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NCT Number: NCT06806462

Biomolecular Markers of Bone Metastasis

The goal of this clinical trial is to characterize the biomolecular profile of bone metastases to define the predisposing profiles of bone metastasis, in patients with breast or lung or renal carcinomas or of the gastroenteric or prostate tract with bone metastasis.

The main question it aims to answer is:

Is it possible to predict the progression of bone metastasis by identifying biomarkers as risk factors for bone metastasis?

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Bologna, 40138, Italy

Location status: Recruiting

Location contact

Andrea Sambri, MD

CONTACT

[email protected]

0512142680

About this study

Metastasization is a process that involves molecular change: potentially colonizable healthy tissues, particularly bone marrow, may "respond" to the production of factors released by the primary tumor, changing some of their funcional molecular characteristics in order to facilitate colonization by circulating tumor cells.

This study aims to describe the biomolecular profile of bone metastases. For this purpose, as per normal clinical practice, patients with carcinomas and who have developed bone metastases will undergo sampling of the metastases and primary tumors.

The activities will have multidisciplinary management. The study will include patients with carcinoma with bone metastases for whom the collection of biological material from the primary lesion and/or bone metastasis is an integral part of the diagnostic-therapeutic procedure or patients for whom, by clinical practice, a biopsy collection is performed because:

  • histologic evaluation of the primary or metastatic lesion has been requested;
  • a pathologic fracture to be treated surgically occurs;
  • prophylactic orthopedic stabilization is required.

These samples will later be analyzed from a molecular point of view in order to identify a biomolecular profile that can help in defining profiles predisposing to bone metastasis and profiles predisposing to pathological fracture risk.

Unsupervised analysis of the emerged transcriptomes will be conducted:

  • regardless of tumor histotype (in order to highlight any common facilitating factors for bone metastasis and osteolytic activity),
  • by histotype,
  • by type of metastasis (osteolytic vs osteosclerotic).

To eliminate analysis error and bias, analyses will be conducted on fresh samples from needle biopsy or intraoperative sampling.

Emerging evidence on transcriptomic analysis will be validated with protein analysis methods and compared with evidence alreadỳ available in the literature.

The analysis being conducted for this study does not influence clinical practice, and all procedures are part of normal clinical practice in the management of patients with bone metastases from carcinoma.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age >= 18 years
  • Patients with breast or lung or renal or gastroenteric tract or prostate with bone metastases
  • Patients who knowingly express willingness to participate in the study after signing the written informed consent

Exclusion criteria

  • None

Treatment and study plan

Biomolecular profile of bone metastases

Genetic

Describe the biomolecular profile of bone metastases

Primary outcomes

  1. Bone metastasis profiling

    Time frame: up to 100 weeks

    Characterizing the biomolecular profile of bone metastasis to define the predisposing profiles of bone metastasis.

    Transcriptional profile of

    • RANK/RANKL
    • OPG
    • PTHLH
    • IL-1/6/7/8/11,
    • TNF-alfa
  2. Fracture pathological profiling

    Time frame: up to 100 weeks

    Characterizing the biomolecular profile of bone metastasis to define the predisposing risk profiles of fracture pathological. Fracture event yes/no and association with primary outcomes.

Secondary outcomes

  1. Comparison between the biomolecular profile of the mestastases and the primary tumor

    Time frame: up to 100 weeks

    Trascriptional profile of:

    • RANK/RANKL,
    • OPG
    • PTHLH
    • IL-1/6/7/8/11
    • TNF-alfa
  2. Comparison between the biomolecular profiles of osteolytic and osteosclerotic metastases

    Time frame: up to 100 weeks

    Trascriptional profile of:

    • RANK/RANKL,
    • OPG
    • PTHLH
    • IL-1/6/7/8/11
    • TNF-alfa
  3. Measuring PTH-rp (parathormone-related peptide) levels and the risk of pathologic facture

    Time frame: Every 3-6 months

    Dosage of PTHrp

Study contacts

Contact information is provided by the study sponsor or research team.

Andrea Sambri, MD

CONTACT

[email protected]

0512142680

Sponsors and collaborators

Lead sponsor

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Other

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Feb 4, 2025
Registry last updated
Feb 4, 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.

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