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吉西他滨、奥沙利铂和聚乙二醇化天冬酰胺酶联合方案(P-gemox方案)治疗新诊断的晚期或复发/难治性结外NK/T细胞淋巴瘤患者的疗效

Efficacy of combined gemcitabine, oxaliplatin and pegaspargase (P-gemox regimen) in patients with newly diagnosed advanced-stage or relapsed/refractory extranodal NK/T-cell lymphoma.

作者信息

Wang Jing-Hua, Wang Liang, Liu Cheng-Cheng, Xia Zhong-Jun, Huang Hui-Qiang, Lin Tong-Yu, Jiang Wen-Qi, Lu Yue

机构信息

Department of Hematologic Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, People's Republic of China.

State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, 510060, People's Republic of China.

出版信息

Oncotarget. 2016 May 17;7(20):29092-101. doi: 10.18632/oncotarget.8647.

Abstract

Extranodal natural killer/T-cell lymphoma (ENKTL) is an aggressive neoplasm with a poor outcome. Asparaginase-based regimens are recommended for patients with advanced-stage or relapsed/refractory ENKTL. We retrospectively investigated the efficacy and toxicity of combined gemcitabine, oxaliplatin, and pegaspargase (P-gemox) in these patients. A total of 35 patients with newly diagnosed stage III-IV, relapsed or refractory ENKTL were treated with 2 to 8 cycles of P-gemox: gemcitabine (1250 mg/m2) and oxaliplatin (85 mg/m2) injected intravenously and pegaspargase (2500 IU/m2) injected intramuscularly on day 1 and repeated every 2 weeks. Upon completion of treatment, the overall response rate was 80.0%, with a complete response in 51.4% of patients. The 1-, 2- and 3- year progression-free survival rates were 45.0%, 38.6% and 38.6%, and overall survival rates were 76.8%, 64.7% and 64.7%, respectively. Patients who attained a complete response showed better progression-free survival than those without a complete response (p = 0.01). The major adverse effects were hematologic toxicity and liver dysfunction. Grade 3/4 leucopenia and neutropenia occurred in 40.0% of patients. No treatment-related deaths occurred. These results indicate the P-gemox regimen is a safe and effective treatment for patients with newly diagnosed advanced-stage or relapsed/refractory ENKTL. We anticipate future prospective trials will confirm the efficacy.

摘要

结外自然杀伤/T细胞淋巴瘤(ENKTL)是一种侵袭性肿瘤,预后较差。对于晚期或复发/难治性ENKTL患者,推荐使用基于门冬酰胺酶的治疗方案。我们回顾性研究了吉西他滨、奥沙利铂和聚乙二醇化门冬酰胺酶(P-gemox)联合方案对这些患者的疗效和毒性。共有35例新诊断的III-IV期、复发或难治性ENKTL患者接受了2至8个周期的P-gemox治疗:第1天静脉注射吉西他滨(1250 mg/m²)和奥沙利铂(85 mg/m²),肌肉注射聚乙二醇化门冬酰胺酶(2500 IU/m²),每2周重复一次。治疗结束时,总缓解率为80.0%,51.4%的患者达到完全缓解。1年、2年和3年无进展生存率分别为45.0%、38.6%和38.6%,总生存率分别为76.8%、64.7%和64.7%。达到完全缓解的患者无进展生存期优于未达到完全缓解的患者(p = 0.01)。主要不良反应为血液学毒性和肝功能障碍。40.0%的患者发生3/4级白细胞减少和中性粒细胞减少。未发生与治疗相关的死亡。这些结果表明,P-gemox方案是新诊断的晚期或复发/难治性ENKTL患者的一种安全有效的治疗方法。我们预计未来的前瞻性试验将证实其疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02ed/5045380/c21d29ea554e/oncotarget-07-29092-g001.jpg

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