Kim Seok Jin, Yang Deok-Hwan, Kim Jin Seok, Kwak Jae-Yong, Eom Hyeon-Seok, Hong Dae Sik, Won Jong Ho, Lee Jae Hoon, Yoon Dok Hyun, Cho Jaeho, Nam Taek-Keun, Lee Sang-Wook, Ahn Yong Chan, Suh Cheolwon, Kim Won Seog
Division of Hematology and Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Irwon-dong, Gangnam-gu, Seoul, 135-710, Korea.
Ann Hematol. 2014 Nov;93(11):1895-901. doi: 10.1007/s00277-014-2137-6. Epub 2014 Jun 20.
We conducted a phase II trial of concurrent chemoradiotherapy (CCRT) followed by 2 cycles of L-asparaginase-containing chemotherapy for patients who were newly diagnosed with stages IE and IIE nasal extranodal NK/T cell lymphoma (ENKTL). CCRT consisted of 40-44 Gy of radiotherapy with weekly administration of 30 mg/m(2) of cisplatin for 4 weeks. Two cycles of VIDL (etoposide (100 mg/m(2)), ifosfamide (1,200 mg/m(2)), and dexamethasone (40 mg) from days 1 to 3, and L-asparaginase (4,000 IU/m(2)) every other day from days 8 to 20) were administered sequentially. CCRT yielded a 90 % overall response rate without significant side effects in 30 patients, including 20 patients with complete response (CR); however, two patients showed distant disease progression. After CCRT, VIDL chemotherapy showed an 87 % final CR rate (26/30). Although grade III or IV hematologic toxicity was frequent during VIDL chemotherapy, no treatment-related mortality was observed, and L-asparaginase-associated toxicity was manageable. With a median follow-up of 44 months, 11 patients showed local (n = 4) and distant (n = 7) relapse or progression. The estimated 5-year progression-free and overall survival rates were 73 and 60 %, respectively. In conclusion, CCRT followed by L-asparaginase-containing chemotherapy is a feasible treatment for newly diagnosed stages IE/IIE nasal ENKTL.
我们对新诊断为IE期和IIE期鼻型结外NK/T细胞淋巴瘤(ENKTL)的患者进行了一项II期试验,采用同步放化疗(CCRT),随后进行2个周期含L-天冬酰胺酶的化疗。CCRT包括40 - 44 Gy的放疗,每周给予30 mg/m²顺铂,共4周。依次给予2个周期的VIDL方案(第1至3天给予依托泊苷(100 mg/m²)、异环磷酰胺(1200 mg/m²)和地塞米松(40 mg),第8至20天每隔一天给予L-天冬酰胺酶(4000 IU/m²))。CCRT在30例患者中产生了90%的总缓解率,且无明显副作用,其中20例患者达到完全缓解(CR);然而,2例患者出现远处疾病进展。CCRT后,VIDL化疗的最终CR率为87%(26/30)。尽管VIDL化疗期间III级或IV级血液学毒性很常见,但未观察到与治疗相关的死亡,且L-天冬酰胺酶相关毒性是可控的。中位随访44个月时,11例患者出现局部(n = 4)和远处(n = 7)复发或进展。估计的5年无进展生存率和总生存率分别为73%和60%。总之,CCRT后序贯含L-天冬酰胺酶的化疗是新诊断的IE/IIE期鼻型ENKTL的一种可行治疗方法。