Integration of personalised ultrasensitive <scp>ctDNA</scp> monitoring of patients with metastatic breast cancer to reduce imaging requirements

Circulating tumour DNA (ctDNA) is an emerging biomarker for monitoring cancers. The personalised disease monitoring in metastatic breast cancer (PDM-MBC) study is an ongoing study instigated to evaluate ctDNA as a biomarker to individualise imaging requirements in patients with MBC. Patients receiving first-line endocrine therapy (aromatase inhibitor + cyclin-dependent kinase 4/6 inhibitor) had plasma samples collected pre-treatment, weeks 2 and 4, and concurrently with imaging until progressive disease (PD). Here, we apply an experimental analytical workflow for ultrasensitive ctDNA analysis, utilising personalised ctDNA panels designed from mutations identified in tumour tissue, and present results for 24 patients. Twenty patients (83%) had detectable ctDNA pre-treatment. The median progression-free survival was 25.6 months, and 13 patients experienced PD, with rising ctDNA detected at or prior to PD in 12 patients (92%). If imaging had been omitted until the detection of rising ctDNA for at least one mutation, 68% (n = 71) of the scans performed amongst ctDNA-positive patients would have been avoided. Our results demonstrate that integration of personalised ctDNA monitoring of patients with MBC has potential to substantially reduce the imaging needs in patients showing ctDNA response to treatment.

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Publication Details

Journal
International Journal of Cancer
Published
2024-12-18
DOI
https://doi.org/10.1002/ijc.35292
Citations
2
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
0.57

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article

Integration of personalised ultrasensitive ctDNA monitoring of patients with metastatic breast cancer to reduce imaging requirements

Maria Ekholm, Ellinor Elinder, Karolina Larsson, Anders Ståhlberg et al.
2 citations
International Journal of Cancer
Cancer Genomics and Diagnostics
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article

Integration of personalised ultrasensitive ctDNA monitoring of patients with metastatic breast cancer to reduce imaging requirements

Maria Ekholm, Ellinor Elinder, Karolina Larsson, Anders Ståhlberg, Sacha J. Howell, Anne Kavanagh, Monika Umińska, Anikó Kovács, Pia Mouhanna, Barbro Linderholm, Tobias Österlund, Daniel Andersson, Olle Eriksson, Ahmed Albu‐Kareem
article en
2 citations

Abstract

Circulating tumour DNA (ctDNA) is an emerging biomarker for monitoring cancers. The personalised disease monitoring in metastatic breast cancer (PDM-MBC) study is an ongoing study instigated to evaluate ctDNA as a biomarker to individualise imaging requirements in patients with MBC. Patients receiving first-line endocrine therapy (aromatase inhibitor + cyclin-dependent kinase 4/6 inhibitor) had plasma samples collected pre-treatment, weeks 2 and 4, and concurrently with imaging until progressive disease (PD). Here, we apply an experimental analytical workflow for ultrasensitive ctDNA analysis, utilising personalised ctDNA panels designed from mutations identified in tumour tissue, and present results for 24 patients. Twenty patients (83%) had detectable ctDNA pre-treatment. The median progression-free survival was 25.6 months, and 13 patients experienced PD, with rising ctDNA detected at or prior to PD in 12 patients (92%). If imaging had been omitted until the detection of rising ctDNA for at least one mutation, 68% (n = 71) of the scans performed amongst ctDNA-positive patients would have been avoided. Our results demonstrate that integration of personalised ctDNA monitoring of patients with MBC has potential to substantially reduce the imaging needs in patients showing ctDNA response to treatment.

International Journal of CancerVol. 156(8)
Linköping University (SE), Sahlgrenska University Hospital (SE), University of Manchester (GB), Stockholm South General Hospital (SE), Region Jönköpings län (SE), The Christie NHS Foundation Trust (GB), Landstinget i Kalmar län (SE), Ryhov Hospital Jönköping (SE), Linköping University Hospital (SE), University of Gothenburg (SE)
Falk Foundation, Forskningsrådet i Sydöstra Sverige, Christie Charity, Sjöbergstiftelsen, Percy Falk Foundation, Cancerfonden, Gunnar Nilssons Cancerstiftelse, Svenska Sällskapet för Medicinsk Forskning, Vetenskapsrådet, Svenska Läkaresällskapet, Medical Research Council, Futurum - Akademin för Hälsa och Vård, Region Jönköpings läns
Good health and well-being
Openalex Percentile: Top 30%
Cancer Genomics and Diagnostics
0.57
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