Efficacy and Safety of the Combination of Low-dose Ibrutinib and Itraconazole in Moderate to Severe Chronic Graft Versus Host Disease: a Phase 2 Trial
试验速览
- 阶段
- 2 期
- 发起方
- 入组人数
- 13
- 试验地点
- 1
- 主要终点
- Treatment safety
研究概览
简要总结
Chronic graft-versus-host disease (cGVHD) affects 30 to 70% of Allogeneic Hematopoietic Cell Transplantation, decreases the quality of life, and increases mortality. First-line treatments for cGVHD are steroids, however, up to 50% of patients do not respond to treatment. There is no well-defined second-line treatment for cGVHD, but ibrutinib, a Bruton tyrosine kinase inhibitor, has been successfully used in phase 2 clinical trials for moderate to severe steroid-refractory cGVHD and has been shown to be safe, showing rates of response of 69% at a median follow-up of 26 months. Therefore, ibrutinib was approved by the FDA for the treatment of steroid-refractory cGVHD. Also, it is known that ibrutinib is metabolized by cytochrome isoenzyme 3A4 and that itraconazole is a potent inhibitor of this hepatic isoenzyme. Therefore, the investigators hypothesized that in subjects with newly diagnosed cGVHD and in patients with steroid-refractory cGVHD, low-dose ibrutinib in combination with itraconazole might be effective and safe.
详细描述
In this phase 2 clinical trial, patients with newly diagnosed cGVHD and refractory cGVHD will receive low-dose ibrutinib (140mg/day) combined with a cytochrome 3A4 inhibitor (itraconazole, 100mg BID) for six months. The follow-up consists of weekly visits for the first months and then monthly for six months. The investigators will address clinical and biochemical parameters in each visit and grade severity using the NIH (2014) scale. Also, patients will answer the modified Lee symptom scale, and grade response to treatment using the National Institutes of Health (NIH) Consensus Panel Chronic GVHD Activity Assessment (2014). The investigators will grade adverse events with the Common Terminology Criteria for Adverse Events [v5.0]. The investigators will report proportion and time to any response, complete response, partial response, stable disease, and progression. Also, the investigators will report the proportion of patients that interrupted steroids for at least one month, the proportion of patients that interrupted every immunosuppressive therapy for at least one month, and the proportion of patients that interrupted ibrutinib specifying the cause of the interruption.
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
- •Age (>18 years)
- •Any type of peripheral blood stem cell transplant (matched-related, match non-related, and haplo)
- •Any conditioning regimen
- •Newly diagnosed moderate to severe chronic graft versus host disease
- •Steroid refractory moderate to severe chronic graft versus host disease defined as progression with prednisone 1mg/kg/day, or stable disease after four to six weeks of prednisone >0.5 mg/kg/day, or disease progression when reducing prednisone below <0.5 mg/kg/día.
- •Eastern Cooperative Oncology Group (ECOG) <= 2
排除标准
- •Disease relapse (excluding positive minimal residual disease)
- •Secondary malignancies
- •Disease progression
- •Use of B lymphocyte cytotoxics in the last month (i.e., rituximab, bortezomib)
- •Advance stages of heart failure (NYHA III o IV)
- •Ventricular arrhythmias
- •Uncontrolled hypertension
- •Ischemic heart diseases such as unstable angina or stable angina in the last six months
- •Hepatitis B or C
- •Hypersensitivity to ibrutinib
- •Active bleeding
- •Uncontrolled acute infection
- •Hepatopathy Child-Pugh C
- •Pregnancy
研究组 & 干预措施
Low-dose ibrutinib
Patients will receive ibrutinib 140mg/day PO in combination with oral itraconazole (100mg/day) continuously for six months.
干预措施: Low-dose ibrutinib (Drug)
结局指标
主要结局
Treatment safety
时间窗: Up to six months of enrollment
Treatment safety will be addressed by obtaining the proportion of patients with grade \>=3 adverse events as defined by the Common Terminology Criteria for Adverse Events \[v5.0\]. If the proportion of \>=3 adverse events is less than 20% then the treatment will be defined as safe.
Overall response rate
时间窗: Up to six months of enrollment
The proportion of patients with partial and/or complete response at six months of follow-up.
次要结局
- Steroid-free cumulative incidence(Up to six months post enrollment)
- Overall treatment-free survival(Up to six months post enrollment)
- Low-dose steroid cumulative incidence(Up to six months post enrollment)
- Immunosuppressive-free cumulative incidence(Up to six months post enrollment)
- Overall survival(Up to six months post enrollment)
- Time to any response(From date of inclusion until the date of first documented response (partial or complete), assessed up to six months.)
- Time to progression(From date of inclusion until the date of first documented progression, assessed up to 6 months.)
- Complete response rate(Up to six months post enrollment)
- Partial response rate(Up to six months post enrollment)
- Progression rate(Up to six months post enrollment)
- Any adverse events rate(Up to six months post enrollment)
- Proportion of therapy interruption(Up to six months post enrollment)
研究者
Cesar Homero Gutierrez-Aguirre
Clinical Professor
Hospital Universitario Dr. Jose E. Gonzalez