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Abemaciclib and Pembrolizumab in Metastatic or Recurrent Head and Neck Cancer

2021年6月16日 更新者:Eddy Yang、University of Alabama at Birmingham

Clinical Trial of Abemaciclib in Combination With Pembrolizumab in Patients With Metastatic or Recurrent Head and Neck Cancer

To assess the objective response rate of tumor lesions to abemaciclib in combination with pembrolizumab in patients with metastatic or recurrent squamous cell carcinoma of head and neck.

研究概览

详细说明

Immunotherapy has been recently approved for patients with metastatic or recurrent squamous cell carcinoma of the head and neck. However, only a small percentage of patients experience long-term control, necessitating new therapeutic strategies. Recently, it was shown preclinically and in breast tumors that abemaciclib stimulates production of type III interferons and hence enhances tumor antigen presentation. Abemaciclib also suppressed the proliferation of regulatory T cells. These events promote cytotoxic T-cell-mediated clearance of tumor cells, which is further enhanced by the addition of immune checkpoint blockade. Based on these data, a phase II trial in patients with metastatic or recurrent head and neck cancer who are eligible for immunotherapy is proposed to investigate the combination of abemaciclib with pembrolizumab. Tumor & blood analysis for interferon gamma signature will be explored as possible biomarkers.

研究类型

介入性

注册 (实际的)

1

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

    • Alabama
      • Birmingham、Alabama、美国、35294
        • University of Alabama at Birmingham

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

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Histologically confirmed (core biopsy proven) metastatic or recurrent squamous cell carcinoma of head and neck
  • Adequate pulmonary and cardiac function
  • Available archived tissue of primary tumor or resected tumor specimen with adequate samples
  • Prior treatment with immune checkpoint inhibitor is not allowed in cohort 1 patients. Patients in cohort 2 should have failed or progressed on prior immune checkpoint inhibitor
  • Eastern Cooperative Oncology Group Performance Status(ECOG PS) = 0 or 1
  • Patients who received chemotherapy must have recovered (Common Terminology Criteria for Adverse [CTCAE] Grade <= 1) from the acute effects of chemotherapy except for residual alopecia or Grade 2 peripheral neuropathy prior to randomization. A washout period of at lease 21 days is required between last chemotherapy dose and randomization (provided the patient did not receive radiotherapy)
  • Patients who received adjuvant radiotherapy must have completed and fully recovered from the acute effects of radiotherapy. A washout period of at least 14 days is required between end of radiotherapy and randomization
  • The patient is able to swallow oral medications
  • Adequate hematologic and end-organ function
  • Absolute Neutrophil Count (ANC) >= 1500/mm3
  • Platelet count ≥ 100,000/mm3
  • Hemoglobin (Hb) ≥ 8g/dl (Patients may receive erythrocyte transfusions to achieve this hemoglobin level at the discretion of the investigator. Initial treatment must not begin earlier than the day after the erythrocyte transfusion)
  • Creatinine (Cr) ≤ 1.5 x Upper Limit of Normal (ULN) or Creatinine Clearance (CrCl) ≥ 60 ml/min
  • Total Bilirubin ≤ 1.5 x ULN (except subjects with Gilbert syndrome, who can have total Bilirubin < 2.0 x ULN and direct bilirubin within normal limits are permitted.)
  • Aspartate Aminotransferase (AST) and Alanine aminotransferase (ALT) and alkaline phosphatase ≤ ULN
  • Agreement to remain abstinent or use appropriate contraception, among women of childbearing potential
  • Willingness and ability to consent for self to participate in study
  • Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures

Exclusion Criteria:

  • Autoimmune disease (Note: Vitiligo, type 1 diabetes mellitus, residual hypothyroidism due to autoimmune thyroiditis only requiring hormone replacement, and conditions not expected to recur in the absence of an external trigger are permitted.)
  • Condition requiring systemic treatment with either corticosteroids (>10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days prior to study treatment (Note: Inhaled and topical steroids, and adrenal replacement steroid doses > 10 mg daily prednisone equivalent, are permitted in the absence of active autoimmune disease.)
  • Preexisting medical condition(s) that would preclude participation in this study (for example, interstitial lung disease, severe dyspnea at rest or requiring oxygen therapy, history of major surgical resection involving the stomach or small bowel, or preexisting Crohn's disease or ulcerative colitis or a preexisting chronic condition resulting in baseline Grade 2 or higher diarrhea).
  • Immunosuppression, of any kind
  • Prior treatment with Cyclin-Dependent Kinase(CDK) 4/6 Inhibitor
  • Major surgical procedure or significant traumatic injury within 4 weeks prior to study treatment, and must have fully recovered from any such procedure
  • Personal history of any of the following conditions: syncope of cardiovascular etiology, ventricular arrhythmia of pathological origin (including, but not limited to, ventricular tachycardia and ventricular fibrillation), or sudden cardiac arrest
  • Angina, myocardial infarction (MI), symptomatic congestive heart failure, cerebrovascular accident, transient ischemic attack TIA), arterial embolism, pulmonary embolism, percutaneous transluminal coronary angioplasty (PTCA), or coronary artery bypass grafting (CABG) within 6 months prior to study treatment
  • Known active viral or non-viral hepatitis or cirrhosis
  • Any active infection requiring systemic treatment, positive tests for Hepatitis B surface antigen or Hepatitis C ribonucleic acid (RNA).
  • History of gastrointestinal perforation or fistula in the 6 months prior to study treatment, unless underlying risk has been resolved (e.g., through surgical resection or repair)
  • Known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS) related illness
  • Pregnancy or breastfeeding - Female patients must be surgically sterile (i.e., ≥6 weeks following surgical bilateral oophorectomy with or without hysterectomy or tubal ligation) or be postmenopausal, or must agree to use effective contraception during the study and for 4 months following last dose of treatment. All female patients of reproductive potential must have a negative pregnancy test (serum or urine) within 7 days prior to study treatment. Male patients must be surgically sterile or must agree to use effective contraception during the study and for 4 months following last dose of treatment.
  • Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or may interfere with the interpretation of study results and, in the judgment of the Investigator, would make the patient inappropriate for this study

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:非随机化
  • 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:Cohort 1 Not Previously Treated
Patients with metastatic or recurrent head and neck cancer who have not been treated previously with immunotherapy.
Abemaciclib 150mg by mouth twice daily Pembrolizumab 200mg IV every 3 weeks
其他名称:
  • CDK4:CDK6
实验性的:Cohort 2 Treated Previously
Patients with metastatic or recurrent head and neck cancer who have been treated previously with immunotherapy.
Abemaciclib 150mg by mouth twice daily Pembrolizumab 200mg IV every 3 weeks
其他名称:
  • CDK4:CDK6

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 the Objective Response Rate of Tumor Lesions Using Scans
大体时间:Baseline
Patients will be evaluated for their tumor response to treatment using RECIST criteria on their scans
Baseline
To Assess the Objective Response Rate of Tumor Lesions Using Scans
大体时间:Baseline to 5 months
Patients will be evaluated for their tumor response to treatment using RECIST criteria on their scans
Baseline to 5 months
To Assess the Objective Response Rate of Tumor Lesions Using Scans
大体时间:Baseline to 8 months
Patients will be evaluated for their tumor response to treatment using RECIST criteria on their scans
Baseline to 8 months

次要结果测量

结果测量
措施说明
大体时间
Number of Participants Experiencing Adverse Events Grade 3 or Greater
大体时间:Baseline to 1 month
Measure adverse events grade 3 or greater to evaluate safety and tolerability
Baseline to 1 month
Number of Participants Experiencing Adverse Events Grade 3 or Greater
大体时间:Baseline to 6 months
Measure adverse events grade 3 or greater to evaluate safety and tolerability
Baseline to 6 months
Number of Participants Experiencing Adverse Events Grade 3 or Greater
大体时间:Baseline to 12 months
Measure adverse events grade 3 or greater to evaluate safety and tolerability
Baseline to 12 months
To Assess Progression Free Survival (PFS)
大体时间:baseline to 6 months
Using scan results to assess whether tumor has progressed and the time;
baseline to 6 months
To Assess Progression Free Survival (PFS)
大体时间:baseline to 12 months
Using scan results to assess whether tumor has progressed and the time;
baseline to 12 months
To Assess Overall Survival
大体时间:baseline to 6 months
time that the patient is experiencing survival
baseline to 6 months
To Assess Overall Survival
大体时间:baseline to 12 months
time that the patient is experiencing survival
baseline to 12 months
To Assess the Time to Tumor Response
大体时间:baseline to 6 months
using scan results to assess the time it takes for the tumor to respond to treatment
baseline to 6 months
To Assess the Time to Tumor Response
大体时间:baseline to 12 months
using scan results to assess the time it takes for the tumor to respond to treatment
baseline to 12 months
To Assess the Duration of Response
大体时间:baseline to 6 months
using scan results to measure the total amount of time that the tumor is responding to treatment
baseline to 6 months
To Assess the Duration of Response
大体时间:baseline to 12 months
using scan results to measure the total amount of time that the tumor is responding to treatment
baseline to 12 months

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。

调查人员

  • 首席研究员:Eddy Yang, MD、University of Alabama at Birmingham

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 (实际的)

2019年10月8日

初级完成 (实际的)

2020年4月3日

研究完成 (实际的)

2020年4月3日

研究注册日期

首次提交

2019年5月2日

首先提交符合 QC 标准的

2019年5月3日

首次发布 (实际的)

2019年5月6日

研究记录更新

最后更新发布 (实际的)

2021年7月9日

上次提交的符合 QC 标准的更新

2021年6月16日

最后验证

2021年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

To Be Determined

IPD 共享时间框架

As long as study record is posted on CT.gov

IPD 共享访问标准

To Be Determined

IPD 共享支持信息类型

  • 研究方案
  • 树液
  • 国际碳纤维联合会

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

在美国制造并从美国出口的产品

是的

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.

Cohort 1 Not Previously Treated的临床试验

3
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