| Literature DB >> 34635570 |
Christoph Kornauth1,2, Tea Pemovska1,3, Gregory I Vladimer3,4, Ingrid Simonitsch-Klupp5, Giulio Superti-Furga3,6, Berend Snijder7, Philipp B Staber8,2, Günther Bayer5, Michael Bergmann9, Sandra Eder10, Ruth Eichner3, Martin Erl11, Harald Esterbauer12, Ruth Exner9, Verena Felsleitner-Hauer13, Maurizio Forte1, Alexander Gaiger1,2, Klaus Geissler14, Hildegard T Greinix15, Wolfgang Gstöttner16, Marcus Hacker17, Bernd Lorenz Hartmann18, Alexander W Hauswirth1, Tim Heinemann7, Daniel Heintel19, Mir Alireza Hoda20, Georg Hopfinger21, Ulrich Jaeger1,2, Lukas Kazianka1, Lukas Kenner5, Barbara Kiesewetter22, Nikolaus Krall3,4, Gerhard Krajnik23, Stefan Kubicek3, Trang Le1, Simone Lubowitzki1, Marius E Mayerhoefer24,25, Elisabeth Menschel26, Olaf Merkel5, Katsuhiro Miura27, Leonhard Müllauer5, Peter Neumeister15, Thomas Noesslinger26, Katharina Ocko28, Leopold Öhler29, Michael Panny26, Alexander Pichler1, Edit Porpaczy1, Gerald W Prager2,22, Markus Raderer2,22, Robin Ristl30, Reinhard Ruckser31, Julius Salamon32, Ana-Iris Schiefer5, Ann-Sofie Schmolke1, Ilse Schwarzinger12, Edgar Selzer33, Christian Sillaber1, Cathrin Skrabs1, Wolfgang R Sperr1,34, Ismet Srndic3, Renate Thalhammer12, Peter Valent1,34, Emiel van der Kouwe1, Katrina Vanura1, Stefan Vogt13, Cora Waldstein33, Dominik Wolf35, Christoph C Zielinski36, Niklas Zojer19.
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. ©2021 The Authors; Published by the American Association for Cancer Research.Entities:
Mesh:
Year: 2021 PMID: 34635570 DOI: 10.1158/2159-8290.CD-21-0538
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397