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NCT03210103Active, not recruiting

Primary Radiotherapy Versus Primary Surgery for HPV-Associated Oropharyngeal Cancer

A Randomized Trial of Treatment De-Escalation for HPV-Associated Oropharyngeal Squamous Cell Carcinoma: Radiotherapy vs. Trans-Oral Surgery (ORATOR II)

Source: ClinicalTrials.gov · Last updated 28 Jan 2026

Brief summary (registry, in English)

The goal of this randomized treatment de-escalation study is to formally compare outcomes in HPV related oropharyngeal cancer tumors treated with a primary radiotherapy versus a primary surgical approach, to provide a high level of evidence to guide the selection of treatment options for a subsequent phase III trial

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
61 (actual)
First submitted
28 Jun 2017
Start date
26 Jan 2018
Primary completion date
15 Aug 2028
Lead sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
NCT number
NCT03210103

What you commit to

  • Study type: Interventional
  • Participants enrolled: 61
  • From 26 Jan 2018 to the primary completion date, 15 Aug 2028
  • 9 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Serious medical comorbidities or other contraindications to radiotherapy, chemotherapy or surgery
  • prior history of head and neck cancer within 5 years
  • prior head and neck radiation at any time
  • inability to attend full course of radiotherapy or follow up visits

Other illness

  • metastatic disease
  • prior invasive malignant disease unless disease-free for at least 5 years or more, with the exception of non-melanoma skin cancer

Other

  • unambiguous clinical or radiological evidence of extranodaal extension on pre-treatment imaging. This includes the presence of matted notes, defined as 3 or more nodes that are abutting with loss of intervening fat planes
  • pregnant or lactating women

Who the study is looking for

  • Age 18 years or older
  • willing to provide informed consent
  • ECOG performance status 0-2
  • Histologically confirmed squamous cell carcinoma
  • P16 positive, or HPV positive
  • Primary tumor site in the oropharynx (includes tonsil, soft palate, base of tongue, walls of oropharynx)
  • Eligible for curative intent treatment, with likely negative resection margins at surgery. For patients where adequate transoral access is in question, they will first undergo an examination under anesthesia prior to randomization to ensure adequate exposure can be obtained.
  • Smokers and non-smokers are included. Patients will be stratified by ,\<10 pack years smoking history versus \> or equal to 10 pack years.
  • Tumor stage (AJCC 8th edition): T1 or T2
  • Nodal stage (AJCC 8th edition): N0, N1, or N2
  • For patients who may require chemotherapy (ie, patients with multiple lymph nodes positive or a single node more than 3 cm in size, in any plane, CBC/differential within 4 weeks prior to randomization with adequate bone marrow function, hepatic, and renal function defined as: Hemoglobin ≥ 80 g/L; Absolute neutrophil count ≥ 1.5 x 10 9/L, platelets ≥ 100 x 10 9/L, bilirubin ≤ 35 umol/L, AST or ALT ≤ 3 x the upper limit of normal; serum creatinine ≤ 130 umol/L or creatinine clearance ≥ 50 ml/min
  • patients assessed at head and neck multidisciplinary clinic (with assessment by radiation oncologist and surgeon) and presented at multidisciplinary tumor board prior to randomization

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Royal Adelaide Hospital
Coordinator of this site? Confirm its status
AdelaideAustraliaUnknown status
Gold Coast University Hospital
Coordinator of this site? Confirm its status
Gold CoastAustraliaUnknown status
Tom Baker Cancer Centre
Coordinator of this site? Confirm its status
CalgaryCanadaUnknown status
London Regional Cancer Program
Coordinator of this site? Confirm its status
LondonCanadaUnknown status
Jewish General Hospital
Coordinator of this site? Confirm its status
MontrealCanadaUnknown status
Ottawa Hospital Research Institute
Coordinator of this site? Confirm its status
OttawaCanadaUnknown status
Sunnybrook Research Institute
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
University Health Network
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
BC Cancer
Coordinator of this site? Confirm its status
VancouverCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.