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The Efficacy and Safety of Apatinib Combined With Etoposide in Heavily Pretreated Advanced Non-small Cell Lung Cancer

T

Third Military Medical University

Status and phase

Unknown
Phase 2

Conditions

Non-small Cell Lung Cancer

Treatments

Drug: Etoposide
Drug: Apatinib

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The development of anti-angiogenesis drugs has led to renewed enthusiasm in lung cancer treatments. Apatinib is a tyrosine kinase inhibitor which selectively inhibits the vascular endothelial growth factor receptor-2 (VEGFR-2). Etoposide is an oral preparation for lung cancer which is recommended by NCCN guideline. The investigators wondered whether these two drugs have synergistic effects when treating advanced non-small cell lung cancer patients who failed to previous at least 2nd line treatments. Thus, the aim of this trial is to investigate the efficacy and safety of apatinib combined with etoposide in heavily pretreated advanced non-small cell lung cancer.

Enrollment

25 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Obtain of informed consent.

  • Histologically or cytologically confirmed non-small cell lung cancer.

  • World Health Organization (WHO) performance status (PS) of 0 to 2.

  • Measurable lesions as defined by RECIST criteria.

  • Second-line or more treatments.

  • Wild type of epidermal-growth-factor receptor (EGFR).

  • Life expectancy ≥12 weeks.

  • Organ functions normal, as defined below, within two weeks of randomization:

    • Hb≥90g/L Absolute neutrophils count(ANC)≥1.5×109/L Platelets≥80×109/L Serum bilirubin≤2×ULN; Aspartate transaminase(AST) and alanine transaminase (ALT)≤2.5×ULN(≤5×ULN if liver metastases) Creatinine clearance≥45ml/min or Cr≤1.25×ULN.

  • Females of child-bearing potential must have negative serum pregnancy test.

  • Sexually active males and females (of childbearing potential) willing to practice contraception during the study.

Exclusion criteria

  • Small cell lung cancer.
  • Newly diagnosed Central Nervous System (CNS) metastases that have not yet been definitively treated with surgery and/or radiation.
  • Uncontrolled hypertension.
  • Myocardial ischemia or infarction more than stage II, cardiac insufficiency.
  • Abnormal coagulation (INR>1.5 or PT>ULN+4, or APTT>1.5 ULN), bleeding tendency or receiving coagulation therapy.
  • Difficulties in taking pills (inability to swallow tablets,GI tract resection, chronic bacillary diarrhea and intestinal obstruction).
  • Hemoptysis, more than 2.5ml daily.
  • Thrombosis in 12 months, including pulmonary thrombosis, stoke, or deep venous thrombosis.
  • Unhealed bone fracture or wound for long time.
  • Received big surgery, had bone fracture or ulcer in 4 weeks.
  • Urine protein≥++, or urine protein in 24 hours≥1.0g.
  • Pregnant or lactating woman.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

Apatinib+Etoposide
Other group
Description:
Apatinib combined with Etoposide
Treatment:
Drug: Etoposide
Drug: Apatinib

Trial contacts and locations

1

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Central trial contact

Xueqin Yang, PHD

Data sourced from clinicaltrials.gov

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