Chronic liver disease and radiation-induced second primary liver malignancy: a retrospective cohort based on SEER database 2010-2021.
코호트
1/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
환자: liver fibrosis
I · Intervention 중재 / 시술
RT had an increased risk for GI SPMs (Observed = 24, O/E = 3
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
However, who received no RT had an 8-fold increased risk for liver SPM. Thus, screening for HCC in cirrhotic patients exposed to RT is a must for early detection and better management outcome.
[INTRODUCTION] Cirrhotic patients are at a high risk of developing radiation-induced liver toxicities despite the modern safe radiation delivery techniques due to the low liver tolerance.
APA
Ellaithy A, Serageldeen A, et al. (2025). Chronic liver disease and radiation-induced second primary liver malignancy: a retrospective cohort based on SEER database 2010-2021.. Annals of medicine and surgery (2012), 87(8), 4742-4750. https://doi.org/10.1097/MS9.0000000000003446
MLA
Ellaithy A, et al.. "Chronic liver disease and radiation-induced second primary liver malignancy: a retrospective cohort based on SEER database 2010-2021.." Annals of medicine and surgery (2012), vol. 87, no. 8, 2025, pp. 4742-4750.
PMID
40787534 ↗
Abstract 한글 요약
[INTRODUCTION] Cirrhotic patients are at a high risk of developing radiation-induced liver toxicities despite the modern safe radiation delivery techniques due to the low liver tolerance. Recent studies demonstrated a potential risk of second primary malignancies (SPMs) following radiotherapy (RT) with further investigations for strategies to decrease RT-induced SPMs. However, it is insufficiently addressed if developing liver SPMs is a serious adverse event following RT for cirrhotic patients. Thus, we aimed to quantitatively assess the risk of gastrointestinal (GI) and liver SPMs following RT in patients with liver fibrosis.
[METHODS] The SEER*Stat beta software version 9.0.32 was used to obtain and analyze the data of patients with chronic liver disease diagnosed from 2010 to 2021. We sub-grouped patients according to the history of receiving RT for prior cancer treatment into two groups and excluded patients with unknown RT administration history.
[RESULTS] We observed 215 cirrhotic patients developed GI SPMs (O/E = 2.76, < 0.05, ER = 45.51), 106 of them developed liver SPMs (O/E = 8.80, < 0.05). Patients with liver cirrhosis who received RT had an increased risk for GI SPMs (Observed = 24, O/E = 3.34, < 0.05) compared to who received no RT (O/E = 2.71, < 0.05, ER = 43.72). Liver SPMs after RT in cirrhotic patients had an O/E of 12.31 (Observed = 13, < 0.05) while the group who received no RT had an O/E of 8.46 (Observed = 93, < 0.05, ER = 29.77).
[CONCLUSION] Cirrhotic patients who received RT before had an increased risk for GI SPMs by three folds and a 12-fold increased risk for liver SPMs. However, who received no RT had an 8-fold increased risk for liver SPM. Thus, screening for HCC in cirrhotic patients exposed to RT is a must for early detection and better management outcome.
[METHODS] The SEER*Stat beta software version 9.0.32 was used to obtain and analyze the data of patients with chronic liver disease diagnosed from 2010 to 2021. We sub-grouped patients according to the history of receiving RT for prior cancer treatment into two groups and excluded patients with unknown RT administration history.
[RESULTS] We observed 215 cirrhotic patients developed GI SPMs (O/E = 2.76, < 0.05, ER = 45.51), 106 of them developed liver SPMs (O/E = 8.80, < 0.05). Patients with liver cirrhosis who received RT had an increased risk for GI SPMs (Observed = 24, O/E = 3.34, < 0.05) compared to who received no RT (O/E = 2.71, < 0.05, ER = 43.72). Liver SPMs after RT in cirrhotic patients had an O/E of 12.31 (Observed = 13, < 0.05) while the group who received no RT had an O/E of 8.46 (Observed = 93, < 0.05, ER = 29.77).
[CONCLUSION] Cirrhotic patients who received RT before had an increased risk for GI SPMs by three folds and a 12-fold increased risk for liver SPMs. However, who received no RT had an 8-fold increased risk for liver SPM. Thus, screening for HCC in cirrhotic patients exposed to RT is a must for early detection and better management outcome.
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