NGS-Guided Precision Oncology in Breast Cancer and Gynecological Tumors—A Retrospective Molecular Tumor Board Analysis

Author:

Gremke Niklas12ORCID,Rodepeter Fiona R.3,Teply-Szymanski Julia3ORCID,Griewing Sebastian1,Boekhoff Jelena1,Stroh Alina12,Tarawneh Thomas S.4,Riera-Knorrenschild Jorge4,Balser Christina5,Hattesohl Akira3,Middeke Martin6,Ross Petra4,Litmeyer Anne-Sophie3,Romey Marcel3,Stiewe Thorsten2ORCID,Wündisch Thomas6,Neubauer Andreas4ORCID,Denkert Carsten3,Wagner Uwe1,Mack Elisabeth K. M.4ORCID

Affiliation:

1. Department of Gynecology, Gynecological Endocrinology and Oncology, University Hospital Gießen and Marburg Campus Marburg, Philipps-University, 35043 Marburg, Germany

2. Institute of Molecular Oncology, Philipps-University, 35043 Marburg, Germany

3. Institute of Pathology, University Hospital Gießen and Marburg Campus Marburg, Philipps-University, 35043 Marburg, Germany

4. Department of Hematology, Oncology and Immunology, University Hospital Gießen and Marburg Campus Marburg, Philipps-University, 35043 Marburg, Germany

5. Practice for Internal Medicine, Hematology and Internal Oncology, 35043 Marburg, Germany

6. Comprehensive Cancer Center Marburg, University Hospital Gießen and Marburg Campus Marburg, Philipps-University, 35043 Marburg, Germany

Abstract

Background: Precision oncology treatments are being applied more commonly in breast and gynecological oncology through the implementation of Molecular Tumor Boards (MTBs), but real-world clinical outcome data remain limited. Methods: A retrospective analysis was conducted in patients with breast cancer (BC) and gynecological malignancies referred to our center’s MTB from 2018 to 2023. The analysis covered patient characteristics, next-generation sequencing (NGS) results, MTB recommendations, therapy received, and clinical outcomes. Results: Sixty-three patients (77.8%) had metastatic disease, and forty-four patients (54.3%) had previously undergone three or more lines of systemic treatment. Personalized treatment recommendations were provided to 50 patients (63.3%), while 29 (36.7%) had no actionable target. Ultimately, 23 patients (29.1%) underwent molecular-matched treatment (MMT). Commonly altered genes in patients with pan-gyn tumors (BC and gynecological malignancies) included TP53 (n = 42/81, 51.9%), PIK3CA (n = 18/81, 22.2%), BRCA1/2 (n = 10/81, 12.3%), and ARID1A (n = 9/81, 11.1%). Patients treated with MMT showed significantly prolonged progression-free survival (median PFS 5.5 vs. 3.5 months, p = 0.0014). Of all patients who underwent molecular profiling, 13.6% experienced a major clinical benefit (PFSr ≥ 1.3 and PR/SD ≥ 6 months) through precision oncology. Conclusions: NGS-guided precision oncology demonstrated improved clinical outcomes in a subgroup of patients with gynecological and breast cancers.

Funder

Stiftung P.E. Kempkes

University Medical Center Giessen and Marburg

von Behring-Röntgen Stiftung

Clinician Scientist program of the Philipps University of Marburg

Carreras leukemia foundation

DFG, German Research Foundation

Publisher

MDPI AG

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