Skip to content

Feasibility study of adjuvant chemotherapy with carboplatin and nab-paclitaxel for resected NSCLC

Feasibility study of adjuvant chemotherapy with carboplatin and nab-paclitaxel for resected NSCLC - Feasibility study of adjuvant chemotherapy with carboplatin and nab-paclitaxel for resected NSCLC

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011910
Enrollment
21
Registered
2013-10-01
Start date
2013-09-27
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

resected NSCLC(stage II - IIIB)

Interventions

CBDCA(AUC 5, day1) plus nab-PTX(100mg/m2,day1,8,15) 4 cycles

Sponsors

Division of Respiratory Medicine, Department of Internal Medicine,Kobe University Graduate School of Medicine
Lead Sponsor
Division of Respiratory surgery, Kobe University Graduate School of Medicine
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)The patient histologically proven as non-small cell lung cancer (2)The patient with p-staged II - IIIB that received segmentectomy, lobectomy, or bi-lobectomy (3) Performance Status is 0 - 1 (ECOG). (4) 20 years of age or older (5) The patient who does not receive any chemotherapy, radiotherapy, or immunotherapy prior to resection (6) The patient who preserves the main organ ( the bone marrow, liver, kidney and so on ) (7) The patient who can receive chemotherapy within 4 - 8 weeks after resection (8) The patient who gives written informed consent

Exclusion criteria

Exclusion criteria: (1)The patient with infection (2)The patient with fever (equal to or more than 38 C) (3)The patient with heavy complication (4)The patient with active double-cancer (5)The patient with uncontrolled pleural effuson (6)The patient with a motor-palsy or figure of peripheral-nerve-disease (7)The patient with drug hypersensitivity (8)The patient with common use of NSAIDs (9)The expectant mother, the woman who has a lactating-woman and the possibility of the pregnancy (10)The patient judged as unsuitable by the doctor

Design outcomes

Primary

MeasureTime frame
safety

Secondary

MeasureTime frame
1.Chemotherapy compliance in the four cycles 2.2-years disease free survival

Countries

Japan

Contacts

Public ContactMotoko Tachihara

Kobe University Graduate School of Medicine Division of Respiratory Medicine, Department of Internal Medicine

mt0318@med.kobe-u.ac.jp078-382-5846

Outcome results

None listed

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