A new view of radiation-induced cancer: integrating short- and long-term processes. Part II: second cancer risk estimation
Year: 2009
Type: article
Abstract: As the number of cancer survivors grows, prediction of radiotherapy-induced second cancer risks becomes increasingly important. Because the latency period for solid tumors is long, the risks of recently introduced radiotherapy protocols are not yet directly measurable. In the accompanying article, we presented a new biologically based mathematical model, which, in principle, can estimate second cancer risks for any protocol. The novelty of the model is that it integrates, into a single formalism, mechanistic analyses of pre-malignant cell dynamics on two different time scales: short-term during radiotherapy and recovery; long-term during the entire life span. Here, we apply the model to nine solid cancer types (stomach, lung, colon, rectal, pancreatic, bladder, breast, central nervous system, and thyroid) using data on radiotherapy-induced second malignancies, on Japanese atomic bomb survivors, and on background US cancer incidence. Potentially, the model can be incorporated into radiotherapy treatment planning algorithms, adding second cancer risk as an optimization criterion.
Language: English
Subfield: Radiology, Nuclear Medicine and Imaging
Field: Medicine
Domain: Health Sciences
Open Access status: hybrid
Estimated APC paid: $3,290
Awards: MODELING THE INTERALATIONS AMONG RADIATION-INDUCED BYSTANDER EFFECTS, GENOMIC INSTABILITY AND CANCER, G222768804, Radiological Research Accelerator Facility (RARAF), G2958910270, G3816247084, Qualifying effectiveness of angiogenic inhibitors, Radiation Bystander Effects: Mechanisms, G5719255924, SOLID TUMOR RISK ESTIMATION: INCORPORATING INTERCELLULAR EFFECTS, Cancer Epidemiology, Biostatistics and Environmental Sciences, SOLID TUMOR RISK ESTIMATION: INCORPORATING INTERCELLULAR INTERACTION EFFECTS
OpenAlex ID: W2170654271
