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.
調査の概要
詳細な説明
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.
研究の種類
介入
入学 (実際)
1
段階
- フェーズ2
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
-
-
Alabama
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Birmingham、Alabama、アメリカ、35294
- University of Alabama at Birmingham
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-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
18年歳以上 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
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
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
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:非ランダム化
- 介入モデル:並列代入
- 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:Cohort 1 Not Previously Treated
Patients with metastatic or recurrent head and neck cancer who have not been treated previously with immunotherapy.
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Abemaciclib 150mg by mouth twice daily Pembrolizumab 200mg IV every 3 weeks
他の名前:
|
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実験的: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
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 |
|---|---|---|
|
To Assess the Objective Response Rate of Tumor Lesions Using Scans
時間枠:Baseline
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Patients will be evaluated for their tumor response to treatment using RECIST criteria on their scans
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Baseline
|
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To Assess the Objective Response Rate of Tumor Lesions Using Scans
時間枠:Baseline to 5 months
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Patients will be evaluated for their tumor response to treatment using RECIST criteria on their scans
|
Baseline to 5 months
|
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To Assess the Objective Response Rate of Tumor Lesions Using Scans
時間枠:Baseline to 8 months
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Patients will be evaluated for their tumor response to treatment using RECIST criteria on their scans
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Baseline to 8 months
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Number of Participants Experiencing Adverse Events Grade 3 or Greater
時間枠:Baseline to 1 month
|
Measure adverse events grade 3 or greater to evaluate safety and tolerability
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Baseline to 1 month
|
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Number of Participants Experiencing Adverse Events Grade 3 or Greater
時間枠:Baseline to 6 months
|
Measure adverse events grade 3 or greater to evaluate safety and tolerability
|
Baseline to 6 months
|
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Number of Participants Experiencing Adverse Events Grade 3 or Greater
時間枠:Baseline to 12 months
|
Measure adverse events grade 3 or greater to evaluate safety and tolerability
|
Baseline to 12 months
|
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To Assess Progression Free Survival (PFS)
時間枠:baseline to 6 months
|
Using scan results to assess whether tumor has progressed and the time;
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baseline to 6 months
|
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To Assess Progression Free Survival (PFS)
時間枠:baseline to 12 months
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Using scan results to assess whether tumor has progressed and the time;
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baseline to 12 months
|
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To Assess Overall Survival
時間枠:baseline to 6 months
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time that the patient is experiencing survival
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baseline to 6 months
|
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To Assess Overall Survival
時間枠:baseline to 12 months
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time that the patient is experiencing survival
|
baseline to 12 months
|
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To Assess the Time to Tumor Response
時間枠:baseline to 6 months
|
using scan results to assess the time it takes for the tumor to respond to treatment
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baseline to 6 months
|
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To Assess the Time to Tumor Response
時間枠:baseline to 12 months
|
using scan results to assess the time it takes for the tumor to respond to treatment
|
baseline to 12 months
|
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To Assess the Duration of Response
時間枠: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
|
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To Assess the Duration of Response
時間枠: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
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
捜査官
- 主任研究者:Eddy Yang, MD、University of Alabama at Birmingham
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2019年10月8日
一次修了 (実際)
2020年4月3日
研究の完了 (実際)
2020年4月3日
試験登録日
最初に提出
2019年5月2日
QC基準を満たした最初の提出物
2019年5月3日
最初の投稿 (実際)
2019年5月6日
学習記録の更新
投稿された最後の更新 (実際)
2021年7月9日
QC基準を満たした最後の更新が送信されました
2021年6月16日
最終確認日
2021年6月1日
詳しくは
本研究に関する用語
その他の研究ID番号
- UAB 1891
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?
はい
IPD プランの説明
To Be Determined
IPD 共有時間枠
As long as study record is posted on CT.gov
IPD 共有アクセス基準
To Be Determined
IPD 共有サポート情報タイプ
- STUDY_PROTOCOL
- SAP
- ICF
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
はい
米国FDA規制機器製品の研究
いいえ
米国で製造され、米国から輸出された製品。
はい
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