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Phase II study of Pemetrexed and Bevacizumab in Performance status 2 patients with advanced non-squamous non-small cell lung cancer.

Phase II study of Pemetrexed and Bevacizumab in Performance status 2 patients with advanced non-squamous non-small cell lung cancer. - Phase II study of Pemetrexed and Bevacizumab in PS2 patients with advanced non-squamous non-small cell lung cancer.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008124
Enrollment
25
Registered
2012-06-08
Start date
2012-06-01
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

Pemetrexed and Bevacizumab administered every 3 week until observation of progression or intolerable toxicity.

Sponsors

Niigata Lung Cancer Treatment Group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) StageIIIB/IV or postoperative recurrence Non-small cell lung cancer and Non-Squamous cell carcinoma proven by histology and/or cytology 2) EGFR mutation or ALK rearrangement status is not required 3) No prior chemotherapy 4) 20 years or older and PS 2 5) At least one or more measurable lesion by RECIST ver1.1 6) Adequate organ function 7) Interval -Palliative radiotherapy >4wks -Surgery >4wks -thoracic drainage>1wks -biopsy with dissection, indwelling port >1wks -blood transfusion >2wks 8) Life expectancy more than three months. 9) Written Informed Consent

Exclusion criteria

Exclusion criteria: 1) History of hemoptysis 2) High risk of bleeding or thrombus events 3) History of anticoagulant within 10 days before enrollment 4) Active radiation pneumonitis or esophagitis 5) Uncontrollable hypertension 6) Symptomatic brain metastasis 7) Scheduled operation 8) Severe complications 9) Problematic infection 10) History of active double cancer 11) No intention to birth control 12) Unstable psychic disorder 13) History of treatment drug 14) Decision of ineligibility by a physician.

Design outcomes

Primary

MeasureTime frame
PFS

Secondary

MeasureTime frame
RR,DCR,OS,TTF,QOL,safety

Countries

Japan

Contacts

Public ContactHirohisa Yoshizawa

Niigata University Medical and Dental Hospital Bioscience Medical Research Center

hy0522@med.niigata-u.ac.jp025-227-2517

Outcome results

None listed

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