Zhu Fang, Liu Tao, Pan Huaxiong, Xiao Yin, Li Qiuhui, Liu Xinxiu, Chen Wangbing, Wu Gang, Zhang Liling
Cancer Center.
Department of pathology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Medicine (Baltimore). 2020 Aug 14;99(33):e21705. doi: 10.1097/MD.0000000000021705.
The optimal treatment strategy of newly diagnosed stage I/II, extranodal nasal-type natural killer/T cell lymphoma (NKTCL) remains unclear. This prospective phase II trial was conducted to explore the short-term and the long-term efficacy and safety of upfront concurrent chemoradiotherapy (CCRT) followed by pegaspargase, gemcitabine, dexamethasone, cisplatin (P-GDP) regimen in patients newly diagnosed with early stage NKTCL.Thirty patients newly diagnosed with stage I/II NKTCL were enrolled from January 2013 to December 2016, and treated as the following strategy: upfront CCRT with cisplatin weekly (25 mg/m) for 5 weeks, followed by 3 cycles of P-GDP regimen chemotherapy (pegaspargase 2500IU/m capped at 3750IU, intramuscular on day 4, gemcitabine 850 mg/m intravenous on days 1 and 8; dexamethasone 40 mg/day intravenous on days 1 to 4; and cisplatin 20 mg/m intravenous on days 1-3) 3 weeks after the completion of CCRT. The objective response rate (ORR) and the complete response (CR) rate were the primary endpoints, and the secondary endpoints were the overall survival (OS), progression-free survival (PFS), and the adverse event (AE).The median follow-up period was 51.5 months (range, 5-78months). The ORR was 93.3% (28/30) and all these 28 patients attained CR at the end of the treatment. Two patients suffered from lymphoma associated hemophagocytic syndrome (LAHS) during the period of consolidation chemotherapy and died within 2 months. The 5-year OS was 93.3%, and the 5-year PFS was 89.4%Mucositis was the most common grades 3/4 nonhematologic AEs (10%, 3/30) of CCRT. During the P-GDP chemotherapy, vomiting (6.7%, 2/30), neutropenia (43.3%, 13/30) and thrombocytopenia (23.3%, 7/30) were the major grades 3/4 toxicities during chemotherapy. No treatment-related deaths occurred.The upfront CCRT followed by P-GDP regimen chemotherapy is an effective and well-tolerated first-line treatment strategy for patients diagnosed with early stage NKTCL. Further investigation of larger sample size is warranted.
新诊断的Ⅰ/Ⅱ期结外鼻型自然杀伤/T细胞淋巴瘤(NKTCL)的最佳治疗策略仍不明确。本前瞻性Ⅱ期试验旨在探讨 upfront 同步放化疗(CCRT)序贯培门冬酶、吉西他滨、地塞米松、顺铂(P-GDP)方案对新诊断的早期NKTCL患者的短期和长期疗效及安全性。2013年1月至2016年12月纳入30例新诊断的Ⅰ/Ⅱ期NKTCL患者,并按以下策略进行治疗: upfront CCRT,顺铂每周(25mg/m)共5周,之后在CCRT完成3周后进行3个周期的P-GDP方案化疗(培门冬酶2500IU/m,最大剂量3750IU,第4天肌肉注射;吉西他滨850mg/m,第1天和第8天静脉滴注;地塞米松40mg/天,第1至4天静脉滴注;顺铂20mg/m,第1至3天静脉滴注)。客观缓解率(ORR)和完全缓解(CR)率为主要终点,次要终点为总生存期(OS)、无进展生存期(PFS)和不良事件(AE)。中位随访期为51.5个月(范围5 - 78个月)。ORR为93.3%(28/30),且所有这28例患者在治疗结束时均达到CR。2例患者在巩固化疗期间发生淋巴瘤相关噬血细胞综合征(LAHS),并在2个月内死亡。5年OS为93.3%,5年PFS为89.4%。黏膜炎是CCRT最常见的3/4级非血液学AE(10%,3/30)。在P-GDP化疗期间,呕吐(6.7%,2/30)、中性粒细胞减少(43.3%,13/30)和血小板减少(23.3%,7/30)是化疗期间主要的3/4级毒性反应。未发生与治疗相关的死亡。 upfront CCRT序贯P-GDP方案化疗是新诊断的早期NKTCL患者有效且耐受性良好的一线治疗策略。有必要进一步开展更大样本量的研究。