Mechanisms of Response and Resistance to Innovative Treatments in Patients With Locally Advanced or Metastatic Breast Cancer (PANDORA)

Hellenic Cooperative Oncology Group

Status: Enrolling

Conditions: Metastatic Breast Cancer

Study type: Observational

Funder types: Other

Identifiers

NCT07066917

HE_11PDR/24

Details and patient eligibility

About

Ample evidence has highlighted the significant clinical benefit of novel therapies for many patients with advanced breast cancer (aBC). The use of CDK inhibitors, antibody-drug conjugates (ADCs), immune checkpoint inhibitors (ICIs), and PARP inhibitors as first-line or subsequent treatments has improved progression-free survival (PFS) rates compared to conventional therapies. In selected cases, these treatments have also increased overall survival (OS), reshaping the therapeutic landscape for advanced breast cancer.

However, several key questions remain unanswered. For example, what should be the first-line treatment when multiple effective options are available? Determining the optimal sequence of drugs in successive lines of therapy is another major challenge. Furthermore, the development of resistance to treatment and the occurrence of severe adverse events that may lead to early discontinuation or fatal outcomes are pressing concerns.

That said, identifying robust predictive biomarkers of response or resistance is crucial for ensuring that patients receive the most effective treatment while avoiding unnecessary exposure to therapies that could cause harm without benefit. Additionally, when multiple effective options exist, selecting the optimal treatment algorithm for each patient based on clinical, pathological, and molecular biomarkers is essential.

We herein, aim at employing high throughput methodologies, such as Whole Exome Sequencing, circulating tumour DNA (ctDNA) analysis, digital pathology and radiomics analyses, as well as real-world data obtained both from patients records for the training of a ML-based algorithm that can predict response or resistance to a specific treatment, based on the genetic make-up of the patient and the molecular profile of the tumour.

Enrollment: 150 estimated patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Eligible patients will be 18 years of age and older
• Histologically confirmed, advanced breast cancer.
• Diagnosis of i) hormone receptor positive and/or ii) HER2-positive or -low or iii) triple negative breast cancer (TNBC).
• Patients will be included in the analysis after receiving at least one treatment cycle.

Exclusion criteria

• Diagnosis of early breast cancer at time of enrollment
• Unwillingness to provide informed consent
• Unwillingness to provide biological specimen
• Lack of comprehensive clinical data

Trial design

150 participants in 3 patient groups

ADCs

Description:

Patients receiving treatment with an Antibody-Drug conjugate (e.g Trastuzumab-Deruxtecan, Sacituzumab-Govitecan)

ICIs

Description:

Patients receiving treatment with an immune checkpoint inhibitor (ICI) (e.g pembrolizumab)

PARPi

Description:

Patients receiving treatment with a PARP inhibitor (e.g Olaparib)