The Efficacy and Drug Resistance Molecular Biology of Apatinib Combined With EGFR-TK1 Treated for Advanced Slow-progressed Non-Small Cell Lung Cancer (NSCLC)

NCT ID: NCT03811054

Last Updated: 2019-01-22

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-12-01
• Study Completion Date: 2020-12-31

Brief Summary

Patients with advanced non-small cell lung cancer (NSCLC) who progress slowly after Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors（EGFR-TKI）resistance. The purpose of this study is to investigate the efficacy and drug resistance mechanism of Apatinib combine with EGFR-TK1 treated for advanced slow progressed non-small cell lung cancer and provide new treatment options.

Detailed Description

Epidermal growth factor receptor Tyrosine kinase inhibitor (EGFR TKI) have been approved to treat NSCLC harboring EGFR mutation as first-line therapy. However, a large proportion of patients would become acquired resistant of EGFR-TKI after about one year although initially sensitivity. Previous studies demonstrated that the anti-angiogenesis combined with EGFR-TKI in slow-progressed EGFR mutation-positive non-small cell lung cancer achieved good efficacy and disease control rates, prolonged the progression free survival. The present study is aim to expand the number of samples to monitor resistance-related genes and tumor cells. Furthermore, to investigate the mechanism of anti-angiogenesis combine with EGFR-TKI and provide the theory for the use and promotion of clinically protocols. In this study, the primary objective is the objective response rates and the secondary goal are disease control rates, overall survival, progression free survival and drug safety.

Conditions

Non Small Cell Lung Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Apatinib combined with EGFR-TKI

Apatinib 250 millgram（mg/day（d））combined with EGFR-TKI

Group Type: EXPERIMENTAL

Apatinib（250mg/d） combined with EGFR-TKI

Intervention Type: DRUG

Patients with advanced non-small cell lung cancer (NSCLC) who had treated with EGFR-TKI and progressed slowly because of resistance are underwent with apatinib mesylate and continuous EGFR-TKI.

Interventions

Apatinib（250mg/d） combined with EGFR-TKI

Patients with advanced non-small cell lung cancer (NSCLC) who had treated with EGFR-TKI and progressed slowly because of resistance are underwent with apatinib mesylate and continuous EGFR-TKI.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Informed consent should be obtained before treatment. Patients with good compliance.

2. Histologically or cytologically confirmed IIIB/IV NSCLC.

3. Progress in the treatment of EGFR TKI.

4. Aged from 18 to 75 years (18 and 75 years are included); Gender Not Required.

5. ECOG PS 0-1.

6. Life expectancy ≥ 3 months.

7. At least one measurable lesion (meet the requirements of the standard Response Evaluation Criteria In Solid Tumors (RESCIST) version 1.1). If the lesions that have received local treatment (radiation, radiofrequency, intervention, etc.) are the only lesions, it is required to have clear imaging progress.

Exclusion Criteria

1. Uncontrolled hypertension (systolic ≥140mmHg and/or diastolic ≥90mmHg after medication treatment); Poor control of blood sugar.

2. Acute phase of cerebral infarction, or recovery period <2 months.

3. A variety of factors that affect the absorption of oral medications (such as inability to swallow, nausea and vomiting, chronic diarrhea, intestinal obstruction, etc.)

4. Patients with a risk of gastrointestinal bleeding may not be enrolled, including the following: (1) active digestive ulcer lesions, and fecal occult blood (++); (2) a history of melena and hematemesis within 2 months. Simple fecal occult blood (+) is not an exclusion criterion.

5. Coagulation abnormality (INR>1.5×ULN, APTT>1.5×ULN), with bleeding tendency.

6. Urine protein ≥ ++ or confirmed 24-hour urine protein quantitation > 1.0 g.

7. Pregnant or lactating women.

8. Severe liver and kidney dysfunction (grade 4) .

9. Allergic to any ingredient of apatinib mesylate.

10. A history of abuse of psychotropic substances and are unable to quit smoking or mental disorders.

11. According to the investigator's judgment, people with concomitant diseases that seriously endanger the safety of the patient or affect the patient's completion of the study.

12. Surgery, major trauma or fracture, within 4 weeks before the treatment or unhealed wound before treatment.

13. Severe heart disease, such as grade III or above (NYHA standard) congestive heart failure, grade III or above (CCS standard) angina, a history of myocardial infarction within 6 months before the treatment, or medication treated arrhythmia.

14. Brain metastasis and meningeal metastasis.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Beijing Chest Hospital

OTHER

Sponsor Role: lead

Responsible Party

Liyan Xu

Chief of Medical Oncology Department

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

The Beijing Chest Hospital

Beijing, , China

Site Status: RECRUITING

Countries

China

Central Contacts

Liyan Xu, MD

Role: CONTACT

xuliyan2009@yahoo.cn

86-89509157

Jing Liu

Role: CONTACT

86-89509157

Facility Contacts

Liyan Xu, MD

Role: primary

xuliyan2009@yahoo.cn

Other Identifiers

BeijingCH002

Identifier Type: -

Identifier Source: org_study_id