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Ojima. Cancer Drug Resist 2021;4:885-7                                           Cancer
               DOI: 10.20517/cdr.2021.86
                                                                                    Drug Resistance




               Editorial                                                                     Open Access



               Recent advances in tumor-targeting chemotherapy
               drugs


               Iwao Ojima

               Institute of Chemical Biology and Drug Discovery, Stony Brook University, Stony Brook, NY 11794-3400, USA.
               Correspondence to: Prof./Dr. Iwao Ojima, Institute of Chemical Biology and Drug Discovery, Stony Brook University, Stony
               Brook, NY 11794-3400, USA. E-mail: iwao.ojima@stonybrook.edu

               How to cite this article: Ojima I. Recent advances in tumor-targeting chemotherapy drugs. Cancer Drug Resist 2021;4:885-7.
               https://dx.doi.org/10.20517/cdr.2021.86

               Received: 30 Aug 2021  Accepted: 7 Sep 2021  First online: 8 Sep 2021

               Academic Editor: Godefridus J. Peters   Copy Editor: Yue-Yue Zhang  Production Editor: Yue-Yue Zhang



               The first antibody-drug conjugate (ADC), Mylotarg, received FDA approval in 2000, and the revolutionary
               targeted cancer chemotherapy drug, Imatinib (Gleevec), was approved by FDA in 2001. Accordingly, it is an
               excellent time to review the recent advances in tumor-targeting chemotherapy drugs by collecting articles
               from leading researchers at the 20th anniversary of the FDA approvals of these two epoch-making
               anticancer drugs with two different approaches to targeting cancer cells specifically. In this Special Issue,
               recent advances in these two approaches are presented.

               Lyons et al.  reviewed recent advances in preclinical research that have significantly increased the
                         [1]
               experimental rigor through which promising candidate molecules are accurately evaluated in parallel to the
               development of ADC technology. For example, preclinical tumor modeling with the development of
               patient-derived tumor organoid models that recapitulate many aspects of the human disease far better than
               conventional subcutaneous xenograft models. The authors also discussed how the application of several
               preclinical molecular imaging techniques has greatly enhanced the quality of experimental data, enabling
               quantitative pre- and post-treatment tumor measurements or the precise assessment of ADCs as effective
               diagnostics.











                           © The Author(s) 2021. Open Access This article is licensed under a Creative Commons Attribution 4.0
                           International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing,
                           adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as
               long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and
               indicate if changes were made.

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