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Published on: February 6, 2019
[Clinical efficacy of combined therapy in children with stage 4 neuroblastoma]
Wei-Ling Liang, Xiao-Fan Ye, Gong Zhong
1Department of Pediatrics, Hong Kong University-Shenzhen Hospital, Shenzhen, Guangdong 518000, China.
Insights
Combined therapy shows promising early clinical efficacy for stage 4 neuroblastoma. Multidisciplinary treatment approaches improve survival rates and prognosis in pediatric patients.
Area of Science:
- Pediatric Oncology
- Cancer Therapeutics
- Clinical Research
Background:
- Stage 4 neuroblastoma is a high-risk pediatric cancer.
- Effective treatment strategies are crucial for improving patient outcomes.
Purpose of the Study:
- To evaluate the early clinical efficacy of combined therapy in children with stage 4 neuroblastoma.
- To assess survival rates and prognosis associated with multidisciplinary treatment.
Main Methods:
- Retrospective analysis of 14 children diagnosed with stage 4 neuroblastoma between January 2016 and June 2021.
- Data included clinical characteristics, pathological findings, treatment regimens (chemotherapy, surgery, stem cell transplantation, radiotherapy, immunotherapy), and follow-up information.
- Analysis of recurrence rates and survival outcomes.
Main Results:
- The median age of onset was 3 years and 7.5 months.
- Common findings included positive bone marrow biopsy (9/14), N-Myc gene amplification (4/14), elevated neuron-specific enolase (13/14), and elevated vanilmandelic acid (7/14).
- Treatments comprised chemotherapy (N7 or Rapid COJEC regimens), surgery, hematopoietic stem cell transplantation, radiotherapy, and Ch14.18/CHO immunotherapy. The 2-year overall survival rate was 100%, with 7 out of 14 children achieving disease-free survival within 3 years.
Conclusions:
- Multidisciplinary combined therapy is recommended for stage 4 neuroblastoma.
- This integrated approach can lead to improved survival and better prognosis for affected children.
Objectives:
To study the early clinical efficacy of combined therapy of stage 4 neuroblastoma.
Methods:
A retrospective analysis was performed on the medical data and follow-up data of 14 children with stage 4 neuroblastoma who were diagnosed in Hong Kong University-Shenzhen Hospital from January 2016 to June 2021.
Results:
The median age of onset was 3 years and 7.5 months in these 14 children. Among these children, 9 had positive results of bone marrow biopsy, 4 had N-Myc gene amplification, 13 had an increase in neuron-specific enolase, and 7 had an increase in vanilmandelic acid in urine. Based on the results of pathological examination, differentiated type was observed in 6 children, undifferentiated type in one child, mixed type, in one child and poorly differentiated type in 6 children. Of all the children, 10 received chemotherapy with the N7 regimen (including 2 children receiving arsenic trioxide in addition) and 4 received chemotherapy with the Rapid COJEC regimen. Thirteen children underwent surgery, 14 received hematopoietic stem cell transplantation, and 10 received radiotherapy. A total of 8 children received Ch14.18/CHO immunotherapy, among whom 1 child discontinued due to anaphylactic shock during immunotherapy, and the other 7 children completed Ch14.18/CHO treatment without serious adverse events, among whom 1 child was treated with Lu177 Dotatate 3 times after recurrence and is still undergoing chemotherapy at present. The median follow-up time was 45 months for all the 14 children. Four children experienced recurrence within 2 years, and the 2-year overall survival rate was 100%; 4 children experienced recurrence within 3 years, and 7 achieved disease-free survival within 3 years.
Conclusions:
Multidisciplinary combined therapy is recommended for children with stage 4 neuroblastoma and can help them achieve better survival and prognosis.
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