Efficacy of a pegaspargase-based regimen in the treatment of newly-diagnosed extranodal natural killer/T-cell lymphoma

被引:26
|
作者
Li, L. [1 ]
Zhang, C. [1 ]
Zhang, L. [1 ]
Li, X. [1 ]
Wu, J. J. [1 ]
Sun, Z. C. [1 ]
Fu, X. R. [1 ]
Wang, X. H. [1 ]
Chang, Y. [1 ]
Wang, R. [1 ]
Qiu, Y. J. [1 ]
Zhang, M. Z. [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Oncol, Zhengzhou 450052, Henan Province, Peoples R China
关键词
pegaspargase; extranodal NK/T-cell lymphoma; non-Hodgkin's lymphoma; medical oncology; ACUTE LYMPHOBLASTIC-LEUKEMIA; L-ASPARAGINASE; NASAL TYPE; T-CELL; (NK)/T-CELL LYMPHOMA; SMILE CHEMOTHERAPY; PHASE-2; TRIAL; STAGE; GEMCITABINE; THERAPY;
D O I
10.4149/neo_2014_029
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Extranodal natural killer (NK)/T-cell lymphoma (ENKL) is an aggressive neoplasm with poor prognosis. Currently, there is no consensus on the optimal treatment of this disease. In this study, we report the efficacy of a pegaspargase (PEG-Asp)based chemotherapy, a DDGP regimen (PEG-Asp, dexamethasone, cisplatin, gemcitabine), for the treatment of newly-diagnosed ENKL. From August 2010 to May 2012, 12 patients with newly-diagnosed stage II - IV ENKL were initially treated with a DDGP regimen in our center. Ten patients (10/12, 83.3%) achieved complete response (CR) and two (2/12, 16.7%) achieved partial response (PR). The objective overall response rate (ORR) was 100%. Three patients (3/12, 25.0%) relapsed, and as a result, two died of disease. Eight patients (8/12, 66.7%) were alive with no evidence of disease (NOD) after a median follow-up of 19 months (range 16 31 months). Hematologic toxicity was the most frequent toxicity reported in this study. Grade 3/4 leukopenia and neutropenia were common and both occurred in eight patients (8/12, 66.7%), respectively. Additionally, six patients (6/12, 50.0%) experienced grade 3/4 thrombocytopenia and three (3/12,25.0%) experienced grade 3/4 anemia. However, no patient died of hematologic toxicity. Our results demonstrate the significant efficacy and safety profile of a DDGP regimen in the treatment of newly-diagnosed ENKL, and indicate the potential of this regimen as a first-line therapy against this disease.
引用
收藏
页码:225 / 232
页数:8
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