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Neutrophil Extracellular Traps (NETs) Formation Following Chemotherapy and Their Role in Antitumor Activity

Neutrophil Extracellular Traps (NETs) Formation Following Chemotherapy for Pediatric Hematological and Solid Tumors, and Its Relation to Other Neutrophil Functions and the Role of NETs in Antitumor Activity

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01533779
Enrollment
50
Registered
2012-02-15
Start date
2012-02-29
Completion date
2015-02-28
Last updated
2012-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric Hematological Malignancies, Pediatric Solid Malignancies

Keywords

children, malignancy, neutrophil, neutrophil extracellular traps, superoxide production, hydrogen peroxide production, chemotaxis, myeloperoxidase, immunosurveillance, cancer cell lines

Brief summary

Examine neutrophil extracellular traps (NETs) formation, in relation to other neutrophil functions like chemotaxis, superoxide production, hydrogen peroxide production, and the presence of myeloperoxidase, in pediatric patients undergoing chemotherpy for solid and hematological malignancies. This data could shed new light on the mechanism responsible for the increased susceptibility to infection among these patients and aid in improving their prophylactic antimicrobial treatment. NETs formation against tumor cell lines and their ability to kill tumor cells will also be examined. The finding of NETs activity against tumor cells could have a major contribution to the investigators understanding of the function of the immune system against cancer.

Detailed description

Neutrophil function, including NETs formation, chemotaxis, superoxide production, hydrogen peroxide production, and the presence of myeloperoxidase, will be examined in 50 pediatric patientsundergoing chemotherapy for solid and hematological malignancies. Children with the following malignancies will be examined: acute lymphoblastic leukemia,acute myelogenous leukemia,Hodgkin's lymphoma,non-Hodgkin's lymphoma, primary bone sarcoma,rhabdomyosarcoma,non-rhabdomyosarcoma,neuroblastoma,Wilms' tumor,hepatoblastoma or hepatocellular carcinoma,germ cell tumors, and hystiocytosis. Also those with brain tumors such as medulloblastom,low grade glioma,high grade glioma,ependymoma,and embryonal and pineal region tumors. Data gathered on the patients will include background data (age, gender, ethnicity) and background diseases, data on current illness (histologic type, grade, stage, response treatment,infectious episodes), and on the use of ranulocyte-colony stimulating factor (G-CSF). The following time points will be examined: 1. At diagnosis, before initiation of chemotherapy. 2. immediately before the 2nd course. 3. After the middle course. 4. A month after the last course. 5. Three months after the last course. 6. In acute myelogenous leukemia and acute lymphoblastic leukemia,time points also include the middle of the maintenance course and 3 months after the end of maintenance. An additional blood examination will be used to examine NETs formation against tumor cell lines and their ability to kill tumor cells.

Interventions

None listed

Sponsors

Max Planck Institute for Infection Biology
CollaboratorOTHER
Meir Medical Center
CollaboratorOTHER
Tel-Aviv Sourasky Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 21 Years
Healthy volunteers
Yes

Inclusion criteria

Included in the study were patients with: * Acute lymphoblastic leukemia or acute myelogenous leukemia. * Hodgkin's lymphoma or non-Hodgkin's lymphoma. * Primary bone sarcoma, rhabdomyosarcoma, non-rhabdomyosarcoma, neuroblastoma, Wilms' tumor, hepatoblastoma or hepatocellular carcinoma, hystiocytosis, and germ cell tumors. * Medulloblastoma, low grade glioma, high grade glioma, ependymoma, and embryonal and pineal region tumors.

Exclusion criteria

* A severe background disease that may affect Neutrophil function (e.g., diabetes, lupus).

Countries

Israel

Contacts

Primary ContactSivan Achituv, MD
sivanbrg@netvision.net.il972-527360718
Backup ContactRonit Elhasid, MD
ronite@tasmc.health.gov.il972-3-6974252

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026