首页> 外文OA文献 >Phase I study of dexamethasone, methotrexate, ifosfamide, l-asparaginase, and etoposide (SMILE) chemotherapy for advanced-stage, relapsed or refractory extranodal natural killer (NK)/T-cell lymphoma and leukemia
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Phase I study of dexamethasone, methotrexate, ifosfamide, l-asparaginase, and etoposide (SMILE) chemotherapy for advanced-stage, relapsed or refractory extranodal natural killer (NK)/T-cell lymphoma and leukemia

机译:I期研究地塞米松,甲氨蝶呤,异环磷酰胺,1-天冬酰胺酶和依托泊苷(smILE)化疗治疗晚期,复发或难治性结外自然杀伤(NK)/ T细胞淋巴瘤和白血病

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摘要

Extranodal natural killer (NK)/T-cell lymphoma, nasal type, and aggressive NK-cell leukemia are rare, and their standard therapy has not been established. They are Epstein-Barr virus-associated lymphoid malignancies, and tumor cells express P-glycoprotein leading to multidrug resistance of the disease. Patients with stage IV, relapsed or refractory diseases have a dismal prognosis, with survival measured in months only. To develop an efficacious chemotherapeutic regimen, we conducted a dose-escalation feasibility study of a new chemotherapeutic regimen, SMILE, comprising the steroid dexamethasone, methotrexate, ifosfamide, L-asparaginase, and etoposide. The components of SMILE are multidrug resistance-unrelated agents and etoposide. Etoposide shows both in vitro and in vivo efficacy for Epstein-Barr virus-associated lymphoproliferative disorders. Eligible patients had newly diagnosed stage IV, relapsed or refractory diseases after first-line chemotherapy, were 15-69 years of age, and had satisfactory performance scores (0-2). Four dose levels of methotrexate and etoposide were originally planned to be evaluated. At level 1, six patients with extranodal NK/T-cell lymphoma, nasal type, were enrolled. Their disease status was newly diagnosed stage IV (n = 3), first relapse (n = 2), and primary refractory (n = 1). All of the first three patients developed dose-limiting toxicities, and one of them died of sepsis with grade 4 neutropenia. A protocol revision stipulating early granulocyte colony-stimulating factor administration was made. Two out of three additional patients developed dose-limiting toxicities that were all manageable and transient. For the six enrolled patients, the overall response rate was 67% and the complete response rate was 50%. Although its safety and efficacy require further evaluation, we recommend a SMILE chemotherapy dose level of 1 for further clinical studies. © 2008 Japanese Cancer Association.
机译:结外自然杀伤(NK)/ T细胞淋巴瘤,鼻型和侵袭性NK细胞白血病很少见,尚未建立其标准疗法。它们是与爱泼斯坦-巴尔病毒相关的淋巴样恶性肿瘤,肿瘤细胞表达P-糖蛋白导致该疾病的多药耐药性。患有IV期,复发或难治性疾病的患者的预后很差,仅以几个月为单位来衡量生存。为了开发有效的化疗方案,我们对一种新的化疗方案SMILE进行了剂量递增的可行性研究,该方案​​包括类固醇地塞米松,甲氨蝶呤,异环磷酰胺,L-天冬酰胺酶和依托泊苷。 SMILE的成分是与多药耐药无关的药物和依托泊苷。依托泊苷显示出与爱泼斯坦-巴尔病毒相关的淋巴增生性疾病的体外和体内功效。符合条件的患者具有一线化疗后新诊断的IV期,复发或难治性疾病,年龄在15-69岁之间,并且表现令人满意(0-2)。最初计划评估甲氨蝶呤和依托泊苷的四个剂量水平。在第1级,招募了6例鼻外结节性NK / T细胞淋巴瘤患者。他们的疾病状态为新诊断的IV期(n = 3),首次复发(n = 2)和原发性难治性(n = 1)。前三名患者均出现了剂量限制性毒性,其中一名死于败血症并伴有4级中性粒细胞减少。进行了协议修订,规定了早期粒细胞集落刺激因子的给药。另外三分之二的患者出现了剂量可控制的暂时性毒性反应。对于这六名入组患者,总缓解率为67%,完全缓解率为50%。尽管其安全性和有效性需要进一步评估,但我们建议将SMILE化疗剂量水平设为1,以进行进一步的临床研究。 ©2008日本癌症协会。

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