跳至主要内容
临床试验/NCT00005780
NCT00005780已完成2 期

Pilot Study of Idiotype Vaccine and EPOCH-Rituximab Chemotherapy in Untreated Mantle Cell Lymphoma

National Cancer Institute (NCI)1 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2000年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
26
试验地点
1
主要终点
Percentage of Participants With an Antibody Response to Idiotype Vaccine

研究概览

简要总结

This study will evaluate the safety and effectiveness of an experimental cancer vaccine for mantle cell lymphoma a form of cancer of the white blood cells called lymphocytes. Although standard treatments for lymphoma may achieve disease remission, none provides a cure.

Patients with mantle cell lymphoma 18 years and older who have not been treated previously with chemotherapy may participate in this study. Candidates will be screened for eligibility with a medical history and physical examination. Other tests that may be required include blood and urine tests; lung function studies; imaging tests such as magnetic resonance imaging, computed tomography and X-rays; and biopsy (surgical removal of a small tissue sample) of tumor, bone marrow, or other tissue.

Patients enrolled in the study will begin treatment with chemotherapy designed to reduce disease to a minimum that is, to achieve remission or shrink the tumor as much as possible. Chemotherapy will be administered on an outpatient basis over a period of around 12 to 18 weeks in 3-week cycles as follows: prednisone by mouth on days 1 through 5; etoposide, doxorubicin and vincristine intravenously through (a vein) on days 1 through 5; and cyclophosphamide intravenously on day 5. Starting day 6, patients receive no chemotherapy for 16 days. In addition, an antibody called rituximab, which attaches to lymphoma cells and may increase the effectiveness of the chemotherapy, will be given on day 1 of the cycle. Patients will also receive a protein called granulocyte colony-stimulating factor (G-CSF) starting day 6 of the cycle and continuing until the white blood cell count recovers or until day 19. G-CSF is naturally produced by bone marrow and may boost the immune system. The chemotherapy drugs and rituximab are infused through a vein by means of a lightweight portable pump, which patients are taught how to use. Patients are also how taught how to give themselves G-CSF injections under the skin, similar to insulin injections.

The first vaccination will be given at least 3 months after chemotherapy ends and will be repeated every 4 weeks for a maximum of 5 vaccinations. The vaccinations will be given in the clinic. Patients will also receive daily injections of granulocyte-macrophage colony-stimulating factor (GM-CSF), a growth factor naturally produced by bone marrow that can boost the immune system. These injections will be given the day of the vaccination and for the next 3 days.

When vaccine therapy is completed, patients who were treated successfully will be followed with periodic clinic visits for follow-up examinations and tests. Patients in whom the lymphoma did not disappear entirely or who have a recurrence of disease will be advised of further treatment possibilities....

详细描述

Background:

  • Mantle cell lymphoma presents a particular clinical challenge because it is aggressive and incurable with chemotherapy. Thus, novel treatment approaches are needed.
  • In follicular center cell lymphomas, another incurable disease, recent evidence suggests that molecular complete remissions may be achieved following idiotype vaccination in patients who have achieved minimal residual disease with combination chemotherapy.
  • These results suggest that idiotype vaccines may be able to induce a clinically significant immune response against lymphoma.

Objectives:

  • To assess if etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab (EPOCH-R)/idiotype vaccination is associated with a median progression-free survival consistent with 36 months;
  • To assess if rituximab affects generation of T-cell immunity against the idiotype.
  • To compare T-cell immunity using two different methods of isolating the idiotype protein.

Eligibility:

研究设计

研究类型
Interventional
分配方式
Na
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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab

Experimental

Etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab (EPOCH-R) followed by idiotype vaccine and granulocyte-macrophage colony-stimulating factor (GM-CSF).

干预措施: EPOCH-R (Drug)

Etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab

Experimental

Etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab (EPOCH-R) followed by idiotype vaccine and granulocyte-macrophage colony-stimulating factor (GM-CSF).

干预措施: GM-CSF (Biological)

Etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab

Experimental

Etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin, and rituximab (EPOCH-R) followed by idiotype vaccine and granulocyte-macrophage colony-stimulating factor (GM-CSF).

干预措施: Idiotype vaccine (Biological)

结局指标

主要结局

Percentage of Participants With an Antibody Response to Idiotype Vaccine

时间窗: Weeks 12 to 32

Participants with an immune response to idiotype vaccine measured by enzyme-linked immunosorbent assay (ELISA) to detect antibody binding to tumor cells. Positive response was defined as at least a fourfold increase in antibody titer.

Median Progression-free Survival (PFS) in Participants Treated With Etoposide, Prednisone, Vincristine, Cyclophosphamide, Doxorubicin, and Rituximab (EPOCH-R)

时间窗: From participants on study date until date of disease relapse or progression, death, or date of last follow-up, assessed up to 245.8 months

PFS is time from on study date until disease relapse or progression, death, or date of last follow-up. Progression was measured by the International Workshop to Standardize Response Criteria for non-Hodgkin's Lymphoma and is defined as ≥50% increase from nadir in the sum of the products of the greatest diameters (SPD) of any previously involved node or the appearance of any new lesion.

次要结局

  • Percentage of Participants With Antibodies to Keyhole Limpet Haemocyanin (KLH)(After vaccinations administered at 0, 1, 2, 3 and 5 months)
  • Time to Recovery of CD4 T Lymphocytes (CD4+)(After chemotherapy before vaccination, up to 6 months)
  • Percentage of Participants Whose Cancer Shrinks or Disappears After Treatment With Etoposide, Prednisone, Vincristine, Cyclophosphamide, Doxorubicin, and Rituximab (EPOCH-R)(After 6 cycles of EPOCH-R therapy, an average of 18 weeks)
  • Percentage of Participants With Grade 3 or Higher Serious and/or Non-serious Toxicity That Occurred That is at Least Possibly Related to Drug or Vaccine(Up to 30 days after last intervention, up to 12.5 months or 1.04 years)
  • Overall Survival (OS)(Time from treatment start date until date of death or date last follow-up, up to 250 months)
  • Percentage of Participants With Induction of Type 1 Cytokine T-cell Response(After vaccinations administered at 0, 1, 2, 3 and 5 months)
  • Progression Free Survival (PFS) in Participants Who Received Idiotype Vaccine(Time from treatment start date until date of disease relapse or progression, death, or date last follow-up, an average of 25 months)

研究者

申办方类型
Nih
责任方
Principal Investigator
主要研究者

Christopher Melani, MD

Principal Investigator

National Cancer Institute (NCI)

研究点 (1)

Loading locations...

相似试验