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multicenter phase II study of chemoradiotherapy with docetaxel for elderly patients with stage II, II esophageal cancer

multicenter phase II study of chemoradiotherapy with docetaxel for elderly patients with stage II, II esophageal cancer - Elderly cStageII, III(non T4) esophageal cancer: DTX-RT PhaseII

Status
Unknown
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000001846
Enrollment
40
Registered
2009-04-04
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

Esophageal cancer

Interventions

Chemoradiaion(Docetaxel+RT)

Sponsors

National Cancer Center Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: patients must fulfill all of the following criteria to be eligible for the trial 1 thoracic esophageal cancer 2 histologically confirmed squamous cell carcinoma or adenocarcinoma or adenosquamous carcinoma 3 clinical stage from II to III except T4 4 patient do not receive any previous therapy for esophageal cancer and previous chemotherapy for any other malignancy 5 age from 70 to 80 years 6 ps of 0 and 1 7 patient do not want to receive esophagectomy 8 adequate organ funcion 9 no evidence to need treatment of ECG within 28 days prior to entering this study 10 written informed consent

Exclusion criteria

Exclusion criteria: patients who fulfill any of the following criteria are not eligible for the study 1 esophageal fistula 2 severe comorbidity 3 active infection 4 history of previous radiotherapy to thorax 5 chest Xray shows obvious interstitial pneumonia and pulmonary fibrosis 6 history of any other malignancy which is including synchronal double cancer or double cancer of disease free for less than 5 years but they are not including the carcinoma in situ or intramucosal cancer diagnosed as cure by local procedure 7 motor paralysis or peripheral neuropathy or edema 8 active men and women unwilling to practice effective contraception 9 evidence of psychological disease and symptom that may affect patient compliance with the study 10 patient who is judged as an inappropriate case by the doctor in charge

Design outcomes

Primary

MeasureTime frame
2-years survival

Secondary

MeasureTime frame
Complete Response Rate, Progression free survival, Adverse Events, Late Adverse Events

Countries

Japan

Contacts

Public Contactken kato

National Cancer Center Hospital Gastrointestinal Oncology

kenkato@ncc.go.jp03-3542-2511

Outcome results

None listed

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