Wen Jing-Yun, Li Mai, Li Xing, Chen Jie, Lin Qu, Ma Xiao-kun, Dong Min, Wei Li, Chen Zhan-Hong, Wu Xiang-Yuan
Department of Medical Oncology, the Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China E-mail :
Asian Pac J Cancer Prev. 2014;15(15):6275-81. doi: 10.7314/apjcp.2014.15.15.6275.
Nasal-type extranodal natural killer (NK)/T-cell lymphoma (ENKL) is a highly invasive cancer with a poor prognosis. More effective and safer treatment regimens for ENKL are needed. Pegaspargase (PEG-Asp) has a similar mechanism of action to L-asparaginase (L-Asp), but presents lower antigenicity. The aim of the present research was to evaluate the safety profile and the latent efficacy of a PEG-Asp-based treatment regimen in patients with ENKL. Data collected from 20 patients with histologically confirmed ENKL, admitted to the Third Affiliated Hospital of Sun Yat-Sen University from January 2009 to August 2013, were included in the study. All patients received 2500 IU/m2/IM PEG-Asp on day 1 of every 21-day treatment cycle. Patients received combination chemotherapy with CHOP (n=5), EPOCH (n=7), GEMOX (n=7) or CHOP with bleomycin (n=1). After 2-5 treatment cycles (median, 4 cycles) of PEG-Asp-based chemotherapy, five patients (25%) showed a complete response (CR), and the overall response rate (ORR) was 60%. Grade 3/4 neutropenia occurred in fourteen patients (70%). Grade 3 alanine aminotransferase (ALT) elevation was observed in two. Grade 1-2 non-hematological toxicity consisted of activated partial thromboplastin time (APTT) elongation (n=9), hypofibrinogenemia (n=6), hypoproteinemia (n=17), hyperglycemia (n=3), and nausea (n=6). No allergic reactions were detected. No treatment related death was reported. Our results suggested that PEG-Asp-based chemotherapy presented an acceptable tolerance and a potential short-term outcome in patients with nasal-type ENKL.
鼻型结外自然杀伤细胞(NK)/T细胞淋巴瘤(ENKL)是一种侵袭性很强、预后较差的癌症。需要更有效且更安全的ENKL治疗方案。聚乙二醇天冬酰胺酶(PEG-Asp)的作用机制与左旋门冬酰胺酶(L-Asp)相似,但抗原性较低。本研究的目的是评估基于PEG-Asp的治疗方案对ENKL患者的安全性和潜在疗效。研究纳入了2009年1月至2013年8月在中山大学附属第三医院住院治疗、经组织学确诊为ENKL的患者。所有患者在每21天治疗周期的第1天接受2500 IU/m²的肌肉注射PEG-Asp。患者接受CHOP(n = 5)、EPOCH(n = 7)、GEMOX(n = 7)或CHOP联合博来霉素(n = 1)的联合化疗。在基于PEG-Asp的化疗进行2 - 5个治疗周期(中位周期数为4个周期)后,5例患者(25%)达到完全缓解(CR),总缓解率(ORR)为60%。14例患者(70%)出现3/4级中性粒细胞减少。2例患者观察到3级丙氨酸氨基转移酶(ALT)升高。1 - 2级非血液学毒性包括活化部分凝血活酶时间(APTT)延长(n = 9)、纤维蛋白原血症(n = 6)、低蛋白血症(n = 17)、高血糖(n = 3)和恶心(n = 6)。未检测到过敏反应。未报告与治疗相关的死亡。我们的结果表明,基于PEG-Asp的化疗对鼻型ENKL患者具有可接受的耐受性和潜在的短期疗效。