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临床试验/NCT00002697
NCT00002697已完成2 期

HIGH DOSE CHEMORADIOTHERAPY WITH PERIPHERAL BLOOD PROGENITOR CELL TRANSPLANTATION FOR PATIENTS WITH PRIMARY REFRACTORY, RELAPSED AND POOR PROGNOSIS NON-HODGKIN'S LYMPHOMA

Memorial Sloan Kettering Cancer Center1 个研究点 分布在 1 个国家开始时间: 1995年9月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
试验地点
1

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with radiation therapy and peripheral stem cell transplantation may kill more tumor cells.

PURPOSE: Phase II trial to study the effectiveness of high-dose combination chemotherapy plus radiation therapy followed by peripheral stem cell transplantation in patients with refractory or recurrent non-Hodgkin's lymphoma.

详细描述

OBJECTIVES:

  • Determine the efficacy of mobilization using filgrastim (G-CSF) with or without standard-dose ifosfamide, carboplatin, and etoposide (ICE), conditioning using ifosfamide and etoposide plus total body irradiation or high-dose ICE, and autologous peripheral blood stem cell (PBSC) transplantation as salvage therapy in patients with refractory, recurrent, or poor prognosis non-Hodgkin's lymphoma.
  • Determine the efficacy of reinduction comprising ICE followed by autologous PBSC transplantation in these patients.
  • Determine the ability of standard-dose ICE combined with hematopoietic growth factors to mobilize PBSC in these patients.
  • Determine the contamination of PBSC by lymphoma cells in patients treated with this mobilization regimen.
  • Determine the quality of life of patients treated with this regimen.

OUTLINE: Patients are stratified according to disease status (relapsed vs refractory), lymphoma grade (low vs intermediate vs high), number of extranodal sites, serum lactic dehydrogenase, performance status, age, and volume of disease.

  • Mobilization/harvest: Patients in first or greater complete remission (CR) are treated on regimen A, whereas patients with recurrent or refractory disease are treated on regimen B.

  • Regimen A: Patients with poor prognosis intermediate-grade lymphoma (IGL) in first CR or IGL or low-grade lymphoma (LGL) in second or greater CR receive mobilization with filgrastim (G-CSF) subcutaneously (SC) daily on days 1-7. Autologous peripheral blood stem cells (PBSC) are harvested and selected for CD34+ cells on days 5 and 6 (and day 7 if needed).

  • Regimen B: Patients who are currently on the MSKCC standard dose salvage therapy protocol with ifosfamide, carboplatin, and etoposide (ICE) for recurrent or refractory IGL receive additional mobilization with G-CSF after completion of the last course of ICE. Patients with recurrent or refractory IGL, immunoblastic lymphoma, or LGL who have not previously received ifosfamide and are not currently on the MSKCC standard dose salvage protocol with ICE receive ifosfamide IV and carboplatin on day 2 and etoposide IV on days 1-3 (standard-dose ICE) followed by G-CSF SC. When blood counts recover, autologous PBSC are harvested and selected for CD34+ cells.

  • Regimens A and B: If additional hematopoietic growth factors (HGFs) become available, they may be administered concurrently with G-CSF. If inadequate CD34+ cells are collected, then autologous bone marrow is harvested.

  • Conditioning: Patients who are under age 60 and have not received dose-limiting radiotherapy are treated on regimen C. Patients who are age 60 and over and patients who are under age 60 and have received dose-limiting radiotherapy are treated on regimen D.

研究设计

研究类型
Interventional
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •DISEASE CHARACTERISTICS:
  • •One of the following diagnoses:
  • •Histologically proven recurrent non-Hodgkin's lymphoma
  • •Previously in complete remission (CR)
  • •Refractory or recurrent intermediate-grade lymphoma (IGL) or high-grade immunoblastic lymphoma (IBL) meeting 1 of the following conditions:
  • •In partial remission (PR) or CR to and currently enrolled on the MSKCC standard dose salvage regimen with ifosfamide, carboplatin, and etoposide (ICE)
  • •In PR or CR after 1-2 other salvage chemotherapy regimens (e.g., 3 courses of dexamethasone, high-dose cytarabine, and cisplatin (DHAP); 2 courses of cyclophosphamide, mechlorethamine, vincristine, procarbazine, and prednisone (C-MOPP))
  • •No prior ifosfamide
  • •Low-grade lymphoma
  • •In second or greater remission or chemosensitive relapse
  • •No HLA identical sibling donor available
  • •IGL or IBL
  • •In first CR
  • •Poor prognosis, defined by age-adjusted international index of 3 or 4 based on lactic dehydrogenase, number of extranodal sites, stage, and performance status
  • •Adequate bone marrow cellularity
  • •No lymphoblastic or small noncleaved cell lymphoma
  • •Ineligible for total body irradiation (TBI) phase of study if prior radiotherapy dose precludes the use of TBI NOTE: A new classification scheme for adult non-Hodgkin's lymphoma has been adopted by PDQ. The terminology of "indolent" or "aggressive" lymphoma will replace the former terminology of "low", "intermediate", or "high" grade lymphoma.However, this protocol uses the former terminology.
  • •PATIENT CHARACTERISTICS:
  • •Physiologic 18 to 65
  • •Performance status:
  • •Not specified
  • •Hematopoietic:
  • •Not specified
  • •Bilirubin no greater than 2.0 mg/dL (if no history of Gilbert's disease)
  • •No chronic active or persistent hepatitis
  • •Hepatitis B positivity allowed provided that the following conditions are met:
  • •Bilirubin same as above*
  • •SGPT no greater than 500 IU/L*
  • •Alkaline phosphatase no greater than 2 times normal* NOTE: * In the absence of liver involvement by lymphoma
  • •Creatinine no greater than 1.5 mg/dL OR
  • •Creatinine clearance at least 60 mL/min
  • •No history of chronic renal insufficiency
  • •Cardiovascular:
  • •LVEF at least 50% by echocardiogram or MUGA scan
  • •No myocardial infarction within the past 6 months
  • •No unstable angina
  • •No arrhythmia other than chronic atrial fibrillation
  • •DLCO at least 50% predicted (corrected for hemoglobin and alveolar ventilation)
  • •HIV negative
  • •No uncontrolled infection
  • •No other malignancy within the past 5 years except curatively treated basal cell skin cancer or carcinoma in situ of the cervix
  • •Not pregnant or nursing
  • •Negative pregnancy test
  • •Fertile patients must use effective contraception
  • •PRIOR CONCURRENT THERAPY:
  • •Biologic therapy
  • •Not specified
  • •Chemotherapy
  • •See Disease Characteristics
  • •Endocrine therapy
  • 另有 4 项未显示

排除标准

  • 未提供

研究者

申办方类型
Other

研究点 (1)

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