A Study of Avastin (Bevacizumab) in Combination With Gemcitabine With or Without Cisplatin in First-Line Treatment of Elderly Patients With Non-Small Cell Lung Cancer

Roche

Status and phase

Completed

Phase 2

Conditions

Non-Squamous Non-Small Cell Lung Cancer

Treatments

Drug: gemcitabine

Drug: bevacizumab [Avastin]

Drug: cisplatin

Study type

Interventional

Funder types

Industry

Identifiers

NCT01077713

2008-008739-27

ML21868

Details and patient eligibility

About

This 2 arm study will evaluate the efficacy and safety of Avastin + gemcitabine, and Avastin + gemcitabine + attenuated doses of cisplatin, as first line treatment in elderly patients with non-squamous non-small cell lung cancer. Patients will be randomised to receive either Avastin 7.5mg/kg iv on day 1 + gemcitabine 1200mg/m2 on days 1-8 of each 3 week cycle, or Avastin 7.5mg/kg iv on day 1 + cisplatin 60mg/m2 on day 1 + gemcitabine 1000mg/m2 on days 1-8 of each 3 week cycle. After 6 cycles of combination therapy, all patients will continue to receive Avastin monotherapy. The anticipated time on study treatment is until disease progression, and the target sample size is <100 individuals.

Enrollment

86 patients

Sex

All

Ages

70+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

adult patients, >=70 years of age;
inoperable, locally advanced, metastatic non-squamous non-small cell lung cancer;
>=1 measurable lesion;
ECOG performance status 0-1.

Exclusion criteria

neoadjuvant/adjuvant chemotherapy within 6 months prior to enrollment;
radical radiotherapy with curative intent within 28 days prior to enrollment;
history of >=grade 2 hemoptysis in 3 months prior to enrollment;
evidence of CNS metastases;
current or recent (within 10 days of first dose of Avastin)use of aspirin (>325 mg/day)or full dose anticoagulants or thrombolytic agents for therapeutic purposes.