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A clinical trial of intra-arterial infusion chemotherapy with cisplatin for head and neck cancer

A clinical trial of intra-arterial infusion chemotherapy with cisplatin for head and neck cancer - A clinical trial of intra-arterial infusion chemotherapy with cisplatin for head and neck cancer

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000017656
Enrollment
18
Registered
2015-05-25
Start date
2015-05-25
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

Head and neck squamous cell carcinoma

Interventions

Combined therapy of intra-arterial infusion chemotherapy with cisplatin and radiotherapy

Sponsors

Department of Radiology Mie University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Head and neck cancer 2)Stage 3, 4A, or 4B 3)Without previous irradiation for head and neck 4)Without previous chemotherapy with cisplatin 5)Squamous cell carcinoma 6)>=20, <=80 7)Performance Status(ECOG) 0-2 8)WBC >3000/mm3, Neutrophil >1500/mm3 9)Hb >9g/dL 10)PLT >=100,000/mm3 11)AST, ALT <3 times the upper limit of normal 12)total bilirubin <2mg/dL 13)Creatinine clearance >50mL/min 14)Provided written informed consent

Exclusion criteria

Exclusion criteria: 1)Prior history of radiotherapy for head and neck 2)History of serious drug allegies 3)With severe complications (hepatic disorder, renal disorder,or heart disease, bowel obstruction, peptic ulcer, severe diabetes) 4)with history of severe mental disorder 5)pregnant or nursing women or women who like be pregnant and men with partner willing to get pregnant 6)Cases that the investigator (subinvestigator) judged as inappropriate as the subject of this clinical study

Design outcomes

Primary

MeasureTime frame
maximum tolerrated dose, recommended dose

Secondary

MeasureTime frame
response rate, toxicity, overall survival, local control time, progression free time

Countries

Japan

Contacts

Public ContactYutaka Toyomasu

Mie University Hospital Department of Radiation Oncology

y-toyomasu@clin.medic.mie-u.ac.jp059-231-5029

Outcome results

None listed

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