- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT03938337
Abemaciclib and Pembrolizumab in Metastatic or Recurrent Head and Neck Cancer
16 juin 2021 mis à jour par: 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.
Aperçu de l'étude
Statut
Résilié
Les conditions
Intervention / Traitement
Description détaillée
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.
Type d'étude
Interventionnel
Inscription (Réel)
1
Phase
- Phase 2
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
-
-
Alabama
-
Birmingham, Alabama, États-Unis, 35294
- University of Alabama at Birmingham
-
-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
18 ans et plus (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Non
Sexes éligibles pour l'étude
Tout
La description
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
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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
Autres noms:
|
|
Expérimental: 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
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
To Assess the Objective Response Rate of Tumor Lesions Using Scans
Délai: 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
Délai: 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
Délai: Baseline to 8 months
|
Patients will be evaluated for their tumor response to treatment using RECIST criteria on their scans
|
Baseline to 8 months
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Number of Participants Experiencing Adverse Events Grade 3 or Greater
Délai: 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
Délai: 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
Délai: 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)
Délai: 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)
Délai: baseline to 12 months
|
Using scan results to assess whether tumor has progressed and the time;
|
baseline to 12 months
|
|
To Assess Overall Survival
Délai: baseline to 6 months
|
time that the patient is experiencing survival
|
baseline to 6 months
|
|
To Assess Overall Survival
Délai: baseline to 12 months
|
time that the patient is experiencing survival
|
baseline to 12 months
|
|
To Assess the Time to Tumor Response
Délai: 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
Délai: 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
Délai: 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
Délai: 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
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: Eddy Yang, MD, University of Alabama at Birmingham
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
8 octobre 2019
Achèvement primaire (Réel)
3 avril 2020
Achèvement de l'étude (Réel)
3 avril 2020
Dates d'inscription aux études
Première soumission
2 mai 2019
Première soumission répondant aux critères de contrôle qualité
3 mai 2019
Première publication (Réel)
6 mai 2019
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
9 juillet 2021
Dernière mise à jour soumise répondant aux critères de contrôle qualité
16 juin 2021
Dernière vérification
1 juin 2021
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- UAB 1891
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
OUI
Description du régime IPD
To Be Determined
Délai de partage IPD
As long as study record is posted on CT.gov
Critères d'accès au partage IPD
To Be Determined
Type d'informations de prise en charge du partage d'IPD
- PROTOCOLE D'ÉTUDE
- SÈVE
- CIF
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Oui
Étudie un produit d'appareil réglementé par la FDA américaine
Non
produit fabriqué et exporté des États-Unis.
Oui
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .