ClinicalTrials.gg
RecruitingNCT07609277Updated May 27, 2026

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

An observational study in Giant Cell Tumor of Bone, TRACP-5b and Disease Surveillance and Monitoring, sponsored by St. Anne's University Hospital Brno, Czech Republic. Recruiting at 1 site in Czechia. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-27.

Sponsored by St. Anne's University Hospital Brno, Czech Republic · Observational

From the registry’s dates

  • Started Jan 2026; still recruiting 10 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
70
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Giant Cell Tumor of Bone
  • TRACP-5b
  • Disease Surveillance and Monitoring
  • Tartrate-Resistant Acid Phosphatase 5b

Keywords

  • Giant Cell Tumor of Bone
  • Tartrate-Resistant Acid Phosphatase 5b
  • Bone Tumor Biomarker
  • Serum Biomarkers
03

In context

Giant Cell Tumor of Bone

23 studies on the registry are indexed under Giant Cell Tumor of Bone; 7 are open to participants now.

Browse Giant Cell Tumor of Bone studies →

Lead sponsor

St. Anne's University Hospital Brno, Czech Republic is the lead sponsor of 25 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

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.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 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

Exclusion criteria

Exclusion Criteria:

  • Concurrent diseases significantly affecting bone metabolism, including metabolic bone disorders
  • Inability or unwillingness to provide
  • 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
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
70 participants (estimated)
Target follow-up
24 Months
Patient registry
Yes
Biospecimen retention
Samples without dna

Interventions

  • Diagnostic testTartrate-Resistant Acid Phosphatase 5b

    Serial measurement of serum TRACP-5b levels in patients with giant cell tumor of bone during routine outpatient follow-up. Peripheral venous blood samples will be collected at scheduled clinical visits and analyzed using a validated immunochemical assay to evaluate the relationship between TRACP-5b levels, disease activity, treatment response, and local recurrence.

06

What researchers measure

Primary outcomes

  1. Serum TRACP-5b concentration measured by chemiluminescent immunoassay in patients with active or recurrent giant cell tumor of bone

    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.

    Time frame: Up to 24 months.

Secondary outcomes

  1. Change in serum TRACP-5b concentration measured by chemiluminescent immunoassay during treatment and follow-up in giant cell tumor of bone

    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.

    Time frame: Up to 24 months.

  2. Correlation between serum TRACP-5b concentration and histopathological findings in giant cell tumor of bone

    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.

    Time frame: Up to 24 months.

  3. Serial serum TRACP-5b concentration measurement by chemiluminescent immunoassay during routine clinical follow-up

    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.

    Time frame: Up to 24 months

07

Study locations

1 of 1 sites recruiting
  • First Department of Orthopaedic Surgery, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czechia
    Brno, 60200, Czechia
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jan 2026 (actual). Primary completion is estimated for Dec 2027, 23 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
May 13, 2026
First posted
May 27, 2026
StartActual
Jan 1, 2026
Primary completionEst.
Dec 31, 2027
CompletionEst.
May 31, 2028
Last update
May 27, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07609277
Lead sponsor
St. Anne's University Hospital Brno, Czech Republic
Collaborators
Department of Clinical Biochemistry, Institute of Laboratory Medicine of the University Hospital Ostrava, Department of Clinical Biochemistry, St. Anne's University Hospital Brno, Czech Republic
Responsible party
Sponsor
First posted
May 27, 2026
Start date
Jan 1, 2026
Primary completion
Dec 31, 2027 (estimated)
Completion
May 31, 2028 (estimated)
Last update
May 27, 2026

Study contacts

Vasileios Apostolopoulos, M.D., Ph.D.
Contact
vasileios.apostolopoulos@fnusa.cz
+420722101065
Vasileios Apostolopoulos, M.D., Ph.D.
principal investigator · First Department of Orthopedic Surgery, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czechia
Michal Mahdal, M.D., Ph.D.
principal investigator · First Department of Orthopedic Surgery, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czechia

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion