L
L.R. Hoes
Researcher at Netherlands Cancer Institute
Publications - 27
Citations - 1033
L.R. Hoes is an academic researcher from Netherlands Cancer Institute. The author has contributed to research in topics: Medicine & Cancer. The author has an hindex of 7, co-authored 16 publications receiving 511 citations.
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Journal ArticleDOI
Patient-derived organoids can predict response to chemotherapy in metastatic colorectal cancer patients.
Salo N. Ooft,Fleur Weeber,Krijn K. Dijkstra,Chelsea M. McLean,Sovann Kaing,Erik van Werkhoven,Luuk J. Schipper,L.R. Hoes,Daniel J. Vis,Joris van de Haar,Warner Prevoo,Petur Snaebjornsson,Daphne L. van der Velden,Michelle Klein,Myriam Chalabi,Henk Boot,Monique E. van Leerdam,Haiko J. Bloemendal,Laurens V. Beerepoot,Lodewyk F. A. Wessels,Lodewyk F. A. Wessels,Edwin Cuppen,Hans Clevers,Emile E. Voest +23 more
TL;DR: An in vitro test based on patient-derived tumor organoids (PDOs) from metastatic lesions to identify nonresponders to standard-of-care chemotherapy in colorectal cancer (CRC) is developed and the feasibility of generating and testing PDOs for evaluation of sensitivity to chemotherapy is shown.
Journal ArticleDOI
Caring for patients with cancer in the COVID-19 era.
Joris van de Haar,L.R. Hoes,Charlotte E. Coles,Kenneth Seamon,Stefan Fröhling,Dirk Jäger,Franco Valenza,Filippo de Braud,Luigi De Petris,Luigi De Petris,Jonas Bergh,Jonas Bergh,Ingemar Ernberg,Benjamin Besse,Fabrice Barlesi,Fabrice Barlesi,Elena Garralda,Alejandro Piris-Giménez,Michael Baumann,Giovanni Apolone,Jean-Charles Soria,Josep Tabernero,Carlos Caldas,Emile E. Voest +23 more
TL;DR: How the seven comprehensive cancer centers of Cancer Core Europe have organized their healthcare systems at an unprecedented scale and pace to make their operations ‘pandemic proof’ is reported.
Journal ArticleDOI
The Drug Rediscovery protocol facilitates the expanded use of existing anticancer drugs
D.L. van der Velden,L.R. Hoes,H. van der Wijngaart,J.M. van Berge Henegouwen,E. van Werkhoven,Paul Roepman,R. L. Schilsky,W. W. J. de Leng,Alwin D. R. Huitema,Alwin D. R. Huitema,Bastiaan Nuijen,Petra M. Nederlof,C.M.L. van Herpen,Derk Jan A. de Groot,Lot A. Devriese,Ann Hoeben,M.J.A. de Jonge,Myriam Chalabi,Egbert F. Smit,A.J. de Langen,Niven Mehra,Mariette Labots,Ellen Kapiteijn,Stefan Sleijfer,Edwin Cuppen,Henk M.W. Verheul,Henk M.W. Verheul,Hans Gelderblom,Emile E. Voest +28 more
TL;DR: The Drug Rediscovery protocol facilitates the defined use of approved drugs beyond their labels in rare subgroups of cancer, identifies early signals of activity in these subgroups, accelerates the clinical translation of new insights into the use of anticancer drugs outside of their approved label, and creates a publicly available repository of knowledge for future decision-making.
Journal ArticleDOI
Prospective experimental treatment of colorectal cancer patients based on organoid drug responses.
Salo N. Ooft,Fleur Weeber,Luuk J. Schipper,Krijn K. Dijkstra,Chelsea M. McLean,Sovann Kaing,J. van de Haar,Warner Prevoo,E. van Werkhoven,Petur Snaebjornsson,L.R. Hoes,Myriam Chalabi,D.L. van der Velden,M E van Leerdam,Henk Boot,Cecile Grootscholten,A. D. R. Huitema,A. D. R. Huitema,Haiko J. Bloemendal,Edwin Cuppen,Emile E. Voest +20 more
TL;DR: The SENSOR trial as mentioned in this paper evaluated the feasibility of patient-derived organoids to allocate patients for treatment with off-label or investigational agents, and the primary endpoint was an objective response rate of ≥20%.
Journal ArticleDOI
Study protocol: Whole genome sequencing Implementation in standard Diagnostics for Every cancer patient (WIDE).
Kris G. Samsom,Linda J.W. Bosch,Luuk J. Schipper,Paul Roepman,Ewart de Bruijn,L.R. Hoes,Immy Riethorst,Lieke Schoenmaker,Lizet E. van der Kolk,Valesca P. Retèl,Geert W.J. Frederix,Tineke E. Buffart,Jacobus J M van der Hoeven,Emile E. Voest,Emile E. Voest,Edwin Cuppen,Kim Monkhorst,Gerrit A. Meijer +17 more
TL;DR: The WIDE study aims to investigate the feasibility and validity of WGS-based diagnostics in clinical practice, and yield the optimal conditions under which WGS can be implemented in a routine molecular diagnostics setting.