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Prospective study about radiation field setting based on 18FDG-PET in definitive chemoradiation for the inoperable local advanced esophageal cancer.

Prospective study about radiation field setting based on 18FDG-PET in definitive chemoradiation for the inoperable local advanced esophageal cancer. - Radiation field setting in chemoradiation for esophageal cancer.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000007209
Enrollment
60
Registered
2012-02-02
Start date
2011-03-01
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

esophageal cancer

Interventions

Duration of chemoradiation was 6 weeks. Radiation consists of 50Gy - 50.4 Gy delivered in 1.8 Gy - 2 Gy per fraction over 5 W - 5.6 weeks. Clinical target volume was defined as the primary tumor
days 29-32, continuous. Nedaplatin consists of 80 mg/m2, day 1 &amp
day 29, bolus.

Sponsors

Department of Radiology, University of Tokyo Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. histopathologically proven invasive esophageal cancer 2. clinical stage I without indicationf of ESD/EMR or clinical stages II - IV 3. PS: 0-2 4. written informed consent 5. WBC: 4000-12000/mm3, Neu > 2000/mm3, Plt > 100,000/mm3, Hb > 9.0g/dL, Tbil < 1.5mg/dL, GOT/GPT < 76/72U/L, Cre < 1.2mg/dL, PaO2 > 70mmHg

Exclusion criteria

Exclusion criteria: 1. having serious complications 2. having synchronism overlap cancer 3. having metastasis to other organs 4. with a history of radiation for the same lesion 5. with a history of chemothrapy 6. having administration contraindication of nedaplatin/5-FU 7. having drug hypersensitivity 8. A woman with the possibility (intention) of the pregnancy, a pregnant woman 9. charging doctor regards as inadequacy because of medical, psychologically, or other factors

Design outcomes

Primary

MeasureTime frame
Isolated lymph node relapse rate

Secondary

MeasureTime frame
Complete response rate, progression free survival time, and frequency and degree of toxicity

Countries

Japan

Contacts

Public ContactHideomi Yamashita

University of Tokyo Hospital Department of Radiology

yamachan07291973@yahoo.co.jp03-5800-8667

Outcome results

None listed

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