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Clinical Outcomes in patients with Esophageal Cancer treated with Definitive Chemoradiotherapy

Definitive Chemoradiotherapy in Esophageal Cancer using Volumetric Modulated Arc Therapy (VMAT) Technique: A Report on Clinical Outcomes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/03/032343
Enrollment
30
Registered
2021-03-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: C159- Malignant neoplasm of esophagus, unspecified

Interventions

None listed

Sponsors

None
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Histologically confirmed non-recurrent non-metastatic squamous cell carcinoma or adenocarcinoma of esophagus or gastroesophageal junction (GEJ). 2. Patients must be considered as having inoperable/unresectable tumor, considered to be unfit for surgery and/or are unwilling for surgery. 3. ECOG performance status less than or equal to 2. 4. Adequate baseline bone marrow, liver and renal functions as determined by routine standard-of-care tests. 5. Patients being treated using VMAT technique. 6. Willingness to participate in the study and provides a voluntary informed consent.

Exclusion criteria

Exclusion criteria: 1. Metastatic disease at presentation. 2. History of prior mediastinal/thoracic malignancy or condition that warranted irradiation or chemotherapy. 3. Patients with tracheoesophageal fistula/bronchoesophageal fistula. 4. Patients with active second malignancy. 5. Uncontrolled co-morbidities that would hamper the patientsâ?? adherence to treatment. 6. Known contraindications to use of concurrent chemotherapy (E.g.: impaired renal/hematological function, known hypersensitivity, etc.)

Design outcomes

Primary

MeasureTime frame
To evaluate the local control rates and disease-free survival (DFS) in esophageal cancer following definitive chemoradiotherapy by VMAT technique.Timepoint: At completion of treatment course, 1 month, 3 months and 6 months

Secondary

MeasureTime frame
To compare target volume coverage and normal tissue exposure dosimetrically between VMAT and 3D-CRT technique.Timepoint: At 6 months.;To correlate between dose exposure to organs-at-risk (OARs) and acute toxicity.Timepoint: At 6 months.;To correlate between radiation dose used and disease outcomes.Timepoint: At 1 month, 3 months and 6 months.;To report on acute and long-term treatment toxicities.Timepoint: At presentation of primary event.

Countries

India

Contacts

Public ContactDr Krishna Sharan

Kasturba Medical College and Hospital, Manipal

tk.sharan@gmail.com9448625116

Outcome results

None listed

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