1. Multiparametric circulating tumor cell analysis to select targeted therapies for breast cancer patients
- Author
-
Mahdi Rivandi, H Asperger, A Franken, Dieter Niederacher, Hans Neubauer, Bernadette Jaeger, Frederic Dietzel, Tanja Fehm, Ellen Honisch, Liwen Yang, Charlotte Proudhon, Natalia Krawczyk, Florian Reinhardt, Irene Esposito, Francesco Marass, Jan-Philipp Cieslik, Natali Schölermann, Bianca Behrens, Nikolas H. Stoecklein, Niko Beerenwinkel, and Emmanuelle Jeannot
- Subjects
Oncology ,Cancer Research ,medicine.medical_specialty ,medicine.medical_treatment ,circulating tumor cells ,Somatic evolution in cancer ,Article ,Targeted therapy ,whole exome sequencing ,Breast cancer ,Circulating tumor cell ,breast cancer ,Internal medicine ,medicine ,AKT1 ,targeted therapy ,Liquid biopsy ,RC254-282 ,Circulating Tumor Cell Analysis ,business.industry ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,medicine.disease ,Metastatic breast cancer ,Primary tumor ,business - Abstract
Background: The analysis of liquid biopsies, e.g., circulating tumor cells (CTCs) is an appealing diagnostic concept for targeted therapy selection. In this proof‐of‐concept study, we aimed to perform multiparametric analyses of CTCs to select targeted therapies for metastatic breast cancer patients. Methods: First, CTCs of five metastatic breast cancer patients were analyzed by whole exome sequencing (WES). Based on the results, one patient was selected and monitored by longitudinal and multiparametric liquid biopsy analyses over more than three years, including WES, RNA profiling, and in vitro drug testing of CTCs. Results: Mutations addressable by targeted therapies were detected in all patients, including mutations that were not detected in biopsies of the primary tumor. For the index patient, the clonal evolution of the tumor cells was retraced and resistance mechanisms were identified. The AKT1 E17K mutation was uncovered as the driver of the metastatic process. Drug testing on the patient’s CTCs confirmed the efficacy of drugs targeting the AKT1 pathway. During a targeted therapy chosen based on the CTC characterization and including the mTOR inhibitor everolimus, CTC numbers dropped by 97.3% and the disease remained stable as determined by computer tomography/magnetic resonance imaging. Conclusion: These results illustrate the strength of a multiparametric CTC analysis to choose and validate targeted therapies to optimize cancer treatment in the future. Furthermore, from a scientific point of view, such studies promote the understanding of the biology of CTCs during different treatment regimens., Cancers, 13 (23), ISSN:2072-6694
- Published
- 2021