Functional Precision Medicine Provides Clinical Benefit in Advanced Aggressive Hematologic Cancers and Identifies Exceptional Responders

Christoph Kornauth(Vienna General Hospital), Tea Pemovska(Austrian Academy of Sciences), Gregory I. Vladimer(Austrian Academy of Sciences), Günther Bayer(Medical University of Vienna), Michael Bergmann(Medical University of Vienna), Sandra Eder(Klinikum Klagenfurt), Ruth Eichner(Austrian Academy of Sciences), Martin Erl(Ordensklinikum Linz Barmherzige Schwestern), Harald Esterbauer(Medical University of Vienna), Ruth Exner(Medical University of Vienna), Verena Felsleitner-Hauer(Fachhochschule Wiener Neustadt), Maurizio Forte(Medical University of Vienna), Alexander Gaiger(Vienna General Hospital), Klaus Geißler(Sigmund Freud Privatuniversität Wien), Hildegard Greinix(Medical University of Graz), Wolfgang Gstöttner(Medical University of Vienna), Marcus Hacker(Medical University of Vienna), Bernd Hartmann(Landeskrankenhaus Feldkirch), Alexander W. Hauswirth(Medical University of Vienna), Tim Heinemann(ETH Zurich), Daniel Heintel(Medical University of Vienna), Mir Alireza Hoda(Medical University of Vienna), Georg Hopfinger(Tirol Kliniken), Ulrich Jaeger(Vienna General Hospital), Lukas Kazianka(Medical University of Vienna), Lukas Kenner(Medical University of Vienna), Barbara Kiesewetter(Medical University of Vienna), Nikolaus Krall(Austrian Academy of Sciences), G. Krajnik(Universitätsklinikum St. Pölten), Stefan Kubicek(Austrian Academy of Sciences), Trang Le(Medical University of Vienna), Simone Lubowitzki(Medical University of Vienna), Marius E. Mayerhoefer(Memorial Sloan Kettering Cancer Center), Elisabeth Menschel(Hanusch Hospital), Olaf Merkel(Medical University of Vienna), Katsuhiro Miura(Nihon University), Leonhard Müllauer(Medical University of Vienna), Peter Neumeister(Medical University of Graz), Thomas Noesslinger(Hanusch Hospital), Katharina Ocko(Vienna General Hospital), Leopold Öhler(Vienna General Hospital), Michael Panny(Hanusch Hospital), Alexander Pichler(Medical University of Vienna), Edit Porpaczy(Medical University of Vienna), Gerald W. Prager(Vienna General Hospital), Markus Raderer(Vienna General Hospital), Robin Ristl(Statistics Austria), Reinhard Ruckser(Donauspital), Julius Salamon(Baidu (China)), Ana‐Iris Schiefer(Medical University of Vienna), Ann-Sofie Schmolke(Medical University of Vienna), Ilse Schwarzinger(Medical University of Vienna), Edgar Selzer(Medical University of Vienna), Christian Sillaber(Medical University of Vienna), Cathrin Skrabs(Medical University of Vienna), Wolfgang R. Sperr(Ludwig Boltzmann Institute for Cancer Research), Ismet Srndic(Austrian Academy of Sciences), Renate Thalhammer(Medical University of Vienna), Peter Valent(Ludwig Boltzmann Institute for Cancer Research), Emiel van der Kouwe(Medical University of Vienna), Katrina Vanura(Medical University of Vienna), Stefan Vogt(Fachhochschule Wiener Neustadt), Cora Waldstein(Medical University of Vienna), Dominik Wolf‎(Innsbruck Medical University), Christoph Zielinski(Comprehensive Cancer Center Vienna), Niklas Zojer(Medical University of Vienna), Ingrid Simonitsch‐Klupp(Medical University of Vienna), Giulio Superti‐Furga(Austrian Academy of Sciences), Berend Snijder(ETH Zurich), Philipp B. Staber(Vienna General Hospital)
Cancer Discovery
October 11, 2021
Cited by 204Open Access
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Abstract

Abstract Personalized medicine aims to match the right drug with the right patient by using specific features of the individual patient's tumor. However, current strategies of personalized therapy matching provide treatment opportunities for less than 10% of patients with cancer. A promising method may be drug profiling of patient biopsy specimens with single-cell resolution to directly quantify drug effects. We prospectively tested an image-based single-cell functional precision medicine (scFPM) approach to guide treatments in 143 patients with advanced aggressive hematologic cancers. Fifty-six patients (39%) were treated according to scFPM results. At a median follow-up of 23.9 months, 30 patients (54%) demonstrated a clinical benefit of more than 1.3-fold enhanced progression-free survival compared with their previous therapy. Twelve patients (40% of responders) experienced exceptional responses lasting three times longer than expected for their respective disease. We conclude that therapy matching by scFPM is clinically feasible and effective in advanced aggressive hematologic cancers. Significance: This is the first precision medicine trial using a functional assay to instruct n-of-one therapies in oncology. It illustrates that for patients lacking standard therapies, high-content assay-based scFPM can have a significant value in clinical therapy guidance based on functional dependencies of each patient's cancer. See related commentary by Letai, p. 290. This article is highlighted in the In This Issue feature, p. 275


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