A Real-World Study of Pyrotinib Maleate in the Treatment of Advanced/Metastatic Non-Small Cell Lung Cancer With Rare Mutations in HER2

Inclusion Criteria:

• 1. Age: 18-70 years old;
• 2. Advanced/metastatic non-small lung cancer (IV) confirmed by pathology with measurable lesions;
• 3. HER2 mutation and amplification confirmed by gene testing of tumor tissue or blood, pleural effusion, cerebrospinal fluid and other specimens;
• 4. ECOG：0-1;
• 5. At least one radiographically measurable lesion
• 6. Expected survival period ≥ 3 months
• 7. Left ventricular ejection fraction (LVEF) ≥ 50% on echocardiography

• 8. Before using the drug for the first time, it was confirmed by laboratory tests that the subject's bone marrow function, liver and kidney function met the following requirements：

  1. Neutrophil count (ANC) ≥ 1,500/mm3 (1.5×109/L);
  2. Platelet count (PLT) ≥ 100,000/mm3 (100×109/L);
  3. Hemoglobin (Hb) ≥ 8 g/dL (80 g/L);
  4. Serum creatinine (SCr) ≤ 1.5 times the upper limit of normal (ULN) or creatinine clearance ≥ 60 ml/min;
  5. Total bilirubin (TBIL) ≤ 1.5 times the upper limit of normal (ULN);
  6. Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) levels ≤ 2.5 times the upper limit of normal (ULN), and subjects with liver metastases should be ≤ 5×ULN;
  7. International normalized ratio (INR) ≤ 1.5, prothrombin time (PT) and activated partial thromboplastin time (APTT) ≤ 1.5 times ULN;
  8. Urine protein <2+; if urine protein ≥2+, the 24-hour urine protein quantification shows that protein must be ≤1g;
• 9. The medication regimen of the subjects during the clinical diagnosis and treatment was pyrotinib as a single drug
• 10. Patients voluntarily entered the study and signed informed consent form (ICF)

Exclusion Criteria:

• Common types of HER2 mutations: YVMA mutations;
• Patients with hypertension that cannot be well controlled by antihypertensive drug treatment (systolic blood pressure>140 mmHg, diastolic blood pressure>90 mmHg); Uncontrolled or severe cardiovascular disease, such as refractory angina pectoris, congestive heart failure occurred within 6 months before screening; Myocardial infarction within 12 months prior to screening; Any history of clinically significant ventricular arrhythmia, prolonged QT interval; History of cerebrovascular accident, symptomatic coronary heart disease requiring drug treatment;
• There are significant digestive tract dysfunction, which may affect the intake, transport or absorption of oral drugs (such as inability to swallow, chronic diarrhea, intestinal obstruction, etc.);
• Subjects with a recent history of active bleeding, clinically significant bleeding symptoms, and a clear bleeding tendency, such as hemoptysis, gastrointestinal bleeding, hemorrhagic gastric ulcer, positive fecal occult blood at baseline and above, etc.;
• Major surgical operations or severe traumatic injuries, fractures, or poorly healing wounds have been received within 4 weeks;
• Uncontrollable history of important respiratory system such as bronchiectasis, chronic obstructive pulmonary disease, lung abscess, pulmonary embolism, etc.;
• Active serious clinical infection (>NCI-CTCAE, 5.0 version 2 infection standard) and viral infections such as hepatitis B, hepatitis C, syphilis and HIV;
• Symptomatic brain metastases or meningeal metastases;
• Combined with previously untreated tumors other than primary lung cancer;
• Participated in clinical trials of other drugs within 4 weeks before the start of the study;
• Received treatment with pyrotinib maleate;
• Those who have serious adverse reactions and allergies to pyrotinib maleate;
• Pregnant or lactating female subjects, female subjects who are fertile and have a positive baseline pregnancy test, or subjects of childbearing age who are unwilling to take effective contraceptive measures throughout the trial;
• Have serious concomitant diseases, or any other conditions that the investigator considers unsuitable to participate in this study.