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A Phase II Study of biweekly Carboplatin, nab-paclitaxel, and concurrent Thoracic radiation therapy for Patients with local advanced Non-small cell Lung Cancer

A Phase II Study of biweekly Carboplatin, nab-paclitaxel, and concurrent Thoracic radiation therapy for Patients with local advanced Non-small cell Lung Cancer - A Phase II Study of biweekly Carboplatin, nab-paclitaxel, and concurrent Thoracic radiation therapy for Patients with local advanced Non-small cell Lung Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000023802
Enrollment
28
Registered
2016-08-28
Start date
2016-08-01
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

locally advanced Non-small cell Lung Cancer

Interventions

Combination of biweekly calboplatin:AUC=4 plus nab-paclitaxel(100mg/m)with concurrent thoracic radiotherapy 2Gy/day for 30 times

Sponsors

Hirosaki University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patient with pathologically or cytologically proven non-small cell lung cancer 2) Patient with stage IIIA or IIIB desease 3) Patient who has not been previously treated for lung cancer, including chemotherapy, radiotherapy, and operation 4) V20 < 35% 5) Patient who has at least one or more measurable lesion 6) ECOG performance status (PS): 0-1 7) Patient aged 20-74 years old 8) Adequate organ function. 9) Patient who are considered to survive for more than 3 months. 10) Written informed consent.

Exclusion criteria

Exclusion criteria: 1) T3N1 2) Superior vena cava syndrome. 3) Lymph node metastases of opposite side hilum, malignant pleuritis, malignant pericarditis, lymphangitis. 4) With active double cancer. 5) Active infection. 6) Other serious disease condition (idiopathic pulmonary fibrosis, interstitial lung disease, renal failure, liver failure, Cerebral Vascular Disorder, unstable angina, cardiac infarction, Myocardial Infarction, poorly controlled diabetes mellitus,etc). 7) Grade2< peripheral neuropathy. 8) Severe drug allergy. 9) Pregnancy or lactation. 10) Patient whose participation in the trial is judged to be inappropriate by the attending doctor.

Design outcomes

Primary

MeasureTime frame
2-year survival rate

Secondary

MeasureTime frame
Response rate, Progression free survival, Over all survival, Adverse events

Countries

Japan

Contacts

Public ContactHisashi Tanaka

Hirosaki University Graduate School of Medicine Department of Respiratory Medicine

xyghx335@gmail.com0172-33-5111

Outcome results

None listed

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