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Clinical impact of induction treatment modalities and optimal timing of radiotherapy for the treatment of limited-stage NK/T cell lymphoma

Authors
Moon, J.-H.Lee, B.-H.Kim, J.-A.Lee, Y.J.Chae, Y.S.Yhim, H.-Y.Kwak, J.-Y.Do, Y.R.Park, Y.Song, Moo KonShin, H.-J.Kim, T.Lee, J.-J.Yang, D.-H.
Issue Date
Oct-2016
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
Chemotherapy; Extranodal NK/T cell lymphoma; Radiotherapy; Relapse
Citation
LEUKEMIA RESEARCH, v.49, pp.80 - 87
Indexed
SCIE
SCOPUS
Journal Title
LEUKEMIA RESEARCH
Volume
49
Start Page
80
End Page
87
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/153728
DOI
10.1016/j.leukres.2016.08.015
ISSN
0145-2126
Abstract
This study retrospectively investigated the optimal timing of radiotherapy (RT) in patients with limited-stage extranodal NK/T-cell lymphoma (ENTKL). Among 158 patients with newly diagnosed stage I/II ENKTL, 61 patients were treated with sequential chemotherapy followed by radiotherapy (SCRT), 55 with concurrent chemoradiotherapy followed by non-anthracycline-based chemotherapy (CCRT/CT), and 42 with chemotherapy (CT) only. The 5-year overall survival (OS) rate did not differ between SCRT (77.7 ± 5.5%) and CCRT/CT (68.9 ± 6.8%; p = 0.234). In the SCRT group, 18 patients (29.5%) relapsed within the RT field and 6 (9.8%) at systemic sites, while in the CCRT/CT group, 9 patients (16.4%) relapsed at the primary site and 14 (25.5%) at systemic sites. The 5-year cumulative incidence of relapse (CIR) at primary sites was 26.3% and 19.2% after SCRT and CCRT/CT (p = 0.308), while the 5-year CIR of systemic sites was 8.7% and 26.5% after SCRT and CCRT/CT, respectively (p = 0.010). In the multivariate analysis, NK/T-cell Prognostic Index score and CR achievement were the most important prognostic factors for survival. Although up-front RT had limitations in systemic disease control and was associated with an increased risk of systemic relapse during RT compared to SCRT, timing of RT did not significantly affect survival outcomes.
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