Dose Escalation Using Hypoxia-adjusted Radiotherapy (DE-HyART)
Head and Neck Squamous Cell Carcinoma
About this trial
This is an interventional treatment trial for Head and Neck Squamous Cell Carcinoma
Eligibility Criteria
Inclusion Criteria: Age: 18 - 70 years Willingness to sign informed consent (written/video documentation) Performance status: ECOG 0 - 2 Histology proved - squamous cell carcinoma Any grade, gender Tumour sites: Oral Cavity, Oropharynx, Hypopharynx and Larynx Sufficient bone marrow reserve within the last 14 days. Hb: > 10g/dl (corrected) TLC: > 4,000 per cumm Platelet: >1.5Lakh per cumm Liver functions and kidney functions within normal limits Nutritional and dental assessment before inclusion into the study Exclusion Criteria: HPV (p16) positive tumours Prior surgery and/or radiation therapy given for any HNC T1/T2 Glottis Metastatic disease or disease not amenable for definitive locoregional treatment. Medical co-morbidity hampering the administration of radiation and/or chemotherapy (cisplatin) Pregnancy or lactation
Sites / Locations
- Rajiv Gandhi Cancer Institute and Research CentreRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
Placebo Comparator
Arm 3 - DE-HyART
Arm 2 - Hypoxic Comparator Arm
Arm 1 - Non-hypoxic arm
The radiation dose will be similar to 'arm 2'. In addition, the HSV identified on baseline FMISO scans will be contoured, and an isotropic margin of 5 mm will be given. This volume will be boosted in phase II to a total dose of 80 Gy. (Addition of 30 Gy in 3 Gy daily fraction added in phase II as a simultaneous integrated boost - SIB).
The prescribed radiotherapy dose will be 70 Gy in 2 Gy per fraction daily. The elective volume will be treated with 50 Gy in 2 Gy per fraction daily till the first 5 weeks. The entire treatment will be delivered in a phased mannered using sequential planning.
The patients will be treated with a standard of care where the treatment will not be controlled, and these patients will act as external control representing clinical practice. However, these patients will be discussed in the head and neck multispeciality clinic and follow the institutional approach. They will be subjected to treatment similar to 'arm 2' but are allowed protocol deviation as per treating radiation oncology discretion.