Proportion of children with cancer that have an indication for genetic counseling and testing based on the cancer type irrespective of other features
- PMID: 33634344
- PMCID: PMC8484228
- DOI: 10.1007/s10689-021-00234-4
Proportion of children with cancer that have an indication for genetic counseling and testing based on the cancer type irrespective of other features
Abstract
In children with cancer, specific clinical features such as physical anomalies, occurrence of cancer in young relatives, specific cancer histologies, and unique mutation/methylation signatures may indicate the presence of an underlying cancer predisposition syndrome (CPS). The proportion of children with a cancer type suggesting a CPS among all children with cancer is unknown. To determine the proportion of children with cancer types suggesting an underlying CPS among children with cancer. We evaluated the number of children with cancer types strongly associated with CPS diagnosed in Germany between 2007 and 2016. Data were obtained from various sources including two national pediatric pathology reference laboratories for brain and solid tumors, respectively, various childhood cancer trial offices as well as the German Childhood Cancer Registry. Among 21,127 children diagnosed with cancer between 2007 and 2016, 2554 (12.1%) had a cancer type strongly associated with a CPS. The most common diagnoses were myelodysplastic syndrome and juvenile myelomonocytic leukemia, retinoblastoma, malignant peripheral nerve sheath tumor, infantile myofibromatosis, medulloblastomaSHH, rhabdoid tumor as well as atypical teratoid/rhabdoid tumor. Based on cancer type only, 12.1% of all children with cancer have an indication for a genetic evaluation. Pediatric oncology patients require access to genetic counselling and testing.
Keywords: Cancer predisposition syndromes; Childhood cancer; Pathology.
© 2021. The Author(s).
Conflict of interest statement
The authors indicate no potential conflicts of interest.
Figures
Similar articles
-
Imaging characteristics of atypical teratoid-rhabdoid tumor in children compared with medulloblastoma.AJR Am J Roentgenol. 2008 Mar;190(3):809-14. doi: 10.2214/AJR.07.3069. AJR Am J Roentgenol. 2008. PMID: 18287456
-
Malignant progression of a peripheral nerve sheath tumor in the setting of rhabdoid tumor predisposition syndrome.Pediatr Blood Cancer. 2018 Jul;65(7):e27030. doi: 10.1002/pbc.27030. Epub 2018 Mar 7. Pediatr Blood Cancer. 2018. PMID: 29512865 Free PMC article.
-
Clinicopathological characteristics of atypical teratoid/rhabdoid tumor.Neurol Med Chir (Tokyo). 1999 Jul;39(7):510-7; discussion 517-8. doi: 10.2176/nmc.39.510. Neurol Med Chir (Tokyo). 1999. PMID: 10437379
-
Advances in the molecular classification of pediatric brain tumors: a guide to the galaxy.J Pathol. 2020 Jul;251(3):249-261. doi: 10.1002/path.5457. Epub 2020 Jun 10. J Pathol. 2020. PMID: 32391583 Review.
-
Pediatric solid tumors and associated cancer predisposition syndromes: Workup, management, and surveillance. A summary from the APSA Cancer Committee.J Pediatr Surg. 2022 Mar;57(3):430-442. doi: 10.1016/j.jpedsurg.2021.08.008. Epub 2021 Aug 24. J Pediatr Surg. 2022. PMID: 34503817 Review.
Cited by
-
A Summary of the Inaugural WHO Classification of Pediatric Tumors: Transitioning from the Optical into the Molecular Era.Cancer Discov. 2022 Feb;12(2):331-355. doi: 10.1158/2159-8290.CD-21-1094. Epub 2021 Dec 17. Cancer Discov. 2022. PMID: 34921008 Free PMC article. Review.
-
Diagnostic Strategies and Algorithms for Investigating Cancer Predisposition Syndromes in Children Presenting with Malignancy.Cancers (Basel). 2022 Jul 31;14(15):3741. doi: 10.3390/cancers14153741. Cancers (Basel). 2022. PMID: 35954404 Free PMC article. Review.
-
Eye Tumors in Childhood as First Sign of Tumor Predisposition Syndromes: Insights from an Observational Study Conducted in Germany and Austria.Cancers (Basel). 2021 Apr 14;13(8):1876. doi: 10.3390/cancers13081876. Cancers (Basel). 2021. PMID: 33919815 Free PMC article.
-
Clinical outcome of pediatric medulloblastoma patients with Li-Fraumeni syndrome.Neuro Oncol. 2023 Dec 8;25(12):2273-2286. doi: 10.1093/neuonc/noad114. Neuro Oncol. 2023. PMID: 37379234 Free PMC article.
-
Germline Predisposition to Pediatric Cancer, from Next Generation Sequencing to Medical Care.Cancers (Basel). 2021 Oct 24;13(21):5339. doi: 10.3390/cancers13215339. Cancers (Basel). 2021. PMID: 34771502 Free PMC article.
References
-
- Sylvester DE, Chen Y, Jamieson RV, Dalla-Pozza L, Byrne JA. Investigation of clinically relevant germline variants detected by next-generation sequencing in patients with childhood cancer: a review of the literature. J Med Genet. 2018;55(12):785–793. doi: 10.1136/jmedgenet-2018-105488. - DOI - PubMed
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources