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Weekly nab-Paclitaxel+Carboplatin with Radiotherapy as First Line Therapy in Patients with Advanced Non-Small-Cell Lung Cancer

Weekly nab-Paclitaxel+Carboplatin with Radiotherapy as First Line Therapy in Patients with Advanced Non-Small-Cell Lung Cancer - Weekly nab-Paclitaxel+Carboplatin with Radiotherapy as First Line Therapy in Patients with Advanced Non-Small-Cell Lung Cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000031017
Enrollment
25
Registered
2019-01-24
Start date
2013-12-01
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

Weekly nab-Paclitaxel+Carboplatin with Radiotherapy

Sponsors

University of Fukui Faculty of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Pathological stage IIIA, IIIB stage that is diagnosed as pathologically non-small cell lung cancer and judged to be resectable on the image. 2) Diagnosis of ipsilateral mediastinal lymph node metastasis (N2) is histologically proven (bronchoscopy, mediastinoscopy), or obvious swelling (minor diameter greater than 20 mm) allowed . 3) For T4, a case clearly showing invasion on the image (CT, MRI, PET - CT). 4) Cases with no resistance to chemotherapy or radiotherapy for non-small cell lung cancer 5) ECOG's Performance Status (PS) is 0 to 1. 6) The age is over 20 years old and under 79 years old. 7) Within 14 days prior to enrollment patients have adequate bone marrow, liver, kidney and lung function

Exclusion criteria

Exclusion criteria: 1) Taxane and CBDCA are contraindicated for administration. 2) A history of severe drug sensitivity. 3) A history of hypersensitivity to albumin. 4)Interstitial pneumonia or pulmonary fibrosis apparent in chest radiography. 5) Active or duplicated cancer with metachronous or simultaneous, multiple cancers. 6) Pleural effusion, drainage and pericardial effusion required drainage. 7) Have serious complications. 8) Patients with peripheral neuropathy of Grade 2 or higher. 9) HBs antigen positive 10) Pregnant women or women who may be pregnant. 11) A man who is willing to conceive. 12) The doctor in charge judged unsuitable for registration of this exam.

Design outcomes

Primary

MeasureTime frame
The complete resection rate

Secondary

MeasureTime frame
2 years no relapse survival rate and progression free survival rate for 2 years.

Countries

Japan

Contacts

Public ContactMasato Sasaki

University of Fukui Faculty of Medical Sciences Division of Thoracic Surgery, Department of Surgery

masato@u-fukui.ac.jp0776-61-3111

Outcome results

None listed

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