- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT00059904
Rituximab and Interleukin-2 in Treating Patients With Relapsed or Refractory Intermediate- or High-Grade Non-Hodgkin's Lymphoma
An Open-Labeled, Phase II Study of Rituximab in Combination With Recombinant IL-2 for Relapsed or Refractory Non-Hodgkin's Lymphoma of Intermediate- or High-Grade Histology
RATIONALE: Monoclonal antibodies such as rituximab can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. Interleukin-2 may stimulate a person's white blood cells to kill cancer cells. Combining rituximab with interleukin-2 may kill more cancer cells.
PURPOSE: Phase II trial to study the effectiveness of combining rituximab with interleukin-2 in treating patients who have relapsed or refractory intermediate- or high-grade non-Hodgkin's lymphoma.
연구 개요
상세 설명
OBJECTIVES:
- Determine the clinical efficacy of rituximab and interleukin-2 in patients with relapsed or refractory intermediate- or high-grade non-Hodgkin's lymphoma.
- Determine the 2-year progression-free survival of patients treated with this regimen.
- Determine the safety of this regimen in these patients.
- Correlate response with natural killer cell numbers and rituximab, interleukin-2 (IL-2), and soluble IL-2 receptor levels in patients treated with this regimen.
OUTLINE: This is an open-label, multicenter study.
Patients receive rituximab IV once weekly on weeks 1-4 and interleukin-2 subcutaneously 3 times weekly on weeks 2-9. Treatment continues in the absence of disease progression or unacceptable toxicity.
Patients are followed every 12 weeks for 2 years.
PROJECTED ACCRUAL: A total of 50-100 patients will be accrued for this study.
연구 유형
단계
- 2 단계
연락처 및 위치
연구 장소
-
-
New York
-
New York, New York, 미국, 10021
- Memorial Sloan-Kettering Cancer Center
-
-
참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
DISEASE CHARACTERISTICS:
Diagnosis of intermediate- or high-grade non-Hodgkin's lymphoma according to the Working Formulation, including the following subtypes:
- Diffuse large cell lymphoma
- Diffuse mixed cell lymphoma
- Immunoblastic large cell lymphoma
- CD20+ disease
- Measurable progressive or refractory disease
- No primary CNS lymphoma or lymphomatous meningitis 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:
Age
- 18 and over
Performance status
- ECOG 0-2
Life expectancy
- Not specified
Hematopoietic
- Lymphocyte count less than 20,000/mm^3
- Absolute neutrophil count at least 1,000/mm^3
- Platelet count at least 75,000/mm^3
- Hemoglobin at least 9.5 g/dL
Hepatic
- SGOT and SGPT no greater than 1.5 times upper limit of normal
- Bilirubin normal
- No liver disease
Hepatitis C-seropositive patients are allowed provided they have no active disease, as demonstrated by any of the following:
- Undetectable hepatitis C viral loads
- Biopsy showing no active disease
- Normal transaminases on at least 3 different occasions within the past year
Renal
- Creatinine normal
Cardiovascular
- No clinically significant cardiac dysfunction
- No myocardial infarction within the past 6 months
- No heart failure within the past 6 months
Pulmonary
- No clinically significant pulmonary dysfunction
- Patients with prior radiotherapy to the lung or autologous transplantation must have FEV greater than 50% and DLCO greater than 50% within 8 weeks before study treatment
Other
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- HIV negative
- No significant infections within the past 2 weeks (including pneumonia or bronchitis)
- No history of autoimmune disease
- No prior or concurrent malignancy except inactive nonmelanoma skin cancer, carcinoma in situ of the cervix, or other solid tumor curatively treated with no evidence of recurrence within the past 2 years
- No symptomatic thyroid disease requiring medical intervention other than replacement treatment for hypothyroidism
- No prior type 1 hypersensitivity or anaphylactic reactions to murine products, rituximab, or radioimmunoconjugated anti-CD20 antibody infusion
PRIOR CONCURRENT THERAPY:
Biologic therapy
- At least 3 months since prior autologous bone marrow transplantation
- No prior allogeneic bone marrow transplantation
- No prior interleukin-2
- No prior interferon (alfa, beta, or gamma)
- No concurrent basiliximab, daclizumab, or monoclonal antibody OKT3
Chemotherapy
- More than 30 days since prior chemotherapy
- No concurrent anticancer chemotherapy
Endocrine therapy
- More than 2 weeks since prior systemic steroids
- No concurrent systemic corticosteroids
Radiotherapy
- More than 30 days since prior radiotherapy
- No concurrent radiotherapy
Surgery
- More than 30 days since prior major surgery
Other
- More than 30 days since other prior investigational drugs
- More than 30 days since prior immunosuppressive medications
No concurrent immunosuppressive medications including the following:
- Cyclosporine
- Mycophenolate mofetil
- Tacrolimus
- Sirolimus
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 마스킹: 없음(오픈 라벨)
공동 작업자 및 조사자
수사관
- 연구 의자: Tarun Kewalramani, MD, Memorial Sloan Kettering Cancer Center
연구 기록 날짜
연구 주요 날짜
연구 시작
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- CHIR-IL2005-A01
- MSKCC-03004
- CDR0000298986 (레지스트리 식별자: PDQ (Physician Data Query))
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