AI Article Synopsis

  • Antibody-drug conjugates (ADCs) are innovative cancer treatments that combine a monoclonal antibody with a toxic drug, specifically designed to target and kill cancer cells while sparing normal cells.
  • They have received regulatory approval for various cancers, marking a significant advancement in cancer therapy, but none are currently approved for renal cell carcinoma (RCC).
  • The paper reviews existing research on ADCs in RCC patients, explores reasons for their limited success, and suggests new strategies to enhance their effectiveness in treating this type of cancer.

Article Abstract

Antibody-drug conjugates (ADCs) are complex chemical structures composed of a monoclonal antibody, serving as a link to target cells, which is conjugated with a potent cytotoxic drug (i.e., payload) through a chemical linker. Inspired by Paul Ehrlich's concept of the ideal anticancer drug as a "magic bullet", ADCs are also highly specific anticancer agents, as they have been demonstrated to recognize, bind, and neutralize cancer cells, limiting injuries to normal cells. ADCs are among the newest pharmacologic breakthroughs in treating solid and hematologic malignancies. Indeed, in recent years, various ADCs have been approved by the Food and Drug Administration and European Medicines Agency for the treatment of several cancers, resulting in a "practice-changing" approach. However, despite these successes, no ADC is approved for treating patients affected by renal cell carcinoma (RCC). In the present paper, we thoroughly reviewed the current literature and summarized preclinical studies and clinical trials that evaluated the activity and toxicity profile of ADCs in RCC patients. Moreover, we scrutinized the potential causes that, until now, hampered the therapeutical success of ADCs in those patients. Finally, we discussed novel strategies that would improve the development of ADCs and their efficacy in treating RCC patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10532725PMC
http://dx.doi.org/10.3390/jpm13091339DOI Listing

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