Journal Article10.3390/cancers16173071
Mechanistic Insights into the Successful Development of Combination Therapy of Enfortumab Vedotin and Pembrolizumab for the Treatment of Locally Advanced or Metastatic Urothelial Cancer
Caroline Taylor,Kamai M. Patterson,Devira Friedman,Silvia M. Bacot,Gerald M. Feldman,Tao Wang +5 more
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TL;DR: This review elucidates the mechanism behind the successful combination therapy of enfortumab vedotin and pembrolizumab for locally advanced or metastatic urothelial cancer, highlighting the enhancement of pembrolizumab-induced immunity by enfortumab vedotin.
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Abstract: Simple Summary Antibody–drug conjugates (ADCs) and immune checkpoint inhibitors (ICIs) are two promising therapeutic modalities against many types of cancers. However, many patients develop resistance. The resistance mechanisms to ADCs and ICIs have been comprehensively illuminated in this review. A combination of ADCs and ICIs has been explored to overcome resistance to ADC or ICI single treatment. Recently, a clinical study demonstrated that a combination of enfortumab vedotin (EV), an ADC against Nectin-4, with the ICI pembrolizumab achieves remarkable clinical efficacy as the first-line therapy for the treatment of locally advanced or metastatic urothelial carcinoma. The underlying mechanism is likely due to the enhancement of pembrolizumab-induced anticancer immunity mediated by EV. With the emerging use of combination therapy strategy, it is critical to understand the mechanism of successful and/or failed clinical studies for the future development of combination therapy of ADCs with ICIs. Abstract Antibody–drug conjugates (ADCs) consist of an antibody backbone that recognizes and binds to a target antigen expressed on tumor cells and a small molecule chemotherapy payload that is conjugated to the antibody via a linker. ADCs are one of the most promising therapeutic modalities for the treatment of various cancers. However, many patients have developed resistance to this form of therapy. Extensive efforts have been dedicated to identifying an effective combination of ADCs with other types of anticancer therapies to potentially overcome this resistance. A recent clinical study demonstrated that a combination of the ADC enfortumab vedotin (EV) with the immune checkpoint inhibitor (ICI) pembrolizumab can achieve remarkable clinical efficacy as the first-line therapy for the treatment of locally advanced or metastatic urothelial carcinoma (la/mUC)—leading to the first approval of a combination therapy of an ADC with an ICI for the treatment of cancer patients. In this review, we highlight knowledge and understanding gained from the successful development of EV and the combination therapy of EV with ICI for the treatment of la/mUC. Using urothelial carcinoma as an example, we will focus on dissecting the underlying mechanisms necessary for the development of this type of combination therapy for a variety of cancers.
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Citations
Real-World Outcomes of Enfortumab Vedotin and Pembrolizumab in Advanced Urothelial Carcinoma: A Multicenter Retrospective Analysis
Prateek Jain,Syed Arsalan Ahmed Naqvi,Nikita Tripathi,Muhammad Abdullah Humayun,Yousef Zakharia,Jacob J Orme,Ruqin Chen,Irbaz B. Riaz,Parminder Singh,Prateek Jain,Nikita Tripathi,Yousef Zakharia,Jacob J Orme,Ruqin Chen,Irbaz B. Riaz,Parminder Singh,Prateek Jain,Syed Arsalan Ahmed Naqvi,Nikita Tripathi,Muhammad Abdullah Humayun,Yousef Zakharia,Jacob J Orme,Ruqin Chen,Irbaz B. Riaz,Parminder Singh +24 more
Abstract: In this real-world cohort, enfortumab vedotin-pembrolizumab combination demonstrated meaningful clinical activity and manageable toxicity in both first-line and subsequent-line settings, consistent with results from the EV-302 trial.
Tumour-Derived Extracellular Vesicles in Chemotherapy Resistance: Molecular Pathways, Clinical Implications and Therapeutic Opportunities
Rupali J. Ghule,Yogeshwari N. Sanap,Mukund M. Pache,Avinash B. Darekar +3 more
Abstract: Background: Chemotherapy remains a central strategy in cancer treatment; however, its effectiveness is often diminished by the emergence of drug resistance, which contributes to over 90% of cancer-related deaths. Traditionally, resistance has been linked to genetic mutations and altered drug metabolism. Recent findings, however, highlight the critical role of extracellular vesicles (EVs) in mediating intercellular communication and facilitating adaptive resistance. Objective: This review examines the involvement of tumour-derived EVs in chemotherapy resistance, focusing on their cargo microRNAs (miRNAs), proteins, and lipids and their impact on drug efflux, apoptosis evasion, and immune suppression. Key Findings: EVs facilitate resistance through various mechanisms. For instance, EVs transfer ATP-binding cassette (ABC) transporters such as P-glycoprotein, enhancing drug efflux and promoting multidrug resistance. Oncogenic miRNAs (e.g., miR-21, miR-155) within EVs suppress pro-apoptotic genes (PTEN, CASP3), impeding cell death. Moreover, EVs contribute to tumour microenvironment remodelling by activating cancer-associated fibroblasts and carrying PD-L1 to suppress T-cell responses. Clinical Relevance: EV-derived biomarkers including circulating miRNAs (miR-192, miR-484, miR-205) and DNA mutations (KRAS, TP53, EGFR) offer potential for non-invasive monitoring. Therapeutic strategies such as EV inhibition (e.g., GW4869, Rab27a inhibitors) and engineered EVs for targeted delivery are promising. Conclusion: EV-targeted approaches may transform personalised cancer therapy. Nonetheless, overcoming challenges related to EV heterogeneity, standardisation, and specificity is essential for clinical translation. Future work should prioritise tumour-selective EV inhibition and AI-based biomarker discovery.
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