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1 Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
2 Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
3 Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York.
4 Department of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia.
5 Division of Hematology/Oncology, Department of Medicine, and Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia.
1 Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
2 Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
3 Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York.
4 Department of Radiation Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia.
5 Division of Hematology/Oncology, Department of Medicine, and Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia.
A, In-field sarcoma after breast radiotherapy (RT) in TP53 pathogenic variance…
Figure.. Secondary Cancer Risk
A, In-field sarcoma after breast radiotherapy (RT) in TP53 pathogenic variance (PV) carriers. The 15-year cumulative incidence risk of developing an in-field sarcoma after breast RT in patients with TP53 PV was 8.8% (IQR, 1.4%-25%). The 15-year risk of the control cohort was 0.0% (P < .001). B, The 10-year cumulative risk of any secondary cancer was not significantly different between TP53 PV carriers who received RT (22.5% [95% CI, 8.8%-40.0%]) and RT-naive PV carriers (38% [95% CI, 15.4%-61%]) (P = .55). The shaded areas indicate 95% CIs.
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