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The Drug Rediscovery protocol facilitates the expanded use of existing anticancer drugs

Author

Listed:
  • D. L. Velden

    (Netherlands Cancer Institute
    Center for Personalized Cancer Treatment)

  • L. R. Hoes

    (Netherlands Cancer Institute
    Center for Personalized Cancer Treatment
    Oncode Institute)

  • H. Wijngaart

    (Center for Personalized Cancer Treatment
    Oncode Institute
    Amsterdam UMC, Vrije Universiteit Amsterdam, Cancer Center Amsterdam)

  • J. M. Berge Henegouwen

    (Center for Personalized Cancer Treatment
    Oncode Institute
    Leiden University Medical Center)

  • E. Werkhoven

    (Netherlands Cancer Institute)

  • P. Roepman

    (Hartwig Medical Foundation)

  • R. L. Schilsky

    (American Society of Clinical Oncology)

  • W. W. J. Leng

    (University Medical Center Utrecht)

  • A. D. R. Huitema

    (University Medical Center Utrecht, Utrecht University
    Netherlands Cancer Institute)

  • B. Nuijen

    (Netherlands Cancer Institute)

  • P. M. Nederlof

    (Molecular Diagnostics Laboratory, Netherlands Cancer Institute)

  • C. M. L. Herpen

    (Radboud University Medical Center)

  • D. J. A. Groot

    (University Medical Center Groningen)

  • L. A. Devriese

    (University Medical Center Utrecht)

  • A. Hoeben

    (Maastricht University Medical Center)

  • M. J. A. Jonge

    (Erasmus MC Cancer Institute)

  • M. Chalabi

    (Netherlands Cancer Institute
    Netherlands Cancer Institute)

  • E. F. Smit

    (Center for Personalized Cancer Treatment
    Netherlands Cancer Institute)

  • A. J. Langen

    (Netherlands Cancer Institute)

  • N. Mehra

    (Radboud University Medical Center)

  • M. Labots

    (Amsterdam UMC, Vrije Universiteit Amsterdam, Cancer Center Amsterdam)

  • E. Kapiteijn

    (Leiden University Medical Center)

  • S. Sleijfer

    (Center for Personalized Cancer Treatment
    Erasmus MC Cancer Institute)

  • E. Cuppen

    (Oncode Institute
    Hartwig Medical Foundation
    University Medical Center Utrecht)

  • H. M. W. Verheul

    (Amsterdam UMC, Vrije Universiteit Amsterdam, Cancer Center Amsterdam
    Radboud University Medical Center)

  • H. Gelderblom

    (Leiden University Medical Center)

  • E. E. Voest

    (Netherlands Cancer Institute
    Center for Personalized Cancer Treatment
    Oncode Institute)

Abstract

The large-scale genetic profiling of tumours can identify potentially actionable molecular variants for which approved anticancer drugs are available1–3. However, when patients with such variants are treated with drugs outside of their approved label, successes and failures of targeted therapy are not systematically collected or shared. We therefore initiated the Drug Rediscovery protocol, an adaptive, precision-oncology trial that aims to identify signals of activity in cohorts of patients, with defined tumour types and molecular variants, who are being treated with anticancer drugs outside of their approved label. To be eligible for the trial, patients have to have exhausted or declined standard therapies, and have malignancies with potentially actionable variants for which no approved anticancer drugs are available. Here we show an overall rate of clinical benefit—defined as complete or partial response, or as stable disease beyond 16 weeks—of 34% in 215 treated patients, comprising 136 patients who received targeted therapies and 79 patients who received immunotherapy. The overall median duration of clinical benefit was 9 months (95% confidence interval of 8–11 months), including 26 patients who were experiencing ongoing clinical benefit at data cut-off. The potential of the Drug Rediscovery protocol is illustrated by the identification of a successful cohort of patients with microsatellite instable tumours who received nivolumab (clinical benefit rate of 63%), and a cohort of patients with colorectal cancer with relatively low mutational load who experienced only limited clinical benefit from immunotherapy. 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.

Suggested Citation

  • D. L. Velden & L. R. Hoes & H. Wijngaart & J. M. Berge Henegouwen & E. Werkhoven & P. Roepman & R. L. Schilsky & W. W. J. Leng & A. D. R. Huitema & B. Nuijen & P. M. Nederlof & C. M. L. Herpen & D. J., 2019. "The Drug Rediscovery protocol facilitates the expanded use of existing anticancer drugs," Nature, Nature, vol. 574(7776), pages 127-131, October.
  • Handle: RePEc:nat:nature:v:574:y:2019:i:7776:d:10.1038_s41586-019-1600-x
    DOI: 10.1038/s41586-019-1600-x
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    Cited by:

    1. Cambrosio, Alberto & Campbell, Jonah & Keating, Peter & Polk, Jessica B. & Aguilar-Mahecha, Adriana & Basik, Mark, 2022. "Healthcare policy by other means: Cancer clinical research as “oncopolicy”," Social Science & Medicine, Elsevier, vol. 292(C).
    2. Denis Horgan & Bettina Borisch & Ivana Cattaneo & Mark Caulfield & Arturo Chiti & Christine Chomienne & Amanda Cole & Karen Facey & Allan Hackshaw & Minna Hendolin & Nadia Georges & Dipak Kalra & Biru, 2022. "Factors Affecting Citizen Trust and Public Engagement Relating to the Generation and Use of Real-World Evidence in Healthcare," IJERPH, MDPI, vol. 19(3), pages 1-18, February.
    3. Perla Pucci & Liam C. Lee & Miaojun Han & Jamie D. Matthews & Leila Jahangiri & Michaela Schlederer & Eleanor Manners & Annabel Sorby-Adams & Joshua Kaggie & Ricky M. Trigg & Christopher Steel & Lucy , 2024. "Targeting NRAS via miR-1304-5p or farnesyltransferase inhibition confers sensitivity to ALK inhibitors in ALK-mutant neuroblastoma," Nature Communications, Nature, vol. 15(1), pages 1-19, December.

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