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      Combination therapies involving checkpoint-inhibitors for treatment of urothelial carcinoma: a narrative review

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          Abstract

          The implementation of immune checkpoint-inhibitors (CPI) has significantly improved the prognosis of a subgroup of patients with urothelial bladder cancer (BC). Still, the majority of patients will progress or experience a recurrence on CPI monotherapy. The next generation of clinical trials is now testing combination therapy with CPI and other agents that target different oncogenic mechanisms in an effort to improve efficacy. The beneficial toxicity profile of CPI but also the approval of CPI combinations in other cancer sites justifies their investigation also in BC. Here we report on clinical trials in muscle-invasive, locally advanced and metastatic BC combining CPI with other therapies, with a focus on the latest results presented at ASCO GU 2020, ASCO 2020 and ESMO 2019 as well as Phase-III trials currently ongoing. Multiple phase I-III clinical trials are investigating the combination of a CPI with a second CPI, with chemotherapy, or with targeted therapies like fibroblast growth factor receptor (FGFR) inhibitors or Nectin-4 inhibitors in different disease states. The results of more than 10 phase-III trials in advanced BC are eagerly awaited. Preliminary data are contradictory, as some trials released promising interim results, while others reported failure to achieve the primary endpoints. Taken together, combining CPI with other therapies is a logical and potentially promising approach, but it is too early to draw conclusions on specific combinations. As combinatorial therapies markedly increase the level of complexity, bedside-to-bench studies are warranted to gain deeper insight of underlying biological mechanisms which can be used to optimize future trials.

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          Most cited references38

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          Nivolumab plus Ipilimumab versus Sunitinib in Advanced Renal-Cell Carcinoma

          Nivolumab plus ipilimumab produced objective responses in patients with advanced renal-cell carcinoma in a pilot study. This phase 3 trial compared nivolumab plus ipilimumab with sunitinib for previously untreated clear-cell advanced renal-cell carcinoma.
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            Overall Survival with Combined Nivolumab and Ipilimumab in Advanced Melanoma

            Nivolumab combined with ipilimumab resulted in longer progression-free survival and a higher objective response rate than ipilimumab alone in a phase 3 trial involving patients with advanced melanoma. We now report 3-year overall survival outcomes in this trial.
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              Atezolizumab as first-line treatment in cisplatin-ineligible patients with locally advanced and metastatic urothelial carcinoma: a single-arm, multicentre, phase 2 trial.

              First-line chemotherapy for patients with cisplatin-ineligible locally advanced or metastatic urothelial carcinoma is associated with short response duration, poor survival, and high toxicity. This study assessed atezolizumab (anti-programmed death-ligand 1 [PD-L1]) as treatment for metastatic urothelial cancer in cisplatin-ineligible patients.
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                Author and article information

                Journal
                Transl Androl Urol
                Transl Androl Urol
                TAU
                Translational Andrology and Urology
                AME Publishing Company
                2223-4683
                2223-4691
                October 2021
                October 2021
                : 10
                : 10
                : 4014-4021
                Affiliations
                [1 ]deptVancouver Prostate Centre , University of British Columbia , Vancouver, Canada;
                [2 ]deptDepartment of Urology , Ludwig-Maximilians-University , Munich, Germany
                Author notes

                Contributions: (I) Conception and design: Both authors; (II) Administrative support: PC Black; (III) Provision of study materials or patients: None; (IV) Collection and assembly of data: Both authors; (V) Data analysis and interpretation: Both authors; (VI) Manuscript writing: Both authors; (VII) Final approval of manuscript: Both authors.

                Correspondence to: Dr. Peter C. Black. Vancouver Prostate Centre, University of British Columbia, Level 6, 2775 Laurel St, Vancouver, BC V5Z 1M9, Canada. Email: pblack@ 123456mail.ubc.ca .
                Article
                tau-10-10-4014
                10.21037/tau-20-1177
                8575593
                34804844
                619bddd9-6be5-4a29-898b-dfb4dbc679de
                2021 Translational Andrology and Urology. All rights reserved.

                Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0.

                History
                : 18 August 2020
                : 19 January 2021
                Categories
                Review Article on Management of Advanced Genitourinary Malignancies

                urothelial carcinoma,immunotherapy,chemotherapy,targeted therapy,antibody drug conjugate

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