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Genetic Risk of Second Malignant Neoplasm after Childhood Cancer Treatment: A Systematic Review
Claire Ducos1, Naïla Aba1, Filippo Rosselli2
1Radiation Epidemiology Team, Center for Research in Epidemiology and Population Health, INSERM Unit 1018, University Paris Saclay, Villejuif, France.
Summary
Genetic factors influence the risk of second malignant neoplasm (SMN) in childhood cancer survivors (CCS). This review compiles genes and variants associated with SMN risk, aiding future research.
Area of Science:
- Oncology
- Genetics
- Cancer Survivorship
Background:
- Second malignant neoplasm (SMN) is a significant long-term risk for childhood cancer survivors (CCS).
- While treatment modalities like radiotherapy and chemotherapy are established risk factors, inter-individual variability suggests a genetic predisposition.
- Understanding these genetic factors is crucial for improving long-term outcomes for CCS.
Conclusions:
- Genetic factors play a role in the susceptibility to SMN among childhood cancer survivors.
- This review offers a valuable compilation of current knowledge on SMN risk-associated genetic variants and genes.
- Further extensive and standardized research is necessary to fully elucidate the genetic basis of SMN risk in CCS.
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