Hereditary cancer risk assessment in a pediatric oncology follow-up clinic

Pediatric Blood and Cancer

Volumn 58, Issue 1, 2012, Pages 85-89

  Knapke, Sara ^a   Nagarajan, Rajaram ^a   Correll, Judy ^a   Kent, Debra ^a   Burns, Karen ^a  

^a CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

Author keywords

Cancer; Genetic; Hereditary; Late effects; Oncology; Pediatric

Indexed keywords

ACUTE LYMPHOCYTIC LEUKEMIA; ADOLESCENT; ADULT; ARTICLE; CANCER RISK; CANCER SURVIVOR; CHILD; CHILDHOOD CANCER; CHOROID PLEXUS CARCINOMA; CHOROID PLEXUS TUMOR; FAMILIAL CANCER; FAMILY HISTORY; FEMALE; FOLLOW UP; GENETIC COUNSELING; GENETIC SCREENING; HEPATOBLASTOMA; HODGKIN DISEASE; HUMAN; MAJOR CLINICAL STUDY; MALE; MEDICAL HISTORY; MEDULLOBLASTOMA; NEPHROBLASTOMA; NEUROBLASTOMA; NONHODGKIN LYMPHOMA; OPTIC NERVE GLIOMA; PHEOCHROMOCYTOMA; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINOBLASTOMA; RISK ASSESSMENT; SCHOOL CHILD;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; FEMALE; FOLLOW-UP STUDIES; GENETIC PREDISPOSITION TO DISEASE; HOSPITALS, PEDIATRIC; HUMANS; MALE; MEDICAL ONCOLOGY; MIDDLE AGED; NEOPLASMS; PROGNOSIS; RISK ASSESSMENT; RISK FACTORS; SURVIVAL RATE; SURVIVORS; YOUNG ADULT;

EID: 81155151775     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.23283     Document Type: Article

References (18)

1. Narod SA, Stiller C, Lenoir GM. An estimate of the heritable fraction of childhood cancer. Br J Cancer 1991; 63: 993-999.
2. Strahm B, Malkin D. Hereditary cancer predisposition in children: Genetic basis and clinical implications. Int J Cancer 2006; 119: 2001-2006.
3. Strong LC. Genetic implications for long-term survivors of childhood cancer. Cancer Suppl 1993; 71: 3435-3440.
4. Rao A, Rothman J, Nichols KE. Genetic testing and tumor surveillance for children with cancer predisposition syndromes. Curr Opin Pediatr 2008; 20: 1-7.
5. Clericuzio C. Recognition and management of childhood cancer syndromes: A systems approach. Am J Med Genet 1999; 89: 81-90.
6. Hampel H, Sweet K, Westman JA, et al. Referral for cancer genetics consultation: A review and compilation of risk assessment criteria. J Med Genet 2004; 41: 81-91.
7. Sweet KM, Bradley TL, Westman JA, et al. Identification and referral of families at high risk for cancer susceptibility. J Clin Oncol 2002; 20: 528-537.
8. American Society of Clinical Oncology. American Society of Clinical Oncology policy statement update: Genetic testing for cancer susceptibility. J Clin Oncol 2003; 21: 1-10.
9. Draper GJ, Sanders BM, Brownbill PA, et al. Patterns of risk of hereditary retinoblastoma and applications to genetic counselling. Br J Cancer 1992; 66: 211-219.
10. Aretz S, Koch A, Uhlhass S, et al. Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations? Pediatr Blood Cancer 2006; 47: 811-818.
11. Tischkowitz M, Rosser E. Inherited cancer in children: Practical/ethical problems and challenges. Eur J Cancer 2004; 40: 2459-2470.
12. Mulvihill JJ, Byrne J. Genetic counseling of the cancer survivor. Semin Oncol Nurs 1989; 29-35.
13. Marees T, Moll AC, Imhof SM, et al. Risk of second malignancies in survivors of retinoblastoma: More than 40 years of follow-up. J Natl Cancer Inst 2008; 100: 1771-1779.
14. Fletcher O, Easton D, Anderson K, et al. Lifetime risks of common cancers among retinoblastoma survivors. J Natl Cancer Inst 2004; 96: 357-363.
15. Wong FL, Boice JD Jr., Abramson DH, et al. Cancer Incidence after retinoblastoma: Radiation dose and sarcoma risk. JAMA 1997; 278: 1284-1285.
16. Hisada M, Garber JE, Fung CY, et al. Multiple primary cancers in families with Li-Fraumeni syndrome. J Natl Cancer Inst 1998; 90: 606-611.
17. Gonzalez KD, Noltner KA, Buzin CH, et al. Beyond Li-Fraumeni syndrome: Clinical characteristics of families with p53 germline mutations. J Clin Oncol 2009; 27: 1250-1256.
18. Merks JH, Caron HN, Hennekam RC, et al. High incidence of malformation syndromes in a series of 1.073 children with cancer. Am J Med Genet 2005; 143A: 132-143.