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Comparison Study of Dendritic Cell Vaccine With and Without Cyclophosphamide to Treat Stage IV Melanoma Patients

2013년 7월 5일 업데이트: Baylor Research Institute

Melanoma Peptide-Loaded Dendritic Cell Vaccine in HLA-A*0201 Patients With Stage IV Melanoma: A Phase II Randomized Trial to Compare Vaccination With and Without Cyclophosphamide Treatment.

The purpose of this study is to determine whether the combination of chemotherapy (Cyclophosphamide) and CD34-DC vaccines results in the improved rate of clinical responses for stage IV melanoma patients.

연구 개요

상세 설명

Vaccination of patients with metastatic melanoma using ex vivo generated dendritic cells (DCs) loaded with tumor-associated antigen(s) have been shown to induce tumor-specific immunity against melanoma antigens measured by in vitro assays and, in some cases, tumor regression. At the present time, the numbers of recorded patients with metastatic melanoma who have been treated with DC vaccinations are too small to predict with certainty the future of overall therapeutic value of DC vaccinations in the management of patients with metastatic melanoma. The purpose of this study is to gather data on feasibility and efficacy of novel combination therapy of CPA and a DC vaccine outlined in this protocol to treat metastatic melanoma.

연구 유형

중재적

등록 (실제)

9

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Texas
      • Dallas, Texas, 미국, 75204
        • Baylor University Medical Center

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

21년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  1. Biopsy-proven metastatic melanoma, Stages M1a, M1b, M1c
  2. HLA-A*0201 phenotype
  3. Age: 21-75 years
  4. ECOG performance status 0-1
  5. Measurable metastatic melanoma lesions by physical examination or radiographs or scans.
  6. Adequate marrow function:

    • White count ≥ 4,000/microliter: Subjects who have recently completed chemotherapy will be allowed study entry with White count ≥ 3,500/microliter
    • Hemoglobin ≥ 10.0 gm: Subjects who have recently completed chemotherapy will be allowed study entry with Hemoglobin ≥ 9.0 gm.
    • Platelets ≥ 100,000/microliter
  7. Adequate hepatic function:

    • Bilirubin ≤ 1.5/mg/dL
    • Alkaline phosphatase ≤ 5 times the upper limit of normal
    • SGOT ≤ 5 times the upper limit of normal
    • SGPT ≤ 5 times the upper limit of normal
  8. Adequate renal function:

    • Serum creatinine ≤ 1.5/mg/dL
  9. No active CNS metastatic disease at screening.

    • Patients with a history of CNS melanoma lesions must have had lesions resected by surgery and/or gamma knife irradiation at least 3 months prior to study entry.
    • The total number of CNS lesions at diagnosis should not have exceeded 3.
  10. Written informed consent

Exclusion Criteria:

  1. Patients who have received > 8 cycles of cytotoxic chemotherapy or metastatic melanoma
  2. Patients who have received any chemotherapy < 4 weeks before the beginning of the trial
  3. Patients who have received interferon alpha (IFNα-2b) or sargramostim (GM-CSF) < 4 weeks before the beginning of the trial
  4. Patients who have received high-dose interleukin-2 (IL-2) < 4 weeks before the beginning of the trial
  5. Patients that have been diagnosed with more than 3 CNS melanoma lesions.
  6. Patients that have been diagnosed with more than 5 hepatic metastases or any hepatic metastasis > 5 cm.
  7. Baseline serum LDH > 1.1 times the upper limit of normal
  8. Patients who are HIV+ (HIV patients are often profoundly immunodeficient because of the viral infection and this additional parameter will interfere with the evaluation of DC induced immune responses in melanoma patients. Furthermore, the safety of collecting DCs, loading them with antigen and re-infusing these cells to HIV+ patients has not yet been determined.)
  9. Pregnancy (Pregnancy is associated with considerable immunosuppression 70 and this additional parameter will interfere with the evaluation of DC induced immune responses in melanoma patients. In addition, the safety and tolerability of cell body-loaded DC given subcutaneously is entirely unknown.)
  10. Patients who have received corticosteroids or other immunosuppressive agents < 4 weeks before beginning the trial
  11. Patients with active asthma and/or on treatment for asthma
  12. Patients with angina pectoris
  13. Patients with congestive heart failure
  14. Patients with a history of autoimmune disease including lupus erythematosus, rheumatoid arthritis or thyroiditis
  15. Patients with active infections including viral hepatitis
  16. Patients with a history of neoplastic disease other than melanoma < 5 years prior to entry on the trial except for patients with carcinomas in situ of the cervix and basal/squamous cell carcinomas of the skin. Patients who have any of these two types of cancer and melanoma can be included.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 더블

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: DC Vaccine & Cyclophosphamide

Patients will receive a fixed dose of about ≥15x106 viable dendritic cells per injection. Patients will receive a total of 8 doses of the vaccination with each individual dose being administered at weeks: 0, 2, 4, 6, 10, 14, 18 and 22. Responses will be evaluated and patients with SD, PR or CR may receive 4 more vaccine at 36, 48, 72 and 96 weeks, if there is vaccine available. The vaccine will be injected subcutaneously, in 3 separate injection sites (3.3.ml per site) in the upper and lower extremities.

Patients will receive either CPA 300mg/m2 for injections administered intravenously over a 2-hour infusion in the outpatient clinic 24 hours prior to DC vaccinations # 1, 3, 5, 6 and 7.

Patients will receive a fixed dose of about ≥15x106 viable dendritic cells per injection. Patients will receive a total of 8 doses of the vaccination with each individual dose being administered at weeks: 0, 2, 4, 6, 10, 14, 18 and 22. Responses will be evaluated and patients with SD, PR or CR may receive 4 more vaccine at 36, 48, 72 and 96 weeks, if there is vaccine available. The vaccine will be injected subcutaneously, in 3 separate injection sites (3.3.ml per site) in the upper and lower extremities.

Patients will receive either CPA 300mg/m2 for injections administered intravenously over a 2-hour infusion in the outpatient clinic 24 hours prior to DC vaccinations # 1, 3, 5, 6 and 7.

다른 이름들:
  • Cyclophosphamide (CPA)
  • DC Vaccine ( Dendritic cell vaccine)
위약 비교기: DC Vaccine & Placebo

Patients will receive a fixed dose of about ≥15x106 viable dendritic cells per injection. Patients will receive a total of 8 doses of the vaccination with each individual dose being administered at weeks: 0, 2, 4, 6, 10, 14, 18 and 22. Responses will be evaluated and patients with SD, PR or CR may receive 4 more vaccine at 36, 48, 72 and 96 weeks, if there is vaccine available. The vaccine will be injected subcutaneously, in 3 separate injection sites (3.3.ml per site) in the upper and lower extremities.

Patients will receive saline for injections administered intravenously over a 2-hour infusion in the outpatient clinic 24 hours prior to DC vaccinations # 1, 3, 5, 6 and 7.

Patients will receive a fixed dose of about ≥15x106 viable dendritic cells per injection. Patients will receive a total of 8 doses of the vaccination with each individual dose being administered at weeks: 0, 2, 4, 6, 10, 14, 18 and 22. Responses will be evaluated and patients with SD, PR or CR may receive 4 more vaccine at 36, 48, 72 and 96 weeks, if there is vaccine available. The vaccine will be injected subcutaneously, in 3 separate injection sites (3.3.ml per site) in the upper and lower extremities.

Patients will receive saline for injections administered intravenously over a 2-hour infusion in the outpatient clinic 24 hours prior to DC vaccinations # 1, 3, 5, 6 and 7.

다른 이름들:
  • DC 백신 - 수지상 세포 백신

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
Induction of melanoma-specific CD8+T Cell Immunity.
기간: 2 years
2 years

2차 결과 측정

결과 측정
기간
Rate of objective clinical responses.
기간: 2 years
2 years

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Joseph Fay, M.D., Baylor Institute for Immunology Research: Baylor University Medical Center

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2008년 6월 1일

기본 완료 (실제)

2011년 4월 1일

연구 완료 (실제)

2012년 7월 1일

연구 등록 날짜

최초 제출

2008년 7월 23일

QC 기준을 충족하는 최초 제출

2008년 7월 24일

처음 게시됨 (추정)

2008년 7월 25일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2013년 7월 8일

QC 기준을 충족하는 마지막 업데이트 제출

2013년 7월 5일

마지막으로 확인됨

2013년 7월 1일

추가 정보

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. .

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