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A Study to Describe the Real-world Treatment Patterns and Associated Outcomes in Patients of China With HER2-positive Unresectable or Metastatic Breast Cancer

A Multicenter, Non-interventional Retrospective Study to Describe the Real-world Treatment Patterns and Associated Outcomes in Patients of China With HER2-positive Unresectable or Metastatic Breast Cancer

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05769751
Enrollment
865
Registered
2023-03-15
Start date
2023-03-15
Completion date
2023-07-25
Last updated
2023-08-16

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

Conditions

HER2-positive Breast Cancer

Keywords

HER2-positive Breast Cancer, Real-world study, Treatment patterns

Brief summary

This is a multicenter, non-interventional, retrospective, real-world study that enrolled patients diagnosed with HER2-positive unresectable or metastatic breast cancer. This study will be conducted to understand the treatment pattern and sequencing of therapies, survival outcomes, and associated burden of toxicities with line of treatment in the real world.

Detailed description

The treatment landscape has changed dramatically with the lack of real-world evidence for usage and the efficacy of newly approved drugs in China. This multicenter, retrospective, non-interventional study will include patients newly diagnosed with HER2-positive unresectable or metastatic breast cancer, or first recurrent from early breast cancer. The primary objective of this real-world study is to describe the treatment patterns of HER2-positive unresectable or metastatic breast cancer in China. Secondary objectives will include describing the demographic and clinicopathological characteristics of patients, efficacy of different treatment regimens, treatment options and efficacy of brain metastases, and safety and tolerability of different treatment regimens in patients with HER2-positive unresectable or metastatic breast cancer.

Interventions

OTHERElectronic medical record and hospital information system or other available resources

This is a non-interventional study. No study medication will be provided to the participants.

Sponsors

Daiichi Sankyo
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male or female patients ≥ 18 years of age at the time of diagnosis of unresectable or metastatic breast cancer * Participants with first diagnosis of unresectable or metastatic breast cancer, or first recurrence of HER2-positive breast cancer since January 1, 2020. Participants were eligible if they were HER2-positive in the early operable stage and HER2-negative in the advanced stage. HER2 positive was defined with the reference to the Chinese guidelines for HER2 positive breast cancer at the time of testing * Participants have received at least one systemic therapy for advanced breast cancer

Exclusion criteria

* Participants with concomitant cancer at the time of diagnosis of HER2-positive unresectable or metastatic breast cancer, except for the non-metastatic non-melanoma skin cancers, or in situ or benign neoplasms; a cancer is considered concomitant if it occurs within 5 years of HER2-positive breast cancer diagnosis. * Participants who are/were currently/previously enrolled in a clinical trial and have not been unblinded during the data collection interval of the study * Participants with critical missing data from their medical records or other patients deemed by the investigator to be ineligible for inclusion

Design outcomes

Primary

MeasureTime frame
Percentage of Participants Receiving Each Regimen in Each Treatment LineAssessed over a 2 year, 8 month time period
Treatment Sequence Since the Time of Diagnosis of HER2-positive Unresectable or Metastatic Breast CancerAssessed over a 2 year, 8 month time period
Percentage of Participants Receiving Endocrine Therapy if Breast Cancer is Hormone Receptor PositiveAssessed over a 2 year, 8 month time period
Percentage of Participants Receiving Local and Regional Treatment for Metastasis (Radiotherapy and/or Surgery) and Osteoprotective TherapyAssessed over a 2 year, 8 month time period

Secondary

MeasureTime frameDescription
Real-world Objective Response Rate (rwORR) in Participants With HER2-positive Unresectable or Metastatic Breast CancerAssessed over a 2 year, 8 month time periodReal-world objective response rate is defined as the percentage of participants who have a partial response or complete response to treatment within a certain period of time.
Real-world Disease Control Rate (rwDCR) in Participants With HER2-positive Unresectable or Metastatic Breast CancerAssessed over a 2 year, 8 month time periodReal-world disease control rate is defined as the percentage of participants with advanced or metastatic cancer who have achieved complete response, partial response, and stable disease.
Real-world Duration of Response (rwDoR) in Participants With HER2-positive Unresectable or Metastatic Breast CancerAssessed over a 2 year, 8 month time periodReal-world duration of response is defined as the time from randomization to disease progression or death in participants who achieve complete or partial response.
Percentage of Participants With Brain Metastases Per Line of Treatment in Participants With HER2-positive Unresectable or Metastatic Breast CancerAssessed over a 2 year, 8 month time period
Percentage of Participants With HER2-positive Unresectable or Metastatic Breast Cancer, Based on Clinical Characteristics of Brain LesionsAssessed over a 2 year, 8 month time period
Percentage of Participants With HER2-positive Unresectable or Metastatic Breast Cancer, Based on Demographic and Clinicopathological CharacteristicsAssessed over a 2 year, 8 month time period
Treatment Pattern After Diagnosis of Brain Metastases in Participants With HER2-positive Unresectable or Metastatic Breast CancerAssessed over a 2 year, 8 month time period
Real-world Progression-free Survival (rwPFS) After Diagnosis of Brain Metastases in Participants With HER2-positive Unresectable or Metastatic Breast CancerAssessed over a 2 year, 8 month time periodReal-world progression-free survival (rwPFS) is defined as the time from initiation of treatment to disease progression or death due to any cause.
Time to Next Treatment (TTNT) After Diagnosis of Brain Metastases in Participants With HER2-positive Unresectable or Metastatic Breast CancerAssessed over a 2 year, 8 month time periodTime to next treatment is defined as the time from initiation of a systemic therapy to the date of initiation of the first subsequent systemic therapy regimen or death.
Percentage of Participants With Adverse Events (AE) Leading to Treatment Discontinuation or Dose ModificationAssessed over a 2 year, 8 month time period
Percentage of Participants Receiving Radiotherapy or Surgery in Participants With HER2-positive Unresectable or Metastatic Breast CancerAssessed over a 2 year, 8 month time period
Real-world Progression-free Survival (rwPFS) in Participants With HER2-positive Unresectable or Metastatic Breast CancerAssessed over a 2 year, 8 month time periodReal-world progression-free survival (rwPFS) is defined as the time from initiation of treatment to disease progression or death due to any cause.
Time to Next Treatment (TTNT) in Participants With HER2-positive Unresectable or Metastatic Breast CancerAssessed over a 2 year, 8 month time periodTime to next treatment is defined as the time from initiation of a systemic therapy to the date of initiation of the first subsequent systemic therapy regimen or death.
Duration of Treatment (DoT) in Participants With HER2-positive Unresectable or Metastatic Breast CancerAssessed over a 2 year, 8 month time periodDuration of treatment is defined as the length of time a patient is treated.

Countries

China

Outcome results

None listed

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