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Transitioning the Molecular Tumor Board from Proof of Concept to Clinical Routine: a German Single-center Analysis
Rouven Höfflin
Adriana Lazarou
Maria Elena Hess
Meike Reiser
Julius Wehrle
Patrick Metzger
Anna-Verena Frey
Heiko Becker
Konrad Aumann
Kai Berner
Martin Boeker
Nico Büttner
Christine Dierks
Jesús Duque Afonso
Michel Eisenblätter
Thalia Erbes
Ralph Fritsch
Isabell Xiang Ge
Anna-Lena Geißler
Markus Tobias Grabbert
Steffen Heeg
Dieter Henrik Heiland
Simone Hettmer
Gian Kayser
Alexander Keller
Anita Kleiber
Alexandra Kutilina
Leman Mehmed
Frank Meiß
Philipp Johann Poxleitner
Justyna Rawluk
Juri Ruf
Henning Sebastian Schäfer
Florian Paul Scherer
Khalid Shoumariyeh
Andreas Tzschach
Christoph Peters
Tilman Brummer
Martin Werner
Justus Duyster
Silke Laßmann
Cornelius Miething
Melanie Börries
Anna Lena Illert
Nikolas von Bubnoff
出版
Universität
, 2021
URL
http://books.google.com.hk/books?id=ox6DzgEACAAJ&hl=&source=gbs_api
註釋
Abstract: Molecular precision oncology faces two major challenges: first, to identify relevant and actionable molecular variants in a rapidly changing field and second, to provide access to a broad patient population. Here, we report a four-year experience of the Molecular Tumor Board (MTB) of the Comprehensive Cancer Center Freiburg (Germany) including workflows and process optimizations. This retrospective single-center study includes data on 488 patients enrolled in the MTB from February 2015 through December 2018. Recommendations include individual molecular diagnostics, molecular stratified therapies, assessment of treatment adherence and patient outcomes including overall survival. The majority of MTB patients presented with stage IV oncologic malignancies (90.6%) and underwent an average of 2.1 previous lines of therapy. Individual diagnostic recommendations were given to 487 patients (99.8%). A treatment recommendation was given in 264 of all cases (54.1%) which included a molecularly matched treatment in 212 patients (43.4%). The 264 treatment recommendations were implemented in 76 patients (28.8%). Stable disease was observed in 19 patients (25.0%), 17 had partial response (22.4%) and five showed a complete remission (6.6%). An objective response was achieved in 28.9% of cases with implemented recommendations and for 4.5% of the total population (22 of 488 patients). By optimizing the MTB workflow, case-discussions per session increased significantly while treatment adherence and outcome remained stable over time. Our data demonstrate the feasibility and effectiveness of molecular-guided personalized therapy for cancer patients in a clinical routine setting showing a low but robust and durable disease control rate over time