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Pemetrexed Monotherapy for Performance Status 2 Patients in Treatment of Non-Small and Non-Squamous Cell Lung Cancer Patients Without EGFR Mutation.

Pemetrexed Monotherapy for Performance Status 2 Patients in Treatment of Non-Small and Non-Squamous Cell Lung Cancer Patients Without EGFR Mutation. - Pemetrexed Monotherapy for Performance Status 2 Patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002622
Enrollment
35
Registered
2009-10-15
Start date
2009-09-01
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

Pemetrexed at a dose of 500mg/m2 every 3 weeks is administered until progression disease.

Sponsors

Kobe Lung Cancer Oncology Study Group (KLOG)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Histologically or cytologically proven non-squamous non-small cell lung cancer (without large cell neuroendocrine carcinoma) 2)Non-squamous non-small cell cancer patients with stage IIIB(with pleural dissemination or malignant pleural effusion),stage IV or recurrent disease after surgery,who have no prior chemoterapy 3)With measurable or inmeasurable lesion 4)If the patient underwent radiotherapy, there should be the following interval between the radiotherapy and the registration i)Radiotherapy including pulmonary field ->3 months ii)Radiotherapy other than thoracic radiation ->1 month 5)over 20 years old 6)ECOG PS 2 7)without (or unknown) EGFR mutation 8)Adequate organ function 9)Life expectancy more than 3 months 10)Written informed consent

Exclusion criteria

Exclusion criteria: 1)Interstitial pneumonia or pulmonary fibrosis detectable on CT scan 2)History of drug induced interstitial pneumonia 3)History of severe drug allergy 4)History of active infection or other serious disease condition (GI bleeding,etc.) 5)History of poorly controlled pleural effusion,pericardial effusion and ascites 6)History of severe heart disease(uncontrollable arrythmia,uncontrollable angina pectoris,herat failure,etc.) 7)Uncontrollable diabetes mellitus 8)History of symptomatic brain metastases 9)Hystory of active double cancer 10)History of active psychological disease 11)Patients whose participation in the trial is judged to be inappropriate by the attending doctor

Design outcomes

Primary

MeasureTime frame
progression free survival

Secondary

MeasureTime frame
response rate overall survival disease control rate safety

Countries

Japan

Contacts

Public ContactAkito Hata

Institute of Biomedical Research and Innovation Integrated Oncology

a-hata@fbri.org078-304-5200

Outcome results

None listed

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