KMID : 0939920190510010357
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´ëÇѾÏÇÐȸÁö 2019 Volume.51 No. 1 p.357 ~ p.367
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Risk Factor Analysis for Secondary Malignancy in Dexrazoxane-Treated Pediatric Cancer Patients
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Kim Hye-Ry
Kang Hyoung-Jin Park Kyung-Duk Koh Kyung-Nam Im Ho-Joon Seo Jong-JIn Lee Jae-Wook Chung Nack-Gyun Cho Bin Kim Hack-Ki Lee Jae-Min Hah Jeong-Ok Lee Jun-Ah Lee Young-Ho Park Sang-Kyu Baek Hee-Jo Kook Hoon Kim Ji-Yoon Kim Heung-Sik Kim Hwang-Min Chueh Hee-Won Park Mee-Rim Yoon Hoi-Soo Lee Mee-Jeong Choi Hyoung-Soo Ahn Hyo-Seop Kawano Yoshifumi Park Ji-Won Hahn Seo-Kyung Shin Hee-Young
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Abstract
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Purpose: Dexrazoxane has been used as an effective cardioprotector against anthracycline cardiotoxicity. This study intended to analyze cardioprotective efficacy and secondary malignancy development, and elucidate risk factors for secondary malignancies in dexrazoxane-treated pediatric patients.
Materials and Methods: Data was collected from 15 hospitals in Korea. Patients who received any anthracyclines, and completed treatment without stem cell transplantation were included. For efficacy evaluation, the incidence of cardiac events and cardiac event-free survival rates were compared. Data about risk factors of secondary malignancies were collected.
Results: Data of total 1,453 cases were analyzed; dexrazoxane with every anthracyclines group (D group, 1,035 patients) and no dexrazoxane group (non-D group, 418 patients). Incidence of the reported cardiac events was not statistically different between two groups; however, the cardiac event-free survival rate of patients with more than 400 mg/m2 of anthracyclines was significantly higher in D group (91.2% vs. 80.1%, p=0.04). The 6-year cumulative incidence of secondary malignancy was not different between both groups after considering follow-up duration difference (non-D, 0.52%¡¾0.37%; D, 0.60%¡¾0.28%; p=0.55). The most influential risk factor for secondary malignancy was the duration of anthracycline administration according to multivariate analysis.
Conclusion: Dexrazoxane had an efficacy in lowering cardiac event-free survival rates in patients with higher cumulative anthracyclines. As a result of multivariate analysis for assessing risk factors of secondary malignancy, the occurrence of secondary malignancy was not related to dexrazoxane administration.
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KEYWORD
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Dexrazoxane, Childhood, Cancer, Anthracyclines, Risk factors, Second neoplasm
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