Pemetrexed Plus Apatinib Maintenance Treatment in Patients With Non-squamous Non-small Cell Lung Cancer Patients Who Have Not Progressed After 4 Cycles of Induction Chemotherapy of Pemetrexed in Combination With Platinum-based Regimen

1. Squamous cell carcinoma (including adenosquamous carcinoma), small cell lung cancer (including small cell carcinoma and non-small cell mixed lung cancer).

2. Patient gene detection is EGFR sensitive mutation, or positive for ALK fusion gene.

3. Symptomatic brain metastasis (a patient with brain metastases who completed treatment and had stable symptoms 21 days before enrollment can be enrolled, but need to be confirmed by brain MRI, CT or venography to have no cerebral hemorrhage symptoms).

4. Imaging (CT or MRI) showed tumor lesions ranging from ≤ 5 mm to large vessels, or central tumors that invaded local large blood vessels; or showed significant pulmonary cavitary or necrotizing tumors.

5. Hypertension (systolic blood pressure ≥140 mmHg or diastolic blood pressure ≥90 mmHg) that is still uncontrollable using a combination of two antihypertensive drugs.

6. Have the following cardiovascular diseases: myocardial ischemia or myocardial infarction above grade II, poorly controlled arrhythmias (including men with QTc interval ≥ 450 ms, women ≥ 470 ms); according to NYHA criteria, grade III to IV cardiac insufficiency, Or cardiac color Doppler ultrasound examination indicates left ventricular ejection fraction (LVEF) \<50%.

7. Patients with a history of pulmonary interstitial disease or a patient with pulmonary interstitial disease.

8. Abnormal coagulation (INR \> 1.5 or prothrombin time (PT) \> ULN + 4 seconds or APTT \> 1.5 ULN), with bleeding tendency or undergoing thrombolysis or anticoagulant therapy.

9. There is obvious cough blood in the 2 months before enrollment, or the daily hemoptysis amount is 2.5ml or more.

10. Into the group of the first 3 months there have been significant clinical significance of bleeding symptoms or have definite bleeding tendency.

11. Events of arterial/venous thrombosis occurring within 12 months prior to enrollment, such as cerebrovascular accidents (including transient ischemic attacks, cerebral hemorrhage, cerebral infarction), deep vein thrombosis, and pulmonary embolism,etc.

12. Known hereditary or acquired bleeding and thrombophilia (such as hemophilia patients, coagulopathy, thrombocytopenia, hypersplenism, etc.)

13. Long-term unhealed wound or fracture.

14. Major surgery or severe traumatic injury, fracture or ulceration within 4 weeks of enrollment.

15. Factors that have a significant impact on oral drug absorption, such as inability to swallow, chronic diarrhea, and intestinal obstruction.

16. Abdominal fistula, gastrointestinal perforation or abdominal abscess occurred within 6 months prior to enrollment.

17. Urine routine indicates urinary protein ≥ ++, or confirmed 24-hour urine protein ≥ 1.0 g.

18. Has a history of psychiatric drugs abuse and can't quit or have a mental disorder.

19. Participated in other clinical trials of anti-tumor drugs within 4 weeks prior to enrollment.

20. Previous or concurrent with other unhealed malignant tumors, except for cured skin basal cell carcinoma, cervical carcinoma in situ, and superficial bladder cancer.

21. Pregnant or lactating women; those who have fertility are unwilling or unable to take effective contraceptive measures.

22. The investigator judges other conditions that may affect the conduct of the clinical study and the determination of the results of the study.

What this study is about