A Phase 1 Trial of Trametinib and Ponatinib in Patients With KRAS Mutant Advanced Non-Small Cell Lung Cancer
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 12
- 试验地点
- 7
- 主要终点
- Maximum Tolerated Dose of Ponatinib, Phase I
研究概览
简要总结
The purpose of this study is to evaluate the safety of the combination of ponatinib and trametinib as well as the most appropriate dosages of the combination.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 19 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Histologically or cytologically proven diagnosis of advanced lung adenocarcinoma
- •KRAS mutation
- •Radiographic progression following prior treatment with platinum doublet chemotherapy and prior treatment with a PD-1/L1 inhibitor. Patients who are deemed not eligible for therapy with a PD-1/L1 inhibitor by their treating physician will also be eligible.
- •Able to take oral medications
- •Measurable disease as per RECIST 1.
- •Previously irradiated sites of tumor may be considered measurable if there is radiographic progression at the site subsequent to the time of completing radiation.
- •Karnofsky performance status (KPS) ≥ 70%
- •Age >18 years old
- •Adequate organ function:
- •AST, ALT ≤ 2.5 x ULN - Total bilirubin ≤ 1.5 x ULN -Albumin ≥ 2.5g/dL
- •Creatinine < 1.5 x ULN OR calculated creatinine clearance ≥ 50mL/min
- •Absolute neutrophil count (ANC) ≥ 1,200 cells/mm^3
- •Hemoglobin ≥ 9.0 g/dL
- •Platelets ≥ 100,000/mm^3
- •Amylase and lipase within normal limits (amylase ≤ 100, lipase ≤ 78)
- •Female patients who:
- •Are postmenopausal for at least 1 year before the screening visit, OR
- •Are surgically sterile, OR
- •If they are of childbearing potential, agree to practice 2 effective methods of contraception, at the same time, from the time of signing the informed consent through 30 days after the last dose of study drug, or agree to completely abstain from heterosexual intercourse
- •Male patients, even if surgically sterilized (i.e., status post-vasectomy), who:
- •Agree to practice effective barrier contraception during the entire study treatment period and through 30 days after the last dose of study drug, or
- •Agree to completely abstain from heterosexual intercourse
排除标准
- •Patients with symptomatic brain metastasis requiring escalating doses of steroids
- •Patients with grade 2 or greater diarrhea prior to study initiation despite maximal medical management
- •History of acute pancreatitis within 1 year of study entry or history of chronic pancreatitis
- •History of or ongoing alcohol abuse that, in the opinion of the Investigator, would compromise compliance or impart excess risks associated with study participation.
- •Pregnant or lactating women
- •Any type of systemic therapy (chemotherapy or experimental drugs) within 2 weeks of starting treatment on protocol
- •Patients who have received prior treatment with MEK inhibitor
- •A history of clinically significant interstitial lung disease or pneumonitis
- •Significant uncontrolled or active cardiovascular disease, specifically including, but not restricted to: History of clinically significant (as determined by the treating physician) atrial arrhythmia; or any ventricular arrhythmia, History of congenital long QT syndrome., Abnormal QTc (≥ 450 msec in males and ≥ 470 msec in females), Ejection fraction ≤ 50% as assessed by echocardiogram.
- •History of arterial thrombotic disease, specifically including, but not restricted to: Myocardial infarction or unstable angina, cerebrovascular event (CVA) or transient ischemic attack (TIA), Peripheral vascular disease or claudication.
- •Uncontrolled hypertension (Diastolic blood pressure > 100 mmHg; Systolic blood pressure > 150 mmHg).
- •History of venous thromboembolism (e.g. deep venous thrombosis or pulmonary embolism) within 6 months of study entry. Note: Participants enrolled after this window must be on appropriate therapeutic anticoagulation.
- •History of central serous retinopathy or retinal vein occlusion
- •Patients with baseline risk factors for central serous retinopathy or retinal vein occlusion such as evidence of new optic disc cupping, evidence of new visual field defects, and intraocular pressure >21 mmHg are excluded from the trial
- •History of prior malignancy within 2 years that requires treatment. Patients who are considered NED from a malignancy may be considered on a case by case basis.
- •Any other condition that, in the opinion of the investigator, may compromise the safety, compliance of the patient, or would preclude the patient from successful completion of the study
研究组 & 干预措施
Phase I: Dose Level 2
Trametinib 2 mg PO q daily Ponatinib 30mg PO q daily
干预措施: Ponatinib 30 MG (Drug)
Phase II
Maximum tolerated dose as established in Phase I portion
干预措施: Trametinib 2 mg (Drug)
Phase I: Dose Level 1
Trametinib 2 mg PO q daily Ponatinib 15mg PO q daily
干预措施: Trametinib 2 mg (Drug)
Phase I: Dose Level 1
Trametinib 2 mg PO q daily Ponatinib 15mg PO q daily
干预措施: Ponatinib 15 MG (Drug)
Phase I: Dose Level -3
Trametinib 0.5mg PO q daily Ponatinib 15mg PO q daily
干预措施: Trametinib 0.5 mg (Drug)
Phase I: Dose Level -3
Trametinib 0.5mg PO q daily Ponatinib 15mg PO q daily
干预措施: Ponatinib 15 MG (Drug)
Phase I: Dose Level 2
Trametinib 2 mg PO q daily Ponatinib 30mg PO q daily
干预措施: Trametinib 2 mg (Drug)
Phase I: Dose Level -2
Trametinib 1.0 mg PO q daily Ponatinib 15mg PO q daily
干预措施: Trametinib 1 MG (Drug)
Phase I: Dose Level -2
Trametinib 1.0 mg PO q daily Ponatinib 15mg PO q daily
干预措施: Ponatinib 15 MG (Drug)
Phase I: Dose Level -1
Trametinib 1.5 mg PO q daily 15mg PO q daily
干预措施: Trametinib 1.5 MG (Drug)
Phase I: Dose Level -1
Trametinib 1.5 mg PO q daily 15mg PO q daily
干预措施: Ponatinib 15 MG (Drug)
Phase II
Maximum tolerated dose as established in Phase I portion
干预措施: Ponatinib 15 MG (Drug)
结局指标
主要结局
Maximum Tolerated Dose of Ponatinib, Phase I
时间窗: maximum of 18 months
In the Phase I portion of the study, a standard 3+3 design will be used to find the maximum tolerated dose.
Overall Response Rate
时间窗: 1 year
In the Phase II portion of the study, RECIST criteria 1.1 will evaluate the overall response rate. Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), \>=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR.
次要结局
未报告次要终点