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A phase I study of chemoradiotherapy (cisplatin and vinorelbine) with use of involved-field conformal radiotherapy and accelerated hyperfractionation for stage III non-small cell lung cancer

A phase I study of chemoradiotherapy (cisplatin and vinorelbine) with use of involved-field conformal radiotherapy and accelerated hyperfractionation for stage III non-small cell lung cancer - A phase I study of chemoradiotherapy with 3DCRT for stage III NSCLC

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000003769
Enrollment
12
Registered
2010-06-21
Start date
2008-09-01
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

cisplatin and vinorelbine

Sponsors

Osaka Lung Cancer Study Group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Histologicaly or cytologicaly proven NSCLC (2) Un-treated patients with IIIA/IIIB NSCLC. When radio-oncologist judged that the patients can tolerable for full dose irradiation. (3) V20 and less 35% (4) ECOG Performance status 0-1 (5) age under than 75 (6) Measurable lesion (RECIST) (7) Adequate organ function (8) Written informed consent

Exclusion criteria

Exclusion criteria: (1) With interstitial pneuminia or pulmonary fibrosis (2) Presence of other active malignancy (3) Pregnancy or lactating patients (4) A male without the intention to contraception (5) With sever cardiac diseases (6) Un-controlled DM (7) With sever infection (8) With high fiver (9) Previous treatment of thoracic irradiation (10) Others

Design outcomes

Primary

MeasureTime frame
recommended dose of radiotherapy

Secondary

MeasureTime frame
Toxicity, response, overall survival

Countries

Japan

Contacts

Public ContactNaruo Yoshimura

Graduate School of Medicine, Osaka City University Department of Respiratory Medicine

y-naruo@sc4.so-net.ne.jp06-6645-3793

Outcome results

None listed

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