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Abemaciclib et thérapie endocrinienne chez les patientes âgées atteintes d'un cancer du sein.

14 octobre 2026 mis à jour par: City of Hope Medical Center

Un essai de phase IIA évaluant la tolérance de l'abémaciclib en association avec une hormonothérapie chez des patientes âgées de 70 ans et plus atteintes d'un cancer du sein métastatique à récepteurs hormonaux positifs qui ont progressé pendant ou après une inhibition antérieure de la CDK 4/6

This phase IIa trial studies the side effects of abemaciclib monotherapy in treating patients age 70 years and older with hormone receptor positive, HER2 negative breast cancer that has spread to other places in the body.

Aperçu de l'étude

Description détaillée

PRIMARY OBJECTIVE:

I. To estimate the incidence of grade 3 or higher toxicities attributed to abemaciclib monotherapy in adults aged 70 or older with hormone receptor positive metastatic breast cancer.

SECONDARY OBJECTIVES:

I. To describe the full toxicity profile including all grade 2 and higher adverse events, and patient-reported adverse events (AEs) using Patients Reported Outcomes (PRO)-Common Terminology Criteria for Adverse Events (CTCAE) measures.

II. To describe rates of dose reductions, dose holds, treatment discontinuations due to factors other than progression, and hospitalizations.

III. To estimate median (and 95% confidence interval [CI]) failure-free survival, progression-free survival and overall survival.

IV. To describe the results of Was It Worth It (WIWI) and Overall Treatment Utility (OTU) questionnaires.

V. To describe the rate of adherence to abemaciclib. VI. To determine average plasma steady-state abemaciclib Ctrough concentrations.

VII. To evaluate the association of adherence rate with abemaciclib plasma t-rough concentrations.

VIII. To describe associations between cancer-specific, comprehensive Geriatric Assessment (cGA) scores and the incidence of toxicities and their grade.

EXPLORATORY OBJECTIVE:

I. To determine the association between biomarkers of aging and grades 3 or higher toxicity.

OUTLINE:

Patients receive abemaciclib orally (PO) twice daily (BID) on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up at 30 days, then every 6 months for 2 years.

Type d'étude

Interventionnel

Inscription (Estimé)

43

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.

Coordonnées de l'étude

  • Nom: Joanne Mortimer, MD
  • Numéro de téléphone: 626-359-8111
  • E-mail: jmortimer@coh.org

Lieux d'étude

    • California
      • Duarte, California, États-Unis, 91010
        • Recrutement
        • City of Hope Medical Center
        • Contact:
          • Mina Sedrak
          • Numéro de téléphone: 89200 626-256-4673
          • E-mail: msedrak@coh.org
        • Chercheur principal:
          • Mina Sedrak
      • Irvine, California, États-Unis, 92618
        • Recrutement
        • City of Hope at Irvine Lennar
        • Contact:
          • Thanh Nga Doan
          • Numéro de téléphone: 6262184673
          • E-mail: tdoan@coh.org
      • Long Beach, California, États-Unis, 90813
        • Recrutement
        • City of Hope at Long Beach Elm
        • Contact:
          • Thanh Nga Doan
          • Numéro de téléphone: 6262184673
          • E-mail: tdoan@coh.org
      • South Pasadena, California, États-Unis, 91030
        • Recrutement
        • City of Hope South Pasadena
        • Contact:
    • Massachusetts
      • Boston, Massachusetts, États-Unis, 02215
    • New York
      • Buffalo, New York, États-Unis, 14203
        • Recrutement
        • Roswell Park Comprehensive Cancer Center
        • Contact:

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

70 ans et plus (Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Documented informed consent of the participant

  • Age >= 70 years

  • Life expectancy > 6 months

  • Ability to read and understand English or Spanish

  • Measurable or non-measurable disease

  • Histologically or cytologically confirmed diagnosis of:

    • Estrogen-receptor positive and/or progesterone receptor positive breast cancer determined by immunohistochemistry (IHC) methods according to the local institution standard protocol
    • HER2-negative breast cancer defined as negative if the IHC status is 0 or 1+, or if IHC is 2+ and in situ hybridization assay is negative per American Society of Clinical Oncology (ASCO)/College of American Pathologists (CAP) guidelines
  • Radiographically confirmed metastatic breast cancer

  • Progressed on prior endocrine therapy or palbociclib or ribociclib or chemotherapy

  • Patients who received chemotherapy recovered from the acute side effects to prior cancer therapy (except alopecia or residual grade 2 peripheral neuropathy) to =< grade 1 or baseline. A washout period of at least 21 days is required between last chemotherapy dose and randomization (provided the patient did not receive radiotherapy)

  • Patients who received 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

  • Absence of central nervous system (CNS) involvement unless they meet ONE of the following criteria:

    • Untreated brain metastases (e.g., lesions < 1 cm) not needing immediate local therapy

    • Previously treated brain metastases not needing immediate local therapy

      • At least 4 weeks from the last date of prior therapy completion (including radiation and/or surgery) to starting the study treatment
      • Clinically stable CNS tumor at the time of screening and not receiving steroids and/or enzyme-inducing anti-epileptic medications for brain metastases
  • Absence of interstitial lung disease/pneumonitis

  • Absolute neutrophil count (ANC) >= 1.5 X 10^9/L

  • Platelets >= 100 x 10^9/L

  • Hemoglobin >= 8 g/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)
  • In the absence of liver metastases, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =< 3.0 x upper limit of normal (ULN)

    • If the patient has liver metastases, ALT and AST < 5 x ULN
  • In patients without Gilbert's syndrome, total bilirubin =< 1.5 x ULN; In patients with Gilbert's syndrome, total bilirubin =< 2.0 x ULN or direct bilirubin within normal limits (WLN)

  • Creatinine clearance of >= 30 mL/min per 24 hour urine test or the Cockcroft-Gault formula

Exclusion Criteria:

  • Major surgery within 14 days prior to receiving study drug or has not recovered from major side effect

  • Patient is currently receiving any of the prohibited medications detailed below and cannot be discontinued 7 days prior to starting study drug

    • Other investigational therapy should be given to participants
    • Anticancer agents other than the study medications administered as part of this study protocol should be given to participants. If such agents are required for a participant then the participant must first be withdrawn from the study
    • Co-medication that may interfere with study results; e.g. immune-suppressive agents other than corticosteroids, such as systemic cyclosporine and tacrolimus are prohibited during the treatment phase of the study, unless discussed with principal investigator felt to be of low clinical risk to the participant
    • Use of herbal medications may have unknown interactions with the metabolism of the study agents, and therefore are prohibited from use during the treatment phase of the trial
  • Known hypersensitivity to any of the excipients of abemaciclib

  • Active systemic bacterial infection (requiring intravenous [IV] antibiotics at time of initiating study treatment), fungal infection, or detectable viral infection (such as known human immunodeficiency virus positivity or with known active hepatitis B or C (for example, hepatitis B surface antigen positive). Screening is not required for enrollment

  • Impairment of gastrointestinal (GI) function or GI disease that in the investigator's opinion may significantly alter the absorption of the study drugs (e.g., ulcerative diseases, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel resection)

  • 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

  • Patient has any other concurrent severe or uncontrolled medical condition that would, in the investigator's judgment, cause unacceptable safety risks, contraindicate patient participation in the clinical study or compromise compliance with the protocol (e.g. chronic pancreatitis, chronic active hepatitis)

  • Inability to swallow oral medications

  • Serious or uncontrolled preexisting medical condition(s) that, in the judgment of the investigator, would preclude participation in this study (for example, interstitial lung disease, severe dyspnea at rest or requiring oxygen therapy, severe renal impairment [e.g. estimated creatinine clearance < 30 ml/min], 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)

  • History of non-compliance to medical regimen

  • Patients with a prior malignancy diagnosed within 2 years and with evidence of disease (except adequately treated, basal or squamous cell carcinoma, non-melanomatous skin cancer or curatively resected cervical cancer

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: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Treatment (abemaciclib)

Patients receive abemaciclib PO BID on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Ancillary studies

Given PO

Autres noms:
  • LY-2835219
  • LY2835219
  • Verzenio

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Incidence of grade 3 or higher toxicities
Délai: Up to 30 days post treatment

Adverse events will be characterized using the descriptions and grading scales found in the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version (v). 5.0.

Up to 30 days post treatment

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Concentrations plasmatiques minimales moyennes d'abemaciclib à l'état d'équilibre
Délai: Jusqu'à 2 ans après le traitement
Jusqu'à 2 ans après le traitement
Incidence of toxicities
Délai: Up to 30 days post treatment

Toxicities will be graded and named according to CTCAE v. 5.0.

Up to 30 days post treatment
Incidence of toxicities
Délai: Up to cycle 6

Toxicities will be captured by Patient Reported Outcome (PRO)-CTCAE.

Up to cycle 6
Dose reductions
Délai: Up to cycle 6

Will assess rates of dose reductions.

Up to cycle 6
Dose holds
Délai: Up to 30 days post treatment

Will assess rates of dose holds.

Up to 30 days post treatment
Treatment discontinuations due to factors other than progression
Délai: Up to 30 days post treatment

Will assess rates of treatment discontinuations.

Up to 30 days post treatment
Hospitalizations
Délai: Up to 2 years post treatment

Will assess rates of hospitalizations.

Up to 2 years post treatment
Time to end of treatment
Délai: Up to end of treatment

Will estimate median (and 95% confidence interval [CI]) failure-free survival using Kaplan-Meier estimates and through Cox regression to adjust for covariates.

Up to end of treatment
Progression free survival
Délai: Up to 2 years post treatment

Will estimate median (and 95% CI) progression-free survival using Kaplan-Meier estimates and through Cox regression to adjust for covariates.

Up to 2 years post treatment
Overall survival
Délai: Up to 2 years post treatment

Will estimate median (and 95% CI) overall survival using Kaplan-Meier estimates and through Cox regression to adjust for covariates.

Up to 2 years post treatment
Was It Worth It (WIWI) response
Délai: Up to end of treatment

Will be assessed using the WIWI questionnaire.

Up to end of treatment
Overall treatment utility (OTU) response
Délai: Up to end of treatment

Will be assessed using the OTU questionnaire.

Up to end of treatment
Adherence to abemaciclib
Délai: Up to end of treatment

Adherence defined as taking 90% of scheduled doses per cycle. Scheduled doses are assigned doses for the participant which may vary per participant depending on whether or not there a hold in treatment. Adherence will be calculated based on consolidation of pill diary with returned unused pills, and, for City of Hope (COH) Duarte patients, Medication Event Monitoring bottle caps.

Up to end of treatment
Pharmacokinetic (PK) parameter of plasma trough concentration
Délai: Up to 2 years post treatment

Will evaluate the association of adherence rate with abemaciclib plasma trough concentrations.

Up to 2 years post treatment
Geriatric assessment scores
Délai: Up to 2 years post treatment

Domains include: functional status, co-morbid medical conditions, cognitive function, nutritional status, social support and psychological state, and a review of medications.

Up to 2 years post treatment
Incidence of toxicities attributable to agent
Délai: Up to 2 years post treatment

Graded by CTCAE v 5.0.

Up to 2 years post treatment

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Âge biologique via le niveau de méthylation de l'acide désoxyribonucléique (ADN)
Délai: Jusqu'à 2 ans après le traitement
Jusqu'à 2 ans après le traitement
Analyses du méthylome et du transcriptome à l'échelle du génome
Délai: Jusqu'à 2 ans après le traitement
Jusqu'à 2 ans après le traitement
Incidence of toxicities at least possibly attributable to agent
Délai: Up to 2 years post treatment

Graded by CTCAE v 5.0.

Up to 2 years post treatment

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Joanne Mortimer, MD, City of Hope Medical Center

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)

5 juin 2020

Achèvement primaire (Estimé)

21 mai 2027

Achèvement de l'étude (Estimé)

21 mai 2027

Dates d'inscription aux études

Première soumission

2 mars 2020

Première soumission répondant aux critères de contrôle qualité

10 mars 2020

Première publication (Réel)

12 mars 2020

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

16 octobre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

14 octobre 2026

Dernière vérification

1 octobre 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • 19206
  • P30CA033572 (Subvention/contrat des NIH des États-Unis)
  • 19206 (Autre identifiant: City of Hope Medical Center)
  • NCI-2019-08847 (Identificateur de registre: CTRP (Clinical Trial Reporting Program))

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

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 .

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