| 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
|
|
|
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
|
|
|
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. |