Primary osteosarcoma of the ribs: A report from the Cooperative Osteosarcoma Study Group

Author:

Bodmer Nicole1,Hecker‐Nolting Stefanie2,Friedel Godehard3,Blattmann Claudia2,Kager Leo4,Kessler Torsten5,Kevric Matthias2,Kühne Thomas6,Mettmann Vanessa2,Müller‐Abt Peter7,Sorg Benjamin2,Theobald Matthias8,Bielack Stefan S.29ORCID

Affiliation:

1. Onkologie Universitätskinderspital Zürich Zurique Switzerland

2. Klinikum Stuttgart‐Olgahospital Stuttgart Cancer Center Zentrum für Kinder‐, Jugend‐, und Frauenmedizin Pädiatrie 5 (Onkologie, Hämatologie, Immunologie) Stuttgart Germany

3. Klinik für Thorax‐, Herz‐, und Gefäßchirurgie Sektion Thoraxchirurgie Universitätsklinikum Tübingen Tübingen Germany

4. Abteilung für Kinder und Jugendheilkunde Medizinische Universität Wien St. Anna Kinderspital and St. Anna Children's Cancer Research Institute Vienna Austria

5. Klinik für Innere Medizin A: Hämatologie, Hämostaseologie, Onkologie und Pneumologie Universitätsklinikum Münster Münster Germany

6. Abteilung Hämatologie/Onkologie Universitätskinderspital Beider Basel Basel Switzerland

7. Radiologisches Institut Zentrum für Kinder‐, Jugend‐, und Frauenmedizin Stuttgart Cancer Center Klinikum Stuttgart‐Olgahospital Stuttgart Germany

8. III. Medizinische Klinik und Poliklinik‐Hämatologie, Internistische Onkologie und Pneumologie Universitäres Centrum für Tumorerkrankungen Universitätsmedizin Mainz Mainz Germany

9. Klinik für Kinder‐und Jugendmedizin Pädiatrische Hämatologie und Onkologie Universitätsklinikum Münster Münster Germany

Abstract

AbstractPurposePrimary rib osteosarcoma has not been investigated extensively, and clinical characteristics and optimal therapeutic strategies have not been defined. The authors used the database of the Cooperative Osteosarcoma Study Group (COSS) to analyze this tumor‐site in depth.MethodsThe COSS database was searched for treatment‐naive, high‐grade osteosarcomas of the rib. Affected patients were analyzed for demographic and tumor‐related factors, treatments, and outcomes.ResultsA total of 44 patients (23 males, 21 females; median age, 23 years [range, 6–59]) were identified. Primary metastases were detected in six of 44 (14%) patients. Surgery was performed in 40 of 44 (91%) patients and rendered 35 of 44 (80%) patients macroscopically disease‐free. Chemotherapy was known to have been administered in 43 of 44 (98%) patients and radiotherapy in seven of 42 (17%) (no data for two patients). A good response to chemotherapy was only noted in five (33%) of those 15 evaluable patients who had received any preoperative chemotherapy. After a median follow‐up of 2.49 (0.22–40.35) years for all patients and 6.61 (0.25–40.35) years for 26 survivors (21 of these in first complete remission), 5‐year actuarial overall and event‐free survival were 53.0% (8.5%) and 42.2% (8.1%), respectively. Incomplete tumor surgery was the most notable negative prognostic factor. Osteoblastic histology and a poor response to chemotherapy may have contributed.ConclusionThis large series provides evidence that patients with costal primaries are older than the average osteosarcoma patient, but appear to share the similar tumor biology and—if treated according to standard protocols—prognostic factors with tumors of other sites. Early, preoperative diagnosis and permanent, definitive local control remain major challenges and should contribute to improved outcomes.

Publisher

Wiley

Subject

Cancer Research,Oncology

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