- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT00652899
Allogeneic Natural Killer Cells in Patients With Recurrent Ovarian Cancer, Fallopian Tube, and Primary Peritoneal Cancer
MT2007-19R: WCC #53 Allogeneic Natural Killer Cells in Patients With Recurrent Ovarian Cancer, Fallopian Tube, and Primary Peritoneal Cancer
RATIONALE: Giving chemotherapy, such as cyclophosphamide and fludarabine, and total-body irradiation before a donor natural killer cell infusion helps stop the growth of tumor cells. It also helps stop the patient's immune system from rejecting the donor's natural killer cells. Aldesleukin may stimulate the natural killer cells to kill ovarian, fallopian tube, or primary peritoneal cancer cells. Treating the donor natural killer cells with aldesleukin may help the natural killer cells kill more tumor cells.
PURPOSE: This phase II trial is studying how well giving laboratory-treated donor natural killer cells together with aldesleukin works when given after cyclophosphamide, fludarabine, and total-body irradiation in treating patients with recurrent and/or metastatic ovarian, fallopian tube, or primary peritoneal cancer.
연구 개요
상태
상세 설명
OBJECTIVES:
Primary
- To evaluate the in vivo expansion of an infused allogeneic natural killer (NK) cell product following a preparative regimen comprising cyclophosphamide, fludarabine phosphate, and total-body irradiation in treating patients with recurrent and/or metastatic ovarian, fallopian tube, or primary peritoneal cancer.
Secondary
- To characterize the quantitative and qualitative toxicities of this treatment regimen.
- To estimate disease response (complete or partial response) or clinical benefit (stable disease for > 6 months) as measured by Response Evaluation Criteria in Solid Tumours (RECIST) criteria.
- To estimate time to progression and overall survival.
- To estimate the association between clinical response and donor/recipient KIR ligand matching status.
Tertiary
- To evaluate immune activation of the in vivo expanded haploidentical allogeneic NK cells and its effect on the immune system.
OUTLINE:
- Preparative regimen: Patients receive fludarabine phosphate IV on days 6 to 2 preceding natural killer (NK) cell infusion and cyclophosphamide IV on days 5 and 4 preceding NK cell infusion. Patients also undergo total-body irradiation on day 1 preceding NK cell infusion.
- Allogeneic natural killer (NK) cell administration and aldesleukin: Patients receive aldesleukin-activated haploidentical allogeneic NK cells intravenously (IV) on day 0. Beginning 4-6 hours after allogeneic NK cell infusion, patients receive aldesleukin subcutaneously (SC) 3 times a week for 6 doses.
Patients achieving any initial response (complete or partial response) or a clinical benefit (stable disease for > 6 months) who progress after 6 months may receive 1 re-treatment course as above.
Blood samples are collected at baseline, on days 0, 7, 14, and 28, and then at 2 and 3 months post NK cell infusion for cytokine measurements, immunophenotyping, functional analyses, and testing for persistence of donor cells.
After completion of study treatment, patients are followed periodically for at least 1 year.
연구 유형
등록 (실제)
단계
- 2 단계
연락처 및 위치
연구 장소
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Minnesota
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Minneapolis, Minnesota, 미국, 55455
- Masonic Cancer Center at University of Minnesota
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Diagnosis of recurrent ovarian cancer, fallopian tube, or primary peritoneal cancer who meets the following criteria:
- Measurable disease (≥ 1 cm) per Response Evaluation Criteria for Solid Tumors (RECIST) - patients with bone as their only site of metastatic disease will not be eligible
- Progression on or failure to respond to at least 2 salvage chemotherapy regimens (2 regimens given for disease recurrence) for recurrent/metastatic ovarian, fallopian tube, or primary peritoneal cancer
- If history of brain metastases, stable for at least 3 months after treatment - A brain computed tomography (CT) scan will only be required in subjects with known brain metastases at the time of enrollment or in subjects with new clinical signs or symptoms suggestive of brain metastases.
- Available related HLA-haploidentical natural killer (NK) cell donor (by at least class I serologic typing). If biologic parents or siblings are available, can proceed with work-up of subject prior to return of human leukocyte antigen (HLA) typing results.
- Age 18 years or older
- Gynecology Oncology Group (GOG) performance status 0 or 1
Adequate organ function as determined by the following criteria within 14 days of study enrollment:
- Bone marrow: platelets ≥ 80,000 x 10^9/L and hemoglobin ≥ 9g/dL, unsupported by transfusions; absolute neutrophil count (ANC) ≥ 1000 x 10^9/L, unsupported by granulocyte-colony stimulating factor (G-CSF) or granulocyte macrophage-colony stimulating factor (GM-CSF)
- Renal function: creatinine (Cr) ≤ 2.0 mg/dL
- Liver function: aspartate aminotransferase (AST), alanine aminotransferase (ALT), total bilirubin, alkaline phosphatase < 5 times upper limit of institutional normal
- Cardiac: Left ventricular ejection fraction >40%
- Pulmonary function: > 50% corrected Carbon Monoxide Diffusing Capacity (DLCO) and Forced expiratory volume in one second (FEV1), if presence of pleural effusion due to metastatic disease >40% corrected DLCO and FEV1 acceptable.
- Able to be off prednisone or other immunosuppressive medications for at least 3 days prior to Day 0
- Voluntary written informed consent signed before performance of any study related procedure not part of normal medical care.
Exclusion Criteria:
- Pregnant or lactating - The agents used in this study may be teratogenic to a fetus and there is no information on the excretion of agents into breast milk. All females of childbearing potential must have a blood test or urine study within 14 days prior to registration to rule out pregnancy.
- Active infection - subjects must be afebrile, off antibiotics, and with no uninvestigated radiologic lesions (infiltrates or lesions with negative cultures or biopsies are allowed).
Human anti-mouse antibody (HAMA) monitoring: All subjects will be questioned about prior exposure to antibody therapy (including OKT3, Rituximab, Trastuzumab, etc). Responses will be recorded and reported to the FDA as part of the annual report. For subjects with no prior antibody therapy exposure, no further action will be taken. For subjects who have received previous antibody therapies 10 ml of serum (red top tube) will be drawn before starting therapy and banked per section 8.1. The presence of HAMA will not exclude a patient from the study.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위화되지 않음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: Total Body Irradiation
This group includes patients that received all chemotherapy, infusion of natural killer (NK) cells and total body irradiation per protocol. 1. Allopurinol 300 mg by mouth daily (unless known allergy) before beginning chemotherapy and continuing through day 14 post NK cell infusion. 2. Cyclophosphamide 60 mg/m^2 on Days 4 and 5 preceding NK cell infusion. 3. Fludarabine phosphate 25 mg/m^2 on Days 6 through 2 preceding NK cell infusion. 4. Radiation: total-body irradiation 200 cGy Day 1 preceding NK cell infusion. 5. Allogeneic natural killer cells- Given day 0 - dose of 1.5-8.0 * 10^7/kg. 6. Aldesleukin 10 million units 3 times/week for a total of 6 doses beginning Day 0. |
All patients are to receive allopurinol 300 mg PO daily (unless known allergy) before beginning chemotherapy and continuing through day 14 post natural killer cell infusion.
다른 이름들:
60 mg/m^2 on Days 4 and 5 preceding natural killer cell infusion.
다른 이름들:
25 mg/m^2 on Days 6 through 2 preceding natural killer cell infusion.
다른 이름들:
200 cGy Day 1 preceding natural killer cell infusion.
다른 이름들:
Given day 0 - dose of 1.5-8.0
* 10^7/kg
다른 이름들:
10 MU 3 times/week for a total of 6 doses beginning Day 0
다른 이름들:
|
|
실험적: No Total Body Irradiation
This group includes patients that received chemotherapy and infusion of natural killer cells, but did not receive total body irradiation. 1. Allopurinol 300 mg by mouth daily (unless known allergy) before beginning chemotherapy and continuing through day 14 post NK cell infusion. 2. Cyclophosphamide 60 mg/m^2 on Days 4 and 5 preceding NK cell infusion. 3. Fludarabine phosphate 25 mg/m^2 on Days 6 through 2 preceding NK cell infusion. 4. Allogeneic natural killer cells- Given day 0 - dose of 1.5-8.0 * 10^7/kg. 5. Aldesleukin 10 million units 3 times/week for a total of 6 doses beginning Day 0. |
All patients are to receive allopurinol 300 mg PO daily (unless known allergy) before beginning chemotherapy and continuing through day 14 post natural killer cell infusion.
다른 이름들:
60 mg/m^2 on Days 4 and 5 preceding natural killer cell infusion.
다른 이름들:
25 mg/m^2 on Days 6 through 2 preceding natural killer cell infusion.
다른 이름들:
Given day 0 - dose of 1.5-8.0
* 10^7/kg
다른 이름들:
10 MU 3 times/week for a total of 6 doses beginning Day 0
다른 이름들:
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Number of Patients With In Vivo Expansion of Infused Allogeneic Natural Killer (NK) Cell Product
기간: Day 12-14
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Detection of an absolute donor derived cell count of > or = 100 cells/mL after NK cell infusion.
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Day 12-14
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Number of Patients Per Disease Response
기간: 1 Month After Natural Killer Cell Infusion (Day 30)
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Response Evaluation Criteria in Solid Tumors (RECIST) criteria: Complete Response (CR)-Disappearance of all target lesions (TL); Partial Response (PR)-< or = 30% decrease in the sum of the longest diameter (LD) of TL, reference baseline sum LD; Stable Disease (SD)-Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD, reference the smallest sum LD since the treatment started; Progressive Disease (PD)- < or = 20% increase in the sum of the LD of TL, reference the smallest sum LD recorded since treatment started or appearance of < or = 1 new lesion.
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1 Month After Natural Killer Cell Infusion (Day 30)
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Median Number of Days to Progression
기간: From date of first treatment to disease progression
|
Median number of days from first date of treatment to date of disease progression (appearance of new metastatic lesions or objective tumor progression).
Defined by computated tomography (CT) imaging based on Response Evaluation Criteria In Solid Tumors (RECIST): Progressive Disease (PD) > or = 20% increase in sum of all target or any new lesions.
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From date of first treatment to disease progression
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Median Overall Survival Number of Days Patients Alive After Treatment
기간: From first date on-study (treatment) to date of death
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Median number of days patients alive from date of treatment to date of death or date of last follow-up if censored.
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From first date on-study (treatment) to date of death
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공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
- 조직학적 유형에 따른 신생물
- 신생물
- 비뇨생식기 신생물
- 부위별 신생물
- 암종
- 신생물, 선상 및 상피
- 생식기 신생물, 여성
- 내분비계 질환
- 난소 질환
- 부속기 질환
- 생식선 장애
- 내분비샘 신생물
- 나팔관 질환
- 난소 신생물
- 나팔관 신생물
- 암종, 난소 상피
- 약물의 생리적 효과
- 약리작용의 분자기전
- 항감염제
- 말초 신경계 작용제
- 항바이러스제
- 효소 억제제
- 항HIV제
- 항레트로바이러스제
- 진통제
- 감각 시스템 에이전트
- 진통제, 비마약성
- 항류마티스제
- 항대사물질, 항종양
- 항대사물질
- 항종양제
- 면역억제제
- 면역학적 요인
- 보호제
- 항종양제, 알킬화제
- 알킬화제
- 골수 파괴 작용제
- 항산화제
- 자유 라디칼 제거제
- 통풍 억제제
- 알데스류킨
- 사이클로포스파마이드
- 플루다라빈
- 플루다라빈 포스페이트
- 알로푸리놀
- 인터루킨-2
기타 연구 ID 번호
- 2007LS138
- UMN-MT2007-19R (기타 식별자: Blood and Marrow Transplantation Program)
- UMN-WCC-53 (기타 식별자: Women's Cancer Center, U of M)
- UMN-0712M23462 (기타 식별자: IRB, University of Minnesota)
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .