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Concurrent chemo-radiotherapy(CCRT) with concomitant boost radiotherapy(CBRT) in locally advanced head and neck cancers.

long term results comparing concurrent chemoradiotherapy with concomitant boost radiotherapy in locally addvanced head and neck cancer.

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/06/034087
Enrollment
100
Registered
2021-06-08
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: C139- Malignant neoplasm of hypopharynx,unspecified Health Condition 2: C109- Malignant neoplasm of oropharynx,unspecified

Interventions

Intervention1: concurrent chemo-radiotherapy,concomitant boost radiotherapy: Study arm (CBRT arm): In CBRT arm, dose of 45 Gy/25 fractions/5 weeks as phase I was given to the primary tumour and the dr

Sponsors

Indira Gandhi Medical College Shimla
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Histology â?? squamous cell carcinoma.17 • Stage III, IV A and IV B. • Previously untreated patients. • Hb > 10gm%. • Pre-treated leucocyte count of > 4000/cu mm. • Platelet count > 100,000/cu mm. • Normal renal and liver function tests. • Karnofsky performance status αα>= 70.

Exclusion criteria

Exclusion criteria: • Histology other than squamous cell carcinoma. • Sites other than oropharynx, hypopharynx, and larynx. • Age > 70yrs. • Deranged RFT / LFT. • Previous treatment with RT/ Chemotherapy. • Any prior/ synchronous malignancy. • Hypersensitivity to platinum agents. • Lymph nodes extending behind the spinal cord. • Karnofsky performance status • Distant metastasis

Design outcomes

Primary

MeasureTime frame
To compare the efficacy of concomitant boost radiotherapy against concurrent chemoradiation in locally advanced head and neck cancer (Oropharynx/Larynx/Hypopharynx). â?¢ To find out the tolerability and toxicity profile of concomitant boost radiotherapy over concurrent chemoradiation in locally advanced head and neck cancer.Timepoint: 6 weeks

Secondary

MeasureTime frame
overall survival and disease free survivalTimepoint: 2 years

Countries

India

Contacts

Public ContactShabnum Thakur

IGMC Shimla

thakurshabnum7@gmail.com9459830966

Outcome results

None listed

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