Lymphoscintigraphy Directed Elective Neck Radiation for p16+ Favorable Risk Oropharynx Cancer

Description

This is a prospective, phase II, stratified single arm investigation for favorable prognosis in p16+ oropharynx cancer patients with either node negative or malignant neck adenopathy with lymphoscintigraphy mapping confined to the ipsilateral neck.

Conditions

Oropharynx Cancer

Study Overview

Study Details

Study overview

This is a prospective, phase II, stratified single arm investigation for favorable prognosis in p16+ oropharynx cancer patients with either node negative or malignant neck adenopathy with lymphoscintigraphy mapping confined to the ipsilateral neck.

A Phase II Investigation of Lymphoscintigraphy Directed Elective Neck Radiation for p16+ Favorable Risk Oropharynx Cancer Patients Managed With Primary (Chemo) Radiation

Lymphoscintigraphy Directed Elective Neck Radiation for p16+ Favorable Risk Oropharynx Cancer

Condition
Oropharynx Cancer
Intervention / Treatment

-

Contacts and Locations

Philadelphia

Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States, 19111

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Pathologically confirmed squamous cell carcinoma of the oropharynx
  • * Patients to be treated with bilateral neck radiation per current guidelines must have either present (see below):
  • * Nodal status (based on staging manual, AJCC (American Joint Committee on Cancer) 8th ed.): N0 (provided the tumor is within 1cm of midline) N1\> 1 lymph nodes (on the same side of the neck as the primary cancer) or cN3 (cranial nerve III) with no contralateral neck adenopathy
  • * Tumor stage T1-2 that approaches within 1 cm but does not cross midline as appreciated radiographically and/or by the treating radiation oncologist or a head and neck surgeon
  • * CT with contrast and/or MRI with contrast performed within 56 days prior to registration that does not demonstrate bilateral neck adenopathy. In the setting of medical contraindication to both CT and MRI contrast please contact the study PI
  • * PET/CT performed with 28 days prior to registration that does not demonstrate bilateral neck adenopathy.
  • * Immunohistochemical staining for p16 that demonstrates moderate to severe staining in at least 70% of cells.
  • * Patients must provide their smoking history prior to registration. Number of pack-years = \[Frequency of smoking (number of cigarettes per day) x duration of cigarette smoking (years)\]/20
  • * Patients must have clinically and/or radiographically evident disease that can be accurately measured in accordance with RECIST criteria v. 1.1.
  • * Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-1 within 56 days prior to registration
  • * Age ≥ 18 years.
  • * Adequate hematologic function within 14 days prior to registration
  • * Adequate renal function within 14 days prior to registration
  • * Adequate hepatic function within 14 days prior to registration
  • * Tumors that cross midline, regardless of T stage
  • * N2 adenopathy (bilateral neck adenopathy)
  • * Gross total excision of the primary site in a diagnostic procedure prior to either imaging and/or physical examination by registering physician.
  • * p16-negative squamous cell carcinoma
  • * Definitive clinical or radiologic evidence of metastatic disease or adenopathy below the clavicles
  • * Prior systemic therapy for the study cancer
  • * Prior head and neck cancer surgery that involved the neck (includes excisional biopsy)
  • * Prior radiation therapy to the head and neck that would result in overlap of treated fields
  • * History of allergic reaction attributed to Technetium-99m-tilmanocept used in lymphoscintigraphy
  • * Uncontrolled intercurrent illness including, but not limited to, any other malignancy, other ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
  • * Pregnant or breast feeding

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Fox Chase Cancer Center,

Thomas Galloway, MD, PRINCIPAL_INVESTIGATOR, Fox Chase Cancer Center

Study Record Dates

2026-09-23