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CTRI Number  CTRI/2026/03/105195 [Registered on: 02/03/2026] Trial Registered Prospectively
Last Modified On: 27/02/2026
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   Role Of G-CSF In Preventing Chemoradiation Induced Mucositis In Locally Advanced Head And Neck Cancer Patients : A Prospective Randomised Study 
Scientific Title of Study   Effect Of Granulocyte Colony Stimulating Factor Administration On Chemoradiation Induced Mucositis In Locally Advanced Head And Neck Cancer Patients – A Prospective Randomized Study 
Trial Acronym  GAMMA-HN  
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  V Bindu Madhavi 
Designation  MD Radiation Oncology, Junior Resident 
Affiliation  Sri Venkateswara Institute of Medical Sciences  
Address  Department of Radiation Oncology Alipiri road Tirupati
Department of Radiation Oncology SVIMS Alipiri road Tirupati
Chittoor
ANDHRA PRADESH
517507
India 
Phone  7989576275  
Fax    
Email  sairam6275@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr.B.V.Subramanian 
Designation  HOD,Professor,MD Radiation Oncology  
Affiliation  Sri Venkateswara Institute of Medical Sciences  
Address  Department of Radiation Oncology Alipiri road Tirupati
Department of Radiation Oncology SVIMS Alipiri road,Tirupati
Chittoor
ANDHRA PRADESH
517507
India 
Phone  9849692950  
Fax    
Email  ravibalasubramanian@hotmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr.B.V.Subramanian 
Designation  HOD.Professor,MD Radiation Oncology  
Affiliation  Sri Venkateswara Institute of Medical Sciences  
Address  Department of Radiation Oncology Alipiri road,Tirupati
Department of Radiation Oncology SVIMS Alipiri road,Tirupati
Chittoor
ANDHRA PRADESH
517507
India 
Phone  9849692950  
Fax    
Email  ravibalasubramanian@hotmail.com  
 
Source of Monetary or Material Support  
Sri Venkateswara Institute of Medical Sciences 
 
Primary Sponsor  
Name  Sri Venkateswara Institute of Medical Sciences 
Address  Alipiri road,Tirupati,Chittoor district,AndhraPradesh,India,517507 Opposite to ASWO office  
Type of Sponsor  Other [SELF] 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
DrBVSUBRAMANIAN  SRI VENKATESWARA INSTITUTE OF MEDICAL SCIENCES  DEPARTMENT OF RADIATION ONCOLOGY SVIMS,TIRUPATI
Chittoor
ANDHRA PRADESH 
9849692950

ravibalasubramanian@hotmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
INSTITUTIONAL ETHICS COMMITTEE  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  ,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  FILGRASTIM  FILGRASTIM GIVEN IN LOCALLY ADVANCED HEAD AND NECK CANCER PATIENTS ON CONCURRENT CHEMORADIATION 
Comparator Agent  FILGRASTIM IN PATIENTS IN EXPERIMENTAL GROUP  FILGRASTIM IN PATIENTS OF LOCALLY ADVANCED HEAD AND NECK CANCER ON CONCURRENT CHEMO RADITION. At the end of first week of Radiation therapy patients in study group will be administered with a dose of 150mcg/day (0.50ml) of Filgrastim subcutaneously on saturday morning throughout the treatment period 6-7 weeks  
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  70.00 Year(s)
Gender  Both 
Details  1.Histopathologically proven head and neck squamous cell carcinoma
2.Patients presenting with AJCC Clinical stage III-IV, nonmetastatic head and neck carcinoma
3.Age between 18 and 70 years.
4.Patients with ECOG performance status of 0–1
5.Patients who are willing to give an approved informed consent.
6.GFR more than 45ml/min/1.73m² 
 
ExclusionCriteria 
Details  1.Patients who had prior underwent surgery or
neoadjuvant chemotherapy for Head and Neck
carcinoma.
2.Patients with proven/known distant metastasis.
3.Patients having hypersensitivity to G-CSF.
4.Patients who have not consented to be a part of
the study.
5.Pregnant women and lactating mother.
 
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   On-site computer system 
Blinding/Masking   Participant, Investigator and Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
•To assess the incidence and severity of oral mucositis in patients receiving concurrent chemo radiotherapy with three weekly cisplatin, with weekend G-CSF administration.  During RT (weekly twice) and Monthly once for 3 months after treatment 
 
Secondary Outcome  
Outcome  TimePoints 
• To compare tumor response between patients receiving concurrent chemo radiotherapy with three weekly cisplatin with weekend G-CSF administration & those receiving concurrent chemo radiotherapy with three weekly cisplatin without G-CSF administration.  3months after treatment  
 
Target Sample Size   Total Sample Size="44"
Sample Size from India="44" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   Phase 3 
Date of First Enrollment (India)   10/03/2026 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="6"
Days="0" 
Recruitment Status of Trial (Global)   Not Yet Recruiting 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

Here is a detailed 500-word summary of the thesis:


Summary: Effect of G-CSF Administration on Chemoradiation-Induced Mucositis in Locally Advanced Head and Neck Cancer Patients

Background and Rationale

This thesis protocol, submitted to Sri Venkateswara Institute of Medical Sciences (SVIMS), Tirupati, Andhra Pradesh, investigates the role of Granulocyte Colony Stimulating Factor (G-CSF) in managing one of the most debilitating side effects of cancer treatment — oral mucositis. Head and neck cancer is the seventh most common cancer globally, representing 26.2% of new cancer cases according to GLOBOCAN 2022. The standard treatment for locally advanced Head and Neck Squamous Cell Carcinoma (HNSCC) is concurrent chemoradiotherapy (CCRT), which, while effective for local tumor control, inevitably causes significant mucosal toxicity.

Oral mucositis — inflammation of the oral mucosa ranging from redness to severe ulceration — is a common and painful complication of CCRT. It can cause excruciating pain, necessitate parenteral nutrition, increase infection risk, lead to septicemia, and cause unscheduled treatment breaks that compromise outcomes. G-CSF (specifically Filgrastim) promotes neutrophil production and modulates the inflammatory environment, potentially aiding mucosal healing by increasing anti-inflammatory cytokines and reducing pro-inflammatory mediators like TNF-alpha.

Aim and Objectives

The primary aim of the study is to evaluate the effect of weekend G-CSF administration on the incidence and severity of oral mucositis in head and neck cancer patients receiving concurrent chemoradiotherapy with three-weekly cisplatin. The secondary objective is to compare tumor response between the G-CSF group and the control group at 3 months post-treatment using RECIST criteria.

Study Design and Methodology

This is a single-center, prospective, randomized interventional study to be conducted over 18 months in the Department of Radiation Oncology at SVIMS, Tirupati, following Institutional Ethics Committee (IEC) approval and CTRI registration. A total of 44 patients (22 per arm) aged 18–70 years with histopathologically proven Stage III–IV non-metastatic HNSCC and ECOG performance status 0–1 will be enrolled. Patients are randomized into a study group (CCRT + weekend G-CSF) and a control group (CCRT alone).

All patients receive radiation therapy using IMRT or VMAT techniques and concurrent cisplatin at 100 mg/m² every three weeks for two cycles. Patients in the study arm receive subcutaneous G-CSF (Filgrastim) at 150 mcg/day every Saturday throughout the treatment (6–7 weekends), maintaining a 24-hour gap from radiotherapy. Mucositis is assessed weekly using the RTOG Acute Radiation Toxicity Grading Scale, and tumor response is assessed at 3 months via contrast-enhanced CT of the head and neck.

Literature Context

Several prior studies have explored GM-CSF and G-CSF for mucositis prevention. A key Indian study (Prathyusha et al., 2019) on 75 patients showed that weekend Filgrastim significantly reduced mucositis severity, with a mean mucositis score of 1.33 in the study group versus 1.62 in controls, and better treatment compliance. The current study builds on this evidence.

Statistical Analysis

Data will be analyzed using SPSS v26.0. Continuous variables will be compared using unpaired t-tests or Mann-Whitney U tests, and categorical variables using chi-square or Fisher’s exact tests. A p-value < 0.05 is considered statistically significant.

Significance

This study addresses a critical unmet need in supportive oncology care — reducing treatment-limiting toxicity in head and neck cancer patients through a cost-effective, weekend-only G-CSF schedule, potentially improving both patient quality of life and treatment completion rates.

 
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