Literature DB >> 19863225

Synchronous and metachronous skeletal osteosarcomas: the Norwegian Radium Hospital experience.

Petter Brandal1, Bodil Bjerkehagen, Oyvind S Bruland, Sigmund Skjeldal, Trond V Bogsrud, Kirsten S Hall.   

Abstract

Background. The purpose of this work was to study clinical and histopathological tumor characteristics of patients treated for synchronous or metachronous skeletal osteosarcoma at The Norwegian Radium Hospital from January 1, 1980 to January 1, 2008. Patients and methods. The hospital sarcoma database and patient records were reviewed to identify cases with synchronous or metachronous skeletal osteosarcoma. Patients with more than one skeletal lesion in the absence of pulmonary or other soft tissue tumor manifestations were included in the study, and histopathological slides from these tumors were reviewed. Results. Among a total of 297 registered osteosarcoma patients, six with synchronous (2.0%) and 10 with metachronous (3.4%) skeletal osteosarcomas were identified. All tumors were of high-grade malignancy. Treatment at the time of the first osteosarcoma diagnosis was in most cases wide resections and multi-agent chemotherapy according to international protocols, whereas the treatment for metachronous tumors was individualized and in general much less intensive. One patient was diagnosed with Li-Fraumeni syndrome, two other individuals may be suspected to have the same syndrome, and yet another patient had previously been treated for a bilateral retinoblastoma. Thirteen patients are dead, 11 from metastatic osteosarcoma, one from myelodysplastic syndrome, and one from wound infection and methotrexate-related nephrotoxicity; whereas three patients are still alive with no evidence of osteosarcoma. Conclusions. The prognosis for patients with synchronous and metachronous skeletal osteosarcoma is poor. However, because long-term survival is seen, aggressive treatment to selected cases, e.g., patients with an osteosarcoma predisposing syndrome and/or late occurring metachronous tumours, is justified. Revealing a possible clonal relationship between these tumors, e.g., by karyotyping, may be of interest for estimating prognosis and guide therapy intensiveness.

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Year:  2009        PMID: 19863225     DOI: 10.3109/02841860903032809

Source DB:  PubMed          Journal:  Acta Oncol        ISSN: 0284-186X            Impact factor:   4.089


  6 in total

1.  Bilateral synchronous tibial periosteal osteosarcoma with familial incidence.

Authors:  Aditya V Maheshwari; James S Jelinek; Nita L Seibel; Aurelia M Meloni-Ehrig; Dhruv Kumar; Robert M Henshaw
Journal:  Skeletal Radiol       Date:  2012-02-17       Impact factor: 2.199

2.  Three Metachronous Osteosarcomas within 22 Years without Pulmonary Metastases: A Case Report and Review of the Literature.

Authors:  Ulrike Michaela Pirker-Frühauf; Jörg Friesenbichler; Katharina Rabitsch; Bernadette Liegl-Atzwanger; Thomas Bauernhofer; Reinhard Windhager; Andreas Leithner
Journal:  Case Rep Orthop       Date:  2013-12-25

3.  Prognostic factors and treatment results of high-grade osteosarcoma in norway: a scope beyond the "classical" patient.

Authors:  Kjetil Berner; Kirsten Sundby Hall; Odd R Monge; Harald Weedon-Fekjær; Olga Zaikova; Øyvind S Bruland
Journal:  Sarcoma       Date:  2015-02-17

4.  Metachronous extraskeletal (soft tissue) epithelioid osteogenic sarcoma: a case report.

Authors:  Gireesha Rawal; Charanjeet Ahluwalia; Amit Kumar Yadav; Rashmi Arora
Journal:  J Med Case Rep       Date:  2019-05-09

5.  Epidemiology and therapies for metastatic sarcoma.

Authors:  Ernest K Amankwah; Anthony P Conley; Damon R Reed
Journal:  Clin Epidemiol       Date:  2013-05-16       Impact factor: 4.790

Review 6.  Metastatic Progression of Osteosarcomas: A Review of Current Knowledge of Environmental versus Oncogenic Drivers.

Authors:  Guillaume Anthony Odri; Joëlle Tchicaya-Bouanga; Diane Ji Yun Yoon; Dominique Modrowski
Journal:  Cancers (Basel)       Date:  2022-01-12       Impact factor: 6.639

  6 in total

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