Tissue Expression of Krüppel-Like Factors 4 and 7 in Bone Tumors

NCT ID: NCT06935864

Last Updated: 2025-04-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-08-16

Study Completion Date

2026-02-28

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The current study is to assess the prognostic value of Krüppel-like factors 4 and 7 in bone tumors, and its role in the disease progression.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Krüppel-like factors are a group of proteins that engage in different cell functions including proliferation, apoptosis, autophagy, invasion, and migration, and have been discovered to play an important role in bone disease development.

Study Setting: Pediatric Hematology, Oncology and Bone Marrow Transplantation Unit at Ain Shams University Children's Hospital.

* Type of Study: Prospective cohort.
* Study Period: 12 months.
* Study Population: Children, adolescents, and young adults diagnosed with localized and metastatic both skeletal and extra-skeletal osteosarcoma and Ewing's sarcoma
* Sampling Method: Convenience
* The medical history by direct interview of participants or from the patients files with a focus on:

* Symptoms such as pain, swelling, and fracture including duration, intensity, and timing of complaint.
* Specific events for bone tumors include prior benign/malignant lesions, family history, and previous radiotherapy for a prior cancer.
* Assessment of the adverse outcomes.
* Treatment protocol, timing of local control, type of local surgical control, need for adjuvant or definitive radiation therapy.
* Examination carried out upon initial patients' presentation (collected from files in the historical group):

* A full physical examination including weight and height, with calculation of body mass index (BMI) and surface area (SA).
* Local examination with specific attention to the size, consistency of the swelling, its location and mobility, the relation of swelling to the involved bone, and the presence of regional/ local lymph nodes.
* Radiologic investigations at initial diagnosis, after induction chemotherapy, after local control, as well as at the end of therapy and every 3 months during 1st 2 years after therapy (collected from files in the historical group):

* Conventional radiographs in two planes
* Magnetic resonance imaging (MRI) of the whole compartment with adjacent joints,
* Computed tomography (CT) should be used only in the case of diagnostic problems or doubt, to visualize more clearly calcification, periosteal bone formation, or cortical destruction
* Stage classification: positron emission tomography (PET)/CT using General Electric device number 5632.
* Laboratory assessment at presentation for cohort group (collected from files in the historical group)

* Complete blood count (CBC)
* Electrolytes including serum Calcium, phosphorus, magnesium, bicarbonate; creatinine, blood urea nitrogen, liver enzymes, and lactate dehydrogenase (LDH)
* Pathological methods:

* Histopathological examination of H\&E-stained sections prepared from paraffin blocks at 4-5 um thickness.
* Immunohistochemical staining of 4 um sections prepared from paraffin blocks using KLF factor (4 and 7); this will be done with automated immunostaining using the streptavidin-biotin technique.
* Interpretation of the stained slides will be done using a semiquantitative score and the results will be statistically analyzed.
* Sample Size: 30 patients

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Osteosarcoma in Children Ewing Sarcoma of Bone or Soft Tissue

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Prospective Arm

Children, young adolescents younger than 15 years, and young adults (15 to 39 years) with histologically confirmed patients with skeletal or extra-skeletal OS or ES with localized or metastatic disease stages.

KLF factor (4 and 7)

Intervention Type DIAGNOSTIC_TEST

Immunohistochemical staining of 4 um sections prepared from paraffin blocks using KLF factor (4 and 7) by automated immunostaining using the streptavidin-biotin technique.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

KLF factor (4 and 7)

Immunohistochemical staining of 4 um sections prepared from paraffin blocks using KLF factor (4 and 7) by automated immunostaining using the streptavidin-biotin technique.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Age: children, young adolescents younger than 15 years, and young adults (15 to 39 years) Gender: Males and female. Histologically confirmed patients with skeletal or extra-skeletal OS or ES. Both localized and metastatic disease stages.

Exclusion Criteria

Patients with second malignant bone sarcoma. Patients with benign bone tumors.
Minimum Eligible Age

1 Month

Maximum Eligible Age

39 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Fatma S E Ebeid

Role: PRINCIPAL_INVESTIGATOR

Faculty of Medicine Ain Shams University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Ain Shams University

Cairo, , Egypt

Site Status RECRUITING

Faculty of Medicine Ain Shams Research Institute- Clinical Research Center (MASRI-CRC)

Cairo, , Egypt

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Fatma S E Ebeid, MD

Role: CONTACT

01095569596

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Fatma Ebeid

Role: primary

01095569596

Fatma Ebeid

Role: primary

01095569596

Related Links

Access external resources that provide additional context or updates about the study.

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

FMASU MD173/2024

Identifier Type: OTHER

Identifier Source: secondary_id

FMASU MD173/2024

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.