Dermatomyositis, polymyositis, giant cell arteritis
    • Autoimmune hemolytic anemia (AIHA), cryoglobulinemia, antiphospholipid antibody syndrome (APLS)
    • Diabetes mellitus type I, myasthenia gravis, Grave's disease
    • Wegener's granulomatosis or other vasculitis
    • A history of Hashimoto's thyroiditis, psoriasis, or eczema, any of which has been inactive for at least one year, or isolated Raynaud's phenomenon is acceptable
  5. History or radiologic evidence of central nervous system metastases.
  6. Medical or psychiatric illness that would preclude participation in the study or the ability of patients to provide informed consent for themselves.
  7. Cardiovascular disease that meets one of the following: congestive heart failure (New York Heart Association Class III or IV), active angina pectoris, or recent myocardial infarction (within the last 6 months).
  8. Concurrent or prior malignancy except for the following:

    • Adequately treated basal or squamous cell skin cancer
    • Adequately treated stage I or II cancer from which the patient is currently in complete remission
    • Any other cancer from which the patient has been disease-free for 5 years
  9. HIV or other history of immunodeficiency disorder.
  10. Prisoners or subjects who are compulsorily detained (involuntarily incarcerated) for treatment of either a psychiatric or medical (e.g. infectious) illness.
  11. Any underlying medical or psychiatric condition, which in the opinion of the investigator will make the administration of ipilimumab hazardous or obscure the interpretation of AEs, such as a condition associated with frequent diarrhea.
  12. A history of prior treatment with ipilimumab or prior CD137 agonist or CTLA 4 inhibitor or agonist.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

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
实验性的:Ipilimumab alone
Ipilimumab 3 mg/kg (IV) will be given every 28 days for six cycles (induction) followed by administration once every three months for patients who are not progressing (maintenance).
Ipilimumab 3 mg/kg on day 1 of a 28 day cycle for 6 cycles.
其他名称:
  • CTLA-4 blockade
实验性的:Ipilimumab with GM-CSF
Ipilimumab 3 mg/kg (IV) will be given every 28 days for six cycles (induction) followed by administration once every three months for patients who are not progressing (maintenance). GM-CSF 250 mcg/m2 SQ will be administered on days 1-14 in Cycles 1-6 and then every 3 months for 14 days beginning on the day of ipilimumab administration during the maintenance therapy phase
Ipilimumab 3 mg/kg on day 1 of a 28 day cycle for 6 cycles.
其他名称:
  • CTLA-4 blockade
GM-CSF 250 mcg/m2 SQ on days 1-14 for 6 cycles.
其他名称:
  • 沙格司亭

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
To assess for clinical activity by PSA response, of both single agent ipilimumab and the combination of GM-CSF and ipilimumab in chemotherapy-naïve patients with metastatic castrate resistant prostate cancer.
大体时间:12 weeks
To assess for clinical activity by PSA (prostate-specific antigen) decline of both single agent ipilimumab in chemotherapy-naïve patients with metastatic castrate resistant prostate cancer (CRPC). The primary endpoint is the proportion of treated patients achieving a >30% decline in PSA.
12 weeks

次要结果测量

结果测量
大体时间
To evaluate the duration of PSA response and time to PSA progression. To quantify the frequency of immune toxicities. To evaluate T cell activation. To assess for clinical activity by objective response.
大体时间:12 weeks
12 weeks

其他结果措施

结果测量
措施说明
大体时间
Assessment of circulating tumor cell (CTC) frequency
大体时间:12 weeks
To assess whether either treatment can modulate the frequency of circulating tumor cells (CTC). Modulation of the frequency of circulating tumor cells (CTC) will be measured from baseline to Cycle 6/off study visit of treatment.
12 weeks
Assessment of the antigen specific immune responses induced with treatment
大体时间:12 weeks
Antigen specific immune responses will be measured by immunoblotting to detect the induction of IgG antibodies and by ELISA and ELISPOT assays to detect antibody and CD4 T cell responses, respectively, against candidate antigens in prostate cancer.
12 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

调查人员

  • 学习椅:Lawrence Fong, MD、University of California, San Francisco

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2015年6月1日

初级完成 (预期的)

2017年12月1日

研究完成 (预期的)

2018年12月1日

研究注册日期

首次提交

2012年2月7日

首先提交符合 QC 标准的

2012年2月7日

首次发布 (估计)

2012年2月10日

研究记录更新

最后更新发布 (估计)

2015年10月5日

上次提交的符合 QC 标准的更新

2015年10月1日

最后验证

2015年10月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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