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A Study to Evaluate a New International Radiation Planning Guideline in Patients with Nasopharyngeal Cancer

Implementation and Outcome Assessment of the 2024 International Clinical Target Volume Delineation Guideline in Locoregionally Advanced Nasopharyngeal Carcinoma: A Prospective Clinical Study - ImpACT-NPC

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/02/102999
Enrollment
55
Registered
2026-02-04
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: C119- Malignant neoplasm of nasopharynx,unspecified

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil

Sponsors

Yanpothung Yanthan
Lead Sponsor
Abhinandan Das
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Biopsy-proven nasopharyngeal carcinoma. Age 18 to 70 years. Stage II to IVA disease (AJCC 9th edition). ECOG performance status 0 to 1 Eligible for induction chemotherapy followed by concurrent chemoradiation. Capable of providing written or witnessed informed consent

Exclusion criteria

Exclusion criteria: Prior head and neck radiotherapy. Previous head and neck malignancy regardless of interval since diagnosis. Previous Non-Head and Neck malignancy (excluding basal cell carcinoma) with disease free interval less than 10 years. Uncontrolled comorbidities or pregnancy.

Design outcomes

Primary

MeasureTime frame
To estimate the 2-year locoregional failure-free survival (LR-FFS) in NPC patients treated using IG-2024 CTV delineation.Timepoint: To estimate the 2-year locoregional failure-free survival (LR-FFS) in NPC patients treated using IG-2024 CTV delineation.

Secondary

MeasureTime frame
To estimate the incidence and severity of acute and late toxicities using CTCAE v6.0Timepoint: Acute till 3 months after treatment completion. Late after 3 months; To analyse dosimetric parameters, including PTV/CTV/GTV coverage and OAR dose metrics.Timepoint: At the time of radiotherapy planning; To compare the estimated 2-year LR-FFS, toxicities, and dosimetric parameters with historical benchmarks based on IG-2018.Timepoint: Acute toxicity till 3 months after treatment completion. Late after 3 months. 2 years LR-FFS

Countries

India

Contacts

Public ContactYanpothung Yanthan

Dr. B. Borooah Cancer Institute

yanyanthan@gmail.com9612551001

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026