KCT0007795招募中未知
azertinib for NSCLC harboring activating EGFR mutations in TKI naïve patients: A single-arm, phase II single-center trial
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 入组人数
- 150
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 19(Year) 至 o Limit(—)
- 性别
- All
入选标准
- •1.Histologically or cytologically confirmed locally advanced or metastatic non-small cell lung cancer which is not amenable to treatment with a curative aim (e.g. surgery or radiation). Patients who underwent curative intent surgery or definitive CRT and experience recurrence after 6 months are eligible.
- •2.Stage IIIC or IV by AJCC 8th edition
- •3.Confirmed EGFR mutations (exon 19 deletion, L858R)
- •(The result from both cell-free DNA or tissue-based DNA from the local test is allowed.)
- •4.Age of 19 or more.
- •5.Performance status of Eastern Cooperative Oncology Group 0 to 2.
- •6.Expected minimum life expectancy of 12 weeks
- •7.Adequate organ function.
- •ANC =1500cells/mm3
- •PLT =100,000cells/mm3
- •Totlal bilirubin =1.5 x (ULN)
- •AST/ALT = 2.5 x ULN ( =5.0 x ULN)
- •Creatinine =1.5 x (ULN) CCr = 45mL/min (Cockcroft– Gault)
- •8.Available to provide the adequate tissue and blood for the genomic tests
- •- At least 15 unstained slide and 20 cc of blood at baseline (mandatory) and disease progression.
- •9.Agreed to perform re-biopsy at the timepoint of disease progression.
- •10. At least two weeks after the chemotherapy
- •11.Female subjects must either be of non-reproductive potential
- •12.Subject willing and able to comply with the protocol
- •13.Signed written informed consent
排除标准
- •1.Previously treatment with any kind of EGFR TKI (Previously chemotherapy treated patients is allowed)
- •2.Any concurrent and/or other active malignancy that has required systemic treatment within 2 years of first dose of study drug. (allowed for participation if investigator decided that previous malignancy is cured and not need for any additional treatment)
- •3.Uncontrolled central nervous system metastases
- •- patient with asymptomatic brain metastases or CNS symptom manageable with TKI and evaluated by investigator can be enrolled.
- •4.Spinal cord compression, leptomeningeal carcinomatosis
- •5.Uncontrolled systemic illness, including uncontrolled hypertension, active bleeding, or active infection
- •6.Radiotherapy with a wide field of radiation within 2 weeks or radiotherapy with a limited field of radiation (localized radiotherapy or gamma knife surgery) for palliation within 1 week
- •7.Any unresolved toxicities from prior therapy, greater than CTCAE grade 1
- •8.Mean QT interval corrected for heart rate (QTc) = 470 ms
- •9.No measurable lesion
- •10.Unable to swallow the product due to refractory nausea, vomiting or chronic gastrointestinal disease.
研究者
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