TREATMENT OUTCOMES OF COMBINED SURGERY AND CHEMOTHERAPY IN CHILDREN WITH RHABDOMYOSARCOMA AT CHILDREN’S HOSPITAL 2 IN 2019 – 2024 PERIOD
Main Article Content
Abstract
Introduction: Rhabdomyosarcoma is a mesenchymal neoplasm with morphology and genetic features similar to skeletal muscle cells. It is the most common subtype of soft-tissue sarcoma. In Southern Vietnam, there are currently no studies evaluating rhabdomyosarcoma cases in detail or assessing survival according to stage and risk stratification. We conducted this study to assess treatment outcomes and survival based on stage and risk groups in children with rhabdomyosarcoma. From this, we aim to draw experience and define more effective treatment objectives for this disease.
Subjects and methods: We conducted a case series describing pediatric patients who were newly diagnosed and treated for rhabdomyosarcoma at Children’s Hospital 2 from January 1st, 2019 to June 30th, 2024.
Results: Among 30 patients, the median age at diagnosis was 3,5 years. Most patients were ≤ 5 years-old (63.3%). The male-to-female ratio was 1:1. A palpable mass was the most common symptom (80%). According to risk stratification, 3,3% (1/30) were in group B; 6,7% (2/30) in group C; 20% (6/30) in group E; 10% (3/30) in group F; 20% (6/30) in group G; 10% (3/30) in group H; and 30% (9/30) had metastatic disease. Regarding surgery, 7 patients (23.3%) underwent upfront tumor resection, 21 patients (70%) underwent delayed resection after chemotherapy, and 2 patients (6.7%) had unresectable tumors, being biopsied only. Surgical margin was tumor-free in 33,3% cases (10/30), while 66,7% (20/30) had residual disease, including 26,7% with microscopic residual tumor and 40% with macroscopic residual tumor. All patients (100%) received chemotherapy following CWS protocol. The rate of complete response at the end of treatment was 47,8%, representing a 39,1% increase compared to after – three – cycle period. Tumor resection was an independent factor associated with treatment response. The overall survival time was 527,3 ± 210 days; event-free survival time was 501,7 ± 208,3 days. The overall survival and event-free survival rates were 54,3% and 66,4%, respectively.
Keywords
Rhabdomyosarcoma, surgery, chemotherapy
Article Details
References
2. Nghiêm Ngọc Linh, “Nghiên cứu đặc điểm dịch tễ học lâm sàng và nhận xét kết quả điều trị Sarcom cơ vân trẻ em” Đại học Y Hà Nội, Hà Nội, 2018.
3. Carola A. S, Sarcomas of Bone and Soft Tissues in Children and Adolescents, Springer, 2021.
4. Gabriela Guillén Burrieza, Marta Martos Rodríguez, “Chapter 14, Soft Tissue Sarcomas” in Survival Handbook in Pediatric Surgical Oncology, Springer, 2024, pp. 85-92.
5. Koscielniak, E.; Klingebiel, M., Cooperative Weichteilsarkom Study Group CWS Der GPOH in Cooperation with the European Paediatric Soft Tissue Sarcoma Study Group EpSSG CWS-Guidance for Risk Adapted Treatment of Soft Tissue Sarcoma and Soft Tissue Tumours in Children. Adolescents, and Young Adults Chair Persons, 2012.
6. Martin-Giacalone, Weinstein, P. Adam, Plon, Sharon E. and Lupo, Philip J., “Pediatric Rhabdomyosarcoma: Epidemiology and Genetic Susceptibility” Journal of Clinical Medicine, vol. 10, no. 9, p. 2028, 2021.