| Eligibility |
Inclusion Criteria:
- =18 years old.
- Locally advanced or metastatic (stage IIIB-IV) NSCLC confirmed histologically or
cytologically, stage III patients are unresectable and are not suitable for radical
concurrent chemoradiotherapy.
- ECOG 0~1.
- Expected survival time =3 months
- Patients with EGFR mutations known to be associated with drug sensitivity (i.e., exon
19 deletion or L858R mutation).
- For advanced NSCLC, 2 or 3 generations of EGFR-TKI or EGFR-TKI (EGFR-TKI monotherapy,
combination chemotherapy or bevacizumab are acceptable) have been treated with
treatment failure, and EGFR-TKI has only been received as first-line therapy: Cohort
1: Third-generation EGFR-TKI therapy failed (EGFR-TKI monotherapy, combination
chemotherapy, or bevacizumab could be used) without first - or second-generation
EGFR-TKI therapy; Cohort 2: EGFR-TKI therapy failed in the first or second generation
(EGFR-TKI monotherapy, combination chemotherapy, or bevacizumab were acceptable), and
the status of T790M was not limited without the third generation of EGFR-TKI therapy
or the first three generations of EGFR-TKI therapy < 4 weeks (28 days);
- Met the following criteria for EGFR-TKI treatment failure (acquired resistance):
Continuous treatment with EGFR-TKI in the past; Treatment with EGFR-TKI resulted in
any of the following objective clinical benefits (RECIST 1.1) ; Documented partial or
complete remission; Clinical benefit for =6 months; Imaging disease progression during
EGFR-TKI treatment (RECIST 1.1).
- Specimens collected after treatment with EGFR-TKI for disease progression meet
criteria for MET amplification (FISH GCN=5 or MET/CEP7=2, or NGS GCN=2.3).
- At least one measurable lesion according to RECIST 1.1 criteria.
- Has recovered from adverse effects of any prior chemotherapy, surgery, radiation, or
other antitumor therapy to CTCAE 5.0 = Grade 1 or baseline (except for toxicities such
as hair loss that the investigator determines are not a safety risk).
- Normal bone marrow and organ function: Neutrophils (ANC) =1.5×10^9/L, platelets (PLT)
=90×10^9/L, hemoglobin (Hb) =90g/L,patients whose hematological indexes were at a
critical value and could not meet the above criteria were determined by the
investigator according to the patient's physical condition; AST, ALT and alkaline
phosphatase (ALP) were all =2.5× upper limit of normal range (ULN), and =5×ULN when
liver metastases occurred;Total bilirubin =1 x ULN or ULN < total bilirubin =1.5 x
ULN, and AST=1 x ULN; Creatinine clearance >50 ml/min (calculated according to
Cockroft-Gault)
- Patients were fully aware of and volunteered to participate in the study.
Exclusion Criteria:
- Patients who had previously been treated with MET inhibitors.
- In addition to EGFR and MET, have gene mutations sensitive to other targeted drugs
such as ALK and ROS1.
- Patients who have previously received EGFR-TKI rechallenge therapy.
- Study patients with neurologically unstable CNS metastases in the central nervous
system who had symptoms related to brain metastases prior to treatment initiation, or
who required increased steroid doses to control CNS disease (patients with controlled
CNS metastases may participate in this trial).
- The following medications are required 2 weeks prior to and during study therapy:
drugs that may lead to prolonged QTc interval or tip torsive ventricular tachycardia,
transporter MATE1, MATE2K substrate, and strong inducers of CYP3A4.
- Present or past 5 years with other malignancies (except cured skin basal cell
carcinoma, carcinoma in situ, etc.).
- Received other antitumor agents (except EGFR-TKI) within 5 half-lives prior to initial
administration of the investigational drug; If the patient's last anti-tumor treatment
prior to screening was third-generation EGFR-TKI, the patient may continue to receive
third-generation EGFR-TKI until admission to the regimen without medication
interruption.
- Adverse effects did not recover after receiving extensive radiation therapy within 4
weeks of study treatment initiation or palliative local radiation therapy within 1
week of study treatment initiation.
- Interstitial lung disease (ILD) or pneumonia requiring systemic steroid treatment.
- Study received major surgery or significant trauma within 4 weeks before the start of
treatment.
- Hyperkinetic/venous thrombotic events or embolic events, such as stroke (including
transient ischemic attack), deep vein thrombosis, pulmonary embolism, occurred within
6 months before the first dose;
- Patients with dysphagia, complete or incomplete digestive obstruction, active
gastrointestinal bleeding, perforation, etc. affecting oral drug absorption (frequent
vomiting, diarrhea, etc.);
- In the 6 months prior to screening, cardiovascular disease met any of the following
criteria: a) congestive heart failure =3 of the New York College of Cardiology (NYHA);
Or left ventricular ejection fraction (LVEF) < 50%; b) severe arrhythmias requiring
medical treatment; c) Screening period mean resting corrected QT interval (QTcF) > 470
ms for women or >450 ms for men (using the Fridericia formula [QTc = QT/(RR^0.33)],
averaging results from three 12-lead ECG tests), or the presence of a risk factor for
tip torsion ventricular tachycardia, For example, a family history of hypokalemia,
long QT syndrome, or familial arrhythmia judged by the investigator to be clinically
significant; d) Uncontrolled hypertension (defined as systolic blood pressure =140
mmHg and/or diastolic blood pressure =90 mmHg after treatment with standardized
antihypertensive drugs); e) acute myocardial infarction, severe or unstable angina
pectoris, coronary or peripheral artery bypass grafting within 6 months prior to
initial administration; f) Clinically significant arrhythmias.
- An active, uncontrolled bacterial, viral, or fungal infection requiring systemic
treatment, defined as persistent signs/symptoms associated with the infection that do
not improve despite the use of appropriate antibiotics, antiviral therapy, and/or
other treatment;
- Patients with active hepatitis B (HbsAg or HBcAb positive and HBV DNA higher than the
upper limit of normal), active hepatitis C (HCV antibody positive and HCV RNA higher
than the upper limit of the study center), HIV antibody positive;
- Known allergy or intolerance to therapeutic drugs or their excipients;
- Pregnant or lactating women;
- The investigator believes that the subjects are not suitable to participate in this
clinical study for other reasons.
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