Erlotinib Versus Vinorelbine/Cisplatin as Adjuvant Treatment in Stage IIIA NSCLC Patients With EGFR Mutations

• Status: Unknown status
• Trial end date: 2017-07-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to assess the effect and safety of erlotinib versus NVB plus cisplatin (NP) as adjuvant treatment in patients with stage IIIA NSCLC after complete resection with EGFR activating mutations and to explore a new treatment strategy for this subset.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Chinese Lung Cancer Surgical Group
• Collaborators: Beijing Cancer Hospital; Chinese PLA General Hospital; Fudan University; Harbin Medical University; Hebei Medical University Fourth Hospital; Qingdao University; Sun Yat-sen University; The First Affiliated Hospital of Soochow University; The Second People's Hospital of Sichuan; Tianjin Medical University Cancer Institute and Hospital; Zhejiang Cancer Hospital
• Treatments: Cisplatin; Erlotinib Hydrochloride; Vinblastine; Vinorelbine

Criteria

Inclusion Criteria:

• Written informed consent provided.

• Males or females aged ≥18 years.

• Chest CT, brain CT or MRI, ECT, abdominal and double-neck B-, or whole body PET-CT examination in 4 weeks before complete resection.

• Pathological diagnosed of non-small cell lung cancer.

• Diagnosed as stage IIIA.

• In 4 weeks after complete resection pts start to accept the adjuvant therapy in this study, previously did not receive any anti-tumor therapy.

• EGFR activating mutation in exon 19 or 21 and KARS

• ECOG performance status 0-1.

• Life expectancy ≥3 months.

• Adequate hematological function:Absolute neutrophil count (ANC) ≥1.5 x 109/L, and Platelet count ≥100 x 109/L, and Hemoglobin ≥9 g/dL (may be transfused to maintain or exceed this level).

• Adequate liver function: Total bilirubin ≤ 1.5 x upper limit of normal (ULN);Aspartate aminotransferase (AST), alanine aminotransferase (ALT) ≤ 2.5 x ULN.

• Adequate renal function:Serum creatinine ≤ 1.25 x ULN, and creatinine clearance ≥ 60 ml/min.

• Able to comply with the required protocol and follow-up procedures, and able to receive oral medications.

• Patients must be nonpregnant and non-lactating.Patients of childbearing potential must implement an effective method of contraception during the study. All female Patients, except those who are postmenopausal or surgically sterilized, must have a negative pre-study serum or urine pregnancy test. .

Exclusion Criteria:

• Patients with prior exposure to agents directed at the HER axis (e.g. erlotinib, gefitinib, cetuximab, trastuzumab).

• Patients with prior chemotherapy or therapy with systemic anti-tumour therapy.

• Patients with prior radiotherapy.

• History of another malignancy in the last 5 years with the exception of the following:Cured basal cell carcinoma of the skin and cured in situ carcinoma of the uterine cervix are permitted.

• Any evidence confirmed tumor recurrence before adjuvant treatment.

• Any unstable systemic disease (including active infection, uncontrolled hypertension, unstable angina, congestive heart failure, myocardial infarction within the previous year, serious cardiac arrhythmia requiring medication, hepatic, renal, or metabolic disease).

• Any evidence of clinically active interstitial lung disease.

• Eye inflammation or eye infection not fully treated or conditions predisposing the subject to this.

• Known human immunodeficiency virus (HIV) infection.

• Known hypersensitivity to Tarceva or NVB or cisplatin.

• Pregnancy or breast-feeding women.

• ECOG performance status ≥ 2.

• Ingredients mixed with small cell lung cancer patients

• Evidence of any other disease, neurological or metabolic dysfunction, physical examination or laboratory finding giving reasonable suspicion of a disease or condition that contraindicated the use of an investigational drug or puts the subject at high risk for treatment-related complications.