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Feasibility study of adjuvant chemotherapy with gemcitabine and cisplatin for completely resected NSCLC

Feasibility study of adjuvant chemotherapy with gemcitabine and cisplatin for completely resected NSCLC - Feasibility study of adjuvant chemotherapy with gemcitabine and cisplatin for completely resected NSCLC

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005256
Enrollment
25
Registered
2011-03-17
Start date
2011-04-01
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

Completely resected NSCLC (stage IB - IIIA including multiple N2)

Interventions

Period: From March 2011 to Febrary 2013 Dose:GEM 1000mg/m2 d1.d8+CDDP 80mg/m2 d1 Cycle: 4 cycles

Sponsors

Kumamoto University Hospital
Lead Sponsor

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 IB - IIIA that received segmentectomy, lobectomy, or bi-lobectomy (including multiple pN2) (3) Performance Status is 0 - 1 (ECOG). (4) 20 years of age or older, 80 years of age or younger. (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 - 12 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 chickenpox (6)The patient with a motor-palsy or figure of peripheral-nerve-disease (7)The patient with drug hypersensitivity (8)The expectant mother, the woman who has a lactating-woman and the possibility of the pregnancy (9)The patient judged as unsuitable by the doctor

Design outcomes

Primary

MeasureTime frame
Chemotherapy compliance in the four cycles

Countries

Japan

Contacts

Public ContactMakoto Suzuki

Kumamoto University Hospital Department of Thoracic Surgery

smakoto@kumamoto-u.ac.jp096-373-5533

Outcome results

None listed

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