The contrasting age-incidence patterns of bone tumours in teenagers and young adults: Implications for aetiology

• Published in: International journal of cancer Vol. 131; no. 7; pp. 1678 - 1685
• Main Authors: Arora, Ramandeep S., Alston, Robert D., Eden, Tim O.B., Geraci, Marco, Birch, Jillian M.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01-10-2012; Wiley-Blackwell; Wiley Subscription Services, Inc
• Subjects: Adolescent; adolescents; Adult; Age Factors; Aged; Aged, 80 and over; Biological and medical sciences; Bone cancer; bone neoplasms; Bone Neoplasms - epidemiology; Cancer; Child; Child, Preschool; Diseases of the osteoarticular system; England; England - epidemiology; Female; Humans; Incidence; Infant; Infant, Newborn; Male; Medical research; Medical sciences; Middle Aged; Sex Factors; Teenagers; Tumors; Tumors of striated muscle and skeleton; Young Adult; Young adults; England; United Kingdom; Great Britain; Europe; Human; adolescents; Diseases of the osteoarticular system; England; Epidemiology; Incidence; Osteoarticular system; Cancerology; Etiology; Bone tumor; bone neoplasms; Bone age; young adults; Adolescent; Young adult; Bone
• ISSN: 0020-7136; 1097-0215
• DOI: 10.1002/ijc.27402

Bone tumours comprise 0.2% of cancers overall but 5.7% in 15–24 year olds. To explore the relationship with adolescence we have analysed age‐incidence patterns of bone tumours in a large national dataset. Data on incident cases of bone tumours in 0–84 year olds in England, 1979–2003, were extracted from national cancer registration data. Incidence rates per million person‐years by 5‐year age‐group, sex, morphology and primary site were calculated and adjusted to the world standard population. Nine thousand one hundred forty‐six cases were identified giving an overall age‐standardized rate of 7.19 per million person‐years. The distribution by morphology was: osteosarcoma, 34.2%; chondrosarcoma, 27.2%; Ewing sarcoma, 19.3%; other, 19.4%. The distribution varied by age. Ewing sarcoma was most common in 0–9 year olds, osteosarcoma in 10–29 year olds and chondrosarcoma in 30–84 year olds. 29.2% of all tumours occurred in 0–24 year olds. Highest incidence of osteosarcoma and Ewing sarcoma in females was in 10–14 year olds. In males, peak incidence occurred at 15–19 years and exceeded that in females. Chondrosarcoma incidence steadily increased with age. The proportions of Ewing sarcomas occurring in respective bones were consistent with those of the adult skeleton by weight. In osteosarcoma tumours of long bones of lower limb were markedly over‐represented in the adolescent peak, being six times more than at any other site. Variation in incidence patterns with age and site suggests pubertal bone growth to be a key factor in osteosarcoma while different biological pathways could be relevant for Ewing sarcoma.