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A Phase II Study of Ifosfamide, Methotrexate, Etoposide, and Prednisolone for Previously Untreated Stage I/II Extranodal Natural Killer/T-Cell Lymphoma, Nasal Type: A Multicenter Trial of the Korean Cancer Study Group

Authors
Kim, Tae MinKim, Dong-WanKang, Yoon-KooChung, JooseopSong, Hong-SukKim, Hyo JungKim, Byung SooLee, Jong-SeokKim, HawkYang, Sung HyunYuh, Young JinBae, Sung HwaHyun, Myung SooJeon, Yoon KyungKim, Chul WooHeo, Dae Seog
Issue Date
Nov-2014
Publisher
ALPHAMED PRESS
Citation
ONCOLOGIST, v.19, no.11, pp.1129 - 1130
Indexed
SCIE
SCOPUS
Journal Title
ONCOLOGIST
Volume
19
Number
11
Start Page
1129
End Page
1130
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/97019
DOI
10.1634/theoncologist.2014-0305
ISSN
1083-7159
Abstract
Background. Combination chemotherapy consisting of ifosfamide, methotrexate, etoposide, and prednisolone (IMEP) was active as first-line and second-line treatment for extranodal natural killer/T-cell lymphoma (NTCL). Methods. Forty-four patients with chemo-naive stage I/IINTCL were enrolled in a prospective, multicenter, phase II study and received six cycles of IMEP (ifosfamide 1.5 g/m(2) on days 1-3; methotrextate 30 mg/m(2) on days 3 and 10; etoposide 100 mg/m(2) on days 1-3; and prednisolone 60 mg/m(2) per day on days 1-5) followed by involved field radiotherapy (IFRT). Results. Overall response rates were 73% (complete remission [CR] in 11 of 41 evaluable patients [27%]) after IMEP chemotherapy and 78% (CR 18 of 27 evaluable patients [67%]) after IMEP followed by IFRT. Neutropenia and thrombocytopenia were documented in 33 patients (75%) and 7 patients (16%), respectively. Only 8 patients (18%) experienced febrile neutropenia. Three-year progression-free survival (PFS) and overall survival (OS) were 66% and 56%, respectively. High Ki-67 (>= 70%) and Ann Arbor stage II independently reduced PFS (p= 5.004) and OS (p =5.001), respectively. Conclusion. Due to the high rate of progression during IMEP chemotherapy, IFRT needs to be introduced earlier. Moreover, active chemotherapy including an L-asparaginase-based regimen should be use to reduce systemic treatment failure in stage I/II NTCL.
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