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Potential of antibody-drug conjugates (ADCs) for cancer therapy

Articolo
Data di Pubblicazione:
2022
Abstract:
The primary purpose of ADCs is to increase the efficacy of anticancer medications by minimizing systemic drug distribution and targeting specific cells. Antibody conjugates (ADCs) have changed the way cancer is treated. However, because only a tiny fraction of patients experienced long-term advantages, current cancer preclinical and clinical research has been focused on combination trials. The complex interaction of ADCs with the tumor and its microenvironment appear to be reliant on the efficacy of a certain ADC, all of which have significant therapeutic consequences. Several clinical trials in various tumor types are now underway to examine the potential ADC therapy, based on encouraging preclinical results. This review tackles the potential use of ADCs in cancer therapy, emphasizing the essential processes underlying their positive therapeutic impacts on solid and hematological malignancies. Additionally, opportunities are explored to understand the mechanisms of ADCs action, the mechanism of resistance against ADCs, and how to overcome potential resistance following ADCs administration. Recent clinical findings have aroused interest, leading to a large increase in the number of ADCs in clinical trials. The rationale behind ADCs, as well as their primary features and recent research breakthroughs, will be discussed. We then offer an approach for maximizing the potential value that ADCs can bring to cancer patients by highlighting key ideas and distinct strategies.
Tipologia CRIS:
01.09 Rassegna della letteratura scientifica in rivista (Literature review)
Keywords:
antibody-drug conjugates; Targeted cancer therapy; Cytotoxic drugs; solid cancer; hematological malignancies
Elenco autori:
Cenciarelli, Carlo
Autori di Ateneo:
CENCIARELLI CARLO
Link alla scheda completa:
https://iris.cnr.it/handle/20.500.14243/416160
Pubblicato in:
CANCER CELL INTERNATIONAL
Journal
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http://www.scopus.com/record/display.url?eid=2-s2.0-85135877697&origin=inward
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