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A clinical trial of application of concomitant late course accelerated hyperfractionation radiochemotherapy with cisplatin and pemetrexed in esophagus cancer

A clinical trial of application of concomitant late course accelerated hyperfractionation radiochemotherapy with cisplatin and pemetrexed in esophagus cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-TRC-09000568
Enrollment
Unknown
Registered
2009-10-27
Start date
2009-11-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

esophagus cancer

Interventions

Case series:to receive concomitant radiochemotherapy with pemetrexed + cisplatin: pemetrexed 400mg/m2, i.v. drip d1
cisplatin 10mg/m2, i.v. drip d1 -5. Radiotherapy carried out in the 1st and 4th week

Sponsors

Shandong Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Signed informed consent; 2. Acquired pathological diagnosis; 3. Life expectancy>=6 months; 4. Age: 18-75 years, male or female; 5. General state of health: ECOG 0-1 grade; 6. Without any chemotherapy or radiotherapy; 7. Subjects meet the following criteria for the clinical laboratory: HG>=100g/L, WBC>=3.5*10^9/L, neutrophilic leukocyte>=1.5*10^9, PLT 10*10^9 /L, CR<=1.5*N, TB<=2.5*N, AST and ALT<=2.5*N, AKP<=2.5*N.

Exclusion criteria

Exclusion criteria: 1. Serious infection; 2. Uncontrollable diabetes; 3. Other serious diseases, such as myocardial infarction in 6 months; 4. Participated other clinical trials in 4 weeks or at present.

Design outcomes

Primary

MeasureTime frame
Response rate;

Countries

China

Contacts

Public ContactBaosheng Li
baoshli@yahoo.com+86 0531 67626161

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 23, 2026