Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

TRACP-5b for Diagnosis and Follow-up of Giant Cell Tumor of Bone

19 de mayo de 2026 actualizado por: St. Anne's University Hospital Brno, Czech Republic

TRACP-5b as a Novel Biomarker for the Diagnosis and Monitoring of Patients With Giant Cell Tumor of Bone

This prospective observational study will evaluate whether the blood biomarker TRACP-5b can help diagnose and monitor patients with giant cell tumor of bone (GCTB). GCTB is a rare but locally aggressive bone tumor that can return even after surgical treatment. Currently, patients require long-term follow-up based mainly on imaging examinations such as CT or MRI, and suspected recurrence often requires invasive biopsy procedures.

TRACP-5b is an enzyme associated with osteoclast activity that can be measured from a blood sample. Previous studies suggest that TRACP-5b levels may reflect disease activity and risk of recurrence in patients with GCTB. In this study, patients with newly diagnosed GCTB and patients already undergoing long-term follow-up after treatment will undergo regular blood sampling for TRACP-5b measurement during routine outpatient visits. Laboratory results will be compared with the patient's clinical condition, imaging findings, and histological results when available.

The goal of the study is to determine whether TRACP-5b could become a reliable and minimally invasive tool for earlier detection of disease recurrence and improved long-term monitoring of patients with giant cell tumor of bone.

Descripción general del estudio

Descripción detallada

Giant cell tumor of bone (GCTB) is a rare, locally aggressive primary bone tumor characterized by osteoclast-like multinucleated giant cells and neoplastic stromal cells. The disease most commonly affects young adults and typically arises in the epiphyseal region of long bones. Although GCTB is classified as an intermediate tumor with limited metastatic potential, it is associated with substantial local bone destruction and a clinically significant risk of local recurrence even after adequate surgical treatment. Standard management consists primarily of surgical treatment, including intralesional curettage with local adjuvant treatment or en bloc resection in selected cases. Despite advances in surgical techniques and the use of systemic therapies such as denosumab in selected patients, long-term surveillance remains essential due to the possibility of recurrence.

Current follow-up strategies are based mainly on periodic imaging examinations, including radiography, computed tomography (CT), and magnetic resonance imaging (MRI). However, imaging-based surveillance may not always detect recurrence at its earliest stage, and suspicious findings frequently require histopathological confirmation through biopsy procedures. At present, there is no routinely established serum biomarker for monitoring disease activity or predicting recurrence in patients with GCTB.

TRACP-5b (tartrate-resistant acid phosphatase isoform 5b) is an enzyme secreted predominantly by activated osteoclasts and reflects osteoclastic bone resorption activity. Since giant cell tumor of bone is characterized by pronounced osteoclast-like giant cell activity, TRACP-5b has emerged as a potential disease-specific biomarker in this patient population. Previous clinical studies have demonstrated significantly elevated serum TRACP-5b levels in patients with active GCTB compared with healthy controls, and several reports suggest that changes in serum TRACP-5b levels may correlate with tumor burden, treatment response, and recurrence risk.

The primary objective of this prospective observational clinical study is to evaluate the diagnostic and predictive value of serum TRACP-5b in patients with histologically confirmed giant cell tumor of bone. The study aims to determine whether serial measurement of TRACP-5b can reliably reflect disease activity and assist in the detection of local recurrence during routine clinical follow-up.

Secondary objectives include evaluation of the temporal dynamics of TRACP-5b during treatment and long-term surveillance, assessment of correlations between TRACP-5b levels and imaging findings, and analysis of the relationship between TRACP-5b levels and histopathological or clinical indicators of disease activity. The study will additionally explore whether implementation of TRACP-5b monitoring could reduce the need for repeated imaging examinations or invasive biopsy procedures in selected clinical situations.

The study is designed as a prospective observational single-center clinical research study conducted at the First Department of Orthopaedic Surgery, St. Anne's University Hospital Brno and Faculty of Medicine, Masaryk University. Approximately 70 patients are expected to be enrolled during the study period. The study population will include both newly diagnosed patients with histologically confirmed giant cell tumor of bone and patients undergoing long-term post-treatment surveillance.

Blood samples for serum TRACP-5b analysis will be collected during routine outpatient visits performed as part of standard clinical care. Approximately 2 mL of venous blood will be obtained at each collection timepoint. In newly diagnosed patients, sampling will be performed at the time of diagnosis and subsequently during scheduled follow-up visits throughout treatment and surveillance. In patients already undergoing long-term follow-up after prior treatment, blood sampling will be performed during routine surveillance visits at approximately 6-month intervals. Samples will be processed and stored at the Department of Clinical Biochemistry of St. Anne's University Hospital Brno and subsequently analyzed using a validated immunochemical assay at the Department of Clinical Biochemistry, University Hospital Ostrava.

TRACP-5b laboratory results will be compared with the patient's clinical condition, including symptoms and physical examination findings, as well as with standard imaging examinations performed during routine oncologic follow-up, including radiography, CT, or MRI where clinically indicated. Available histopathological findings obtained from diagnostic or follow-up biopsy procedures will also be evaluated in relation to TRACP-5b levels when applicable.

The primary outcome measure will be the ability of serum TRACP-5b to detect active disease and local recurrence of giant cell tumor of bone. Secondary outcome measures will include longitudinal changes in TRACP-5b levels during treatment and surveillance, correlations between TRACP-5b and radiologic findings, and evaluation of the feasibility of incorporating TRACP-5b testing into routine clinical management of GCTB patients.

Tipo de estudio

De observación

Inscripción (Estimado)

70

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

      • Brno, Chequia, 60200
        • Reclutamiento
        • First Department of Orthopaedic Surgery, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czechia
        • Contacto:
          • Vasileios Apostolopoulos
          • Número de teléfono: 722101065
          • Correo electrónico: Vasilis.apo@email.cz

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Método de muestreo

Muestra no probabilística

Población de estudio

The study population consists of adult patients with histologically confirmed Giant Cell Tumor of Bone treated or followed at the First Department of Orthopaedic Surgery, St. Anne's University Hospital Brno. The study will include both newly diagnosed patients and patients undergoing long-term surveillance after previous treatment for giant cell tumor of bone. Approximately 70 participants are expected to be enrolled during the study period.

Descripción

Inclusion Criteria:

  • Histologically confirmed Giant Cell Tumor of Bone
  • Newly diagnosed patients or patients undergoing long-term follow-up after previous treatment
  • Age ≥18 years
  • Ability to understand the study procedures and provide written informed consent

Exclusion Criteria:

  • Concurrent diseases significantly affecting bone metabolism, including metabolic bone disorders
  • Inability or unwillingness to provide informed consent
  • Patients unable to comply with routine follow-up procedures
  • Active conditions that may substantially influence serum TRACP-5b levels independently of Giant Cell Tumor of Bone evaluation

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Serum TRACP-5b concentration measured by chemiluminescent immunoassay in patients with active or recurrent giant cell tumor of bone
Periodo de tiempo: Up to 24 months.
Serum TRACP-5b concentration (U/L) measured using a chemiluminescent immunoassay will be evaluated in patients with clinically, radiologically, or histologically confirmed active disease or local recurrence during routine follow-up.
Up to 24 months.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in serum TRACP-5b concentration measured by chemiluminescent immunoassay during treatment and follow-up in giant cell tumor of bone
Periodo de tiempo: Up to 24 months.
Serial serum TRACP-5b concentrations (U/L), measured using a chemiluminescent immunoassay, will be evaluated over time during routine clinical surveillance, treatment, and follow-up in patients with giant cell tumor of bone.
Up to 24 months.
Correlation between serum TRACP-5b concentration and histopathological findings in giant cell tumor of bone
Periodo de tiempo: Up to 24 months.
Correlation between serum TRACP-5b concentration (U/L), measured using a chemiluminescent immunoassay, and histopathological findings obtained from biopsy or surgical specimens when clinically indicated in patients with giant cell tumor of bone.
Up to 24 months.
Serial serum TRACP-5b concentration measurement by chemiluminescent immunoassay during routine clinical follow-up
Periodo de tiempo: Up to 24 months
Evaluation of the feasibility and practical applicability of serial serum TRACP-5b concentration measurements (U/L), performed using a chemiluminescent immunoassay, as a minimally invasive biomarker for long-term surveillance of patients with giant cell tumor of bone.
Up to 24 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Michal Mahdal, M.D., Ph.D., First Department of Orthopedic Surgery, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czechia
  • Investigador principal: Vasileios Apostolopoulos, M.D., Ph.D., First Department of Orthopedic Surgery, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czechia

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de enero de 2026

Finalización primaria (Estimado)

31 de diciembre de 2027

Finalización del estudio (Estimado)

31 de mayo de 2028

Fechas de registro del estudio

Enviado por primera vez

13 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

19 de mayo de 2026

Publicado por primera vez (Actual)

27 de mayo de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

27 de mayo de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

19 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Suscribir