Your browser doesn't support javascript.
loading
Ultra-Late Osteosarcoma Recurrences: An Analysis of 17 Cooperative Osteosarcoma Study Group Patients with a First Recurrence Detected More Than 10 Years After Primary Tumor Diagnosis.
Hecker-Nolting, Stefanie; Kager, Leo; Kühne, Thomas; Baumhoer, Daniel; Blattmann, Claudia; Friedel, Godehard; von Kalle, Thekla; Kevric, Mathias; Mayer-Steinacker, Regine; Schwarz, Rudolf; Sorg, Benjamin; Wirth, Thomas; Bielack, Stefan S.
Affiliation
  • Hecker-Nolting S; Cooperative Osteosarcoma Study Group, Pediatrics 5 (Oncology, Hematology, Immunology), Center for Pediatric, Adolescent and Women's Medicine, Stuttgart Cancer Center, Klinikum Stuttgart-Olgahospital, Stuttgart, Germany.
  • Kager L; Department of Pediatrics, Medical University Vienna and St. Anna Children's Cancer Research Institute (CCRI), St. Anna Children's Hospital, Vienna, Austria.
  • Kühne T; Department of Oncology/Hematology, University Children's Hospital Basel, Basel, Switzerland.
  • Baumhoer D; Bone Tumor Reference Center, Institute of Medical Genetics and Pathology, University Hospital Basel and University of Basel, Basel, Switzerland.
  • Blattmann C; Cooperative Osteosarcoma Study Group, Pediatrics 5 (Oncology, Hematology, Immunology), Center for Pediatric, Adolescent and Women's Medicine, Stuttgart Cancer Center, Klinikum Stuttgart-Olgahospital, Stuttgart, Germany.
  • Friedel G; Clinic for Thoracic, Heart and Vascular Surgery, University Hospital Tuebingen, Tuebingen, Germany.
  • von Kalle T; Center for Pediatric, Adolescent and Women's Medicine, Stuttgart Cancer Center, Radiologic Institute, Klinikum Stuttgart-Olgahospital, Stuttgart, Germany.
  • Kevric M; Cooperative Osteosarcoma Study Group, Pediatrics 5 (Oncology, Hematology, Immunology), Center for Pediatric, Adolescent and Women's Medicine, Stuttgart Cancer Center, Klinikum Stuttgart-Olgahospital, Stuttgart, Germany.
  • Mayer-Steinacker R; Division of Hematology and Oncology, Department of Internal Medicine, Ulm University Hospital, Ulm, Germany.
  • Schwarz R; Department of Radiation Oncology, University Medical Center Eppendorf, Hamburg, Germany.
  • Sorg B; Cooperative Osteosarcoma Study Group, Pediatrics 5 (Oncology, Hematology, Immunology), Center for Pediatric, Adolescent and Women's Medicine, Stuttgart Cancer Center, Klinikum Stuttgart-Olgahospital, Stuttgart, Germany.
  • Wirth T; Department of Orthopaedics, Center for Pediatric, Adolescent and Women's Medicine, Stuttgart Cancer Center, Klinikum Stuttgart-Olgahospital, Stuttgart, Germany.
  • Bielack SS; Cooperative Osteosarcoma Study Group, Pediatrics 5 (Oncology, Hematology, Immunology), Center for Pediatric, Adolescent and Women's Medicine, Stuttgart Cancer Center, Klinikum Stuttgart-Olgahospital, Stuttgart, Germany.
J Adolesc Young Adult Oncol ; 12(1): 76-82, 2023 02.
Article in En | MEDLINE | ID: mdl-36454220
ABSTRACT

Purpose:

Osteosarcoma is a typical malignancy of childhood and adolescence. Recurrences usually occur early, but rarely may arise after decades of remission. Little is known about these very late events and we set out to fill this knowledge gap.

Methods:

The database of the Cooperative Osteosarcoma Study Group (COSS) was searched for patients with a first recurrence of a high-grade central osteosarcoma occurring >10 years after diagnosis of the primary disease. Identified patients were analyzed for demographic, tumor-, and treatment-related factors as well as outcomes.

Results:

Among a total of 1,178 10-year relapse-free survivors, 17 affected patients were identified. Only five of these had a documented good response to initial chemotherapy. No presenting factor was identified to predict these very late events. Prognosis was generally very poor despite intensive multimodal therapy. Inoperability of the recurrences seems to have constituted a major limiting factor.

Conclusion:

Osteosarcoma patients should be followed for potential recurrences for well >10 years from initial diagnosis. Only through such an extended truly long-term follow-up and a structured transition of young patients can these be detected while they are still operable and, hence, potentially curable.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Neoplasms / Osteosarcoma Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Humans Language: En Journal: J Adolesc Young Adult Oncol Year: 2023 Type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Neoplasms / Osteosarcoma Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Humans Language: En Journal: J Adolesc Young Adult Oncol Year: 2023 Type: Article Affiliation country: Germany