EGFR Mutation Positive NSCLC Patients With Gefitinib and Thalidomide

• Status: Unknown status
• Trial end date: 2020-11-01
• Target enrollment: 0
• Participant gender: All

Summary

EGFR-TKIs are the standard first-line treatment option for EGFR-mutant NSCLC. After a randomized phase II trial, JO25567 was presented at 2014 ASCO, the synergistic effect of progression-free survival(PFS) could be expected when EGFR TKI, Gefitinib is combined with Antiangiogenesis agent thalidomide, Therefore Chinese data of treating EGFR mutation positive NSCLC patients with Gefitinib and thalidomide is significantly necessary for developing new standard treatment in first-line therapy in Chinese EGFR mutant NSCLC patients.

In this study, The investigators will investigate the efficacy and safety of Gefitinib and thalidomide combination compare to Gefitinib alone in Chinese EGFR-mutant NSCLC patients.

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

Details

• Lead Sponsor: Fujian Cancer Hospital
• Treatments: Gefitinib; Thalidomide

Criteria

Inclusion Criteria:

• Pathologically confirmed stage IIIB & IV non-small cell lung cancer other than squamous cell carcinoma

• Patients with one or more measurable lesion based on Response Evaluation Criteria in Solid Tumors (RECIST 1.1)

• Locally diagnosed sensitive EGFR mutation positive (Exon 19 deletion or L858R)

• ECOG performance 0~1

• Age ≥ 19 years and - No previous treatment

Adequate organ function by following:

• ANC ≥1,500/uL, hemoglobin ≥9.0g/dL, platelet ≥100,000/uL

• Serum bilirubin < 1 x UNL, AST (SGOT) and ALT (SGPT) < 2.5 x UNL, If Liver metastasis, Serum bilirubin < 3 x UNL, AST (SGOT) and ALT (SGPT) < 5 x UNL

• Serum Cr ≤ 1 x UNL

• Patients who have had undergone radiotherapy are acceptable if patients meet all of the following criteria:

• No history of irradiation to pulmonary tumor lesions.

• In case of palliative irradiation to bone lesions in lung: at least 12 weeks must have passed at the date of registration since the last irradiation of the sites.

• In case of irradiation to non-pulmonary sites: at least two weeks must have passed at the date of inclusion since the last irradiation of the sites

• At the time of registration, at least the following period has passed since last date of the prior therapy or procedure:

• Surgery(including exploratory/ examination thoracotomy): 4 weeks

• Pleural cavity drainage: 1 weeks

• Pleurodesis without anti-neoplastic agents (inclusive of BRM such as Picibanil):

2 week

• Biopsy accompanied by incision (including thoracoscopic biopsy): 2 week

• Procedure for trauma (exclusive of patients with unhealed wound): 2 weeks

• Transfusion of blood, preparation of hematopoietic factor: 2 week

• Puncture and aspiration cytology: 1 week

• Other investigational product: 4 weeks

• Written informed consent form

Exclusion Criteria:

• • Previous history of malignancy within 3 years from study entry except treated non-melanomatous skin cancer, uterine cervical cancer in situ, or thyroid cancer

• Prior chemotherapy or systemic anti-cancer therapy for metastatic disease but postoperative adjuvant or neoadjuvant therapy of 6 months or more previously is allowed

• Patients who received previous treatment for lung cancer with drugs

• Symptomatic or uncontrolled central nervous system (CNS) metastases

• Patients with increased risk of bleeding, clinically significant cardiovascular diseases, a history of thrombosis or thromboembolism in the 6 months prior to treatment, gastrointestinal problems, and neurologic problems

• Any significant ophthalmologic abnormality

• Pre-existing parenchymal lung disease such as pulmonary fibrosis

• Known allergic history of Erlotinib or Bevacizumab

• Interstitial lung disease or fibrosis on chest radiogram

• Active infection, uncontrolled systemic disease (cardiopulmonary insufficiency, fatal arrhythmias, hepatitis)

• Pregnant or nursing women