Skip to content

Effect of difinitive chemoradiation with cisplatin-irrinotecan or carboplatin-paclitaxol in esophageal cancer

A survey on different chemoradiation of esophageal cancer with cisplatin and irrinotecan compered with paclitaxol /carboplatin and evaluation of their effect and toxicity

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014110219783N1
Enrollment
100
Registered
2017-07-24
Start date
2016-05-12
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Chemoradiation Protocols. ??? ???????_??? ????_??????

Interventions

Intervention 1: Patients in the arm 1 treat with the combination of cisplatin 30mg/m2 and irrinotecan 65mg/m2 days 1,8 every 3 weeks at least 2 cycles during radiotherapy and 1 cycle before and 2 cycl
Treatment - Drugs
Diagnosis
Patient in the control arme treat with the combination of paclitaxel 50mg\m2 and carboplatin AUC:2 ,weekly during radiotherapy .
Patients in the arm 1 treat with the combination of cisplatin 30mg/m2 and irrinotecan 65mg/m2 days 1,8 every 3 weeks at least 2 cycles during radiotherapy and 1 cycle before and 2 cycles after chemora

Sponsors

Vice chancellor for research, Mashhad University of Medical Sciencesice
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Iinclusion criteria:Primery Esophageal or Cardioesoohageal ?Cancer(Adenocarcinoma or Scc);Without eny distant metastas;Maximum age 75 years ;Performance Status>70% ;Hemotologically Stable; Normal liver and kidney function; Patient Satisfaction; Unfit patient for surgery. Exclusion Criteria;Metastatic disease; Cervical Esophageal Cancer; Thracheoesophageal fistula; Another previous or current malignant disease ; Any surgery performed within the past 4 weeks; According to the judgment of physition.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Survival Rate. Timepoint: 1-Every 3 monthes after start of intervention2-Following every cycle of chemothrapy. Method of measurement: 1-Monthes that patients survive after intervention2-Questionnaire.

Secondary

MeasureTime frame
1-Disease Free Survival 2-toxcicity. Timepoint: 1-Every 3 months after start of intervention 2-Following every cycle of chemothrapy. Method of measurement: Monthes that patients survive after start of intervention-qestionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMitra Fazl Ersi

Cancer Research Center

fazlm1@mums.ac.ir+98 51 3846 1518

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026