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NCT Number: NCT03963531

Patterns of Care and Outcomes in Patients With Metastatic Bone Tumors (METABONE)

Bone tumors make up about 3-5% of childhood cancers and less than 1% of cancers in adults. Of these, osteosarcoma (OSS) is the most commonly diagnosed primary malignant bone tumor. OSS is a primary mesenchymal malignant tumor of bone characterized by the production of osteoid or immature bone by the malignant cells. Despite its rarity, OSS is the most common primary malignancy of bone in children and adolescents, and the fifth most common malignancy among adolescents and young adults aged 15 to 19 years.

Ewing sarcoma (ES) is the second most frequent bone tumors in children and may arise also in soft tissues. This disease encompasses tumors formerly known as Askin's tumor, Peripheral Neuroectodermal Tumor (PNET) and the Ewing Sarcoma Family of Tumors (ESFT).

Chondrosarcoma are rare sarcoma reputed chemorefractory in the non-operable setting and for which little is known in terms of palliative management with systemic treatments.

Despite adequate loco-regional treatment, up to 40% of patients with sarcoma, soft tissue or bone, will develop metastatic disease. When metastases are detected, the standard of care is based on palliative chemotherapy with a median survival in this setting of only 18 months.

A slight improvement has been obtained over years thank to registration of a couple of drugs such as Trabectedin and Pazopanib, the first antiangiogenic registered for soft tissue sarcoma patients. Pazopanib is routinely prescribed worldwide after failure of first line chemotherapy in soft tissue sarcoma. However, bone tumors have not benefited from these small advances yet and treatment still rely on chemotherapy combining doxorubicine cisplatinum and ifosfamide. There is no standard in relapse and palliative settings, and after failure of these agents the survival is very poor. Bone sarcomas are therefore tumors with very little available data and low level of evidence on palliative systemic treatments in clinical trials and in the real life setting.

The primary objective of the METABONE study is to conduct a retrospective descriptive analysis of clinic-biological profiles, patterns of care and modalities of treatment for a set of patients with malignant bone tumors in a real-life national setting.

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Key information

Age range

12 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Institut Bergonié, Comprehensive Cancer Center

Bordeaux, 33076, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged >= 12 years
  • Informed consent obtained for inclusion in the databases
  • Histology of Ewing's sarcoma type, osteosarcoma, chondrosarcoma
  • Diagnostic between 2008 and 2018

Treatment and study plan

Any cancer treatment

Other

chemotherapy, surgery, radiotherapy, interventional radiology.

Other names: intervention as per recommendations

Primary outcomes

  1. Overall Survival (OS)

    Time frame: 5 years

    Interval between the diagnosis of metastatic disease or the first-line systemic therapy onset and the time of death.

  2. Time to Next Treatment (TNT)

    Time frame: 5 years

    time from the systemic treatment onset to the next treatment or death due to any cause, whichever comes first

Sponsors and collaborators

Lead sponsor

Institut Bergonié

Other

Collaborators

  • French Sarcoma Group

Registry information

Official study title

Patterns of Care and Outcomes of Patients With METAstatic BONE Tumors in a Real-life Setting

Acronym: METABONE

Important dates

Study start
2008
Primary completion
2024
Study completion
2025
First posted
May 24, 2019
Registry last updated
Dec 10, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.