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Feasibility study of Carboplatin plus Pemetrexed in patients with recurrent and postoperative non-small cell lung cancer

Feasibility study of Carboplatin plus Pemetrexed in patients with recurrent and postoperative non-small cell lung cancer - Carboplatin plus Pemetrexed in patients with recurrent and postoperative non-small cell lung cancer

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000004866
Enrollment
30
Registered
2011-01-14
Start date
2010-04-01
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 and non squamous lung cancer

Interventions

Pemetrexed, Carboplatin

Sponsors

Department of Thoracic Surgery, University of Tsukuba
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Initial chemottherapy 2.ECOG performance status0-1 3.Stage IIor III after complete resection 4.Age of 20 years or older 5.Laboratory parameters obtained before registation WBC count:>4000/uL, <12000/uL neutrophil count:>2000/uL Platelet count:>10*10000/uL Hemoglobin:>9.5g/dL GOT,GPT:<100 IU/L Total bilirubin:<2.0mg/dL PaO2:>60 torr creatinine:<1.5mg/dL 6.Anticipated life expectancy of at least 3 months 7.Capable to registrate in 30days after surgery 8.Capable to stay in the hospital 9.Obtained informed consent

Exclusion criteria

Exclusion criteria: 1.Interstitial pneumonia or pulmonary fibrosis on Chest Xray 2.Unstable pleural effusion formation 3.Superior vena cava syndrome 4.Uncotrolled diabetes mellitus, hypertension, liver dysfunction, angina pectoris, and acute myocardial infarction 5.Severe infection, a sign of severe infection 6.Grade2 or worse peripheral nerve disorder at the time of enrollment 7.Regular user of NSAIDs 8.Pregnant woman, lactating woman, woman of child-bearing potential, woman who wish to pregnancy 9.Severe drug allergy 10.Severe complication 11Other inadequate reasons 12.New lesion that is recognized before enrollment

Design outcomes

Primary

MeasureTime frame
feasibility study (4 courses)

Secondary

MeasureTime frame
1-year recurrence-free survival

Countries

Japan

Contacts

Public ContactMitsuaki Sakai

University of Tsukuba Department of Thoracic Surgery

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

Outcome results

None listed

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