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Multicenter phase II study of docetaxel/cisplatin/bevacizumab combination therapy in patients with advanced non-squamous non-small cell lung cancer (TORG1016)

Multicenter phase II study of docetaxel/cisplatin/bevacizumab combination therapy in patients with advanced non-squamous non-small cell lung cancer (TORG1016) - Multicenter phase II study of docetaxel/cisplatin/bevacizumab combination therapy in patients with advanced non-squamous non-small cell lung cancer (TORG1016)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004368
Enrollment
47
Registered
2010-10-12
Start date
2010-10-01
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-small cell lung cancer

Interventions

docetaxel/cisplatin/bevacizumab combination therapy

Sponsors

Thoracic Oncology Research Group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) pathologically diagnosed non-squamous non-small cell cancer 2) stage III/IV without indication for curative radiothrapy or post-operative reccurent disease 3) aged 20 years or older, under 75 years 4) ECOG PS: 0-1 5) measurable lesion meeting RECIST criteria (version 1.1) 6) no prior treatment except for surgery,EGFR-TKI, palliative radiotherapy 7) adequate organ function 8) life expectancy more than 3 months 9) adequate interval after prior treatments; 2 weeks from radiotherapy, 8 weeks from lobectomy, 4 weeks from exploratory thoracotomy, 2 weeks pleural drainage 10) written informed consent

Exclusion criteria

Exclusion criteria: 1) brain metastasis 2) histroy of hemoptysis 3) serious complication; cardiac disea se, interstitial peumonia, diabetes, active infection 4) massive pleural or pericardial effusion, ascites 5) concomitant malignancy 6) uncontrollable peptic ulcer or GI perforaion within 1 year 7) uncontrollable hypertension 8) anticoagulation therapy 9) inappropriate for this study judged by the attending physician

Design outcomes

Primary

MeasureTime frame
response rate

Secondary

MeasureTime frame
adverse events, progression free survival, overall survival

Countries

Japan

Contacts

Public ContactTerufumi Kato

Kanagawa Cardiovascular and Respiratory Center Department of Respiratory Medicine

t-kato@kanagawa-junko.jp045-701-9581

Outcome results

None listed

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