A Study of Tarceva vs. Avastin+Tarceva for Advanced NSCLC With EGFR m(+)

EGFR Positive Non-small Cell Lung Cancer Clinical Trial

— AvaTa  

Official title:

A Randomized Phase II Study of Erlotinib Alone Versus Erlotinib Plus Bevacizumab for Advanced Non-small Cell Lung Cancer With Epidermal Growth Factor Receptor Activating Mutations

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03126799
• Other study ID #: NCC-2016-0107
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: November 1, 2016
• Est. completion date: July 20, 2023

Study information

• Verified date: April 2022
• Source: National Cancer Center, Korea
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Korean data of treating EGFR mutation positive NSCLC patients with Erlotinib and Bevacizumab is significantly necessary for developing new standard treatment in first-line therapy in Korean EGFR mutant NSCLC patients.

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

Description:

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, Erlotinib is combined with Antiangiogenesis agent, Bevacizumab. Even Korean and Japanese are classified as Asian based on location, the figure of Korean is more tended to Western people due to the dietary life in recent years. However the incidence rate of EGFR mutation positive patients in Korea is much higher than Western countries.

Therefore Korean data of treating EGFR mutation positive NSCLC patients with Erlotinib and Bevacizumab is significantly necessary for developing new standard treatment in first-line therapy in Korean EGFR mutant NSCLC patients.

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

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 128
• Est. completion date: July 20, 2023
• Est. primary completion date: December 31, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 19 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• EGFR Positive Non-small Cell Lung Cancer
• Lung Neoplasms

Intervention

Drug:
• Erlotinib plus Bevacizumab
Erlotinib 150mg, po, daily, q 3weeks plus Bevacizumab 15mg/kg, IV, on D1 Q 3 weeks
• Erlotinib
Erlotinib 150mg, po, daily, Q weeks

Locations

Country	Name	City	State
Korea, Republic of	National Cancer Center	Goyang-Si	Gyeonggi-do

Sponsors (2)

Lead Sponsor	Collaborator
National Cancer Center, Korea	Roche Korea co.,Ltd.

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	PFS	Progression Free Survival	From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to at least 36 months.
Secondary	ORR	Overall Response Rate	through study completion, and average of 2 years
Secondary	OS	Overall Survival	From date of randomization until the date of death or date of last visit/contact, whichever came first, assessed to at least 36 months