Clinical trial · Observational
Clinical Value of Next Generation Sequencing in Chinese Childhood Solid Tumors
Clinical Value of Next Generation Sequencing in Chinese Childhood Solid Tumors: A Multicenter Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Samples of 200 patients with pediatric malignant solid tumors will prospectively be collected. Selected samples are sufficient for next generation sequencing(NGS) and available for follow-up information. Multi-omics techniques such as DNA and RNA panel will be used to study driver genes for the development of malignant solid tumors in children, and to explore the pathogenic mechanism. The aim of this study is to explore new biomarkers for the diagnosis and treatment for childhood malignant solid tumors.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Pediatric, Solid Tumors, NGS | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| NGS | Genetic | — | UNRESOLVED |
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Mutation characteristics of malignant solid tumors in Chinese children.
- timeFrame
- 2021.8-2023.8
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 0 Years
- Maximum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patients are diagnosed by histology and pathology as pediatric malignant solid tumors (including soft tissue sarcoma, osteosarcoma, pediatric glioma, neuroblastoma, nephroblastoma, retinoblastoma, hepatoblastoma, atypical teratoid/rhabdomymoma, embryonal tumor, etc.); 2. Age: \< 18 years old; 3. Eastern Cooperative Oncology Group (ECOG) PS score: 0-2, estimated survival \>6 months; 4. Complete clinical laboratory examination and pathological examination information of patients; 5. Patients can be evaluated on time, and samples can be obtained throughout the whole test process; 6. Informed consent signed by the patient or his/her legal representative shall be obtained after the patient is informed of the project; Exclusion Criteria: 1. As determined by the investigator, the patient had other major diseases that might affect follow-up and short-term survival; 2. Any social/psychological problems that the researcher determines are not suitable for the study;
References
Publications (1)
- DERIVEDLu S, Zhang Y, Zhang W, Huang J, Yang C, Wang J, Gao J, Guo X, Yuan X, Chen S, Sun F, Cheng H, Yao W, Dong K, Guo H, Sun X, Li H, Chen K, Lan H, Zhen Z, Zhu J, Zhang X, Que Y, Yan S, Ma J, Li J, Zhu D, Wang H, Wang S, Zhang Y. Precision Medicine Program in Chinese Pediatric Patients With Sarcoma. JCO Precis Oncol. 2026 Jan;10:e2500428. doi: 10.1200/PO-25-00428. Epub 2026 Jan 14. PMID 41533994