Neoadjuvant Pemetrexed, Carboplatin and Bevacizumab in Unresectable, Locally Advanced Lung Adenocarcinoma

Si-Yu Wang42 enrolled

Overview

The prognosis of patients with unresectable, locally advanced non-small cell lung cancer (NSCLC) is poor. Chemoradiotherapy is the main treatment modality for this disease. The newer drug regimens can be expected to improve survival in this subset of NSCLC patients. Modern targeted therapies have enhanced the outcomes of lung cancer treatment, especially for advanced NSCLC. Among the targeted approaches for the inhibition of angiogenesis is bevacizumab, a monoclonal antibody that represses vascular endothelial growth factor (VEGF). Bevacizumab in combination with platinum-based chemotherapy used as neoadjuvant chemotherapy may change the previous treatment modality. It allows some lung cancer patients to be downstaged to surgery rather than radiotherapy. Thus, survival of these patients may be improved.

This trial investigates the role of neoadjuvant pemetrexed, carboplatin and bevacizumab in unresectable, locally advanced lung adenocarcinoma.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Lung Cancer

Interventions

Eligibility

Sex: ALLMin age: 18 YearsMax age: 65 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Histologically confirmed unresectable, locally advanced (III A (bulky N2), III B) lung adenocarcinoma * No previous chemotherapy, radiotherapy, surgery or biological therapy for lung cancer * Adequate organ and bone marrow function Exclusion Criteria: * Prior chemotherapy or radiation therapy for NSCLC * Prior treatment with bevacizumab or other agents specifically targeting vascular endothelial growth factor (VEGF) * Patients with known hypersensitivity to other recombinant human antibodies * History of stroke or transient ischemic attack (TIA). * History of myocardial infarction or unstable angina within the past 12 months. * Other serious illness or medical condition including unstable cardiac disease requiring treatment, history of significant neurologic or psychiatric disorders (including psychotic disorders, dementia, or seizures), symptomatic diverticulitis, or active uncontrolled infection. * Women who are pregnant or breast-feeding

Outcomes

Primary Outcomes

Resectability rate

Time frame: 3 months

Secondary Outcomes

Number of participants with perioperative complications

Time frame: 4 months

Disease-free survival

Time frame: 2 years

Overall survival