Trial Evaluating Hypo-fractionated Accelerated Versus Conventional Fractionated Adjuvant RT in Head & Neck Malignancies

Trial statusRecruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age18-80
SponsorAll India Institute of Medical Sciences

About this trial

Hypo-fractionated radiotherapy reduces the OTT (overall treatment time) which may in turn reduce rapid accelerated repopulation of clonogenic cells during waiting period after surgery. If this holds true, there is a potential to achieve better loco-regional control in with PORT for HNSCC. There is a strong radiobiological and economic rationale for delivery hypo-fractionated radiotherapy in HNSCC. The HYPCON III trial will be aimed to reduce the number of fractions by 50% (30 fr to 15 fr)

Eligibility criteria

Qualifiers

Positive lymph node (s)

Perineural invasion

Lympho-vascular invasion

Close margins

Disqualifiers

High risk factors following resection: positive-margin(s)and/or extra nodal extension (ENE)

pT1-2disease and no high-risk features (LVSI, PNI, Close margins,pN0)

Patients receiving Neo-adjuvant or concurrent Chemotherapy

Non-Squamous Histology

Trial design

Treatments tested in this trial

  • Standard conventionally fractionated PORT
  • hypo-fractionated PORT

Treatment groups

369 Participants
are divided into 2 treatment groups

Sponsors and collaborators

All India Institute of Medical Sciences

Lead sponsor

Indian Council of Medical Research

Collaborator