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Abemaciclib and Pembrolizumab in Metastatic or Recurrent Head and Neck Cancer

16. Juni 2021 aktualisiert von: 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.

Studienübersicht

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

1

Phase

  • Phase 2

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Alabama
      • Birmingham, Alabama, Vereinigte Staaten, 35294
        • University of Alabama at Birmingham

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

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

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Nicht randomisiert
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 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
Andere Namen:
  • CDK4:CDK6
Experimental: 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
Andere Namen:
  • CDK4:CDK6

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
To Assess the Objective Response Rate of Tumor Lesions Using Scans
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: Baseline to 8 months
Patients will be evaluated for their tumor response to treatment using RECIST criteria on their scans
Baseline to 8 months

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Number of Participants Experiencing Adverse Events Grade 3 or Greater
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: baseline to 12 months
Using scan results to assess whether tumor has progressed and the time;
baseline to 12 months
To Assess Overall Survival
Zeitfenster: baseline to 6 months
time that the patient is experiencing survival
baseline to 6 months
To Assess Overall Survival
Zeitfenster: baseline to 12 months
time that the patient is experiencing survival
baseline to 12 months
To Assess the Time to Tumor Response
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Hauptermittler: Eddy Yang, MD, University of Alabama at Birmingham

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Tatsächlich)

8. Oktober 2019

Primärer Abschluss (Tatsächlich)

3. April 2020

Studienabschluss (Tatsächlich)

3. April 2020

Studienanmeldedaten

Zuerst eingereicht

2. Mai 2019

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

3. Mai 2019

Zuerst gepostet (Tatsächlich)

6. Mai 2019

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

9. Juli 2021

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

16. Juni 2021

Zuletzt verifiziert

1. Juni 2021

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

JA

Beschreibung des IPD-Plans

To Be Determined

IPD-Sharing-Zeitrahmen

As long as study record is posted on CT.gov

IPD-Sharing-Zugriffskriterien

To Be Determined

Art der unterstützenden IPD-Freigabeinformationen

  • STUDIENPROTOKOLL
  • SAFT
  • ICF

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Ja

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Ja

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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