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Risk Factor Analysis for Secondary Malignancy in Dexrazoxane-Treated Pediatric Cancer Patientsopen access

Authors
Kim, HyeryKang, Hyoung JinPark, Kyung DukKoh, Kyung-NamIm, Ho JoonSeo, Jong JinLee, Jae WookChung, Nack-GyunCho, BinKim, Hack KiLee, Jae MinHah, Jeong OkLee, Jun AhLee, Young HoPark, Sang KyuBaek, Hee JoKook, HoonKim, Ji YoonKim, Heung SikKim, Hwang MinChueh, Hee WonPark, MeerimYoon, Hoi SooLee, Mee JeongChoi, Hyoung SooAhn, Hyo SeopKawano, YoshifumiPark, Ji WonHahn, SeokyungShin, Hee Young
Issue Date
Jan-2019
Publisher
KOREAN CANCER ASSOCIATION
Keywords
Dexrazoxane; Childhood; Cancer; Anthracyclines; Risk factors; Second neoplasm
Citation
CANCER RESEARCH AND TREATMENT, v.51, no.1, pp 357 - 367
Pages
11
Journal Title
CANCER RESEARCH AND TREATMENT
Volume
51
Number
1
Start Page
357
End Page
367
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/74879
DOI
10.4143/crt.2017.457
ISSN
1598-2998
2005-9256
Abstract
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/m(2) 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%+/- 0.37%; D, 0.60%+/- 0.28%; 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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