Proton Spatially Fractionated Radiotherapy or Photon Stereotactic Body Radiotherapy in Combination With Pembrolizumab Before Surgery for the Treatment of Locally Advanced and Radiation-Naive Locoregionally Recurrent Oral Cavity Cancer, OSPRI Trial

Phase 2Not Yet RecruitingNCT07783581

Mayo Clinic30 enrolled

Overview

This phase II trial compares the effect of adding proton spatially fractionated radiotherapy (SFRT) or photon stereotactic body radiotherapy (SBRT) to standard immunotherapy pembrolizumab before surgery (neoadjuvant) in treating patients with oral cavity squamous cell cancer that has spread to nearby tissue or lymph nodes (locally advanced) or that has come back where it first started (primary site) or near it (locoregionally recurrent) and have not had (naive) prior radiation. Radiation therapy uses high energy x-rays, particles, or radioactive seeds to kill tumor cells and shrink tumors. Proton SFRT is a type of external beam radiation treatment that uses streams of protons (tiny particles with a positive charge) to deliver different doses of radiation to different parts of the tumor in a grid like pattern. This type of radiation kills tumor cells but does not damage nearby tissues. SBRT is a type of external radiation therapy that uses special equipment to position a patient and precisely deliver radiation to tumors in the body (except the brain). The total dose of radiation is divided into smaller doses given over several days. This type of radiation therapy helps spare normal tissue. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the tumor, and may interfere with the ability of tumor cells to grow and spread. Giving neoadjuvant proton SFRT or SBRT in combination with pembrolizumab may be safe and tolerable and may be an effective approach to shrink the tumor, reduce the extent of surgery and/or the need for further treatment in patients with locally advanced or locoregionally recurrent oral cavity squamous cell cancer.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Interventions

Biopsy ProcedurePROCEDURE

Undergo tissue biopsy

Biospecimen CollectionPROCEDURE

Undergo blood sample collection

Computed TomographyPROCEDURE

Undergo CT or PET/CT

Magnetic Resonance ImagingPROCEDURE

Undergo PET/MRI

PembrolizumabBIOLOGICAL

Given IV

Photon Stereotactic Body Radiation TherapyRADIATION

Receive photon SBRT

Positron Emission TomographyPROCEDURE

Undergo PET/CT or PET/MRI

Spatially-fractionated Radiation TherapyRADIATION

Receive proton SFRT

Surgical ProcedurePROCEDURE

Undergo surgical resection

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patients with histologically confirmed human papillomavirus (HPV)/p16-unrelated squamous cell carcinoma of the oral cavity and: * Either locally advanced (T3-T4) non-metastatic disease, or * Radiation-naïve locoregionally recurrent disease (prior radiation to a site outside of the treatment fields is permitted) * Age ≥ 18 years old * Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≤ 2 * Eligible to receive immunotherapy on multidisciplinary evaluation * Ability to complete questionnaire(s) by themselves or with assistance * Provide signed written informed consent in accordance with ethical, regulatory, and institutional requirements * Willing to return to enrolling institution for follow-up (during the active monitoring phase of the study) * Willing to consent to and provide tissue and blood samples for correlative research purposes (not the optional Riskguard and OncoExtra testing) * PD-L1 combined positive score ≥ 1 Exclusion Criteria: * Participation in another clinical study with an investigational product during the last 3 months (12 weeks) * Exception: Unless it is an observational (non-interventional) clinical study during the follow-up period of the study * Contraindications to pembrolizumab * Prior radiation therapy to the head and neck * Previous anticancer therapeutic received ≤ 30 days prior to registration, or adequate washout period on a per-agent basis, or concurrent anti-cancer therapeutic not specified by this protocol * Uncontrolled pre-existing condition(s), such as infection, congestive heart failure, hypertension, angina, arrhythmia, chronic diarrhea, psychiatric conditions, or others, that in the opinion of the treating investigator limits the ability to provide consent or longitudinal participation in this study * Inability to place 2 or more SFRT spheres within the tumor target * Prophylactic placement of feeding tubes is not allowed

Outcomes

Primary Outcomes

Improvement in major pathologic response rate (MPR)

MPR is defined from pathologic evaluation of the surgically resected tumor, demonstrating less than 10% of residual tumor in the resection sample (≥90% disease reduction). Will be assessed using a Bayesian pick-the-winner randomized phase-II clinical trial design.

Time frame: At the time of surgical resection

Secondary Outcomes

Pathologic complete response rate

Pathologic complete response rate is defined from pathologic evaluation of the surgically resected tumor, demonstrating no signs of residual disease following immuno-radiation. This will be calculated separately for Arm A and for Arm B.

Time frame: At the time of surgical resection

Percent of patients receiving the prescribed therapy

Will be defined as the number of patients who received the prescribed therapy divided by the number of evaluable patients who signed a consent form and began treatment. This will be calculated separately for Arm A and Arm B.

Time frame: Up to 1 year

Incidence of Adverse Events (AEs) Prior to Surgery:

Overall AEs, overall toxicities, and by maximum grade per type of AE per patient of the AEs that occur before surgery will be explored and summarized descriptively, mainly through the use of frequency tables. Toxicity is defined as an adverse event that is classified as possibly, probably, or definitely related to study treatment. AEs are graded per National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 6.0.

Time frame: From the time of registration until surgery