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Phase II Study of neoadjuvant chemotherapy with carboplatin,pemetrexed and bevacizumab in patients with non-squemous non-small-cell lung cancer

Phase II Study of neoadjuvant chemotherapy with carboplatin,pemetrexed and bevacizumab in patients with non-squemous non-small-cell lung cancer - Phase II Study of neoadjuvant chemotherapy with carboplatin,pemetrexed and bevacizumab in patients with non-squemous non-small-cell lung cancer

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000006759
Enrollment
30
Registered
2011-11-24
Start date
2011-11-01
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 AUC6(day1)+Pemetrexed 500mg/m2(day1)+Bevacizumab 15mg/kg(day1) q3weeks x2cycles CBDCA AUC6(day1)+ Pemetrexed 500mg/m2 (day1) q3weeks x1cycles Surgical operation is performed over 3 weeks

Sponsors

University of Tsukuba, Faculty of Medicine, Department of Thoracic Surgery
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 StageII(exclusing N0)/III 3)Without previously treatment for lung cancer 4)ECOG Performance status 0-1 5)Age:20 years to less than 75 years 6)Patients who has measurable by RECIST(ver 1.1)criteria 7)Adequate organ function 8)Life expectancy more than 3 months 9)Signed written informed consent

Exclusion criteria

Exclusion criteria: 1)Uncontrolled infection or Serious medical complications 2)Uncontrollable diabetes mellitus 3)Uncontrollable hypertension 4)Therapeutic anticoagulopathy (except Aspirin within 325mg/day) 5)Current or previous history of hemoptysis 6)Evidence of bleeding diathesis or hemoptysis 7)With great vessel invasion 8)Cavity in tumor 9)Uncontrollable gastrointestinal ulceration 10)Current or previous(within the last 1 year) history of GI perforration 11)History of severe heart disease 12)Interstitial pneumonia or pulmonary fibrosis detectableon chest X-ray 13)Multiple primary cancer 14)With a history of drug sensitivity 15)Patients who do not want to take vitamin preparation 16)Serious psychiatric illness or psychological symptom 17)Women who are pregnant, lactating or with childbearing potential 18)Ineligible based on decision of an investigator.

Design outcomes

Primary

MeasureTime frame
Down staging rate

Secondary

MeasureTime frame
2year survival rate,2-years relapse free survival,Progression free survival,rate of completion of the protocol treatment,Pathologic complete response rate,Complete resection rate,Safety

Countries

Japan

Contacts

Public ContactYukio Sato

University of Tsukuba Faculty of Medicine, Department of Thoracic Surgery

ysato@md.tsukuba.ac.jp029-853-3097

Outcome results

None listed

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