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Abstract
Accurate prediction of response to neoadjuvant chemotherapy (NAC) can help tailor treatment to individual patients’ needs. Little is known about the combination of liquid biopsies and computer extracted features from multiparametric magnetic resonance imaging (MRI) for the prediction of NAC response in breast cancer. Here, we report on a prospective study with the aim to explore the predictive potential of this combination in adjunct to standard clinical and pathological information before, during and after NAC. The study was performed in four Dutch hospitals. Patients without metastases treated with NAC underwent 3 T multiparametric MRI scans before, during and after NAC. Liquid biopsies were obtained before every chemotherapy cycle and before surgery. Prediction models were developed using penalized linear regression to forecast residual cancer burden after NAC and evaluated for pathologic complete response (pCR) using leave-one-out-cross-validation (LOOCV). Sixty-one patients were included. Twenty-three patients (38%) achieved pCR. Most prediction models yielded the highest estimated LOOCV area under the curve (AUC) at the post-treatment timepoint. A clinical-only model including tumor grade, nodal status and receptor subtype yielded an estimated LOOCV AUC for pCR of 0.76, which increased to 0.82 by incorporating post-treatment radiological MRI assessment (i.e., the “clinical-radiological” model). The estimated LOOCV AUC was 0.84 after incorporation of computer-extracted MRI features, and 0.85 when liquid biopsy information was added instead of the radiological MRI assessment. Adding liquid biopsy information to the clinical-radiological resulted in an estimated LOOCV AUC of 0.86. In conclusion, inclusion of liquid biopsy-derived markers in clinical-radiological prediction models may have potential to improve prediction of pCR after NAC in breast cancer.
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1 Utrecht University, Image Sciences Institute, University Medical Centre Utrecht, Utrecht, The Netherlands (GRID:grid.5477.1) (ISNI:0000000120346234)
2 Utrecht University, Julius Center for Health Sciences and Primary Care, University Medical Centre Utrecht, Utrecht, The Netherlands (GRID:grid.5477.1) (ISNI:0000000120346234)
3 St Antonius Hospital, Department of Radiology, Nieuwegein, The Netherlands (GRID:grid.415960.f) (ISNI:0000 0004 0622 1269)
4 Philips Research, Eindhoven, The Netherlands (GRID:grid.417284.c) (ISNI:0000 0004 0398 9387)
5 Agena Bioscience GmbH, Hamburg, Germany (GRID:grid.417284.c)
6 Stilla Technologies, Villejuif, France (GRID:grid.417284.c)
7 St. Antonius Hospital, Department of Medical Oncology, Nieuwegein, The Netherlands (GRID:grid.415960.f) (ISNI:0000 0004 0622 1269)
8 Alexander Monro Hospital, Department of Medical Oncology, Bilthoven, The Netherlands (GRID:grid.491135.b)
9 Albert Schweitzer Hospital, Department of Medical Oncology, Dordrecht, The Netherlands (GRID:grid.413972.a) (ISNI:0000 0004 0396 792X)
10 Utrecht University, Department of Pathology, University Medical Centre Utrecht, Utrecht, The Netherlands (GRID:grid.5477.1) (ISNI:0000000120346234)
11 Utrecht University, Department of Medical Oncology, University Medical Centre Utrecht, Utrecht, The Netherlands (GRID:grid.5477.1) (ISNI:0000000120346234)