Kim Tae Min, Kim Dong-Wan, Kang Yoon-Koo, Chung Jooseop, Song Hong-Suk, Kim Hyo Jung, Kim Byung Soo, Lee Jong-Seok, Kim Hawk, Yang Sung Hyun, Yuh Young Jin, Bae Sung Hwa, Hyun Myung Soo, Jeon Yoon Kyung, Kim Chul Woo, Heo Dae Seog
Seoul National University Hospital, Seoul, Republic of Korea;
Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea;
Oncologist. 2014 Nov;19(11):1129-30. doi: 10.1634/theoncologist.2014-0305. Epub 2014 Oct 3.
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).
Forty-four patients with chemo-naïve stage I/II NTCL 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).
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 = .004) and OS (p = .001), respectively.
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.
由异环磷酰胺、甲氨蝶呤、依托泊苷和泼尼松龙组成的联合化疗(IMEP)作为结外自然杀伤/T细胞淋巴瘤(NTCL)的一线和二线治疗具有活性。
44例初治的I/II期NTCL患者参加了一项前瞻性、多中心、II期研究,接受6个周期的IMEP治疗(异环磷酰胺1.5 g/m²,第1 - 3天;甲氨蝶呤30 mg/m²,第3天和第10天;依托泊苷100 mg/m²,第1 - 3天;泼尼松龙60 mg/m²,第1 - 5天),随后进行受累野放疗(IFRT)。
IMEP化疗后总缓解率为73%(41例可评估患者中有11例完全缓解[CR] [27%]),IMEP联合IFRT后总缓解率为78%(27例可评估患者中有18例CR [67%])。分别有33例患者(75%)和7例患者(16%)记录到中性粒细胞减少和血小板减少。仅8例患者(18%)发生发热性中性粒细胞减少。三年无进展生存期(PFS)和总生存期(OS)分别为66%和56%。高Ki-67(≥70%)和Ann Arbor II期分别独立降低PFS(p = 0.004)和OS(p = 0.001)。
由于IMEP化疗期间进展率高,需要更早引入IFRT。此外,应使用包括基于L-天冬酰胺酶的方案在内的积极化疗来减少I/II期NTCL的全身治疗失败。