Treatment Monitoring of a Patient with Synchronous Metastatic Angiosarcoma and Breast Cancer Using ctDNA

Author:

Vannas Christoffer12ORCID,Escobar Mandy1ORCID,Österlund Tobias134ORCID,Andersson Daniel1ORCID,Mouhanna Pia15ORCID,Soomägi Amanda1,Molin Claes2,Wennergren David6,Fagman Henrik17,Ståhlberg Anders134ORCID

Affiliation:

1. Sahlgrenska Center for Cancer Research, Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, 40530 Gothenburg, Sweden

2. Department of Oncology, Sahlgrenska University Hospital, Region Västra Götaland, 41345 Gothenburg, Sweden

3. Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Region Västra Götaland, 41345 Gothenburg, Sweden

4. Wallenberg Centre for Molecular and Translational Medicine, University of Gothenburg, 40530 Gothenburg, Sweden

5. Department of Oncology, Ryhov County Hospital, 55185 Jönköping, Sweden

6. Department of Orthopaedics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, 40530 Gothenburg, Sweden

7. Department of Clinical Pathology, Sahlgrenska University Hospital, Region Västra Götaland, 41345 Gothenburg, Sweden

Abstract

Angiosarcoma is a rare and aggressive type of soft-tissue sarcoma with high propensity to metastasize. For patients with metastatic angiosarcoma, prognosis is dismal and treatment options are limited. To improve the outcomes, identifying patients with poor treatment response at an earlier stage is imperative, enabling alternative therapy. Consequently, there is a need for improved methods and biomarkers for treatment monitoring. Quantification of circulating tumor-DNA (ctDNA) is a promising approach for patient-specific monitoring of treatment response. In this case report, we demonstrate that quantification of ctDNA using SiMSen-Seq was successfully utilized to monitor a patient with metastatic angiosarcoma. By quantifying ctDNA levels using 25 patient-specific mutations in blood plasma throughout surgery and palliative chemotherapy, we predicted the outcome and monitored the clinical response to treatment. This was accomplished despite the additional complexity of the patient having a synchronous breast cancer. The levels of ctDNA showed a superior correlation to the clinical outcome compared with the radiological evaluations. Our data propose a promising approach for personalized biomarker analysis to monitor treatment in angiosarcomas, with potential applicability to other cancers and for patients with synchronous malignancies.

Funder

Swedish Cancer Society

Swedish Childhood Cancer Foundation

Assar Gabrielsson Research Foundation

Johan Jansson Foundation for Cancer Research

Wilhelm and Martina Lundgren Foundation for Scientific Research

Anna-Lisa and Bror Björnsson Foundation,

the Sarcoma patient union research fund

the memorial fund of Elvira Trané

Lions Cancer Fund West

the Foundation in memory of Bernt Katina

Region Västra Götaland

Swedish Research council

Sweden’s Innovation Agency

the Sjöberg Foundation

the Swedish state under the agreement between the Swedish government and the county councils

ALF-agreement

Publisher

MDPI AG

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