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      Gemcitabine and cisplatin plus nivolumab as organ-sparing treatment for muscle-invasive bladder cancer: a phase 2 trial

      research-article
      1 , 2 , , 3 , 1 , 4 , 5 , 6 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 , 25 , 1 , 2 , 14 , 15 , 15 , 15 , 2 , 16 , 14 , 17 , 18 , 16 , 16 , 16 , 19 , 1 , 20 , 21 , 22 , 23 , 2 , 15 , 16 , 24 , 24 , 2 , 15 , 16 , 2 , 17 , 18 , 1 , 20 , 2 , 15 , 16 , 23 , 7
      Nature Medicine
      Nature Publishing Group US
      Phase II trials, Translational research, Bladder cancer, Cancer immunotherapy, Chemotherapy

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          Abstract

          Cystectomy is a standard treatment for muscle-invasive bladder cancer (MIBC), but it is life-altering. We initiated a phase 2 study in which patients with MIBC received four cycles of gemcitabine, cisplatin, plus nivolumab followed by clinical restaging. Patients achieving a clinical complete response (cCR) could proceed without cystectomy. The co-primary objectives were to assess the cCR rate and the positive predictive value of cCR for a composite outcome: 2-year metastasis-free survival in patients forgoing immediate cystectomy or <ypT1N0 in patients electing immediate cystectomy. Seventy-six patients were enrolled; of these, 33 achieved a cCR (43%, 95% confidence interval (CI): 32%, 55%), and 32 of 33 who achieved a cCR opted to forgo immediate cystectomy. The positive predictive value of cCR was 0.97 (95% CI: 0.91, 1), meeting the co-primary objective. The most common adverse events were fatigue, anemia, neutropenia and nausea. Somatic alterations in pre-specified genes ( ATM, RB1, FANCC and ERCC2) or increased tumor mutational burden did not improve the positive predictive value of cCR. Exploratory analyses of peripheral blood mass cytometry and soluble protein analytes demonstrated an association between the baseline and on-treatment immune contexture with clinical outcomes. Stringently defined cCR after gemcitabine, cisplatin, plus nivolumab facilitated bladder sparing and warrants further study. ClinicalTrials.gov identifier: NCT03451331.

          Abstract

          In a phase 2 trial, the combination of gemcitabine, cisplatin and anti-PD-1 led to a clinical complete response in 43% of patients with muscle-invasive bladder cancer, which facilitated bladder sparing and was associated with long-term bladder-intact metastasis-free survival.

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          Most cited references49

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Standards and Guidelines for the Interpretation of Sequence Variants: A Joint Consensus Recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology

            The American College of Medical Genetics and Genomics (ACMG) previously developed guidance for the interpretation of sequence variants. 1 In the past decade, sequencing technology has evolved rapidly with the advent of high-throughput next generation sequencing. By adopting and leveraging next generation sequencing, clinical laboratories are now performing an ever increasing catalogue of genetic testing spanning genotyping, single genes, gene panels, exomes, genomes, transcriptomes and epigenetic assays for genetic disorders. By virtue of increased complexity, this paradigm shift in genetic testing has been accompanied by new challenges in sequence interpretation. In this context, the ACMG convened a workgroup in 2013 comprised of representatives from the ACMG, the Association for Molecular Pathology (AMP) and the College of American Pathologists (CAP) to revisit and revise the standards and guidelines for the interpretation of sequence variants. The group consisted of clinical laboratory directors and clinicians. This report represents expert opinion of the workgroup with input from ACMG, AMP and CAP stakeholders. These recommendations primarily apply to the breadth of genetic tests used in clinical laboratories including genotyping, single genes, panels, exomes and genomes. This report recommends the use of specific standard terminology: ‘pathogenic’, ‘likely pathogenic’, ‘uncertain significance’, ‘likely benign’, and ‘benign’ to describe variants identified in Mendelian disorders. Moreover, this recommendation describes a process for classification of variants into these five categories based on criteria using typical types of variant evidence (e.g. population data, computational data, functional data, segregation data, etc.). Because of the increased complexity of analysis and interpretation of clinical genetic testing described in this report, the ACMG strongly recommends that clinical molecular genetic testing should be performed in a CLIA-approved laboratory with results interpreted by a board-certified clinical molecular geneticist or molecular genetic pathologist or equivalent.
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              Association of tumour mutational burden with outcomes in patients with advanced solid tumours treated with pembrolizumab: prospective biomarker analysis of the multicohort, open-label, phase 2 KEYNOTE-158 study

              Tumour mutational burden (TMB) has been retrospectively correlated with response to immune checkpoint blockade. We prospectively explored the association of high tissue TMB (tTMB-high) with outcomes in ten tumour-type-specific cohorts from the phase 2 KEYNOTE-158 study, which assessed the anti-PD-1 monoclonal antibody pembrolizumab in patients with selected, previously treated, advanced solid tumours.
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                Author and article information

                Contributors
                matthew.galsky@mssm.edu
                Journal
                Nat Med
                Nat Med
                Nature Medicine
                Nature Publishing Group US (New York )
                1078-8956
                1546-170X
                2 October 2023
                2 October 2023
                2023
                : 29
                : 11
                : 2825-2834
                Affiliations
                [1 ]Division of Hematology and Medical Oncology, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) New York, NY USA
                [2 ]Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) New York, NY USA
                [3 ]GRID grid.488628.8, Department of Urology, , Keck School of Medicine of USC, Norris Comprehensive Cancer Center, ; Los Angeles, CA USA
                [4 ]Department of Oncological Sciences, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) New York, NY USA
                [5 ]Department of Urology, City of Hope Comprehensive Cancer Center, ( https://ror.org/00w6g5w60) Duarte, CA USA
                [6 ]Department of Radiology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) New York, NY USA
                [7 ]Department of Medical Oncology & Therapeutics, City of Hope Comprehensive Cancer Center, ( https://ror.org/00w6g5w60) Duarte, CA USA
                [8 ]Division of Hematology and Medical Oncology, Oregon Health and Science University, ( https://ror.org/009avj582) Portland, OR USA
                [9 ]Department of Urology, University of Utah, ( https://ror.org/03r0ha626) Salt Lake City, UT USA
                [10 ]GRID grid.488628.8, Division of Hematology and Medical Oncology, , Keck School of Medicine of USC, Norris Comprehensive Cancer Center, ; Los Angeles, CA USA
                [11 ]Division of Hematology and Medical Oncology, University of Pennsylvania Abramson Cancer Center, ( https://ror.org/00b30xv10) Philadelphia, PA USA
                [12 ]Division of Hematology and Medical Oncology, University of Wisconsin Carbone Cancer Center, ( https://ror.org/01e4byj08) Madison, WI USA
                [13 ]Genentech, ( https://ror.org/04gndp242) South San Francisco, CA USA
                [14 ]Department of Pathology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) New York, NY USA
                [15 ]Human Immune Monitoring Center, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) New York, NY USA
                [16 ]Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) New York, NY USA
                [17 ]Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) New York, NY USA
                [18 ]Icahn Institute for Data Science and Genomic Technology, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) New York, NY USA
                [19 ]Department of Pathology, Molecular and Cell-based Medicine, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) New York, NY USA
                [20 ]Gene Dx, Stamford, CT USA
                [21 ]GRID grid.38142.3c, ISNI 000000041936754X, Department of Radiation Oncology, , Dana-Farber Cancer Institute/Brigham & Women’s Hospital, Harvard Medical School, ; Boston, MA USA
                [22 ]Department of Radiation Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) New York, NY USA
                [23 ]Department of Urology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, ( https://ror.org/04a9tmd77) New York, NY USA
                [24 ]Department of Biostatistics and Medical Informatics, University of Wisconsin Carbone Cancer Center, ( https://ror.org/01e4byj08) Madison, WI USA
                [25 ]GRID grid.59734.3c, ISNI 0000 0001 0670 2351, Present Address: Formerly with the Icahn School of Medicine at Mount Sinai, ; New York, NY USA
                Author information
                http://orcid.org/0000-0001-7655-9378
                http://orcid.org/0000-0001-8948-5689
                http://orcid.org/0000-0002-6948-0626
                http://orcid.org/0000-0001-6041-1344
                http://orcid.org/0000-0002-6452-7405
                http://orcid.org/0000-0001-6982-2078
                http://orcid.org/0000-0001-6860-2401
                http://orcid.org/0000-0003-1865-4187
                http://orcid.org/0000-0001-9267-2426
                http://orcid.org/0000-0003-0834-8178
                http://orcid.org/0000-0001-5643-9520
                http://orcid.org/0000-0002-1712-0848
                Article
                2568
                10.1038/s41591-023-02568-1
                10667093
                37783966
                c2ffe183-60da-4d04-ac57-d31ed102d332
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 10 January 2023
                : 24 August 2023
                Funding
                Funded by: FundRef https://doi.org/10.13039/100001368, V Foundation for Cancer Research (V Foundation);
                Award ID: T2019-011
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100002491, Bristol-Myers Squibb (Bristol-Myers Squibb Company);
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award ID: CA209-9AU
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100000054, U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI);
                Award ID: P30 CA196521
                Award ID: U24CA224319
                Award Recipient :
                Funded by: Foundation for the National Institutes of Health (FNIH)/Partnership for Accelerating Cancer Therapies (PACT)
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                © Springer Nature America, Inc. 2023

                Medicine
                phase ii trials,translational research,bladder cancer,cancer immunotherapy,chemotherapy
                Medicine
                phase ii trials, translational research, bladder cancer, cancer immunotherapy, chemotherapy

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