N-of-1 Trials in Cancer Drug Development

Author:

Gouda Mohamed A.1ORCID,Buschhorn Lars2ORCID,Schneeweiss Andreas2ORCID,Wahida Adam2ORCID,Subbiah Vivek134ORCID

Affiliation:

1. 1Department of Investigational Cancer Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

2. 2Division of Gynecological Oncology, National Center for Tumor Diseases (NCT), Heidelberg, Germany.

3. 3Division of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

4. 4MD Anderson Cancer Network, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Abstract

Summary: The current approaches for cancer drug development lag behind an accelerated need in the field for a fast and efficient method for evaluating drugs in the personalized medicine era. In that regard, N-of-1 studies emerge as a potential addition to the drug development arsenal, although there are several considerations before its broad application becomes feasible. In essence, N-of-1 trials are a departure from the traditional “drug-centric” model to a “patient-centric” model. Herein, we review the concept of N-of-1 trials and provide real-world examples of their use in the developmental therapeutics field. N-of-1 trials offer an exceptional opportunity for fast-tracking of cancer drug development in the precision oncology era.

Funder

National Institutes of Health

University of Texas MD Anderson Cancer Center

Publisher

American Association for Cancer Research (AACR)

Subject

Oncology

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