Targeted Therapy With Lapatinib in Patients With Recurrent Pituitary Tumors Resistant to Standard Therapy
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 9
- 试验地点
- 3
- 主要终点
- Change in Tumor Volume
研究概览
简要总结
This study focuses on new therapies for a challenging disease in pituitary medicine, that of aggressive pituitary tumors which have limited therapeutic options beyond standard surgical, radiotherapy, and select medical therapies, each incurring significant morbidity and mortality, and each not optimally effective. To improve this gap in knowledge, we seek to translate findings from the laboratory into clinical practice and hone in on therapies directed at pituitary molecular targets, namely ErbB receptors. We have shown that human prolactinomas express nuclear EGFR and membranous ErbB2, ErbB3 and ErbB4, and expression correlates with tumor invasion. Pituitary tumor cell lines transfected with EGFR and ErbB2 translated to downstream effects on prolactin (PRL) gene expression and secretion,as well as cell proliferation. Animal models implanted with these cell lines developed larger tumors and PRL elevations. Treatment with ErbB tyrosine kinase inhibitors (TKIs) led to regression of tumors xenografted into these animals and attenuated PRL secretion. Primary culture of human prolactinomas confirmed expression of ErbB receptors and inhibitory effects of TKIs on PRL secretion and cell proliferation. Based on these exciting preliminary data, the objective of this new proposal is to conduct a Phase IIa clinical trial as a trenchant test of our translational hypothesis that tyrosine kinase inhibition constitutes highly effective targeted biologic therapy for these hitherto refractory pituitary adenomas. Specifically, our aims are to test the: 1) efficacy of TKI therapy with a clinical trial; 2) threshold level of tumor receptor expression to achieve TKI clinical response. Nineteen subjects will be treated with lapatinib for 6 months in combination with their current dopamine agonist therapy, with monthly measurements of PRL levels and MRI imaging every 3 months to evaluate the primary endpoints of achieving 40% reduction in tumor size and 50% reduction in PRL and secondary endpoints of radiologic stabilization and/or reduction and PRL normalization. Mean ErbB receptor protein expression will be compared between responders to lapatinib and non-responders by immunohistochemistry in pituitary tumor samples of these subjects collected from prior surgeries.
详细描述
PURPOSE
The drug Lapatinib has been shown to inhibit both epidermal growth factor receptor (EGFR) and erbB2 tyrosine kinases resulting in an effective slowing of disease progression in breast cancer. It has also been demonstrated that erbB is overexpressed in human pituitary adenomas. The investigators are therefore assessing tumor size stabilization and pituitary tumor secretory profiles during the course of a six month therapy of lapatinib. The purpose of this trial will be to estimate the activity of lapatinib in slowing the growth rate of pituitary tumors. Lapatinib is an FDA approved drug used to treat breast cancer. However, in this study, the drug will be used to treat pituitary cancer.
STUDY POPULATION
This study will recruit patients from the Pituitary Center at CSMC who are over the age of 18 that have a recurrent nonfunctioning adenoma after at least one surgical resection as well as patients with prolactinomas who are resistant to dopamine agonist therapy and patients with recurrent Cushing's disease.
PARTICIPANT'S JOURNEY THROUGH THE RESEARCH
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
- 否
入选标准
- •Patients with nonfunctioning adenomas who have undergone at least one prior surgical resection and have demonstrated recurrence on MRI
- •Patients with prolactinomas who are resistant to dopamine agonist therapy
- •Patients with malignant pituitary tumors
- •Patients with visual field deficits and/or compression of the optic chiasm must be stable for at least 6 months
排除标准
- •Patients with compromised visual fields and/or compression of the optic chiasm on MRI that has not been stable for last 6 months.
- •Patients that have reduced left ventricular ejection fraction less than 50%
- •Patients with moderate to severe hepatic impairment
- •Patients that are pregnant or lactating
- •Patients under the age of 18
- •Active hepatitis
- •Known previous HIV Positive
- •Concurrent cancers
- •Life expectancy less than one year
研究组 & 干预措施
Lapatinib
All participants will be asked to take Lapatinib daily for a total of six months during the research study.
干预措施: Lapatinib (Drug)
结局指标
主要结局
Change in Tumor Volume
时间窗: baseline and at 6 months
Tumor volume will be assessed on MRI at 6 months on therapy and compared to baseline MRI.
Number of Participants With 50% Reduction in Prolactin Levels
时间窗: every month, up to 6 months
50% reduction in prolactin level measured monthly on 6 months therapy compared to baseline level.
次要结局
- % Change in Prolactin From Baseline to Study End(Baseline and at 6 months)
- ErbB Receptor Expression(at 6 months)
研究者
Odelia Cooper
Principal investigator
Cedars-Sinai Medical Center
