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Phase II Trial of Preoperative Chemotherapy and Bevacizumab in Patients With Stage IIIA Non-Squamous Non-Small Cell Lung Cancer

Phase II Trial of Preoperative Chemotherapy and Bevacizumab in Patients With Stage IIIA Non-Squamous Non-Small Cell Lung Cancer - Phase II Trial of Preoperative Chemotherapy and Bevacizumab

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004487
Enrollment
30
Registered
2010-11-01
Start date
2010-11-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-squamous, Non-small cell lung cancer

Interventions

CBDCA AUC=5 (Day1) Paclitaxel 200mg/m2 (Day1) Bevacizumab 15mg/kg (Day0 or1) and Surgery

Sponsors

Osaka International Cancer Institute
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Histologically or cytologically proven non-squamous non-small cell lung cancer 2) Patients with resectable stage IIIA (UICC-7th edition) 3) Without previously treatment for lung cancer 4) Age:20-74 5) PS:0-1 6) Expected FEV 1.0 > 1.0L after lung resection 7) Adequate organ function 8) Written informed consent

Exclusion criteria

Exclusion criteria: 1) Active double cancer 2) Current history of hemoptysis 3) Evidence of bleeding diathesis or coagulopathy 4) With great vessel invasion 5) Cavity in tumor 6) History of uncontrollable pericardial effusion 7) History of severe heart disease 8) Current or previous history (within the last 1 year) of symptomatic cerebrovascular disease 9) Active infectious disease in need of intravenous administration of anti-bacterial, anti-fungal, or anti-viral drugs 10) Receiving anticoagulant drug (except Aspirin within 324 mg/day) 11) Uncontrollable Gastrointestinal ulceration 12) Current or previous(within the last 1 year)history of GI perforation 13) Uncontrollable systemic disease (hyper tension or diabetes mellitus) 14) Interstitial pneumonia or pulmonary fibrosis detectable on chest Xp 15) Peripheral neuropathy > Grade2 16) With a history of drug sensitivity 17) History of pregnancy or lactation 18) No intention to practice birth control 19) Patients whose participation in the trial is judged to be inappropriate by the attending doctor

Design outcomes

Primary

MeasureTime frame
3-year disease free survival

Secondary

MeasureTime frame
Rate of completion of the protocol treatment Overall survival Disease-free survival clinical and pathologic response Complete resection rate Toxicity Intraoperative and postoperative complications

Countries

Japan

Contacts

Public ContactJiro Okami

Osaka International Cancer Institute General thoracic surgery

okami-ji@mc.pref.osaka.jp06-6945-1181

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026