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. 2019 Jan;24(1):110-116.
doi: 10.1634/theoncologist.2017-0574. Epub 2018 Aug 6.

Outcome of First-Line Systemic Treatment for Unresectable Conventional, Dedifferentiated, Mesenchymal, and Clear Cell Chondrosarcoma

Affiliations

Outcome of First-Line Systemic Treatment for Unresectable Conventional, Dedifferentiated, Mesenchymal, and Clear Cell Chondrosarcoma

Annemiek van Maldegem et al. Oncologist. 2019 Jan.

Abstract

Background: Chondrosarcoma is a heterogeneous group of primary bone sarcoma with an excellent overall survival after local therapy. However, the small percentage of patients who have no surgical treatment options have a very poor prognosis. We retrospectively collected data from these patients in four sarcoma centers and compared the progression-free survival (PFS) for the different treatment regimens used for the four chondrosarcoma subtypes.

Materials and methods: Patients diagnosed with unresectable chondrosarcoma in all four major sarcoma centers were included, and data on first-line systemic therapy were retrospectively collected for analysis.

Results: A total of 112 patients were enrolled in this retrospective analysis: 50 conventional, 25 mesenchymal, 34 dedifferentiated, and 3 clear cell chondrosarcoma patients. In conventional chondrosarcoma patients, the longest mean PFS (6.7 months) was found in the group treated with antihormonal therapy. Patients diagnosed with mesenchymal chondrosarcoma were all treated with multidrug chemotherapy, and the mean PFS was 6.7 months. Doxorubicin monotherapy seems to have an unexplained better PFS than doxorubicin-based combination therapy in patients with dedifferentiated chondrosarcoma (5.5 vs. 2.8 months, respectively; p = .275).

Conclusion: Prospective studies need to be conducted based on preclinical work to develop a uniform regimen to treat advanced chondrosarcoma patients according to the diagnosed subtype and improve survival.

Implications for practice: Currently, there are no uniform treatment lines for advanced chondrosarcoma patients, which results in a very diverse group of treatment regimens being used. In this study, the data of 112 patients was collected. It was concluded that some treatment regimens seem to have a better progression-free survival compared with others, and that these results also differ between the chondrosarcoma subtypes. Prospective studies need to be conducted based on preclinical work to develop a uniform regimen to treat advanced chondrosarcoma patients according to the diagnosed histological subtype to improve their survival.

Keywords: Chondrosarcoma; Progression‐free survival; Retrospective; Systemic treatment; Unresectable.

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Conflict of interest statement

Disclosures of potential conflicts of interest may be found at the end of this article.

Figures

Figure 1.
Figure 1.
Swimmers plot for the different regimens used (PFS in months). Swimmer plot of the different treatment regimens used after unresectability comparing the PFS for conventional (A), dedifferentiated (B), mesenchymal (C), and clear cell (D) subtype.Abbreviations: VAC/IE, vincristine, doxorubicin, cyclofosfamide/ifosfamide, etoposide; VDC/VID, vincristine, doxorubicin, cyclophosphamide/vincristine, doxorubicin, ifosfamide; VID, vincristine, ifosfamide, doxorubicin; VIDE, vincristine, ifosfamide, doxorubicin, etoposide; VID/IE, vincristine, ifosfamide, doxorubicin/ifosfamide, etoposide.
Figure 2.
Figure 2.
Progression‐free survival for first treatment regimen after unresectability for patients divided in the different chondrosarcoma subtypes.
Figure 3.
Figure 3.
Overall survival after unresectability for all patients subdivided in chondrosarcoma subtypes.

References

    1. Fletcher CDM, Bridge JA, Hogendoorn PC. et al., eds. WHO Classification of Tumours of Soft Tissue and Bone. 4th ed Lyon, France: IARC Press, 2013:264.
    1. Cesari M, Bertoni F, Bacchini P et al. Mesenchymal chondrosarcoma. An analysis of patients treated at a single institution. Tumori 2007;93:423–427. - PubMed
    1. Dantonello TM, Int‐Veen C, Leuschner I et al. Mesenchymal chondrosarcoma of soft tissues and bone in children, adolescents, and young adults: Experiences of the CWS and COSS study groups. Cancer 2008;112:2424–2431. - PubMed
    1. Grimer RJ, Gosheger G, Taminiau A et al. Dedifferentiated chondrosarcoma: Prognostic factors and outcome from a European group. Eur J Cancer 2007;43:2060–2065. - PubMed
    1. Staals EL, Bacchini P, Bertoni F. Dedifferentiated central chondrosarcoma. Cancer 2006;106:2682–2691. - PubMed

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