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      Bladder cancer, a unique model to understand cancer immunity and develop immunotherapy approaches

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          Abstract

          With the mechanistic understanding of immune checkpoints and success in checkpoint blockade using antibodies for the treatment of certain cancers, immunotherapy has become one of the hottest areas in cancer research, with promise of long‐lasting therapeutic effect. Currently, however, only a proportion of cancers have a good response to checkpoint inhibition immunotherapy. Better understanding of the cancer response and resistance mechanisms is essential to fully explore the potential of immunotherapy to cure the majority of cancers. Bladder cancer, one of the most common and aggressive malignant diseases, has been successfully treated both at early and advanced stages by different immunotherapeutic approaches, bacillus Calmette–Guérin (BCG) intravesical instillation and anti‐PD‐1/PD‐L1 immune checkpoint blockade, respectively. Therefore, it provides a good model to investigate cancer immune response mechanisms and to improve the efficiency of immunotherapy. Here, we review bladder cancer immunotherapy with equal weight on BCG and anti‐PD‐1/PD‐L1 therapies and demonstrate why and how bladder cancer can be used as a model to study the predictors and mechanisms of cancer immune response and shine light on further development of immunotherapy approaches and response predictive biomarkers to improve immunotherapy of bladder cancer and other malignancies. We review the success of BCG and anti‐PD‐1/PD‐L1 treatment of bladder cancer, the underlying mechanisms and the therapeutic response predictors, including the limits to our knowledge. We then highlight briefly the adaptation of immunotherapy approaches and predictors developed in other cancers for bladder cancer therapy. Finally, we explore the potential of using bladder cancer as a model to investigate cancer immune response mechanisms and new therapeutic approaches, which may be translated into immunotherapy of other human cancers. © 2019 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

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          Tumor mutational load predicts survival after immunotherapy across multiple cancer types

          Immune checkpoint inhibitor (ICI) treatments benefit some patients with metastatic cancers, but predictive biomarkers are needed. Findings in select cancer types suggest that tumor mutational burden (TMB) may predict clinical response to ICI.To examine this association more broadly, we analyzed the clinical and genomic data of 1662 advanced cancer patients treated with ICI, and 5371 non-ICI treated patients, whose tumors underwent targeted next-generation sequencing (MSK-IMPACT). Among all patients, higher somatic TMB (highest 20% in each histology) was associated with better OS (HR 0.52; p=1.6 ×10 −6 ). For most cancer histologies, an association between higher TMB and improved survival was observed. The TMB cutpoints associated with improved survival varied markedly between cancer types. These data indicate that TMB is associated with improved survival in patients receiving ICI across a wide variety of cancer types, but that there may not be one universal definition of high TMB.
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            Adaptive resistance to therapeutic PD-1 blockade is associated with upregulation of alternative immune checkpoints

            Despite compelling antitumour activity of antibodies targeting the programmed death 1 (PD-1): programmed death ligand 1 (PD-L1) immune checkpoint in lung cancer, resistance to these therapies has increasingly been observed. In this study, to elucidate mechanisms of adaptive resistance, we analyse the tumour immune microenvironment in the context of anti-PD-1 therapy in two fully immunocompetent mouse models of lung adenocarcinoma. In tumours progressing following response to anti-PD-1 therapy, we observe upregulation of alternative immune checkpoints, notably T-cell immunoglobulin mucin-3 (TIM-3), in PD-1 antibody bound T cells and demonstrate a survival advantage with addition of a TIM-3 blocking antibody following failure of PD-1 blockade. Two patients who developed adaptive resistance to anti-PD-1 treatment also show a similar TIM-3 upregulation in blocking antibody-bound T cells at treatment failure. These data suggest that upregulation of TIM-3 and other immune checkpoints may be targetable biomarkers associated with adaptive resistance to PD-1 blockade.
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              High-dimensional single-cell analysis predicts response to anti-PD-1 immunotherapy

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                Author and article information

                Contributors
                y.j.lu@qmul.ac.uk
                Journal
                J Pathol
                J. Pathol
                10.1002/(ISSN)1096-9896
                PATH
                The Journal of Pathology
                John Wiley & Sons, Ltd (Chichester, UK )
                0022-3417
                1096-9896
                24 June 2019
                October 2019
                : 249
                : 2 ( doiID: 10.1002/path.v249.2 )
                : 151-165
                Affiliations
                [ 1 ] Department of Urology The First Affiliated Hospital and Academy of Medical Sciences, Zhengzhou University Zhengzhou PR China
                [ 2 ] Centre for Experimental Cancer Medicine, Barts Cancer Institute Queen Mary University of London London UK
                [ 3 ] Department of Medical Oncology Barts Health NHS London UK
                [ 4 ] Department of Pharmacology, School of Basic Medical Sciences Zhengzhou University Zhengzhou PR China
                [ 5 ] Department of Immunology Institut Pasteur Paris France
                [ 6 ] Inserm U1223 Paris France
                [ 7 ] Centre for Molecular Oncology Barts Cancer Institute, Queen Mary University of London London UK
                Author notes
                [*] [* ]Correspondence to: Y‐J Lu, Centre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London, John Vane Science Centre, Charterhouse Square, London EC1M 6BQ, UK. E‐mail: y.j.lu@ 123456qmul.ac.uk
                Author information
                https://orcid.org/0000-0001-6174-6621
                Article
                PATH5306
                10.1002/path.5306
                6790662
                31102277
                bc68cdbc-4749-46da-b943-d54a8a4a06ce
                © 2019 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 07 January 2019
                : 02 May 2019
                : 15 May 2019
                Page count
                Figures: 2, Tables: 1, Pages: 15, Words: 9943
                Categories
                Review
                Review
                Custom metadata
                2.0
                October 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.0 mode:remove_FC converted:14.10.2019

                Pathology
                bladder cancer,immune response,immunotherapy,bacillus calmette–guérin,intravesical instillation,immune checkpoint blockade,pd‐1/pd‐l1 inhibitors,biomarkers,model system

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