Background: A significant proportion of patients with poor prognosis squamous cell cancer of the oropharynx relapse loco-regionally despite radical (chemo)radiotherapy. If a predictive biomarker for disease control can be identified during treatment then individualised and adaptive treatment strategies may be employed. The aim of this study is to assess the feasibility of adaptive and dose-escalated RT to the gross tumour volume without increasing surrounding planning target volume doses and maintaining clinically acceptable organs at risk doses.Materials and methods: Twenty representative patients with poor prognosis locally advanced OPSCC who were known to have relapsed post RT, were re-planned retrospectively using Eclipse TPS v15.5, RapidPlanTM and multi-criteria optimisation. In our centre, areas of gross disease (PTV65) are treated with 65Gy in 30# while areas at risk of containing microscopic disease (PTV54) are treated synchronously to 54Gy in 30#. The original clinical plans were re-optimised to act as controls (Group I). These plans were split into two plans of 15# each, with the latter 15# used to escalate the dose to the GTV to 73Gy (Group II) and 82Gy (Group III). Plan sums were created for the total 30# to record plan evaluation parameters along with assessments of plan deliverability.Results: For all groups, the dose coverage at D98% and D50% for the PTVs were comparable. As expected, the D2% dose levels for PTV65 increased. All dose levels associated with PTV54 remained largely unaffected by the dose escalation regimens. Conformity indices for PTV65 and PTVAll reveal comparable conformity across all three groups. Despite the GTV being escalated by 12.3% and 26.2% in groups II and III, the volume of GTV receiving > 84 Gy was considerably less than 1.75 cc. While OAR doses increased for the escalated groups, these increases were not clinically significant. Conclusion: This planning feasibility study exploring RapidPlanTM combined with multi-criteria optimisation has demonstrated that doses to the GTV may be escalated without increasing PTV or OAR doses considerably, suggesting an interventional clinical trial using this approach would be feasible. Given loco-regional control remains an unmet need, response-adaptive dose-escalated RT has the potential to improve outcomes for poor-prognosis patients.