Combined Focused Next-Generation Sequencing Assays to Guide Precision Oncology in Solid Tumors: A Retrospective Analysis from an Institutional Molecular Tumor Board

Cancers (Basel). 2022 Sep 12;14(18):4430. doi: 10.3390/cancers14184430.

Abstract

Background: Increasing knowledge of cancer biology and an expanding spectrum of molecularly targeted therapies provide the basis for precision oncology. Despite extensive gene diagnostics, previous reports indicate that less than 10% of patients benefit from this concept.

Methods: We retrospectively analyzed all patients referred to our center's Molecular Tumor Board (MTB) from 2018 to 2021. Molecular testing by next-generation sequencing (NGS) included a 67-gene panel for the detection of short-sequence variants and copy-number alterations, a 53- or 137-gene fusion panel and an ultra-low-coverage whole-genome sequencing for the detection of additional copy-number alterations outside the panel's target regions. Immunohistochemistry for microsatellite instability and PD-L1 expression complemented NGS.

Results: A total of 109 patients were referred to the MTB. In all, 78 patients received therapeutic proposals (70 based on NGS) and 33 were treated accordingly. Evaluable patients treated with MTB-recommended therapy (n = 30) had significantly longer progression-free survival than patients treated with other therapies (n = 17) (4.3 vs. 1.9 months, p = 0.0094). Seven patients treated with off-label regimens experienced major clinical benefits.

Conclusion: The combined focused sequencing assays detected targetable alterations in the majority of patients. Patient benefits appeared to lie in the same range as with large-scale sequencing approaches.

Keywords: gene panels; molecular tumor board; next-generation sequencing; precision oncology; solid tumors; ultra-low-coverage whole-genome sequencing.

Grants and funding

C.D. reports grants from European Commission H2020, German Cancer Aid Translational Oncology, German Breast Group, Myriad and Roche, all outside the submitted work. E.K.M.M. and A.N. were funded by the Deutsche José-Carreras Leukämie-Stiftung (Grant Numbers AR 07/2017 and AH 06-01 to A.N.). E.K.M.M. was supported by the Clinician Scientist program of the Philipps University of Marburg and the University Hospital Gießen and Marburg.