FIND: Transoral Robotic Surgery and Tailored Radiotherapy in Unknown Primary and Small Squamous Cell Head and Neck Cancer

Sponsor
University Health Network, Toronto (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03281499
Collaborator
(none)
22
1
1
59.5
0.4

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the use of Transoral Robotic Surgery (TORS) to identify small oropharyngeal carcinomas. Findings from this study will be used to better determine which patients may be suitable for more targeted radiotherapy that would lead to a reduction in the total amount of radiotherapy needed as part of their treatment. Reducing the amount of radiotherapy received has been found to reduce the risk of late complications and toxicity to the patient.The pathologic findings will then be used to determine patients who may be candidates for de-intensification of radiotherapy.

Condition or Disease Intervention/Treatment Phase
  • Other: da Vinci Surgical System Model IS4000
N/A

Detailed Description

Patients who present with carcinomas of unknown primary site (CUP) of the head and neck represent a challenging problem for clinicians both from a diagnostic and therapeutic perspective. Traditional techniques for identification of primary tumors involved a Positron Emission Tomography scan (PET)/ computerized tomography scan(CT) followed by examination under anesthesia with biopsies of the nasopharynx, tongue base, piriform sinuses in conjunction with a tonsillectomy may identify as many as 44% of primary tumors, the remaining unidentified tumors are treated with mucosal irradiation to all high risk mucosal sites. The addition of a lingual tonsillectomy with Transoral Robotic Surgery (TORS) may identify almost 70% of primary tumours that have otherwise escaped initial identification at this timepoint,. Historically, for those whose primary would not be discovered at the PET/CT, the discovery would have been made later during follow up visits.

The investigators propose to integrate Transoral Robotic Surgery into the diagnostic evaluation of participants presenting with metastatic squamous cell carcinoma to the neck of unknown primary origin. The investigators will localize small hidden oropharyngeal carcinomas, determine their laterality, and based on the laterality of the tumour, laterality of neck nodes, and completeness of resection, will offer reduced radiotherapy to the primary site and/or to the neck (de-intensification)to the participant. The investigators hypothesize that this approach to unknown primary carcinomas will be both safe and effective.

Study Design

Study Type:
Interventional
Actual Enrollment :
22 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Intervention Model Description:
There will only be a single group of participants in this studyThere will only be a single group of participants in this study
Masking:
None (Open Label)
Masking Description:
No masking will be used in this study for both participants and the study team
Primary Purpose:
Treatment
Official Title:
A Pilot Study Integrating Transoral Robotic Surgery, Histopathologic Localization, and Tailored De-Intensification of Radiotherapy for Unknown Primary and Small Oropharyngeal Head and Neck Squamous Cell Carcinoma(FIND Trial)
Actual Study Start Date :
Aug 15, 2017
Anticipated Primary Completion Date :
Aug 1, 2022
Anticipated Study Completion Date :
Aug 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: da Vinci Surgical System Model IS4000

Transoral robotic surgery, followed by tailored radiotherapy

Other: da Vinci Surgical System Model IS4000
tailored radiotherapy regimen following transoral robotic surgery
Other Names:
  • tailored radiotherapy regimen
  • Outcome Measures

    Primary Outcome Measures

    1. Determination of the rate of out-of-field failures following treatment [2 years]

      The primary outcome for the study is to determine the rate of out-of-field failures following treatment as determined by use of morphologic imaging (contrast enhanced CT or MRI of the head) and confirmed by biopsy.

    Secondary Outcome Measures

    1. Adverse Events (AE) monitoring [2 years]

      To determine the profile of TORS related complications and Surgical Adverse Events within 30 days of surgery using National Cancer Institute Common Terminology Criteria (CTC) for Adverse Events (NCI CTC-AE v 4.0)

    2. Determination of proportions of occult oropharyngeal cancers identified [2 years]

      To determine the proportion of patients with occult oropharyngeal cancers identified

    3. Location of primary tumours identified through enumeration of patients in each identified site group [2 years]

      To determine the location of primary tumours identified through enumeration of patients in each identified site group. The study data will be sorted by location of primary tumour and the proportions for each location calculated

    4. Determination of the proportion of patients with completely resected primary tumours [2 years]

      To determine the location of primary tumours identified, the proportion of patients with primary oropharyngeal carcinomas completely resected (with negative margins), and the proportion of patients amenable to de-intensification treatment (ie, patients who receive no radiotherapy to the primary site and/or unilateral neck radiotherapy).

    5. Determination of the proportion of patients patients amenable to de-intensification treatment [2 years]

      Determination of the proportion of patients patients amenable to de-intensification treatment

    6. Exploration of expert rated swallowing impairment [2 years]

      To explore expert rated swallowing impairment on video fluoroscopic swallow studies (VFSS) using the Modified Barium Swallow Impairment (MBS-Imp)instrument tool 2 years

    7. Exploration of patient reported swallowing related quality of life [2 years]

      To explore patient reported swallowing related quality of life using the MD Anderson Dysphagia Inventory (MDADI)

    8. Exploration of speech and swallowing performance status [2 years]

      To explore observer rated speech and swallowing using the Performance Status Scale for Head and Neck (PSS-HN) instrument

    9. Exploration of patient reported neck impairment [2 years]

      To explore patient reported neck impairment using the Neck Dissection Impairment Index (NDII) instrument

    10. Determination of patterns of failure by location [2 years]

      To determine patterns of failure by location (local, regional, distant) as determined by CT/MRI of the Head and Neck and/or biopsy.

    11. Rates of survival after treatment [2 years]

      To determine rates of survival at 2 years

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age >= 18

    • Metastatic squamous cell carcinoma (T0,N1-3,M0) to at least one regional lymph node of the neck (includes N1-N3) based on fine needle aspiration (FNA) biopsy, core biopsy, excisional biopsy, or neck dissection

    • Ability to understand and willing to sign a written informed consent document

    • Women of child-producing potential must agree to use effective contraceptive methods prior to study entry, during study participation, and for at least 30 days after the last administration of study medication.

    Exclusion Criteria:
    • Evidence of a nasopharyngeal carcinoma by one or more of the following methods: endoscopic examination, imaging, positive nasopharyngeal biopsy or core lymph node biopsy staining for Epstein Barr Encoded RNA (EBER) by In Situ Hybridization.

    • Prior non-cutaneous head and neck squamous cell carcinoma

    • Prior head and neck radiotherapy

    • History of neck dissection - contralateral to the side of the nodal disease

    • Presence of lymphadenopathy on CT unlikely to originate from a primary oropharyngeal carcinoma (i.e., parotid, isolated low (level IV/low level V)

    • Radiologically abnormal/enlarged retropharyngeal adenopathy.

    • Poor performance status (ECOG status 3 - 5)

    • Severe comorbidity or uncontrolled inter-current illness (i.e., unstable angina or heart failure in last 6 months, myocardial infarction in last 6 months, chronic obstructive pulmonary disease with exacerbations necessitating hospitalization or emergency room visit in the past 3 months, history of pneumonia in the past 3 months, use of home oxygen, uncorrectable coagulopathy)

    • Not a surgical candidate

    • Pregnancy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Princess Margaret Cancer Centre Toronto Ontario Canada

    Sponsors and Collaborators

    • University Health Network, Toronto

    Investigators

    • Principal Investigator: John de Almeida, MD, University Health Network, Toronto

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    University Health Network, Toronto
    ClinicalTrials.gov Identifier:
    NCT03281499
    Other Study ID Numbers:
    • FIND Trial
    First Posted:
    Sep 13, 2017
    Last Update Posted:
    Apr 19, 2021
    Last Verified:
    Apr 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 19, 2021