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A Real-world Study of Effectiveness and Safety in HR+/HER2- Breast Cancer Patients Treated With Ribociclib or Alpelisib

Real-world Effectiveness and Safety in HR+/HER2- Advanced or Metastatic BC Patients Treated With Ribociclib or Alpelisib: A European Non-interventional Retrospective Study (REASSURE)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06705504
Enrollment
435
Registered
2024-11-26
Start date
2021-06-11
Completion date
2023-11-30
Last updated
2024-11-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hormone Receptor Positive HER-2 Negative Breast Cancer

Brief summary

This study was a multinational and multicenter cohort study of patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced or metastatic breast cancer (aBC/mBC) treated with ribociclib or alpelisib between the period of 01 January 2018 and 30 September 2021. Patients who were receiving active treatment for malignancies other than BC or participating in a clinical trial were excluded. This study was conducted retrospectively with secondary use of data.

Interventions

None listed

Sponsors

Novartis
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Confirmed diagnosis of locally advanced/metastatic not amenable to surgery HR+/HER2- BC (progressed following prior therapy or de novo) for whom the treating physician took the decision to initiate treatment with ribociclib or alpelisib. * Patients with at least one prescription for ribociclib or alpelisib during the index period (01 January 2018 to 30 September 2021).

Exclusion criteria

* Patients who were participating in any interventional clinical trial that included investigational or marketed products at the time of index (ribociclib, alpelisib, and other); patients who were participating in other investigator-initiated research or non-interventional study (NIS) could be included as long as their standard of care was not altered by the study. * Patients on active treatment for malignancies other than HR+/HER2- aBC/mBC at the time of index. * IPO-Porto cohort only: * Patients who had participated or were participating in any interventional clinical trial that included investigational or marketed products at the time of index (ribociclib, alpelisib, and others). * Patients who underwent part of the treatment for locally advanced/metastatic not amenable to surgery HR+/HER2- BC outside the center.

Design outcomes

Primary

MeasureTime frameDescription
Real-world Progression-free Survival (rwPFS)Up to 51 monthsrwPFS was defined as the time from the index date to the date of the first documented progression or death due to any cause. If a patient did not have an event, rwPFS was censored at the date of the last adequate tumor assessment. The index date was defined as the date of the first treatment with ribociclib or alpelisib.

Secondary

MeasureTime frameDescription
Number of Patients by Age GroupBaselineAge groups: * Younger than 65 years * 65 years or older
GenderBaseline
Number of Patients Categorized by Year of Index DateBaselineThe index date was defined as the date of the first treatment with ribociclib or alpelisib.
Number of Patients With a History of Breast CancerBaseline
Number of Patients by ComorbidityBaselineComorbidities included: * Diabetes mellitus * Cardiovascular disease * Cerebrovascular disease * Chronic obstructive pulmonary disease (COPD) * Dementia * Depression * Heart Failure * Hypertension * Hypothyroidism * Ischemic heart disease * Liver disease * Myocardial infarction * Osteoporosis * Peripheral vascular disease * Renal Disease * Rheumatological disease * Ulcer disease * Other
Body Mass Index (BMI)Baseline
Number of Patients per BMI CategoryBaselineBMI Categories: * Underweight: below 18.5 kilograms per meter squared (kg/m\^2) * Healthy/normal weight: 18.5 to 24.9 kg/m\^2 * Pre-obesity: 25 to 29.9 kg/m\^2 * Obesity: 30 kg/m\^2 and higher
Number of Patients by Menopausal StatusBaselineMenopausal status: * Pre- or peri-menopausal * Post-menopausal
Number of patients per Charlson Comorbidity Index (CCI) Score CategoryBaselineCCI predicts the ten-year mortality for a patient who may have a range of comorbid conditions. Comorbidity was assessed using the CCI, categorized as low (0-1) and high (≥2).
Number of Patients Categorized by Duration of Disease RecurrenceBaselineDisease recurrence categories: * 12 months or less * More than 12 months
Number of Patients by Smoking StatusBaselineSmoking status: * Current smoker * Former smoker * Never smoked
Number of Patients Categorized by Primary Tumor TypeBaselineTumor types: * Invasive ductal * Lobular carcinoma * Other
Number of Patients Categorized by Disease SiteBaselineDisease site categories: * Non-visceral * Visceral * Multiple
Number of Patients With Primary Metastatic DiseaseBaseline
Number of Patients Categorized by Number of Metastatic SitesBaselineCategories for number of metastatic sites: 0, 1, 2, 3, 4 or more.
AgeBaseline
Number of Patients Categorized by Time From Diagnosis to MetastasisBaselineCategories: * 24 months or less * More than 24 months * Metastatic BC at diagnosis
Number of Patients With Asymptomatic DiseaseBaseline
Number of Patients Categorized by Tumor GradeBaselineTumor Grades: * Grade 1 * Grade 2 * Grade 3
Number of Patients Categorized by Stage of CancerBaselineCancer Stages: I, IIA, IIB, IIIA, IIIB, IIIC, and IV.
Number of Patients by Eastern Cooperative Oncology Group (ECOG) Performance ScoreBaselineECOG performance score describes a patient's level of functioning in terms of their ability to care for themself, daily activity, and physical ability (walking, working, etc.). Scores ranged from a lower value of 0 (fully active, able to carry out all pre-disease performance without restriction) up to 4 (completely disabled; cannot carry out any selfcare; totally confined to bed or chair).
Number of Patients Categorized by Previous Types of TreatmentBaselineTreatment categories: * Chemotherapy * Surgery * Radiotherapy * Adjuvant endocrine therapy * Everolimus treatment
Number of Patients Categorized by the Number of Prior Lines of Endocrine Therapy (ET)BaselineCategories for number of lines of ET: 0, 1, 2, and 3 or more.
Number of Patients Resistant to ETBaseline
Number of Patients Sensitive to Hormonal TherapyBaseline
Number of Patients Categorized by Line of Cyclin-dependent Kinase 4/6 Inhibitor (CDK4/6i) Treatment ReceivedBaselineCDK4/6i lines of treatment: * Adjuvant * 1st metastatic line * 2nd metastatic line * 3rd metastatic line or later
Number of Patients Categorized by the Number of Previous Lines of TreatmentBaselineCategories for number of lines of treatment: 0, 1, 2, and 3 or more.
Baseline Neutrophil-to-lymphocyte Ratio (NLr)Baseline
Baseline Platelet-to-lymphocyte Ratio (PLr)Baseline
Baseline Lymphocytes-to-monocytes Ratio (LMr)Baseline
Number of Patients Categorized by Type of MetastasesBaselineMetastases: * Local/breast metastases * Bone metastases * Lung metastases * Liver metastases * Central nervous system metastases * Lymph node metastases * Other metastases

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026