21
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Primary cardiac sarcomas: A clinicopathologic study in a single institution with 25 years of experience with an emphasis on MDM2 expression and adjuvant therapy for prognosis

      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

          Background

          Primary cardiac sarcomas are rare and their clinicopathologic features are heterogeneous. Among them, particularly intimal sarcoma is a diagnostic challenge due to nonspecific histologic features. Recently, MDM2 amplification reported to be a characteristic genetic event in the intimal sarcoma. In this study, we aimed to identify the types and incidence of primary cardiac sarcomas that occurred over 25 years in tertiary medical institutions, and to find clinicopatholgical significance through reclassification of diagnoses using additional immunohistochemistry (IHC).

          Methods

          We reviewed the primary cardiac sarcoma cases between January 1993 and June 2018 at Asan Medical Center, South Korea, with their clinicopathologic findings, and reclassified the subtypes, especially using IHC for MDM2 and then, analyzed the significance of prognosis.

          Results

          Forty‐eight (6.8%) cases of a primary cardiac sarcoma were retrieved. The tumors most frequently involved the right atrium ( n = 25, 52.1%), and the most frequent tumor subtype was angiosarcoma ( n = 23, 47.9%). Seven cases (53.8%) were newly reclassified as an intimal sarcoma by IHC for MDM2. Twenty‐nine (60.4%) patients died of disease (mean, 19.8 months). Four patients underwent a heart transplantation and had a median survival of 26.8 months. This transplantation group tended to show good clinical outcomes in the earlier stages, but this was not statistically significant ( p = 0.318). MDM2 positive intimal sarcoma showed the better overall survival ( p = 0.003) than undifferentiated pleomorphic sarcoma. Adjuvant treatment is beneficial for patient survival ( p < 0.001), particularly in angiosarcoma ( p < 0.001), but not in intimal sarcoma ( p = 0.154).

          Conclusion

          Our study supports the use of adjuvant treatment in primary cardiac sarcoma, as it was associated with a significantly better overall survival rate. Further consideration of tumor histology may be important in determining the optimal use of adjuvant treatment for different types of sarcomas. Therefore, accurate diagnosis by MDM2 test is important condsidering patient's prognosis and treatment.

          Related collections

          Most cited references36

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

          Pembrolizumab in advanced soft-tissue sarcoma and bone sarcoma (SARC028): a multicentre, two-cohort, single-arm, open-label, phase 2 trial.

          Patients with advanced sarcomas have a poor prognosis and few treatment options that improve overall survival. Chemotherapy and targeted therapies offer short-lived disease control. We assessed pembrolizumab, an anti-PD-1 antibody, for safety and activity in patients with advanced soft-tissue sarcoma or bone sarcoma.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Amplification of a gene encoding a p53-associated protein in human sarcomas.

            Despite extensive data linking mutations in the p53 gene to human tumorigenesis, little is known about the cellular regulators and mediators of p53 function. MDM2 is a strong candidate for one such cellular protein; the MDM2 gene was originally identified by virtue of its amplification in a spontaneously transformed derivative of mouse BALB/c cells and the MDM2 protein subsequently shown to bind to p53 in rat cells transfected with p53 genes. To determine whether MDM2 plays a role in human cancer, we have cloned the human MDM2 gene. Here we show that recombinant-derived human MDM2 protein binds human p53 in vitro, and we use MDM2 clones to localize the human MDM2 gene to chromosome 12q13-14. Because this chromosomal position appears to be altered in many sarcomas, we looked for changes in human MDM2 in such cancers. The gene was amplified in over a third of 47 sarcomas, including common bone and soft tissue forms. These results are consistent with the hypothesis that MDM2 binds to p53, and that amplification of MDM2 in sarcomas leads to escape from p53-regulated growth control. This mechanism of tumorigenesis parallels that for virally-induced tumours, in which viral oncogene products bind to and functionally inactivate p53.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Nivolumab with or without ipilimumab treatment for metastatic sarcoma (Alliance A091401): two open-label, non-comparative, randomised, phase 2 trials

              Patients with metastatic sarcoma have limited treatment options. Nivolumab and ipilimumab are monoclonal antibodies targeting PD-1 and CTLA-4, respectively. We investigated the activity and safety of nivolumab alone or in combination with ipilimumab in patients with locally advanced, unresectable, or metastatic sarcoma.
                Bookmark

                Author and article information

                Contributors
                songjs@amc.seoul.kr
                Journal
                Cancer Med
                Cancer Med
                10.1002/(ISSN)2045-7634
                CAM4
                Cancer Medicine
                John Wiley and Sons Inc. (Hoboken )
                2045-7634
                03 July 2023
                August 2023
                : 12
                : 16 ( doiID: 10.1002/cam4.v12.16 )
                : 16815-16828
                Affiliations
                [ 1 ] Department of Pathology University of Ulsan College of Medicine, Asan Medical Center Seoul Republic of Korea
                [ 2 ] Department of Radiology and Research Institute of Radiology University of Ulsan College of Medicine, Asan Medical Center Seoul Republic of Korea
                [ 3 ] Department of Thoracic and Cardiovascular Surgery University of Ulsan College of Medicine, Asan Medical Center Seoul Republic of Korea
                Author notes
                [*] [* ] Correspondence

                Joon Seon Song, Department of Pathology, University of Ulsan College of Medicine, Asan Medical Center, 88, Olympic‐ro 43‐gil, Songpa‐gu, Seoul 05505, Republic of Korea.

                Email: songjs@ 123456amc.seoul.kr

                Author information
                https://orcid.org/0000-0001-6783-4016
                https://orcid.org/0000-0002-7429-4254
                Article
                CAM46303 CAM4-2022-10-4558.R2
                10.1002/cam4.6303
                10501235
                37395142
                04a337e1-5384-418b-87d9-dca0303ac70b
                © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

                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
                : 04 June 2023
                : 18 October 2022
                : 22 June 2023
                Page count
                Figures: 5, Tables: 2, Pages: 14, Words: 6591
                Funding
                Funded by: Asan Institute for Life Sciences, Asan Medical Center , doi 10.13039/501100005006;
                Award ID: 2018IL‐0664
                Categories
                Research Article
                RESEARCH ARTICLES
                Clinical Cancer Research
                Custom metadata
                2.0
                August 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.3.3 mode:remove_FC converted:14.09.2023

                Oncology & Radiotherapy
                cardiac sarcoma,heart transplantation,intimal sarcoma,mdm2,survival
                Oncology & Radiotherapy
                cardiac sarcoma, heart transplantation, intimal sarcoma, mdm2, survival

                Comments

                Comment on this article