RecruitingPhase 2NCT05894083

A Phase II Study for p16+ Oropharyngeal Cancer PerSonalized De-escalation Treatment at University of MIchigan (CuSToMIze)


Sponsor

University of Michigan Rogel Cancer Center

Enrollment

150 participants

Start Date

Apr 27, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

Single center, non-randomized Phase II study enrolling Stage I-II p16+ oropharyngeal cancer patients to one of two de-escalation treatment paradigms: (1) receive surgery followed by observation or risk-adjusted adjuvant radiation (+/-chemo), or (2) individualized adaptive definitive chemoradiation (CRT).


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This Phase 2 study tests whether patients with HPV-related oropharyngeal cancer (tonsil or base of tongue cancer) can receive a less intensive, personalized treatment plan based on how their tumor responds early on, without sacrificing survival. **You may be eligible if...** - You have confirmed squamous cell carcinoma of the oropharynx or an unknown primary that is HPV-positive or p16-positive - Your cancer is early to intermediate stage (Stage I or II by AJCC 8th edition) - Your tumor shows high activity on a PET scan (SUV ≥ 4.0) **You may NOT be eligible if...** - Your cancer is HPV-negative or p16-negative - Your cancer is stage III or higher - Your PET scan activity is below the required threshold Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURESurgery

Cohort A will undergo initial surgical resection of the primary and neck dissection with pathologic features directing predetermined adjuvant treatment. Pathology of the primary and nodal specimens will then be reviewed as to determine the next intervention per protocol. Based on operative findings including degree of nodal involvement, extracapsular spread, perineural invasion, and lymphovascular involvement, patients will be designated to adjuvant treatment arms consisting of observation, adjuvant radiation, or adjuvant chemoradiation.

COMBINATION_PRODUCTChemoradiation

Patients will receive an initial plan with a single prescription of 30 Gy in 15 fractions to PTV\_High and PTV\_Low with RT given once daily, 5 days a week (Monday through Friday). After analysis of mid-treatment PET/CT, the remaining radiation treatment will be delivered as a conedown to the gross disease only. Patients will be planned to receive a total dose of 70 Gy, 54 Gy, or 44 Gy to PTV\_High in 2 Gy per fraction.

OTHERObservation

Cohort A will undergo initial surgical resection of the primary and neck dissection with pathologic features directing predetermined adjuvant treatment. Pathology of the primary and nodal specimens will then be reviewed as to determine the next intervention per protocol. Based on operative findings including degree of nodal involvement, extracapsular spread, perineural invasion, and lymphovascular involvement, patients will be designated to adjuvant treatment arms consisting of observation, adjuvant radiation, or adjuvant chemoradiation.

RADIATIONPost-operative radiation

Patients will receive adjuvant radiation based on pathologic features.Total radiation treatment doses and prescriptions will include 36 Gy in 18 fractions, 50 Gy in 25 fractions and 60 Gy in 30 fractions.


Locations(1)

University of Michigan Rogel Cancer Center

Ann Arbor, Michigan, United States

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NCT05894083


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