Skip to content

Study of a childhood cancer Neuroblastoma: documenting how it behaves and underlying biology.

India Neuroblastoma Registration and Biology Study InPOG-NB-18-01

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/01/023088
Enrollment
300
Registered
2020-01-31
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: C749- Malignant neoplasm of unspecifiedpart of adrenal gland

Interventions

None listed

Sponsors

Vikramjit S Kanwar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 5.1 Diagnosisâ?¨All newly diagnosed patients with suspected neuroblastoma (NB), or ganglioneuroblastoma seen at participating InPOG institutions are eligible for this study. 5.2. Patients may have received emergent chemotherapy. However documentation of such exposure is needed as excessive exposure may yield samples that have inadequate tumor to analyze. 5.3 Specimens required for eligibility:â?¨It is mandatory that an effort be made to submit a neuroblastoma tissue slides of sufficient quality and quantity for genomic analysis. For patients with stage 4 disease confirmed on marrow histopathology and urine catecholamine testing, tissue biopsy is not required for registration but marrow biopsy specimen slides or aspirate sample should be sent. Similarly for low risk neuroblastoma patients followed with imaging tissue biopsy may not be available, however should they undergo a biopsy or resection at a later date tumor needs to be submitted for testing at that time. 5.4 All patients and/or their parents or legal guardians must sign a written informed consent. â?¨ 5.5 All institutional ethics requirements must be met. â?¨

Exclusion criteria

Exclusion criteria: 1. Patients who are not diagnosed with neuroblastoma.

Design outcomes

Primary

MeasureTime frame
1) Overall survival of neuroblastoma patients 2) Correlation with initial stage, treatment administered, and biologic risk factors.Timepoint: Samples and patient registration to be submitted Staging and biology assessed at time of initial diagnosis, patient outcome will be assessed 3 years from patient registration

Secondary

MeasureTime frame
To follow all patients for a period of 5 years to gain a better understanding of survival. Timepoint: Follow up to complete 2 years after last patient accrued

Countries

India

Contacts

Public ContactVikramjit S Kanwar

Division Chief Pediatric Hematology-Oncology CIMS Hospital

vikramjit.kanwar@cimshospital.org9650707275

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026