Skip to main content
OpenTrials
Recruiting

NCT Number: NCT07476170

Real-World Treatment Pattern and Clinical Outcome With Influential Factors of HR+/HER2-aBC 1L Patients in China

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Novartis Investigative SIte

Bingjie, Beijing Municipality, 100021, China

Location status: Recruiting

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed with HR+/HER2- ABC:

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.

  • Initiation of 1L anti-cancer treatment between Jan. 1, 2024 and Jan. 1, 2027; Defined as having records of systemic anti-cancer treatment in disease course records or order records within 90 days after the initial diagnosis of ABC, and receiving the first dose between Jan. 1, 2024 and Jan. 1, 2027, as recorded in the NATDSS database.
  • Aged 18 years or older at the time of receiving the 1L treatment; Definition: The initiation date (index date) of 1L treatment is defined as the initiation date of systemic anti-cancer treatment for HR+/HER2- ABC first recorded in the database. Age will be preferentially calculated based on the date of birth (or year of birth) and the initiation date of 1L treatment in the database. If the birth information is not included in the database but shown in an "Age" field in the medical visit/hospitalization record associated with 1L treatment, this age field will be used as the basis for age.
  • At least 3 months of follow-up records after the initiation of 1L treatment. Defined as having at least one outpatient or inpatient medical visit record in the NATDSS at least 3 months after the index date.

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.

Treatment and study plan

Primary outcomes

  1. Distribution of first-line treatment regimens

    Time frame: Up to 39 months

    Proportion of patients receiving each first line treatment category and specific regimen

  2. Proportion of patients with treatment changes

    Time frame: Up to 39 months

    Proportion of patients who discontinue or switch first line treatment

  3. Time to treatment initiation, time to discontinuation, and time to next line therapy

    Time frame: Up to 39 months

    Time to treatment initiation (TTI), time to discontinuation (TTD), and time to next-line therapy (TTNT)

  4. Proportion of patients by initial CDK4 6 inhibitor dose

    Time frame: Up to 39 months

    Proportion of patients treated with a CDK4 6 inhibitor, stratified by initial dose level

  5. Proportion of patients with dose modifications of CDK4/6 inhibitor therapy

    Time frame: Up to 39 months

    Proportion of patients treated with CDK4/6 inhibitor who experience any dose modification (including dose reduction and interruption)

  6. Time to first dose modification of CDK4/6 inhibitor therapy

    Time frame: Up to 39 months

    Time from initiation of CDK4/6 inhibitor therapy to the first dose modification, including dose reduction or interruption

Secondary outcomes

  1. rwPFS of 1L treatment patterns

    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

  2. rwPFS of HR+/HER2- ABC patients

    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

  3. rwPFS of HR+/HER2- ABC patients receiving ribociclib-based 1L treatment regimens

    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

  4. Number of subjects with AESIs

    Time frame: Up to 39 months

    AESIs under different treatment patterns, including:

    • Hematology: neutropenia, leukopenia, anemia, and thrombocytopenia;
    • Gastrointestinal tract: diarrhea, nausea, vomiting, stomatitis/mucositis;
    • QTc prolongation;
    • Hepatotoxicity: alanine transaminase (ALT)/aspartate transaminase (AST) increased, and total bilirubin increased.
  5. Baseline demographics

    Time frame: Baseline

Study contacts

Contact information is provided by the study sponsor or research team.

Novartis Pharmaceuticals

CONTACT

[email protected]

+41613241111

Novartis Pharmaceuticals

CONTACT

Sponsors and collaborators

Lead sponsor

Novartis Pharmaceuticals

Industry

Registry information

Official study title

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

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Mar 17, 2026
Registry last updated
Apr 2, 2026

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.

Published trials that share one or more normalized conditions with this study.