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      Expression of Nectin-4 and PD-L1 in Upper Tract Urothelial Carcinoma

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          Abstract

          Enfortumab vedotin is a novel antibody–drug conjugate targeting Nectin-4, which is highly expressed in urothelial carcinoma. However, the expression status of Nectin-4 in upper tract urothelial carcinoma (UTUC) remains unclear. The relationship between Nectin-4 and Programmed Death Ligand 1 (PD-L1) in UTUC is also ambiguous. We performed immunohistochemical analysis of 99 UTUC tissue microarray to assess the expression of Nectin-4 and PD-L1 in UTUC. Nectin-4-positivity was detected in 65 (65.7%) samples, and PD-L1 was detected in 24 (24.2%) samples. There was no correlation between the expression of Nectin-4 and PD-L1. Patients with strong Nectin-4-expressing tumors had a significantly higher risk of progression ( p = 0.031) and cancer-specific mortality ( p = 0.036). Strong Nectin-4 expression was also an independent predictor of disease progression in the high-risk group (pT3 ≤ or presence of lymphovascular invasion or lymph node metastasis) (Hazard ratio, 3.32 [95% confidence interval, 1.20–7.98; p = 0.027]). In conclusion, we demonstrated that Nectin-4 expression rate in UTUC was 65.7% and independent of PD-L1 expression. Strong Nectin-4 expression was associated with worse progression-free survival in high-risk UTUC. These findings suggested that enfortumab vedotin may be effective in a broad range of patients with UTUC, regardless of PD-L1 expression.

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          Atezolizumab with or without chemotherapy in metastatic urothelial cancer (IMvigor130): a multicentre, randomised, placebo-controlled phase 3 trial

          Atezolizumab can induce sustained responses in metastatic urothelial carcinoma. We report the results of IMvigor130, a phase 3 trial that compared atezolizumab with or without platinum-based chemotherapy versus placebo plus platinum-based chemotherapy in first-line metastatic urothelial carcinoma.
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            Pivotal Trial of Enfortumab Vedotin in Urothelial Carcinoma After Platinum and Anti-Programmed Death 1/Programmed Death Ligand 1 Therapy

            PURPOSE Locally advanced or metastatic urothelial carcinoma is an incurable disease with limited treatment options, especially for patients who were previously treated with platinum and anti–programmed death 1 or anti–programmed death ligand 1 (PD-1/L1) therapy. Enfortumab vedotin is an antibody–drug conjugate that targets Nectin-4, which is highly expressed in urothelial carcinoma. METHODS EV-201 is a global, phase II, single-arm study of enfortumab vedotin 1.25 mg/kg (intravenously on days 1, 8, and 15 of every 28-day cycle) in patients with locally advanced or metastatic urothelial carcinoma who were previously treated with platinum chemotherapy and anti–PD-1/L1 therapy. The primary end point was objective response rate per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 by blinded independent central review. Key secondary end points were duration of response, progression-free survival, overall survival, safety, and tolerability. RESULTS Enfortumab vedotin was administered to 125 patients with metastatic urothelial carcinoma. Median follow-up was 10.2 months (range, 0.5 to 16.5 months). Confirmed objective response rate was 44% (95% CI, 35.1% to 53.2%), including 12% complete responses. Similar responses were observed in prespecified subgroups, such as those patients with liver metastases and those with no response to prior anti–PD-1/L1 therapy. Median duration of response was 7.6 months (range, 0.95 to 11.30+ months). The most common treatment-related adverse events were fatigue (50%), any peripheral neuropathy (50%), alopecia (49%), any rash (48%), decreased appetite (44%), and dysgeusia (40%). No single treatment-related adverse events grade 3 or greater occurred in 10% or more of patients. CONCLUSION Enfortumab vedotin demonstrated a clinically meaningful response rate with a manageable and tolerable safety profile in patients with locally advanced or metastatic urothelial carcinoma who were previously treated with platinum and anti–PD-1/L1 therapies.
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              Enfortumab Vedotin Antibody-Drug Conjugate Targeting Nectin-4 Is a Highly Potent Therapeutic Agent in Multiple Preclinical Cancer Models.

              The identification of optimal target antigens on tumor cells is central to the advancement of new antibody-based cancer therapies. We performed suppression subtractive hybridization and identified nectin-4 (PVRL4), a type I transmembrane protein and member of a family of related immunoglobulin-like adhesion molecules, as a potential target in epithelial cancers. We conducted immunohistochemical analysis of 2,394 patient specimens from bladder, breast, lung, pancreatic, ovarian, head/neck, and esophageal tumors and found that 69% of all specimens stained positive for nectin-4. Moderate to strong staining was especially observed in 60% of bladder and 53% of breast tumor specimens, whereas the expression of nectin-4 in normal tissue was more limited. We generated a novel antibody-drug conjugate (ADC) enfortumab vedotin comprising the human anti-nectin-4 antibody conjugated to the highly potent microtubule-disrupting agent MMAE. Hybridoma (AGS-22M6E) and CHO (ASG-22CE) versions of enfortumab vedotin (also known as ASG-22ME) ADC were able to bind to cell surface-expressed nectin-4 with high affinity and induced cell death in vitro in a dose-dependent manner. Treatment of mouse xenograft models of human breast, bladder, pancreatic, and lung cancers with enfortumab vedotin significantly inhibited the growth of all four tumor types and resulted in tumor regression of breast and bladder xenografts. Overall, these findings validate nectin-4 as an attractive therapeutic target in multiple solid tumors and support further clinical development, investigation, and application of nectin-4-targeting ADCs. Cancer Res; 76(10); 3003-13. ©2016 AACR.
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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                29 July 2020
                August 2020
                : 21
                : 15
                : 5390
                Affiliations
                [1 ]Department of Urology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan; tomiyama@ 123456uro.med.osaka-u.ac.jp (E.T.); kato@ 123456uro.med.osaka-u.ac.jp (T.K.); hatano@ 123456uro.med.osaka-u.ac.jp (K.H.); kawashima@ 123456uro.med.osaka-u.ac.jp (A.K.); ujike@ 123456uro.med.osaka-u.ac.jp (T.U.); uemura@ 123456uro.med.osaka-u.ac.jp (M.U.); nono@ 123456uro.med.osaka-u.ac.jp (N.N.)
                [2 ]Department of Urology, Kindai University Faculty of Medicine, 377-2, Ohno-Higashi, Sayama, Osaka 589-8511, Japan; ebanno@ 123456med.kindai.ac.jp (E.B.); yoshimur@ 123456med.kindai.ac.jp (K.Y.); huemura@ 123456med.kindai.ac.jp (H.U.)
                [3 ]Department of Pathology, Johns Hopkins University, Baltimore, MD 21287, USA
                [4 ]Department of Pathology, University of Alabama at Birmingham, Birmingham, AL 35233-7331, USA; mdcrodriguez@ 123456uabmc.edu (M.D.C.R.P.); gnetto@ 123456uabmc.edu (G.J.N.)
                [5 ]Department of Pathology, Kidney Diseases Research Center, Isfahan University of Medical Sciences, Isfahan 8174673461, Iran; diana1380@ 123456yahoo.com
                [6 ]Department of Urological Immuno-Oncology, Osaka University Graduate School of Medicine, Osaka 565-0871, Japan
                [7 ]Department of Urology, Osaka General Medical Center, Osaka 558 8558, Japan; takao@ 123456gh.opho.jp (T.T.); syamaguchi@ 123456gh.opho.jp (S.Y.)
                [8 ]Department of Pathology, Osaka General Medical Center, Osaka 558 8558, Japan; hiroaki-fushimi@ 123456gh.opho.jp
                Author notes
                [* ]Correspondence: kfujita@ 123456med.kindai.ac.jp ; Tel.: + (81)-7-2366-0221
                Author information
                https://orcid.org/0000-0002-6774-7497
                https://orcid.org/0000-0002-3439-7013
                https://orcid.org/0000-0001-9369-4264
                Article
                ijms-21-05390
                10.3390/ijms21155390
                7432817
                32751328
                e7d45198-425e-4e52-8ddc-5e2c7b214837
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 03 July 2020
                : 27 July 2020
                Categories
                Article

                Molecular biology
                nectin-4,programmed death ligand 1,upper tract urothelial carcinoma,enfortumab vedotin

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