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临床试验/NCT00418535
NCT00418535已完成2 期

A Phase II Study of Concurrent Chemoradiation Followed by VIPD (Etoposide/Ifosfamide/Cisplatin/Dexamethasone) in Stage I, II Nasal NK/T-cell Lymphoma

Samsung Medical Center2 个研究点 分布在 2 个国家开始时间: 2006年4月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
试验地点
2

研究概览

简要总结

Nasal NK/T-cell lymphoma is a peculiar clinico-pathologic subtype of non-Hodgkin's lymphoma (NHL). Although most patients present with stage I/II, only 30-60% of the patients remain disease-free. The efficacy of the conventional anthracycline-based chemotherapy (cyclophosphamide, doxorubicin, vincristine, prednisone [CHOPP]) has been unsatisfactory.

The optimal treatment of localized NK/T-cell lymphoma has not been defined yet. The optimal dose, sequence, and multi-modality treatment with involved field radiotherapy still need to be refined. This trial is to evaluate the efficacy of concurrent chemoradiotherapy with cisplatin followed by VIPD (etoposide, ifosfamide, cisplatin, dexamethasone) in localized NK/T-cell lymphoma patients.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Pathologically confirmed NK/T-cell lymphoma
  • Localized (Ann Arbor stage I/II) disease
  • At least one measurable lesion
  • Age > 18
  • ECOG performance status 0 - 2
  • Expected life span of at least 12 weeks
  • Normal marrow function (hemoglobin ≥ 9.0 g/dL; absolute neutrophil count ≥ 1,500/mm3; platelet count ≥ 100,000/mm3)
  • Normal liver function (total bilirubin < 2x upper limit of normal [ULN], transaminase < 3x ULN)
  • Normal renal function (serum creatinine ≤ 1.5 mg/dL, creatinine clearance ≥ 50 mL/min)
  • Written informed consent

排除标准

  • Other malignancies except for treated non-melanoma skin cancers and cervical cancer in situ
  • Serious medical illnesses (congestive heart failure, angina, respiratory failure, and renal failure)
  • Acute or active infection requiring intravenous (IV) antibiotics
  • Pregnant, lactating women
  • Previous history of chemotherapy or radiotherapy
  • Concomitant medication that may influence the study drugs
  • Allergic reaction to study drugs
  • Grade 2 or greater peripheral neuropathy

研究者

申办方类型
Other

研究点 (2)

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