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1.
Int J Radiat Oncol Biol Phys ; 97(2): 278-286, 2017 02 01.
Article in English | MEDLINE | ID: mdl-28068236

ABSTRACT

BACKGROUND AND PURPOSE: The aim of this study was to investigate the role of radiation dose received to the circle of Willis (WC) during radiation therapy (RT) and of potential dose-response modifiers on the risk of stroke after treatment of childhood cancer. METHODS: We evaluated the risk factors for stroke in a cohort of 3172 5-year survivors of childhood cancer who were followed up for a median time of 26 years. Radiation doses to the WC and brain structures were estimated for each of the 2202 children who received RT. RESULTS: Fifty-four patients experienced a confirmed stroke; 39 were ischemic. Patients not receiving RT had a stroke risk similar to that of the general population, whereas those who received RT had an 8.5-fold increased risk (95% confidence interval [CI]: 6.3-11.0). The excess of incidence of stroke increased yearly. The dose of radiation to the WC, rather than to other brain structures, was found to be the best predictor of stroke. The relative risk was 15.7 (95% CI: 4.9-50.2) for doses of 40 Gy or more. At 45 years of age, the cumulative stroke incidence was 11.3% (95% CI: 7.1%-17.7%) in patients who received 10 Gy or more to the WC, compared with 1% expected from general population data. Radiation doses received to the heart and neck also increased the risk. Surgery for childhood brain cancer was linked to hemorrhagic strokes in these patients. CONCLUSION: The WC should be considered as a major organ at risk during RT for childhood brain cancers. The incidence of radiation-induced ischemic stroke strongly increases with long-term follow-up.


Subject(s)
Circle of Willis/radiation effects , Organs at Risk/radiation effects , Stroke/etiology , Survivors , Adolescent , Adult , Age Factors , Antineoplastic Agents/administration & dosage , Antineoplastic Agents/classification , Brain Ischemia/epidemiology , Brain Ischemia/etiology , Brain Neoplasms/prevention & control , Brain Neoplasms/radiotherapy , Cause of Death , Cerebral Hemorrhage/epidemiology , Cerebral Hemorrhage/etiology , Cerebrovascular Disorders/etiology , Child , Child, Preschool , Dose-Response Relationship, Radiation , Female , Follow-Up Studies , France , Heart/radiation effects , Hodgkin Disease/radiotherapy , Humans , Incidence , Infant , Male , Middle Aged , Neck/radiation effects , Radiation Dosage , Retrospective Studies , Stroke/epidemiology , Survivors/statistics & numerical data , Time Factors , United Kingdom
2.
Int J Radiat Oncol Biol Phys ; 93(3): 658-67, 2015 Nov 01.
Article in English | MEDLINE | ID: mdl-26461008

ABSTRACT

PURPOSE: To investigate the roles of radiation therapy and chemotherapy in the occurrence of subsequent leukemia after childhood cancer. METHODS AND MATERIALS: We analyzed data from a case-control study with 35 cases and 140 controls. The active bone marrow (ABM) was segmented into 19 compartments, and the radiation dose was estimated in each. The chemotherapy drug doses were also estimated to enable adjustments. Models capable of accounting for radiation dose heterogeneity were implemented for analysis. RESULTS: Univariate analysis showed a significant trend in the increase of secondary leukemia risk with radiation dose, after accounting for dose heterogeneity (P=.046). This trend became nonsignificant after adjustment for doses of epipodophyllotoxins, alkylating agents, and platinum compounds and the first cancer on multivariate analysis (P=.388). The role of the radiation dose appeared to be dwarfed, mostly by the alkylating agents (odds ratio 6.9, 95% confidence interval 1.9-25.0). Among the patients who have received >16 Gy to the ABM, the radiogenic risk of secondary leukemia was about 4 times greater in the subgroup with no alkylating agents than in the subgroup receiving ≥10 g/m(2). CONCLUSIONS: Notwithstanding the limitations resulting from the size of our study population and the quite systematic co-treatment with chemotherapy, the use of detailed information on the radiation dose distribution to ABM enabled consideration of the role of radiation therapy in secondary leukemia induction after childhood cancer.


Subject(s)
Antineoplastic Agents/adverse effects , Bone Marrow/drug effects , Bone Marrow/radiation effects , Leukemia, Radiation-Induced , Leukemia/chemically induced , Neoplasms/therapy , Adolescent , Analysis of Variance , Antineoplastic Agents, Alkylating/adverse effects , Case-Control Studies , Child , Child, Preschool , Confidence Intervals , Female , Humans , Infant , Male , Neoplasms, Second Primary/etiology , Odds Ratio , Platinum Compounds/adverse effects , Podophyllotoxin/adverse effects , Radiation Dosage
3.
J Clin Endocrinol Metab ; 100(11): 4282-90, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26327481

ABSTRACT

CONTEXT: Thyroid carcinoma is a frequent complication of childhood cancer radiotherapy. The dose response to thyroid radiation dose is now well established, but the potential modifier effect of other factors requires additional investigation. OBJECTIVE: This study aimed to investigate the role of potential modifiers of the dose response. DESIGN: We followed a cohort of 4338 5-year survivors of solid childhood cancer treated before 1986 over an average of 27 years. The dose received by the thyroid gland and some other anatomical sites during radiotherapy was estimated after reconstruction of the actual conditions in which irradiation was delivered. RESULTS: Fifty-five patients developed thyroid carcinoma. The risk of thyroid carcinoma increased with a radiation dose to the thyroid of up to two tenths of Gy, then leveled off for higher doses. When taking into account the thyroid radiation dose, a surgical or radiological splenectomy (>20 Gy to the spleen) increased thyroid cancer risk (relative risk [RR] = 2.3; 95% confidence interval [CI], 1.3-4.0), high radiation doses (>5 Gy) to pituitary gland lowered this risk (RR = 0.2; 95% CI, 0.1-0.6). Patients who received nitrosourea chemotherapy had a 6.6-fold (95% CI, 2.5-15.7) higher risk than those who did not. The excess RR per Gy of radiation to the thyroid was 4.7 (95% CI, 1.7-22.6). It was 7.6 (95% CI, 1.6-33.3) if body mass index at time of interview was equal or higher than 25 kg/m(2), and 4.1 (95% CI, 0.9-17.7) if not (P for interaction = .1). CONCLUSION: Predicting thyroid cancer risk following childhood cancer radiation therapy probably requires the assessment of more than just the radiation dose to the thyroid. Chemotherapy, splenectomy, radiation dose to pituitary gland, and obesity also play a role.


Subject(s)
Neoplasms, Radiation-Induced/epidemiology , Radiotherapy/adverse effects , Thyroid Neoplasms/epidemiology , Adolescent , Antineoplastic Agents/adverse effects , Child , Child, Preschool , Cohort Studies , Dose-Response Relationship, Radiation , Humans , Incidence , Infant , Infant, Newborn , Nitrosourea Compounds/adverse effects , Obesity/complications , Obesity/epidemiology , Pituitary Gland/radiation effects , Radiation Dosage , Retrospective Studies , Risk Factors , Splenectomy , Thyroid Gland/radiation effects
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