Locally advanced or metastatic non-small cell lung cancer with EGFR classical mutations
Conditions
Interventions
treatment group:Furmonertinib 160mg, PO, QD
Sponsors
Peking Union Medical College Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.= 18 years old, Male or Female; 2.Histologically or cytologically confirmed locally advanced or metastatic lung adenocarcinoma not amenable to curative surgery or radiotherapy; 3.Patients have been confirmed by local laboratory to have one of the following EGFR mutations: 19Del or L858R (single or compound); 4.Patients had locally advanced NSCLC or metastatic NSCLC without any systemic antitumor therapy; 5.Having at least one measurable lesion (in accordance with RECIST1.1). Note: measurable lesion can neither be subject to local therapy as radiotherapy nor used for biopsy in screening period; if there is only one measurable lesion, this lesion will be permitted to be biopsied. However, the baseline radiological examination can be performed for this lesion at least 14 days after biopsy; 6.Adequate organ function as shown in the laboratory test, including: (1) ANC >= 1.5 x 10^9/L; PLT >= 100 x 10^9/L; HGB >= 90 g/L; (2) TBIL = 50 mL/min (according to Cockcroft-Gault formula); 7.ECOG PS 0-1, and there was no obvious disease deterioration within 2 weeks prior to screening; 8.Life expectancy > 12 weeks after the first dose of investigational product; 9.Female of childbearing age are not pregnant and have no pregnancy plan. Female subjects at childbearing age and male subjects agree to take effective contraceptive measures during the study and within 6 months after drug discontinuation; 10.Being able to understand and voluntarily participate in the study, and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1.NSCLC with predominant squamous cell histology, small cell lung cancer or neuroendocrine carcinoma indicated by histology or cytology test; 2.Patients with other driver oncogenes (ALK fusion, ROS1 fusion, RET rearrangement, BRAF mutation, NTRK fusion, MET mutation, KRAS mutation, but not TP53, RB1, BRAC mutation, etc.); 3.Expected to receive other anti-tumor therapy other than the investigational product during the study; 4.Having received the following therapies: (1) Having been irradiated for > 30% bone marrow or a large area within 4 weeks prior to the first dose of investigational product; (2) Having received major surgery within 4 weeks prior to the first dose of investigational product or plan to receive major surgery during the study with exception of the surgical procedures to establish vascular access, biopsy through mediastinoscopy or thoracoscopy; (3) Use of a potent CYP3A4 inhibitor within 7 days prior to the first dose of investigational product or a potent CYP3A4 inducer within 21 days prior to the first dose of investigational product; use of the traditional Chinese medicine or traditional Chinese medicine preparation with tumor indication, or traditional Chinese medicine or traditional Chinese medicine preparation with adjuvant anti-tumor effect within two weeks prior to the first dose of investigational product or expected to be required during the study; (4) Having participated in the clinical trial and received the investigational product or device within 4 weeks or at least 5 half-lives prior to the first dose of investigational product; (5) Having received other anti-tumor drugs within 14 days prior to the first dose of investigational product; 5.Concurrent spinal cord compression or symptomatic brain metastasis; 6.The toxicity caused by previous anti-tumor therapy has not recovered to 470 ms on ECG at resting state; 12.Clinically significant prolonged QT interval or other arrhythmia or clinical status considered by investigators that may increase the risk of prolonged QT interval; for example, complete left bundle branch block, degree III atrioventricular block, congenital long QT syndrome, serious hypokalemia, or current use of drugs that may lead to prolonged QT interval; 13.Serious gastrointestinal dysfunction, or disease that may a
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Progression Free Survival according to RECIST 1.1 by investigator; | — |
Secondary
| Measure | Time frame |
|---|---|
| Disease Control Rate;Overall survial;Safety;Analysis of recurrence type and location of recurrence;CNS ORR;CNS DCR;CNS PFS;Objective Response Rate; | — |
Countries
China
Contacts
Public ContactWang Mengzhao
Peking Union Medical College Hospital
Outcome results
None listed