Risk of hematologic malignancies after breast ductal carcinoma in situ treatment with ionizing radiation

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作者
Kang Wang
Zhuyue Li
Xingxing Chen
Jianjun Zhang
Yongfu Xiong
Guochao Zhong
Yang Shi
Qing Li
Xiang Zhang
Hongyuan Li
Tingxiu Xiang
Theodoros Foukakis
Tomas Radivoyevitch
Guosheng Ren
机构
[1] The First Affiliated hospital of Chongqing Medical University,Department of Endocrine and Breast Surgery
[2] Chongqing Medical University,Key Laboratory of Molecular Oncology and Epigenetics
[3] The First Affiliated Hospital of Chongqing Medical University,Department of Oncology
[4] Karolinska Institutet,Pathology
[5] Sichuan University,West China Hospital/West China School of Nursing
[6] Fudan University,Department of Oncology, Shanghai Medical College
[7] Fudan University Shanghai Cancer Center,Department of Radiation Oncology
[8] Indiana University,Department of Epidemiology, Fairbanks School of Public Health and Melvin and Bren Simon Comprehensive Cancer Center
[9] Affiliated Hospital of North Sichuan Medical College,The First Department of Hepatobiliary Surgery
[10] the Second Affiliated Hospital of Chongqing Medical University,Department of Hepatobiliary Surgery
[11] Augusta University,Division of Biostatistics and Data Science, Department of Population Health Sciences, Medical College of Georgia
[12] Karolinska University Hospital,Breast Center, Theme Cancer
[13] Quantitative Health Sciences,undefined
[14] Lerner Research Institute,undefined
[15] Cleveland Clinic,undefined
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摘要
The increased incidence of secondary hematologic malignancies (SHM) is a well-known, potentially fatal, complication after cancer treatment. It is unknown if patients with ductal carcinoma in situ (DCIS) of the breast treated with external beam radiotherapy (RT) and who survive long-term have increased risks of secondary hematologic malignancies (SHM), especially for low/intermediate-risk subsets with limited benefits from RT. DCIS patients in Surveillance, Epidemiology, and End Results (SEER) registries (1975–2016) were identified. Relative risks (RR), hazard ratio (HR), and standardized incidence ratios (SIR) were calculated to assess the SHM risk and subsequent survival times. SHM development, defined as a nonsynchronous SHM occurring ≥1 year after DCIS diagnosis, was our primary endpoint. Of 184,363 eligible patients with DCIS, 77,927 (42.3%) in the RT group, and 106,436 (57.7%) in the non-RT group, 1289 developed SHMs a median of 6.4 years (interquartile range, 3.5 to 10.3 years) after their DCIS diagnosis. Compared with DCIS patients in the non-RT group, RT was associated with increased early risk of developing acute lymphoblastic leukemia (ALL; hazard ratio, 3.15; 95% CI, 1.21 to 8.17; P = 0.02), and a delayed risk of non-Hodgkin lymphoma (NHL; hazard ratio, 1.33; 95% CI, 1.09 to 1.62; P < 0.001). This increased risk of ALL and NHL after RT was also observed in subgroup analyses restricted to low/intermediate-risk DCIS. In summary, our data suggest that RT after breast conserving surgery for DCIS patients should be cautiously tailored, especially for low and intermediate-risk patients. Long-term SHM surveillance after DCIS diagnosis is warranted.
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