De-escalation of Radiation Dose in HPV-associated OPC Utilising FMISO PET (DE-RADIATE)

Not Applicable

Not yet recruiting

• Conditions: HPV Positive Oropharyngeal Squamous Cell Carcinoma
• Interventions: Radiation: Standard of care; Radiation: De-escalation

• Registration Number: NCT06307015
• Lead Sponsor: Royal North Shore Hospital

Brief Summary

The goal of this prospective clinical trial is to determine if HPV-associated oropharyngeal squamous cell carcinoma that is non-hypoxic on FMISO PET can be successfully treated with a lower dose of radiation therapy.

The main questions it aims to answer are:

1. What is the pathologic complete response rate in patients selected for radiation dose de-escalation and neck dissection?

2. What is the correlation between MRI and FMISO PET assessment of hypoxia before and during RT?

3. What are the acute and late toxicities in patients selected for radiation dose de-escalation?

4. What are the quality of life scores in patients selected for radiation dose de-escalation?

5. What are the local, regional and distant failure rates of patients selected for radiation dose de-escalation?

Patients with cT1-2N1-2b (AJCC 7th edition) oropharyngeal tumours will undergo surgical resection of the primary tumour. Following this, they will be allocated to standard radiation therapy (70Gy with concurrent cisplatin chemotherapy) or de-escalation radiation therapy (30Gy with concurrent cisplatin chemotherapy) based on the results of FMISO PET. Patients with non-hypoxic tumours at baseline OR after two weeks of radiation therapy will be allocated to the de-escalated group. 3-4 months after completion of radiation therapy, all patients in the de-escalated group will undergo mandatory neck dissection to assess pathologic response.

Researchers will assess the pathologic response rate after surgery in the de-escalation group. They will also compare the outcomes (oncological outcomes and quality of life) between the group receiving the standard treatment (70Gy) and the group receiving de-escalated radiation therapy (30Gy).

Detailed Description

This study is designed to evaluate the role of FMISO PET in selecting patients for de-escalated RT. Patients with cT1-2N-1-2b HPV+ OPC or cTxN1-2 CUP, who are suitable for surgical management of the primary (if applicable) and/or RT to the primary and ipsilateral neck will be included. All patients will undergo surgical resection or core biopsy of the primary site if applicable (negative margins and robotic surgery not mandated) or EUA and tonsillectomy (CUP) and FNA or core biopsy of the cervical lymph node (all patients). Patients will be eligible for inclusion if histopathology is consistent with HPV-associated squamous cell carcinoma or CUP, with p16 positivity (IHC) and HPV positivity (PCR).

Patients enrolled will undergo FMISO PET/CT (after surgery to the primary or EUA/biopsy of suspected primary site) to assess for tumour hypoxia, which will stratify patients into two groups. Determination for the presence or absence of hypoxia will be made on the basis of visual inspection and in accordance with well-established tumour-muscle activity ratio (\>1.2) on the late static 18F-FMISO PET by 1 nuclear medicine physician. FMISO PET will be repeat after 5-10 fractions of RT (1-2 weeks of treatment) with the same assessment for hypoxia.

Absence of pre-treatment hypoxia or intra-treatment resolution of hypoxia on FMISO PET will be deemed as an indicator of radiosensitivity and qualify a patient for de-escalation (i.e., to total dose 30Gy). The remainder of patients (i.e., with evidence of tumour hypoxia at the FMISO PET performed after 5-10 fractions of RT) will continue to standard of care RT to a total dose of 70Gy.

Additional MRI images (including T1, T2 and dynamic contract-enhanced and oxygen enhanced sequences) before and during RT (at the same time as 18F FMISO PET). These will not change the patient's management.

All patients will undergo routine FDG-PET/CT scan three months after RT (as part of standard of care). Patients in the de-escalation arm will undergo mandatory ipsilateral neck dissection within 3-4 months of completing RT to assess for pathologic response. Patients will be followed up for a minimum of five years post treatment.

Study Timeline

• Study First Submitted: 2024-03-01
• Study First Submitted QC: 2024-03-06
• Study First Posted: 2024-03-12
• Status Verified: 2025-04
• Study Start: 2025-04-01
• Last Update Submitted: 2025-04-07
• Last Update Posted: 2025-04-09
• Primary Completion: 2027-12
• Study Completion: 2031-12

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

• Age > 18 years
• Histologically confirmed cT1-2N1-2b oropharyngeal squamous cell carcinoma or cTxN1-2 carcinoma of unknown primary
• p16 positive (70% nuclear and cytoplasmic staining) and HPV positive (genotyping via PCR) tumours of the tonsil, base of tongue, glossotonsillar sulcus, or unknown primary site (suspected mucosal origin).
• No contraindications to radiotherapy, platinum-based chemotherapy or surgery
• No contraindications to PET/CT or MRI
• Eastern Cooperative Oncology Group (ECOG) performance status score 0-2 (KPS > 70%)
• Ability to understand and willingness to sign a written informed consent document

Exclusion Criteria

• Women lactating, pregnant or of childbearing potential who are not willing to avoid pregnancy during the study
• Patients with a history of severe renal disease(s) (eGFR <20) than cannot tolerate gadolinium chelate contrast agents.)
• ECOG ≥ 3
• Previous high dose radiation therapy to the head or neck
• Patients unwilling or unable to have PET/CT or MRI
• Geographically remote patients unable to agree to imaging schedule
• Patients with a history of psychological illness or condition such as to interfere with the patient's ability to understand the requirements of the study.
• Patients with significant cardiac or pulmonary disease including cardiac arrythmias or Chronic Obstructive Pulmonary Disease (COPD) that are unable to tolerate high flow O2 for oxygen contrast.
• Patients taking carbonic anhydrase inhibitors (acetazolamide)
• History of glaucoma
• Any implant, foreign body, 3T MRI incompatible device, or other contraindication to MRI imaging

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Standard of care	Standard of care	Standard of care treatment for patients undergoing definitive chemoradiation for oropharyngeal squamous cell carcinoma
De-escalation	De-escalation	De-escalated radiation therapy for patients undergoing surgery to the primary site followed by chemoradiation to the primary site and neck for oropharyngeal squamous cell carcinoma

Primary Outcome Measures

Name	Time	Method
Pathologic complete response	4 months after completion of radiation therapy	Pathologic complete response in surgical neck dissection

Secondary Outcome Measures

Name	Time	Method
Quality of Life of patients undergoing de-escalation radiation therapy	Baseline, then 3 months post completion of treatment, then 3-monthly post to 2 years, then 6-monthly to 5 years	Quality of Life - Head \& Neck Specific (assessment by EORTC HN-35)
Acute toxicities	From date of commencement of RT, measured weekly during RT, fortnightly post treatment (up to 3 months post treatment)	Acute toxicities of radiation therapy +/- chemotherapy (assessed by CTCAE V 5.0)
Late toxicities	Commencing from 3 months post treatment and measured 3-monthly to 2 years, then 6-monthly to 5 years	Acute toxicities of radiation therapy +/- chemotherapy (assessed by CTCAE V 5.0)
Local control	3-monthly to 2 years, 6-monthly to 5 years	Failure rate at primary site (oropharynx) (calculated from date of commencing RT)
Correlation between MRI and FMISO PET assessment of hypoxia	Baseline and after 2 weeks of radiation therapy	Correlation between MRI and FMISO PET assessment of hypoxia at baseline and during radiation therapy
Regional control	3-monthly to 2 years, 6-monthly to 5 years	Failure rate in neck (calculated from date of commencing RT)
Distant metastases	3-monthly to 2 years, 6-monthly to 5 years	Number of participants with radiologically confirmed distant metastases (calculated from date of commencing RT)

Trial Locations

Locations (1)

Northern Sydney Cancer Centre, Royal North Shore Hospital; 🇦🇺 Saint Leonards, New South Wales, Australia