Skip to content

Liquid Biopsies and Imaging in Breast Cancer

Liquid Biopsies and Imaging in Breast Cancer

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04223492
Acronym
LIMA
Enrollment
61
Registered
2020-01-10
Start date
2019-01-02
Completion date
2022-05-16
Last updated
2023-12-28

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

Conditions

Breast Cancer

Keywords

Breast Cancer, Neoadjuvant, Response Prediction, Liquid Biopsies, Magnetic resonance imaging, Circulating Tumor DNA

Brief summary

The aim of the study is to show proof of concept for combining multi-parametric MRI with liquid biopsies in addition to conventional clinical and pathologic information, to accurately predict response to neoadjuvant treatment for patients with primary breast cancer.

Detailed description

The response to neoadjuvant chemotherapy (NAC) in early stage breast cancer has important prognostic implications. Early, dynamic prediction of response allows for adaption of the treatment plan before completion, or even before the start of treatment. This strategy can help prevent overtreatment and related toxicity and correct for undertreatment with an ineffective regimen. The hypothesis of this study is that accurate dynamic response prediction may be reached by combining multi-parametric MRI with liquid biopsies prior to, during and after NAC, in addition to conventional clinical and pathological information. Magnetic resonance imaging (MRI) is non-invasive and is typically used for response evaluation in current clinical practice. It shows the size and perfusion of the tumor as they change during treatment. However, tumor size on MRI has limited predictive value for response to therapy. Multi-parametric MRI uses different imaging protocols in one session to measure more functional items than perfusion alone, addressing different aspects of tumor biology, and possibly improving predictive value. With this improvement, imaging still only visualizes macroscopic disease. Therefore, in the LIMA study, MRI will be combined with liquid biopsies containing circulating tumor cells (CTCs) and circulating tumor DNA (ctDNA), which have both shown prognostic and predictive values in early stage breast cancer. Since the ctDNA may originate from cells in every part of the tumor, it may capture tumor heterogeneity. Liquid biopsies are minimally invasive and provide insight into microscopic tumor load and the tumor's genetic picture. The aim of the study is to show proof of concept for combining multi-parametric MRI with liquid biopsies in addition to conventional clinical and pathologic information, to accurately predict response to neoadjuvant treatment for patients with primary breast cancer. The LIMA is a multicenter prospective observational cohort study. Multi-parametric MRI will we performed prior to NAC, halfway and after completion of NAC. Liquid biopsies will be obtained before start of treatment, every 2 weeks during treatment and after completion of NAC. 100 patients will be enrolled in different hospitals. Funding from the European Union Horizon 2020 research and innovation program under grant agreement no. 755333 (LIMA)

Interventions

DIAGNOSTIC_TESTLiquid biopsy

A blood sample containing circulating tumor DNA and circulating tumor cells.

DIAGNOSTIC_TESTMulti-parametric MRI

Multi-parametric MRI combines different imaging protocols in one session to measure more functional items than perfusion alone, addressing different aspects of tumor biology.

Sponsors

Horizon 2020 - European Commission
CollaboratorOTHER
Philips Electronics Nederland BV
CollaboratorINDUSTRY
Agena Bioscience GmbH
CollaboratorUNKNOWN
DiaDx
CollaboratorUNKNOWN
Stilla Technologies
CollaboratorUNKNOWN
ANGLE Europe Limited
CollaboratorUNKNOWN
ALS Automated Lab Solutions GmbH
CollaboratorUNKNOWN
Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
Philips GmbH Innovate Technologies
CollaboratorUNKNOWN
Institut du Cancer de Montpellier - Val d'Aurelle
CollaboratorOTHER
UMC Utrecht
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* Histologically proven invasive breast carcinoma * Planned for neoadjuvant chemotherapy (and in case of a Her2-positive tumor: addition of trastuzumab and/or pertuzumab)

Exclusion criteria

* Luminal A breast cancer (defined as: ER-positive and HER2-negative by immunohistochemistry and Bloom and Richardson grade 1 or 2) * Inflammatory breast cancer * Distant metastases on PET/CT * Other active malignant disease in the past 5 years (excluded squamous cell or basal cell carcinoma of the skin) * Pregnant or lactating women * Contra-indications for MRI according to standard hospital guidelines * Contra-indications for gadolinium-based contrast-agent, including known prior allergic reaction to any contrast-agent, and renal failure, defined by GFR \< 30 mL/min/1.73m2

Design outcomes

Primary

MeasureTime frameDescription
Residual Cancer Burden index in surgical resection specimenAfter neoadjuvant treatment and surgery (approx. 6 months from diagnosis)The following parameters are required from pathologic examination in order to calculate Residual Cancer Burden (RCB) after neoadjuvant treatment: Primary tumor bed area, overall cancer cellularity (as percentage of area), percentage of cancer that is in situ disease, number of positive lymph nodes and diameter of largest metastasis. These parameters are filled in in the calculator that is available online to calculate the Residual Cancer Burden index: http://www3.mdanderson.org/app/medcalc/index.cfm?pagename=jsconvert3

Secondary

MeasureTime frameDescription
Radiological lesion volume on DCE MRI after NACAfter neoadjuvant treatment (approx. 6 months from diagnosis)Measured in three dimensions as described in ACR BI-RADS Atlas® 5th Edition
pathological complete response, defined as ypT0/ypN0After neoadjuvant treatment and surgery (approx. 6 months from diagnosis)Pathological complete response, defined as ypT0/ypN0

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026