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RecruitingNCT07060261Updated Sep 22, 2026

Pre-Op MRI on Margin Status for Transoral Robotic Surgery for HPV+ Tonsillar Squamous Cell Carcinoma

An interventional study of Transoral robotic surgery+MRI in Human Papilloma Virus Related Carcinoma and Tonsillar Squamous Cell Carcinoma, sponsored by Case Comprehensive Cancer Center. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-22.

Sponsored by Case Comprehensive Cancer Center · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

This prospective research study aims to see if pre-operative MRI can predict the margin status after transoral robotic surgery (TORS) for human papillomavirus positive (HPV+) tonsillar squamous cell carcinoma (SCC). The pre-operative MRI will have a standard MR neck without and with contrast, with added axial T2 weighted sequence and T2 SPACE sequence through the tonsils. Three neuroradiologists will grade the thickness of the pharyngeal constrictor muscle (the muscle that surrounds the tonsils) on a five-point scale. The study will determine if the pre-operative MRI grading will correlate with positive, insecure (\<1mm), or secure (>1mm) margin during TORS surgery for your HPV+ tonsillar SCC.

Read the detailed description

There has been a marked increase in the incidence on oropharyngeal SCC in recent decades because of the rise of HPV+ disease1-3. Stage I or II tonsillar SCC can be treated by either surgery or radiation with similar good outcomes. For tumors treated surgically, transoral robotic surgery has replaced open surgery due to decreased morbidity and improved local control. It has been shown that margin status of 1.1mm of healthy tissue around the tumor is sufficient for adequate local control. However, approximately 8.1% of the time there is a positive or insecure margin, resulting in added adjuvant radiation and possibly chemotherapy, with increasing morbidity for each added treatment modality.

Therefore, there is a need to determine pre-operatively the chance of positive or insecure margin at surgery to avoid increased morbidity with added adjuvant treatment. Currently, the most commonly used imaging modality is computed tomography (CT) or magnetic resonance imaging (MRI), but this is to rule out absolute contraindications such as internal carotid artery encasement, involvement of the mandibular periosteum, prevertebral fascia/musculature, or masticator space musculature. Recently, a retrospective study used a novel five-point grading scale (1, normal constrictor; 2, bulging constrictor; 3, thinning constrictor; 4, obscured constrictor; and 5, tumor protrusion into the parapharyngeal fat) to evaluate the pharyngeal constrictor muscle, showing that higher scores with obscured constrictor or tumor protrusion into the parapharyngeal fat resulted in increased risk of positive or insecure margin. Given this, there is need for a prospective study to estimate the accuracy of the five-point MRI score with respect to distinguishing patients who go onto have secure surgical margins versus patients who go on to have insecure/positive surgical margins including surgical report of violation of anatomic boundaries (pharyngeal constrictor muscle)

02

Conditions studied

  • Human Papilloma Virus Related Carcinoma
  • Tonsillar Squamous Cell Carcinoma

Keywords

  • Transoral robotic surgery (TORS)
  • MRI
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Adults ≥ 18 years of age.
  2. Participants being considered for TORS for HPV+ tonsillar SCC.

Exclusion criteria

Exclusion Criteria:

  1. Participants \< 18 years of age.
  2. Participants who cannot provide informed consent.
  3. Participants who do not wish to participate.
  4. Vulnerable populations, including but not limited to cognitively impaired persons, pregnant women, and students or house staff under the direct supervision of the investigator.
  5. Participants in whom MRI is contraindicated.
04

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Pre-operative MRI

    Procedure: Transoral robotic surgery+MRI

Interventions

  • ProcedureTransoral robotic surgery+MRI

    During the standard of care MRI, there will be an added T2 and T2 SPACE sequences. These sequences are estimated to take an additional 6 minutes, with no added risk to the patient.

05

What researchers measure

Primary outcomes

  1. Accuracy as assessed by 5-point MRI score

    Accuracy will be summarized using the area under the receiver operating characteristics curve (AUC)

    Time frame: Perioperative

Secondary outcomes

  1. Number of Grade 5 cases missed by pre-operative CT versus pre-operative MRI

    Time frame: Perioperative

  2. Percentage of patients who received adjuvant treatment, stratified by MRI grade.

    Time frame: Perioperative

  3. Percentage of participants who received adjuvant therapy, stratified by MRI grade.

    Time frame: Perioperative

  4. Predictive value of tumor size and diffusion/perfusion MRI parameters for post-operative surgical margin status

    Time frame: Perioperative

06

Study locations

1 of 1 sites recruiting
  • Case Comprehensive Cancer Center, Cleveland Clinic Foundation
    Cleveland, Ohio 44195, United States
    • Lee Jonathan, MD · Contact
    Recruiting
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07060261
Lead sponsor
Case Comprehensive Cancer Center
Responsible party
Sponsor
First posted
Jul 11, 2025
Start date
Nov 26, 2025
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Sep 22, 2026

Study contacts

Jonathan Lee, MD
Contact
LEEJ13@ccf.org
216-445-9390

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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