2
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      A phase I/Ib trial and biological correlate analysis of neoadjuvant SBRT with single-dose durvalumab in HPV-unrelated locally advanced HNSCC

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Five-year survival for human papilloma virus-unrelated head and neck squamous cell carcinomas remain below 50%. We assessed the safety of administering combination hypofractionated stereotactic body radiation therapy with single-dose durvalumab (anti-PD-L1) neoadjuvantly ( n = 21) ( NCT03635164). The primary endpoint of the study was safety, which was met. Secondary endpoints included radiographic, pathologic and objective response; locoregional control; progression-free survival; and overall survival. Among evaluable patients at an early median follow-up of 16 months (448 d or 64 weeks), overall survival was 80.1% with 95% confidence interval (95% CI) (62.0%, 100.0%), locoregional control and progression-free survival were 75.8% with 95% CI (57.5%, 99.8%), and major pathological response or complete response was 75% with 95% exact CI (51.6%, 100.0%). For patients treated with 24 Gy, 89% with 95% CI (57.1%, 100.0%) had MPR or CR. Using high-dimensional multi-omics and spatial data as well as biological correlatives, we show that responders had: (1) an increase in effector T cells; (2) a decrease in immunosuppressive cells; and (3) an increase in antigen presentation post-treatment.

          Abstract

          Karam and colleagues report a phase I/Ib trial in patients with HNSCC treated with neoadjuvant SBRT and anti-PD-L1, and perform high-dimensional analyses of immune correlates of response in the tissue microenvironment and peripheral blood.

          Related collections

          Most cited references70

          • Record: found
          • Abstract: not found
          • Article: not found

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

            Bookmark
            • Record: found
            • Abstract: found
            • Article: found

            Hallmarks of Cancer: The Next Generation

            The hallmarks of cancer comprise six biological capabilities acquired during the multistep development of human tumors. The hallmarks constitute an organizing principle for rationalizing the complexities of neoplastic disease. They include sustaining proliferative signaling, evading growth suppressors, resisting cell death, enabling replicative immortality, inducing angiogenesis, and activating invasion and metastasis. Underlying these hallmarks are genome instability, which generates the genetic diversity that expedites their acquisition, and inflammation, which fosters multiple hallmark functions. Conceptual progress in the last decade has added two emerging hallmarks of potential generality to this list-reprogramming of energy metabolism and evading immune destruction. In addition to cancer cells, tumors exhibit another dimension of complexity: they contain a repertoire of recruited, ostensibly normal cells that contribute to the acquisition of hallmark traits by creating the "tumor microenvironment." Recognition of the widespread applicability of these concepts will increasingly affect the development of new means to treat human cancer. Copyright © 2011 Elsevier Inc. All rights reserved.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Cytoscape: a software environment for integrated models of biomolecular interaction networks.

              Cytoscape is an open source software project for integrating biomolecular interaction networks with high-throughput expression data and other molecular states into a unified conceptual framework. Although applicable to any system of molecular components and interactions, Cytoscape is most powerful when used in conjunction with large databases of protein-protein, protein-DNA, and genetic interactions that are increasingly available for humans and model organisms. Cytoscape's software Core provides basic functionality to layout and query the network; to visually integrate the network with expression profiles, phenotypes, and other molecular states; and to link the network to databases of functional annotations. The Core is extensible through a straightforward plug-in architecture, allowing rapid development of additional computational analyses and features. Several case studies of Cytoscape plug-ins are surveyed, including a search for interaction pathways correlating with changes in gene expression, a study of protein complexes involved in cellular recovery to DNA damage, inference of a combined physical/functional interaction network for Halobacterium, and an interface to detailed stochastic/kinetic gene regulatory models.
                Bookmark

                Author and article information

                Contributors
                sana.karam@cuanschutz.edu
                Journal
                Nat Cancer
                Nat Cancer
                Nature Cancer
                Nature Publishing Group US (New York )
                2662-1347
                25 November 2022
                25 November 2022
                2022
                : 3
                : 11
                : 1300-1317
                Affiliations
                [1 ]GRID grid.430503.1, ISNI 0000 0001 0703 675X, Radiation Oncology, , University of Colorado Denver at Anschutz Medical Campus, ; Aurora, CO USA
                [2 ]GRID grid.430503.1, ISNI 0000 0001 0703 675X, Department of Immunology, , University of Colorado Denver at Anschutz Medical Campus, ; Aurora, CO USA
                [3 ]GRID grid.430503.1, ISNI 0000 0001 0703 675X, Department of Biostatistics and Informatics, Colorado School of Public Health, , University of Colorado Denver, ; Aurora, CO USA
                [4 ]GRID grid.430503.1, ISNI 0000 0001 0703 675X, Department of Anesthesiology, , University of Colorado Anschutz Medical Campus, ; Aurora, CO USA
                [5 ]GRID grid.430503.1, ISNI 0000 0001 0703 675X, Department of Pathology, , University of Colorado Denver at Anschutz Medical Campus, ; Aurora, CO USA
                [6 ]GRID grid.430503.1, ISNI 0000 0001 0703 675X, Department of Neurology, , University of Colorado Denver at Anschutz Medical Campus, ; Aurora, CO USA
                [7 ]GRID grid.430503.1, ISNI 0000 0001 0703 675X, Department of Biochemistry and Molecular Genetics, , University of Colorado Denver at Anschutz Medical Campus, ; Aurora, CO USA
                [8 ]GRID grid.415147.2, ISNI 0000 0004 0402 8537, Department of Radiation Oncology, , University of Colorado, Poudre Valley Hospital, ; Fort Collins, CO USA
                [9 ]GRID grid.430503.1, ISNI 0000 0001 0703 675X, Division of Medical Oncology, , University of Colorado School of Medicine, ; Aurora, CO USA
                [10 ]GRID grid.430503.1, ISNI 0000 0001 0703 675X, Department of Radiology, , University of Colorado Denver at Anschutz Medical Campus, ; Aurora, CO USA
                [11 ]GRID grid.266186.d, ISNI 0000 0001 0684 1394, Department of Otolaryngology Head and Neck Surgery, , University of Colorado, Memorial South Hospital, ; Colorado Springs, CO USA
                [12 ]GRID grid.430503.1, ISNI 0000 0001 0703 675X, Department of Otolaryngology Head and Neck Surgery, , University of Colorado Denver at Anschutz Medical Campus, ; Aurora, CO USA
                Author information
                http://orcid.org/0000-0002-6445-7988
                http://orcid.org/0000-0002-5786-9837
                http://orcid.org/0000-0002-9905-9998
                http://orcid.org/0000-0001-5238-0429
                http://orcid.org/0000-0002-6059-2429
                http://orcid.org/0000-0003-1676-5967
                Article
                450
                10.1038/s43018-022-00450-6
                9701140
                36434392
                66df209e-3435-476d-976b-828c9fc75dd6
                © The Author(s) 2022

                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
                : 26 February 2022
                : 21 September 2022
                Funding
                Funded by: FundRef https://doi.org/10.13039/100000072, U.S. Department of Health & Human Services | NIH | National Institute of Dental and Craniofacial Research (NIDCR);
                Award ID: F31 DE029997
                Award ID: 1R01DE028282-01
                Award ID: 1R01DE028529-01
                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: 1P50CA261605-01
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s), under exclusive licence to Springer Nature America, Inc. 2022

                oral cancer,tumour immunology,cancer,immunotherapy
                oral cancer, tumour immunology, cancer, immunotherapy

                Comments

                Comment on this article