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The Efficacy and Safety of Dalpiciclib Plus Endocrine Therapy in HR-positive / HER2-negative Advanced Breast Cancer Patients With Visceral Crisis

An Exploratory Trial of Dalpiciclib in Combination With Endocrine Therapy in HR-positive / HER2-negative Advanced Breast Cancer Patients With Visceral Crisis

This is a multicenter, single-arm, open-label, Simon's two-stage exploratory clinical trial. 18 eligible patients with advanced breast cancer with visceral crisis will enroll in stage I. If the study enter stage 2 and continue to include 53 assessable subjects (35 in stage 2). All eligible patients will receive Dalpiciclib plus endocrine therapy chosen by the Physicians until disease progression, death or intolerable toxicity. Tumor assessment was conducted according to RECIST 1.1 criteria.

Aperçu de l'étude

Statut

Pas encore de recrutement

Les conditions

Type d'étude

Interventionnel

Inscription (Anticipé)

53

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: Fei Ma
  • Numéro de téléphone: 86-10-87788060
  • E-mail: drmafei@126.com

Lieux d'étude

    • Beijing
      • Beijing, Beijing, Chine, 100021
        • Cancer Hospital, Chinese Academy of Medical Sciences

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

Femelle

La description

Inclusion Criteria:

  1. Postmenopausal or premenopausal/perimenopausal women aged ≥18 meet one of the following:

    A) Previous bilateral oophorectomy, or age ≥60 years; or B) age<60. Natural postmenopausal status (defined as spontaneous cessation of regular menstruation for at least 12 consecutive months without other pathological or physiological causes), E2 and FSH at postmenopausal levels; or C) premenopausal/perimenopausal women must receive LHRH agonists therapy during the study.

  2. Female breast cancer patients diagnosed as HR-positive or HER2-negative by pathological examination are not suitable for surgical resection or radiotherapy for the purpose of cure.

    A) ER-positive and/or PR-positive are defined as: ≥ 1% of all tumor cells are positively stained (confirmed by investigator review at the site); B) HER2-negative are defined as: 0/1 + by standard immunohistochemistry (IHC); HER2/CEP17 ratio less than 2.0 by ISH or HER2 gene copy number less than 4 (confirmed by investigator review at the site).

  3. Any clinical signs or symptoms of symptomatic brain metastasis or visceral metastasis (at least one of the following: carcinomatous meningitis or leptomeningeal metastasis; pleural effusion; ascites; abdominal pain caused by liver or peritoneal metastasis; dyspnea caused by pleural effusion or pulmonary lymphangitis; elevated liver enzymes (> 2 × ULN); rapid elevation of bilirubin > 1.5 × ULN in the absence of Gilbert's syndrome or biliary obstruction; pathologically confirmed bone marrow metastasis; hemoglobin less than 10 g) and patients who cannot tolerate chemotherapy or are considered by the investigator to be inappropriate for chemotherapy or chemotherapy.
  4. Adequate bone marrow function. Definitions are as follows: a) neutrophil count (ANC) ≥ 1,500/mm3 (1.5 x 109L) (14 without growth factors); b) platelet count (PLT) ≥ 100,000/mm3 (100 x 109L) (7 without correction); c) hemoglobin (Hb) ≥ 8 g/dL (80 g/L) (7 without correction).
  5. Female subjects who are not postmenopausal or surgically sterile must have a serum pregnancy test within 7 days before the first dose and have a negative result, and are willing to abstain from sexual intercourse or use a medically recognized highly effective contraceptive measure after signing the informed consent, during the study, and for 1 year after administration of the study drug.
  6. Voluntarily participate in this study, sign informed consent, have good compliance and are willing to cooperate with follow-up.

Exclusion Criteria:

  1. Patients contraindicated with dalpiciclib.
  2. Patients with primary resistance to endocrine therapy. Relapse within 2 years of adjuvant endocrine therapy, or disease progression within 6 months of advanced first-line endocrine therapy.
  3. Patients with more than 3 lines of prior endocrine therapy.
  4. Patients previously treated with any CDK4/6 inhibitor.
  5. Patients with simple bone metastasis.
  6. Human immunodeficiency virus (HIV) infection or known acquired immunodeficiency syndrome (AIDS), active hepatitis B (HBV DNA ≥ 1000 IU/ml), hepatitis C (hepatitis C antibody positive, and HCV-RNA above the lower limit of detection of the analytical method) or combined hepatitis B and C co-infection.
  7. Within 6 months before enrollment, the following conditions occur: myocardial infarction, severe/unstable angina pectoris, NYHA grade 2 or higher cardiac insufficiency, ≥ grade 2 persistent arrhythmia (according to NCI CTCAE v5.0), atrial fibrillation of any grade, coronary/peripheral artery bypass grafting, symptomatic congestive heart failure, cerebrovascular accident (including transient ischemic attack) or symptomatic pulmonary embolism.
  8. Severe infection occurring within 4 weeks (such as intravenous drip of antibiotics, antifungal or antiviral drugs according to clinical practice) before the first dose, or unexplained fever > 38.5℃ during screening/before the first dose.
  9. Inability to swallow, intestinal obstruction, or other factors affecting drug administration and absorption.
  10. Known hypersensitivity to dalpiciclib and any of its excipients.
  11. Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation;
  12. Known history of psychiatric drug abuse or drug use;
  13. Female patients who are pregnant or lactating.
  14. Any other condition that the investigator considers the subject unsuitable 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: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Treatment group
Dalpiciclib in combination with endocrine therapy by physicians choice

Dalpiciclib 150 mg orally once daily for 3 weeks, followed by 1 week off in each 4-week cycle.

Endocrine therapy including but not limited to fulvestran, tanastrozole, letrozole or exemestane In regular doses

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
6-month-OS rate
Délai: From the start of treatment to 6 month
6-month-Overall Survival rate. Overall Survival , defined as the time from the start of treatment to the date of death, regardless of the cause of death.
From the start of treatment to 6 month

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Overall Survival (OS)
Délai: From the start of treatment to 36 month

Overall Survival , defined as the time from the start of treatment to the date of death, regardless of the cause of death.

The OS will be estimated using Kaplan-Meier method. A Kaplan-Meier curve, median OS, hazard ratio with appropriate confidence intervals will be reported.

From the start of treatment to 36 month
1-year-OS rate
Délai: From the start of treatment to 12 month
1-year-Overall Survival rate. Overall Survival , defined as the time from the start of treatment to the date of death, regardless of the cause of death.
From the start of treatment to 12 month
Progression-Free Survival (PFS)
Délai: From the start of treatment to 36 month

Progression-Free Survival is defined as the time from randomization to first documented disease progression (PD) using Response Evaluation Criteria in Solid Tumors 1.1 (RECIST 1.1) or death from any cause, whichever occurred first.

The PFS will be will be estimated using Kaplan-Meier method. A Kaplan-Meier curve, median PFS, hazard ratio with appropriate confidence intervals will be reported.

From the start of treatment to 36 month
Time to treatment failure (TTF)
Délai: From the start of treatment to 36 month

TTF is defined as date of treatment start until permanent treatment discontinuation due to progressive disease or unacceptable toxicity.

The TTF will be estimated using Kaplan-Meier method. A Kaplan-Meier curve, median TTF, hazard ratio with appropriate confidence intervals will be reported.

From the start of treatment to 36 month
Objective Overall Response Rate (ORR)
Délai: From the start of treatment to 36 month

ORR is defined as percentage of participants with best (confirmed) overall response (BOR) of either CR or PR. ORR was assessed by the investigator according to RECIST version 1.1 and is based on BOR, which is defined as best response recorded from start of study treatment until disease progression/recurrence or death.

The ORR will be reported by percentage with each arms and appropriate confidence intervals.

From the start of treatment to 36 month
Clinical Benefit Response (CBR)
Délai: From the start of treatment to 36 month

CBR is percentage of participants with best (confirmed) PR or CR or SD for at least 6 months. PR or CR or SD is according to RECIST version 1.1.

The CBR will be reported by percentage with each arms and appropriate confidence intervals.

From the start of treatment to 36 month
Duration of Response (DoR)
Délai: From the start of treatment to 36 month

DoR is defined as date of initial confirmed PR/CR until date of progressive disease or death from any cause. PR or CR or SD is according to RECIST version 1.1.

The DoR will be estimated using Kaplan-Meier method. Kaplan-Meier curves, median DoR, hazard ratio with appropriate confidence intervals will be reported.

From the start of treatment to 36 month
Time to response(TTR)
Délai: From the start of treatment to 36 month

TTR, defined as the time from the date of randomization to the date of first CR or PR. CR or PR is according to RECIST version 1.1.

The TTR will be estimated using Kaplan-Meier method. A Kaplan-Meier curve, median TTR, hazard ratio with appropriate confidence intervals will be reported.

From the start of treatment to 36 month
Adverse events (AEs)
Délai: From the start of treatment to 36 month

AEs were graded according to the National Cancer Institute's Common Toxicity Criteria for Adverse Events (CTCAE) version 5.0.

The type, grade and frequency of AEs will be reported.

From the start of treatment to 36 month

Collaborateurs et enquêteurs

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

Les enquêteurs

  • Chercheur principal: Fei Ma, Cancer Institute and Hospital, Chinese Academy of Medical Sciences

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 (Anticipé)

1 juin 2022

Achèvement primaire (Anticipé)

1 décembre 2025

Achèvement de l'étude (Anticipé)

1 décembre 2027

Dates d'inscription aux études

Première soumission

19 juin 2022

Première soumission répondant aux critères de contrôle qualité

19 juin 2022

Première publication (Réel)

24 juin 2022

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

24 juin 2022

Dernière mise à jour soumise répondant aux critères de contrôle qualité

19 juin 2022

Dernière vérification

1 avril 2022

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • MA-BC-II-033

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

Non

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

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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