Real-World Study of Post-Resistance Treatment Strategies in Advanced Breast Cancer Following CDK4/6i, PIK3CA Inhibitors, or T-DXd
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Metastatic Breast Cancer, Drug Resistance, Hormone Receptor-Positive Breast Cancer, HER2-positive Breast Cancer. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
A Real-World Observational Study on Post-Resistance Treatment Outcomes in Advanced Breast Cancer Patients After CDK4/6 Inhibitors, PIK3CA Inhibitors, or Trastuzumab Deruxtecan Therapy
Overview
This is a real-world observational study aiming to evaluate the effectiveness of post-progression treatment strategies in patients with advanced breast cancer who have developed resistance to prior targeted therapies, including CDK4/6 inhibitors, PIK3CA inhibitors, trastuzumab deruxtecan (T-DXd), or other targeted agents commonly used in clinical practice. As resistance to these therapies becomes increasingly common, optimal sequencing strategies for subsequent treatment remain unclear. This study will collect clinical information on post-resistance systemic treatments and their outcomes, including progression-free survival, overall survival, and response rate. Baseline patient and tumor characteristics will also be collected to explore potential prognostic and predictive factors and to develop outcome prediction models that may help guide future clinical decision-making. This is a non-interventional study based on retrospective and prospective data from routine medical care. The results are expected to provide real-world evidence to inform personalized treatment strategies for patients with advanced breast cancer following resistance to targeted therapies.
Detailed description
Breast cancer is a heterogeneous disease, and advances in targeted therapies have significantly improved clinical outcomes, especially in hormone receptor-positive (HR+), HER2-positive, and selected triple-negative breast cancer (TNBC) subtypes. However, disease progression following treatment with targeted agents such as CDK4/6 inhibitors, PIK3CA inhibitors, and antibody-drug conjugates like trastuzumab deruxtecan (T-DXd) remains a major clinical challenge. With a growing number of post-resistance treatment options available, real-world data are urgently needed to inform evidence-based sequencing strategies in routine clinical practice.
This real-world observational study aims to investigate the treatment patterns and clinical outcomes of patients with advanced or metastatic breast cancer who experience disease progression after receiving CDK4/6 inhibitors, PIK3CA inhibitors, T-DXd, or other relevant targeted agents. The study will focus on characterizing the effectiveness of subsequent treatment regimens, including chemotherapy, endocrine therapy, additional targeted therapies, or their combinations.
In addition to evaluating clinical outcomes such as progression-free survival (PFS), overall survival (OS), objective response rate (ORR), and duration of response (DoR), the study will collect detailed baseline patient characteristics, tumor biological features, and prior treatment histories. These data will be used to identify potential prognostic and predictive factors and to develop outcome prediction models that may support personalized treatment planning in the post-resistance setting.
Patients will be identified based on medical record review, with retrospective and/or prospective data collection depending on institutional capabilities. Treatment decisions are made at the discretion of the treating physicians as part of standard clinical care. The study does not involve any experimental intervention, and no additional diagnostic or therapeutic procedures will be imposed on participants.
The ultimate goal of this study is to generate clinically relevant, real-world evidence to guide optimal treatment sequencing after resistance to targeted therapy in advanced breast cancer, and to support future clinical research and decision-making frameworks.
Primary outcome measures
- Progression-Free Survival (PFS) [Time frame: From the start of post-resistance systemic treatment until documented disease progression or death, up to 36 months.]
Secondary outcome measures (4)
- Overall Response Rate (ORR) [Time frame: From start of post-resistance systemic treatment to best documented response, assessed up to 24 months.]
- Disease Control Rate (DCR) [Time frame: From treatment initiation to disease progression or last follow-up, assessed up to 24 months.]
- Overall Survival (OS) [Time frame: From start of post-progression treatment to death or last follow-up, up to 48 months.]
- Treatment-Related Adverse Events [Time frame: From the start of post-resistance treatment until 30 days after treatment discontinuation, assessed up to 24 months.]
Eligibility criteria
Inclusion criteria
- Adults (≥18 years old) with histologically or cytologically confirmed advanced or metastatic breast cancer
- Received prior treatment with at least one of the following: CDK4/6 inhibitors, PIK3CA inhibitors, trastuzumab deruxtecan (T-DXd), or other targeted therapies
- Documented disease progression following prior targeted therapy
- Initiated a subsequent line of systemic therapy (chemotherapy, endocrine therapy, targeted therapy, or combination) after resistance
- Available clinical data including baseline characteristics and treatment details
- At least one follow-up evaluation after initiation of post-resistance therapy
Exclusion criteria
- Incomplete medical records or missing key clinical follow-up data
- Concurrent diagnosis of other active malignancies (except non-melanoma skin cancer or in situ cervical cancer)
- Known central nervous system disease requiring immediate local treatment (unless clinically stable)
- Poor general condition with an Eastern Cooperative Oncology Group (ECOG) performance status ≥2
- Life expectancy estimated to be less than 6 months based on clinical judgment
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
China · 1 center
- Hunan Cancer Hospital — Changsha
Identifiers
NCT: NCT07073755 · HNCA-PoReBC