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A Phase II Study of Simultaneous modulated accelerated radiation therapy cocurrent with chemotherapy in patients with esophageal squamous cell carcinoma

A Phase II Study of Simultaneous modulated accelerated radiation therapy cocurrent with chemotherapy in patients with esophageal squamous cell carcinoma

Status
Recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-12002356
Enrollment
Unknown
Registered
2012-07-17
Start date
2012-07-25
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

Esophageal cancer

Interventions

Study:Simultaneous modulated accelerated radiation therapy corrent with chemotherapy

Sponsors

Cancer Hospital of Shantou University Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) pathological proven diagnosis of primary squamous cell carcinoma of the esophagus; (2) the primary disease located in cervical, upper or middle thoracic esophagus; (3) no distant metastases; (4) Zubrod performance status: 0~2; (5) Age > 18 and 6 months; (7) absence of another malignancy; (8) adequate liver, renal and bone marrow function; (9) women of childbearing potential and male participants must practice adequate contraception; (10) patient must provide study-specific informed consent prior to study entry?

Exclusion criteria

Exclusion criteria: (1) Evidence of tracheoesophageal or Mediastinal-esophageal fistula; (2) Prior invasive malignancy (except non-melanomatous skin cancer) unless disease free for a minimum of 2 years; (3) Prior radiation therapy that would result in overlap of planned radiation therapy fields; (4) Severe, active comorbidity; (5) Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception; (6) Women who are nursing.

Design outcomes

Primary

MeasureTime frame
Acute toxicities;2-year late toxicitie;

Secondary

MeasureTime frame
2-year local control rate;2-year overall survival rate;

Countries

China

Contacts

Public ContactChuangzhen Chen
stccz@139.com+86 13923995569

Outcome results

None listed

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