Management of Refractory Pediatric Sarcoma: Current Challenges and Future Prospects
Open accessAbstract
Paediatric sarcomas are a heterogeneous group of disorders constituting bone sarcoma and various soft tissue sarcomas. Almost one-third of these presents with metastasis at baseline and another one-third recur after initial curative treatment. There is a huge unmet need in this cohort in terms of curative options and/or prolongation of survival. In this review, we have discussed the current treatment options, challenges and future strategies of managing relapsed/refractory paediatric sarcomas. Upfront risk-adapted treatment with multidisciplinary management remains the main strategy to prevent future recurrence or relapse of the disease. In the case of limited local and/or systemic relapse or late relapse, initial multimodality management can be administered. In treatment-refractory cases or where cure is not feasible, the treatment options are limited to novel therapeutics, immunotherapeutic approach, targeted therapies, and metronomic therapies. A better understanding of disease biology, mechanism of treatment refractoriness, identifications of driver mutation, the discovery of novel targeted therapies, cellular vaccine and adapted therapies should be explored in relapsed/refractory cases. Close national and international collaboration for translation research is needed to fulfil the unmet need.
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Pediatric sarcomas are a biologically heterogeneous group of aggressive solid tumors with a persistently high risk of relapse and metastatic progression.
“Among childhood malignancies, pediatric sarcomas including Ewing sarcoma, osteosarcoma, and rhabdomyosarcoma represent a biologically heterogeneous group of aggressive solid tumors with a persistently high risk of relapse and metastatic progression [2,3,4,5].”
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Cited by
Sorted by citations
Kurdi, M., Hassan, A., Reda, B., Nooh, A., Alsobaie, M., Alkhotani, A., Mirdad, D. S., Almansouri, M., Khashoggi, K., Halwani, M., et al. (2026) · Oncology Research · doi:10.32604/or.2026.078833 · Cited by 2 · see citing works
- Authors
- Pushpam, D., Garg, V., Ganguly, S., & Biswas, B.
- Affiliations
- All India Institute of Medical Sciences (IN)
- Tata Medical Center (IN)
- Corresponding author
- Biswas, Bivas
- Venue
- OncoTargets and Therapy
- Publisher
- Informa UK Limited
- Published
- 2020-06
- Volume
- Volume 13
- Pages
- 5093-5112
- ISSN
- 1178-6930 (ISSN-L)
- PMC
- PMC7293381
- OpenAlex
- W3033206180
- Cited by
- 16
- References
- 7
- Citations by year
- 2026: 7 · 2025: 1 · 2024: 1 · 2023: 2 · 2022: 1 · 2021: 2 · 2020: 2
- FWCI
- 0.25
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- OncoTargets and Therapy (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Dove Medical Press (Taylor and Francis Group) (submittedVersion, cc-by-nc)
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Sarcoma Diagnosis and Treatment
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Acute Lymphoblastic Leukemia research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- pediatric sarcoma, refractory sarcoma, relapsed sarcoma, bone sarcoma, soft tissue sarcoma, risk-adapted treatment, multimodality management, immunotherapy, targeted therapy, driver mutations, cellular vaccine, treatment resistance mechanisms, unmet medical needs
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