Overview

Phase I Study of the Combination of Anlotinib With Gefitinib

Status:
Unknown status
Trial end date:
2019-02-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this clinical study is to evaluate the tolerability and toxicity of different dose of Anlotinib puls Gefitinib in First-line Treatment of Advanced Gene Positive Non-squamous Non-small Cell Lung Cancer , to provide a reference of dosage for Phase II clinical trials
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Second Affiliated Hospital of Nanchang University
Treatments:
Gefitinib
Criteria
Inclusion Criteria:

- Be≥18 years of age on the day of signing informed consent and With good compliance and
agree to accept follow-up of disease progression and adverse events.

- Patients with histologic or cytologic confirmation of advanced or metastatic NSCLC
with stage III or IV disease.(For recurrent patients, adjuvant chemotherapy,
neoadjuvant chemotherapy or neoadjuvant chemotherapy plus adjuvant were assessed for
eligibility, and the last treatment time must be more than 6 months before enrollment)

- Epidermal Growth Factor Receptor(EGFR)mutations confirmed by molecular detection
(including, but not limited to, 20 exon, 19 exon deletion and L858R) external
pathological examination was accepted (including pathological or blood test results)

- Patients have not been received systematic treatment,including chemotherapy and EGFR
-TKIs(Tyrosine kinase inhibitors)

- There were at least one target lesions in the past three months has not yet accepted
radiotherapy, and could be recorded by magnetic resonance imaging (MRI) or computer
tomography (CT) measuring accurately at least in one direction(The maximum diameter
needs to be recorded), including conventional CT ≥20 mm or spiral CT ≥10 mm.

- Life expectancy ≥3 months.

- Have a performance status of 0 or 2 on the Eastern Cooperative Oncology Group (ECOG)
Performance Status.

- With normal marrow, liver ,renal and coagulation function:

- The blood routine examination need to be standard (no blood transfusion and blood
products within 14 days, no g-csf and other hematopoietic stimulating factor
correction)

- Hemoglobin(HB)≥90 g/L

- A Neutrophil count of (ANC)≥1.5×109/L

- A Platelet count of (PLT)≥80×109/L

- A Total bilirubin (TBil) of ≤1.5 upper normal limitation (UNL)

- A alanine aminotransferase (ALAT) and a aspartate aminotransferase (ASAT) of ≤2.5 UNL,
in case of liver metastasis ALAT and ASAT≤5 UNL

- A creatinine (Cr) of ≤1.5 UNL; a creatinine clearance rate ≥ 60ml/min
(Cockcroft-Gault)

- Doppler echocardiography: left ventricular ejection fraction (LVEF) is lower than
normal (50%)

- Female subjects of child-bearing potential must agree to use contraceptive measures
starting 1 week before the administration of the first dose of apatinib until 8 weeks
after discontinuing study drug. Male subjects must agree to use contraceptive measures
during the study and 8 weeks after last dose of study drug.

Exclusion Criteria:

- Small cell lung cancer (include Small cell lung cancer mixture of NSCLC).

- Iconography (CT or MRI) shows that the tumor vessels have 5 mm or less, or
Cardiovascular involvement by Central tumor ; Or obvious lung empty or necrotic tumor.

- Patients has a history of malignant tumors. Patients with basal cell carcinoma,
superficial bladder cancer, skin squamous cell carcinoma, or cervical cancer in situ
who have undergone possible curative treatment and have not suffered any recurrence of
the disease within 5 years from the start of treatment.

- Patients with Other active malignant tumors requiring concurrent treatment

- Patients who have not recovered to grade 1 or below after previous systemic antitumor
therapy (except alopecia)

- Patients with brain or central nervous system metastases, including leptomeningeal
disease, or CT/MRI examination revealed brain or leptomeningeal disease) (14 days
before the random treatment has been completed and the symptoms of patients with brain
metastases from stable can into the group, but need to the cerebral MRI, CT or vein
angiography confirmed as without symptoms of cerebral hemorrhage)

- Uncontrollable hypertensive (systolic blood pressure or greater 140 mmHg or diastolic
blood pressure or greater 90 mmHg, despite the best drug treatment)

- Significant cardiac disease as defined as: grade II or greater myocardial infarction,
unstable arrhythmia(Including corrected QT interval (QTc )period between male or
greater 450 ms, female or greater 470 ms); New York Heart Association (NYHA) grade II
or greater heart dysfunction , or Echocardiography reveal left ventricular ejection
fraction (LVEF)Less than 50%

- Patients with grade II or greater peripheral neuropathy, except due to trauma

- Abnormal coagulation (INR > 1.5 or prothrombin time (PT) >Upper Limit of Normal( ULN)+
4 seconds or APTT(activated partial thromboplastin time ) ULN > 1.5, with bleeding
tendency or be treated with thrombolysis and anticoagulation.

Note: under the premise of International Normalized ratio (INR) of prothrombin time (PT)
Less than or equal to 1.5, allow to administrate low-dose heparin (adult daily dose is
06000 ~ 12000 U) or low-dose aspirin (100 mg daily dosage or less) , for prophylactic
purposes

- Urine routines show urine protein≥ ++, or urine protein quantity≥ 1.0 g during 24
hours

- Patients with respiratory syndrome (difficulty breathing of level 2 or higher ),
serous cavity effusion need to surgical treatment ( including pleural of level 2 or
higher with respiratory distress and anoxia, need for intubation or pleurodesis
treatment, severe ascites of level 2 need to surgery invasive treatment, pericardial
of level 2 and affect physiological function)

- Patients with severe infections , and need to receive systemic antibiotic treatment.(
the infection with grade 2 or above and requiring intravenous antibacterial therapy
);Decompensated diabetes or other contraindication with high dose glucocorticoid
therapy)

- Active or chronic hepatitis c and/or Hepatitis B virus (HBV) infection

- Serious, non-healing wound, ulcer, or bone fracture

- Has an obvious factor influencing oral drug absorption, such as unable to swallow,
chronic diarrhea and intestinal obstruction, etc

- Has received major surgery or severe traumatic injury, fractures or ulcer Within
4weeks before Random

- Patients have participated in other antitumor drug clinical trials Within 4 weeks
before enrollment or prepare to receive systemic anti-tumor treatment during the study
or Within 4 weeks before randomization, including cytotoxic therapy cellular, Signal
transduction inhibitors, immune therapy (or receiving mitomycin C Within six weeks
before taking experimental drug therapy).Field overspread radiotherapy (ef-rt) was
carried out within 4 weeks before the grouping or limited field radiotherapy was
carried out within 2 weeks before the grouping to evaluate tumor lesions

- Severe weight loss (> 10%) Within 6 weeks before Random

- Has Clinically significant hemoptysis Within 3 months before Random (daily hemoptysis
than 50 ml;Or significant clinical significance of bleeding symptoms or have definite
bleeding tendency, such as gastrointestinal bleeding, bleeding ulcers, baseline period
+ + and above of fecal occult blood, or vasculitis, etc.

- Has venous thromboembolism events Within 12 months before Random, such as
cerebrovascular accident (including transient ischemic attack, cerebral hemorrhage,
cerebral infarction), deep vein thrombosis and pulmonary embolism, etc.

- Patients who have a history of mental drug abuse and cannot be cured or have mental
disorders

- There are any contraindications with receiving anlotinib or gefitinib treatment

- There are allergic reaction to contrast media, anlotinib, and/or excipient of
experimental drug

- There are allergic reaction to the contrast agent

- Patients with any other medical condition or reason, in that investigator's opinion,
makes the patient unstable to participate in a clinical trial.