- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03938337
Abemaciclib and Pembrolizumab in Metastatic or Recurrent Head and Neck Cancer
16. juni 2021 opdateret af: 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.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
1
Fase
- Fase 2
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Alabama
-
Birmingham, Alabama, Forenede Stater, 35294
- University of Alabama at Birmingham
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
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
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: 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
Andre navne:
|
|
Eksperimentel: 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
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
To Assess the Objective Response Rate of Tumor Lesions Using Scans
Tidsramme: 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
Tidsramme: 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
Tidsramme: Baseline to 8 months
|
Patients will be evaluated for their tumor response to treatment using RECIST criteria on their scans
|
Baseline to 8 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Number of Participants Experiencing Adverse Events Grade 3 or Greater
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: baseline to 12 months
|
Using scan results to assess whether tumor has progressed and the time;
|
baseline to 12 months
|
|
To Assess Overall Survival
Tidsramme: baseline to 6 months
|
time that the patient is experiencing survival
|
baseline to 6 months
|
|
To Assess Overall Survival
Tidsramme: baseline to 12 months
|
time that the patient is experiencing survival
|
baseline to 12 months
|
|
To Assess the Time to Tumor Response
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Eddy Yang, MD, University of Alabama at Birmingham
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
8. oktober 2019
Primær færdiggørelse (Faktiske)
3. april 2020
Studieafslutning (Faktiske)
3. april 2020
Datoer for studieregistrering
Først indsendt
2. maj 2019
Først indsendt, der opfyldte QC-kriterier
3. maj 2019
Først opslået (Faktiske)
6. maj 2019
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
9. juli 2021
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
16. juni 2021
Sidst verificeret
1. juni 2021
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- UAB 1891
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
JA
IPD-planbeskrivelse
To Be Determined
IPD-delingstidsramme
As long as study record is posted on CT.gov
IPD-delingsadgangskriterier
To Be Determined
IPD-deling Understøttende informationstype
- STUDY_PROTOCOL
- SAP
- ICF
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ja
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
produkt fremstillet i og eksporteret fra U.S.A.
Ja
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Cohort 1 Not Previously Treated
-
Bristol-Myers SquibbCardioxyl Pharmaceuticals, IncAfsluttetHjertefejlForenede Stater