Novartis Investigative SIte
Bingjie, Beijing Municipality, 100021, China
Location status: Recruiting
NCT Number: NCT07476170
This study aims to fill the current gap in data regarding HR+/HER2- ABC 1L treatment patterns and outcomes in the real-world setting in China, especially in the context of the widespread application of CDK4/6is and the lack of sufficient evidence for ribociclib as a most recently marketed drug in the real-world setting.
Interested in participating?
Request Info18 year–99 year
All sexes
Observational
Bingjie, Beijing Municipality, 100021, China
Location status: Recruiting
This study is a longitudinal, non-interventional, retrospective, and observational study based on secondary real-world data in the National Anti-Tumor Drug Surveillance System (NATDSS) database. The study will not involve any active intervention, randomization, or control group.
All analyses will be conducted using Electronic Health Record (EHR) routinely collected in clinical practice and additional secondary data sources
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
HR+ is defined as ER+ or PR+, and HER2+ is defined as immunohistochemistry 3+, or 2+ with positive in situ hybridization (amplification). Advanced or metastatic breast cancer is defined as having a documented inoperable clinical or pathological stage IIIB, IIIC, or IV, or the records indicating distant metastasis.
Exclusion criteria
(1) Patients with any other concomitant invasive malignancies Defined as patients meeting any of the following conditions based on their diagnosis records in the cancer registry/medical database used for the study: 1. Within 5 years before the diagnosis of HR+/HER2- ABC, there is a diagnosis record of invasive malignancy other than breast cancer in the database (based on the International Classification of Diseases [ICD] diagnosis code or cancer registry code), and the diagnosis is not carcinoma in situ or benign/borderline tumor; 2. On the day of, or within 3 months after, the diagnosis of HR+/HER2- ABC, there is a new diagnosis record of invasive malignancy at another site (also based on the ICD diagnosis code or cancer registry code) indicating a concomitant active malignancy.
Time frame: Up to 39 months
Proportion of patients receiving each first line treatment category and specific regimen
Time frame: Up to 39 months
Proportion of patients who discontinue or switch first line treatment
Time frame: Up to 39 months
Time to treatment initiation (TTI), time to discontinuation (TTD), and time to next-line therapy (TTNT)
Time frame: Up to 39 months
Proportion of patients treated with a CDK4 6 inhibitor, stratified by initial dose level
Time frame: Up to 39 months
Proportion of patients treated with CDK4/6 inhibitor who experience any dose modification (including dose reduction and interruption)
Time frame: Up to 39 months
Time from initiation of CDK4/6 inhibitor therapy to the first dose modification, including dose reduction or interruption
Time frame: Up to 39 months
rwPFS is defined as the duration from the initiation date of 1L treatment to documented disease progression or death from any cause. If a patient has not experienced disease progression or death, the last confirmed survival time will be used as the censoring time to calculate the rwPFS censoring duration
Time frame: Up to 39 months
rwPFS of HR+/HER2- ABC patients adhering or not adhering to the highest level of first-line treatment recommendation in the guidelines in the real-world setting based on the NATDSS database
Time frame: Up to 39 months
rwPFS of HR+/HER2- ABC patients receiving ribociclib-based 1L treatment regimens in the real-world setting based on the NATDSS database
Time frame: Up to 39 months
AESIs under different treatment patterns, including:
Time frame: Baseline
Contact information is provided by the study sponsor or research team.
Novartis Pharmaceuticals
Industry
Real-World Treatment Pattern and Clinical Outcome With Influential Factors of HR+/HER2-aBC 1L Patients in China: A Retrospective Analysis Based on a Database
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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