Phase Ib Trial of HER2/Neu Peptide (E75) Vaccine in Breast Cancer Patients at Risk for Recurrence After Surgical and Medical Therapies
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 100
- 试验地点
- 4
- 主要终点
- The primary endpoints are the safety and optimal dosing of the vaccine to induce an in vivo peptide-specific immune response.
研究概览
简要总结
The purposes of this study are the following:
- To assess safety and document local and systemic toxicity to the peptide vaccine (E75)
- To determine maximum tolerated dose (MTD) and optimal biologic dose (OBD) for the peptide vaccine
- To evaluate the in vivo cellular immune response to the peptide vaccine
- To evaluate time to recurrence in the vaccinated patients vs. matched controls
详细描述
Breast cancer is the most common malignancy and second most common cause of cancer-specific death among women in the United States. Despite advances in the diagnosis and treatment of breast cancer, one third of the women who develop the disease will die of the disease, accounting for approximately 46,300 deaths/year. While good primary therapies are available to treat early stage breast cancer, there is a substantial failure rate to these therapies in more advanced disease.
Advances in the understanding of the immune response to cancer have lead to the genesis of immunotherapeutic approaches. Specifically, the development of anti-cancer vaccines holds promise as an adjuvant and preventive therapy for patients after both primary surgical and medical treatment for breast cancer, but who are at a high risk for recurrence. Patients with greater than four lymph nodes positive have an 87% chance of recurrence post standard surgical and medical therapies at 10 years. While patients with hormone receptor positive tumors have the option to undergo hormonal therapy, recurrence is especially high among estrogen receptor/progesterone receptor (ER/PR) negative patients. For these patients, currently there is no good treatment option after completion of primary therapy; close surveillance and watchful waiting is the standard.
It is this population of patients that a vaccine strategy to induce cellular immunity would target. We propose to vaccinate these patients with an immunogenic peptide from the HER2/neu protein. If successful, this vaccine strategy could be utilized as an adjuvant to currently accepted first line therapy in future clinical trials.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 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
- 否
入选标准
- •HER2/neu expressing tumor
- •HLA-A2+ and/or HLA-A3+ to receive the vaccine. HLA-A2- and/or HLA-A3- patients will be eligible to be included in the control group.
- •Immunologically intact with a good performance status
- •Identified as being high or intermediate risk for recurrence
- •Without evidence of disease
- •Completion of all standard first-line therapies (but may still be on hormonal therapy)
排除标准
- •Tumor does not express HER2/neu
- •Not HLA-A2+ and/or HLA-A3+
- •Receiving immunosuppressive therapy
- •In poor health (Karnofsky <60%, ECOG >2 and Tbili >1.5 and creatinine>2)
- •Pregnant (beta HCG+)
- •Metastatic disease or have refused standard therapies
- •Patients enrolled in other experimental protocols may enroll to this study only with the permission of the other study PI.
结局指标
主要结局
The primary endpoints are the safety and optimal dosing of the vaccine to induce an in vivo peptide-specific immune response.
时间窗: Time period needed to determine the maximum tolerated and optimal biologic doses.
次要结局
- The clinical endpoint is time to disease recurrence.(30 days after each monthly vaccine, then per standard of care for breast cancer.)
研究者
COL George Peoples, MD, FACS
Chief, Surgical Oncology, Brooke Army Medical Center
Walter Reed Army Medical Center
