TY - JOUR
T1 - Absolute risk prediction of second primary thyroid cancer among 5-year survivors of childhood cancer
AU - Kovalchik, Stephanie A.
AU - Ronckers, Cécile M.
AU - Veiga, Lene H.S.
AU - Sigurdson, Alice J.
AU - Inskip, Peter D.
AU - De Vathaire, Florent
AU - Sklar, Charles A.
AU - Donaldson, Sarah S.
AU - Anderson, Harald
AU - Bhatti, Parveen
AU - Hammond, Sue
AU - Leisenring, Wendy M.
AU - Mertens, Ann C.
AU - Smith, Susan A.
AU - Stovall, Marilyn
AU - Tucker, Margaret A.
AU - Weathers, Rita E.
AU - Robison, Leslie L.
AU - Pfeiffer, Ruth M.
PY - 2013/1/1
Y1 - 2013/1/1
N2 - Purpose: We developed three absolute risk models for second primary thyroid cancer to assist with long-term clinical monitoring of childhood cancer survivors. Patients and Methods: We used data from the Childhood Cancer Survivor Study (CCSS) and two nested case-control studies (Nordic CCSS; Late Effects Study Group). Model M1 included self-reported risk factors, model M2 added basic radiation and chemotherapy treatment information abstracted from medical records, and model M3 refined M2 by incorporating reconstructed radiation absorbed dose to the thyroid. All models were validated in an independent cohort of French childhood cancer survivors. Results: M1 included birth year, initial cancer type, age at diagnosis, sex, and past thyroid nodule diagnosis. M2 added radiation (yes/no), radiation to the neck (yes/no), and alkylating agent (yes/no). Past thyroid nodule was consistently the strongest risk factor (M1 relative risk [RR], 10.8; M2 RR, 6.8; M3 RR, 8.2). In the validation cohort, 20-year absolute risk predictions for second primary thyroid cancer ranged from 0.04% to 7.4% for M2. Expected events agreed well with observed events for each model, indicating good calibration. All models had good discriminatory ability (M1 area under the receiver operating characteristics curve [AUC], 0.71; 95% CI, 0.64 to 0.77; M2 AUC, 0.80; 95% CI, 0.73 to 0.86; M3 AUC, 0.75; 95% CI, 0.69 to 0.82). Conclusion: We developed and validated three absolute risk models for second primary thyroid cancer. Model M2, with basic prior treatment information, could be useful for monitoring thyroid cancer risk in childhood cancer survivors.
AB - Purpose: We developed three absolute risk models for second primary thyroid cancer to assist with long-term clinical monitoring of childhood cancer survivors. Patients and Methods: We used data from the Childhood Cancer Survivor Study (CCSS) and two nested case-control studies (Nordic CCSS; Late Effects Study Group). Model M1 included self-reported risk factors, model M2 added basic radiation and chemotherapy treatment information abstracted from medical records, and model M3 refined M2 by incorporating reconstructed radiation absorbed dose to the thyroid. All models were validated in an independent cohort of French childhood cancer survivors. Results: M1 included birth year, initial cancer type, age at diagnosis, sex, and past thyroid nodule diagnosis. M2 added radiation (yes/no), radiation to the neck (yes/no), and alkylating agent (yes/no). Past thyroid nodule was consistently the strongest risk factor (M1 relative risk [RR], 10.8; M2 RR, 6.8; M3 RR, 8.2). In the validation cohort, 20-year absolute risk predictions for second primary thyroid cancer ranged from 0.04% to 7.4% for M2. Expected events agreed well with observed events for each model, indicating good calibration. All models had good discriminatory ability (M1 area under the receiver operating characteristics curve [AUC], 0.71; 95% CI, 0.64 to 0.77; M2 AUC, 0.80; 95% CI, 0.73 to 0.86; M3 AUC, 0.75; 95% CI, 0.69 to 0.82). Conclusion: We developed and validated three absolute risk models for second primary thyroid cancer. Model M2, with basic prior treatment information, could be useful for monitoring thyroid cancer risk in childhood cancer survivors.
UR - http://www.scopus.com/inward/record.url?scp=84871769704&partnerID=8YFLogxK
U2 - 10.1200/JCO.2012.41.8996
DO - 10.1200/JCO.2012.41.8996
M3 - Article
C2 - 23169509
AN - SCOPUS:84871769704
SN - 0732-183X
VL - 31
SP - 119
EP - 127
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 1
ER -