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临床试验/KCT0007795
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

Samsung Medical Center0 个研究点目标入组 150 人开始时间: 待定最近更新:
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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