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FDG-PET/CT in Assessing the Tumor and Planning Neck Surgery in Patients With Newly Diagnosed H&N Cancer (ACRIN6685)

Primary Purpose

Head and Neck Cancer

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
therapeutic conventional surgery
fludeoxyglucose F 18
Sponsored by
American College of Radiology Imaging Network
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Head and Neck Cancer focused on measuring stage II squamous cell carcinoma of the larynx, stage II squamous cell carcinoma of the lip and oral cavity, stage II squamous cell carcinoma of the oropharynx, stage III squamous cell carcinoma of the larynx, stage III squamous cell carcinoma of the lip and oral cavity, stage III squamous cell carcinoma of the oropharynx, stage IV squamous cell carcinoma of the larynx, stage IV squamous cell carcinoma of the lip and oral cavity, stage IV squamous cell carcinoma of the oropharynx, stage II verrucous carcinoma of the oral cavity, stage III verrucous carcinoma of the oral cavity, stage IV verrucous carcinoma of the oral cavity, tongue cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

DISEASE CHARACTERISTICS:

  • Histologically confirmed newly diagnosed squamous cell carcinoma (SCC) of the head and neck , including any of the following sites:

    • Oral cavity
    • Oropharynx, including base of tongue and tonsils
    • Larynx
    • Supraglottis
  • Stage T2-T4, N0-N3 disease

    • Unilateral or bilateral neck dissection planned

      • No N2c disease (if bilateral disease is present)
    • Has ≥ 1 clinically N0 neck side as defined by clinical exam (physical exam with CT scan and/or MRI)

      • A N0 neck must be planned to be dissected for the patient to be eligible
      • . The N0 neck can be either ipsilateral to the head and neck tumor or the contralateral N0 neck if a bilateral neck dissection is planned
  • CT scan and/or MRI taken within the past 4 weeks to confirm SCC of the head and neck

    • Simultaneous diagnostic CT with PET scan allowed; however, PET cannot be used as part of the criteria to define the N0 neck disease
    • For CT scan and/or MR images from other institutions, ACRIN recommends a re-read by a local neuro-radiologist to ensure compliance
  • No sinonasal cancer, salivary gland cancer, thyroid cancer, nasopharyngeal cancer, or advanced skin cancer

PATIENT CHARACTERISTICS:

  • Not pregnant or nursing
  • Negative pregnancy test
  • Weight ≤ 350 lbs
  • No poorly controlled diabetes (defined as fasting glucose level > 200 mg/dL) despite attempts to improve glucose control by fasting duration and adjustment of medications (optimally, patients will have glucose < 150 mg/dL)
  • No underlying medical condition that would preclude surgery (neck dissection)

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics

Sites / Locations

  • Arkansas Cancer Research Center at University of Arkansas for Medical Sciences
  • USC/Norris Comprehensive Cancer Center and Hospital
  • Morton Plant Mease Cancer Care at Mease Countryside Hospital
  • H. Lee Moffitt Cancer Center and Research Institute at University of South Florida
  • Jewish Hospital Heart and Lung Institute
  • Mayo Clinic Cancer Center
  • Siteman Cancer Center at Barnes-Jewish Hospital - Saint Louis
  • Wake Forest University Comprehensive Cancer Center
  • Abramson Cancer Center of the University of Pennsylvania
  • Kimmel Cancer Center at Thomas Jefferson University - Philadelphia
  • Fox Chase Cancer Center - Philadelphia
  • Peking Union Medical College Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

FDG PET/CT

Arm Description

Planning for Therapeutic conventional surgery of the N0 neck is documented prior to and immediately after review of the fludeoxyglucose F 18 (FDG)-PET/CT scan completed per protocol.

Outcomes

Primary Outcome Measures

Negative predictive value of PET/CT imaging for staging the N0 neck based upon pathologic sampling of the neck lymph nodes
True negative cases will be determined by histopathology reports. The test will be defined as positive when SUVmax value of ≥ 2.0; and negative otherwise.

Secondary Outcome Measures

Sensitivity and diagnostic yield of PET/CT imaging for detecting occult metastasis in the clinically N0 neck (both by neck and lymph node regions) or other local sites
True positive cases will be determined by histopathology reports. The test will be defined as positive when SUVmax value of ≥ 2.0; and negative otherwise. The diagnostic yield is defined as the ratio of cancers to total screened
Determine which factors (e.g., tumor size, secondary primary tumors, location, or intensity of FDG uptake) may identify patients who can forego neck dissection
True positive cases will be determined by histopathology reports. The test will be defined as positive when SUVmax value of ≥ 2.0; and negative otherwise. The diagnostic yield is defined as the ratio of cancers to total screened
Cost-effectiveness and cost-benefit of using PET/CT imaging for staging of head and neck cancer vs current good clinical practices
The outcome measure will use the total cost of care for each participant to compute the incremental cost-effectiveness ratio (ICER)
Incidence of occult distant body metastasis discovered by whole body PET/CT imaging
this outcome will count the distant body metastasis not previously seen and report the results as a percentage.
Correlation of PET/CT imaging findings with CT/MRI findings and biomarker results
the outcome measure will consist of paired proportions of dichotomized PET/CT and CT/MRI test results; and biomarker test results
Quality of life (QOL), particularly in patients whose management could have been altered by imaging results
QOL will be assessed using SF-36, Non-Utility HUI, and UW-QoL scores
Evaluation of the PET/CT imaging and biomarker data for complementary contributions to metastatic disease prediction
the metastatic disease status is the response variable and PET/CT test results and biomarker data are predictors.
Comparison of baseline PET/CT imaging and biomarker data with 2-year follow up as an adjunct assessment of their prediction of recurrence
model the associations of PET/CT test results and biomarker data (predictors) to recurrence
Comparison of baseline PET/CT imaging and biomarker data with 2-year follow up as an adjunct assessment of their prediction of disease-free survival
model the associations of PET/CT test results and biomarker data (predictors) to disease-free survival
Comparison of baseline PET/CT imaging and biomarker data with 2-year follow up as an adjunct assessment of their prediction of overall survival
model the associations of PET/CT test results and biomarker data (predictors) to overall survival (censored responses)
Proportion of neck dissections that are extended based on local-reader PET/CT imaging findings shared with the surgeon before dissection
Outcome is defined as the number patients who surgeons intend to dissect levels beyond the initial surgery plan
Optimum cutoff value of standardized uptake values for diagnostic accuracy of PET/CT imaging
ROC analysis will be used to maximize the youden index and estimate the optimum cutoff value of SUV for diagnostic accuracy of PET/CT on N0 neck
Impact of PET/CT imaging on the N0 neck across different tumor subsites (defined by anatomic location)
Diagnostic Accuracy measures will be calculated using ROC analysis, subset by anatomic location

Full Information

First Posted
September 23, 2009
Last Updated
October 22, 2020
Sponsor
American College of Radiology Imaging Network
Collaborators
National Cancer Institute (NCI)
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1. Study Identification

Unique Protocol Identification Number
NCT00983697
Brief Title
FDG-PET/CT in Assessing the Tumor and Planning Neck Surgery in Patients With Newly Diagnosed H&N Cancer
Acronym
ACRIN6685
Official Title
A Multicenter Trial of FDG-PET/CT Staging of Head and Neck Cancer and Its Impact on the N0 Neck Surgical Treatment in Head and Neck Cancer Patients
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
April 1, 2010 (Actual)
Primary Completion Date
January 15, 2019 (Actual)
Study Completion Date
December 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
American College of Radiology Imaging Network
Collaborators
National Cancer Institute (NCI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
RATIONALE: Diagnostic procedures, such as fludeoxyglucose F 18-PET/CT scan, may help doctors find head and neck cancer and find out how far the disease has spread. It may also help doctors plan the best treatment. PURPOSE: This phase II trial is studying fludeoxyglucose F 18-PET/CT imaging to see how well it works in assessing the tumor and planning neck surgery in patients with newly diagnosed head and neck cancer.
Detailed Description
OBJECTIVES: Primary Determine the negative predictive value of PET/CT imaging based upon pathologic sampling of the neck lymph nodes in patients with head and neck cancer planning to undergo N0 neck surgery. Determine the potential of PET/CT imaging to change treatment. Secondary Estimate the sensitivity and diagnostic yield of PET/CT imaging for detecting occult metastasis in the clinical N0 neck (both by neck and lymph node regions) or other local sites. Determine the effect of other factors (e.g., tumor size, location, secondary primary tumors, or intensity of FDG uptake) that can lead to identification of subsets of patients that could potentially forego neck dissection or that can provide preliminary data for subsequent studies. Compare the cost-effectiveness of using PET/CT imaging for staging head and neck cancer vs current good clinical practices. Evaluate the incidence of occult distant body metastasis discovered by whole-body PET/CT imaging. Correlate PET/CT imaging findings with CT/MRI findings and biomarker results. Evaluate the quality of life of these patients, particularly of those patients whose management could have been altered by imaging results. Evaluate PET/CT imaging and biomarker data for complementary contributions to metastatic disease prediction. Compare baseline PET/CT imaging and biomarker data with 2-year follow up as an adjunct assessment of their prediction of recurrence, disease-free survival, and overall survival. Determine the proportion of neck dissections that are extended (i.e., additional levels that clinicians intend to dissect beyond the initial surgery plan) based on local-reader PET/CT imaging findings shared with the surgeon before dissection. Estimate the optimum cutoff value of standardized uptake values for diagnostic accuracy of PET/CT imaging. Evaluate the impact of PET/CT imaging on the N0 neck across different tumor subsites (defined by anatomic location). OUTLINE: This is a multicenter study. Patients undergo fludeoxyglucose F 18-PET/CT imaging. Approximately 14 days later, patients undergo unilateral or bilateral neck dissection. Patients complete quality-of-life questionnaires at baseline and at 1, 12, and 24 months after surgery. Patients undergo blood and tissue sample collection periodically for biomarker analysis. Patients are followed up periodically for up to 2 years after surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Head and Neck Cancer
Keywords
stage II squamous cell carcinoma of the larynx, stage II squamous cell carcinoma of the lip and oral cavity, stage II squamous cell carcinoma of the oropharynx, stage III squamous cell carcinoma of the larynx, stage III squamous cell carcinoma of the lip and oral cavity, stage III squamous cell carcinoma of the oropharynx, stage IV squamous cell carcinoma of the larynx, stage IV squamous cell carcinoma of the lip and oral cavity, stage IV squamous cell carcinoma of the oropharynx, stage II verrucous carcinoma of the oral cavity, stage III verrucous carcinoma of the oral cavity, stage IV verrucous carcinoma of the oral cavity, tongue cancer

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
292 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
FDG PET/CT
Arm Type
Experimental
Arm Description
Planning for Therapeutic conventional surgery of the N0 neck is documented prior to and immediately after review of the fludeoxyglucose F 18 (FDG)-PET/CT scan completed per protocol.
Intervention Type
Procedure
Intervention Name(s)
therapeutic conventional surgery
Intervention Type
Radiation
Intervention Name(s)
fludeoxyglucose F 18
Primary Outcome Measure Information:
Title
Negative predictive value of PET/CT imaging for staging the N0 neck based upon pathologic sampling of the neck lymph nodes
Description
True negative cases will be determined by histopathology reports. The test will be defined as positive when SUVmax value of ≥ 2.0; and negative otherwise.
Time Frame
Within Two Weeks Before Surgery and after sampling of neck lymph nodes
Secondary Outcome Measure Information:
Title
Sensitivity and diagnostic yield of PET/CT imaging for detecting occult metastasis in the clinically N0 neck (both by neck and lymph node regions) or other local sites
Description
True positive cases will be determined by histopathology reports. The test will be defined as positive when SUVmax value of ≥ 2.0; and negative otherwise. The diagnostic yield is defined as the ratio of cancers to total screened
Time Frame
Within Two Weeks Before Surgery and after sampling of neck lymph nodes
Title
Determine which factors (e.g., tumor size, secondary primary tumors, location, or intensity of FDG uptake) may identify patients who can forego neck dissection
Description
True positive cases will be determined by histopathology reports. The test will be defined as positive when SUVmax value of ≥ 2.0; and negative otherwise. The diagnostic yield is defined as the ratio of cancers to total screened
Time Frame
Within Two Weeks Before Surgery and after sampling of neck lymph nodes
Title
Cost-effectiveness and cost-benefit of using PET/CT imaging for staging of head and neck cancer vs current good clinical practices
Description
The outcome measure will use the total cost of care for each participant to compute the incremental cost-effectiveness ratio (ICER)
Time Frame
2 years post-surgery
Title
Incidence of occult distant body metastasis discovered by whole body PET/CT imaging
Description
this outcome will count the distant body metastasis not previously seen and report the results as a percentage.
Time Frame
Within Two Weeks Before Surgery
Title
Correlation of PET/CT imaging findings with CT/MRI findings and biomarker results
Description
the outcome measure will consist of paired proportions of dichotomized PET/CT and CT/MRI test results; and biomarker test results
Time Frame
Within Two Weeks Before Surgery
Title
Quality of life (QOL), particularly in patients whose management could have been altered by imaging results
Description
QOL will be assessed using SF-36, Non-Utility HUI, and UW-QoL scores
Time Frame
2 years post-surgery
Title
Evaluation of the PET/CT imaging and biomarker data for complementary contributions to metastatic disease prediction
Description
the metastatic disease status is the response variable and PET/CT test results and biomarker data are predictors.
Time Frame
Within Two Weeks Before Surgery
Title
Comparison of baseline PET/CT imaging and biomarker data with 2-year follow up as an adjunct assessment of their prediction of recurrence
Description
model the associations of PET/CT test results and biomarker data (predictors) to recurrence
Time Frame
2 years post-surgery
Title
Comparison of baseline PET/CT imaging and biomarker data with 2-year follow up as an adjunct assessment of their prediction of disease-free survival
Description
model the associations of PET/CT test results and biomarker data (predictors) to disease-free survival
Time Frame
2 years post-surgery
Title
Comparison of baseline PET/CT imaging and biomarker data with 2-year follow up as an adjunct assessment of their prediction of overall survival
Description
model the associations of PET/CT test results and biomarker data (predictors) to overall survival (censored responses)
Time Frame
2 years post-surgery
Title
Proportion of neck dissections that are extended based on local-reader PET/CT imaging findings shared with the surgeon before dissection
Description
Outcome is defined as the number patients who surgeons intend to dissect levels beyond the initial surgery plan
Time Frame
Within Two Weeks Before Surgery
Title
Optimum cutoff value of standardized uptake values for diagnostic accuracy of PET/CT imaging
Description
ROC analysis will be used to maximize the youden index and estimate the optimum cutoff value of SUV for diagnostic accuracy of PET/CT on N0 neck
Time Frame
Within Two Weeks Before Surgery
Title
Impact of PET/CT imaging on the N0 neck across different tumor subsites (defined by anatomic location)
Description
Diagnostic Accuracy measures will be calculated using ROC analysis, subset by anatomic location
Time Frame
Within Two Weeks Before Surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically confirmed newly diagnosed squamous cell carcinoma (SCC) of the head and neck , including any of the following sites: Oral cavity Oropharynx, including base of tongue and tonsils Larynx Supraglottis Stage T2-T4, N0-N3 disease Unilateral or bilateral neck dissection planned No N2c disease (if bilateral disease is present) Has ≥ 1 clinically N0 neck side as defined by clinical exam (physical exam with CT scan and/or MRI) A N0 neck must be planned to be dissected for the patient to be eligible . The N0 neck can be either ipsilateral to the head and neck tumor or the contralateral N0 neck if a bilateral neck dissection is planned CT scan and/or MRI taken within the past 4 weeks to confirm SCC of the head and neck Simultaneous diagnostic CT with PET scan allowed; however, PET cannot be used as part of the criteria to define the N0 neck disease For CT scan and/or MR images from other institutions, ACRIN recommends a re-read by a local neuro-radiologist to ensure compliance No sinonasal cancer, salivary gland cancer, thyroid cancer, nasopharyngeal cancer, or advanced skin cancer PATIENT CHARACTERISTICS: Not pregnant or nursing Negative pregnancy test Weight ≤ 350 lbs No poorly controlled diabetes (defined as fasting glucose level > 200 mg/dL) despite attempts to improve glucose control by fasting duration and adjustment of medications (optimally, patients will have glucose < 150 mg/dL) No underlying medical condition that would preclude surgery (neck dissection) PRIOR CONCURRENT THERAPY: See Disease Characteristics
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Val J. Lowe, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Study Chair
Facility Information:
Facility Name
Arkansas Cancer Research Center at University of Arkansas for Medical Sciences
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72205
Country
United States
Facility Name
USC/Norris Comprehensive Cancer Center and Hospital
City
Los Angeles
State/Province
California
ZIP/Postal Code
90089-9181
Country
United States
Facility Name
Morton Plant Mease Cancer Care at Mease Countryside Hospital
City
Safety Harbor
State/Province
Florida
ZIP/Postal Code
34695
Country
United States
Facility Name
H. Lee Moffitt Cancer Center and Research Institute at University of South Florida
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612-9497
Country
United States
Facility Name
Jewish Hospital Heart and Lung Institute
City
Louisville
State/Province
Kentucky
ZIP/Postal Code
40245
Country
United States
Facility Name
Mayo Clinic Cancer Center
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States
Facility Name
Siteman Cancer Center at Barnes-Jewish Hospital - Saint Louis
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Facility Name
Wake Forest University Comprehensive Cancer Center
City
Winston-Salem
State/Province
North Carolina
ZIP/Postal Code
27157
Country
United States
Facility Name
Abramson Cancer Center of the University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104-4283
Country
United States
Facility Name
Kimmel Cancer Center at Thomas Jefferson University - Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Facility Name
Fox Chase Cancer Center - Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19111-2497
Country
United States
Facility Name
Peking Union Medical College Hospital
City
Beijing
ZIP/Postal Code
100730
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
See ACRIN data sharing policy: https://www.acrin.org/RESEARCHERS/POLICIES/DATAANDIMAGESHARINGPOLICY.aspx
IPD Sharing Time Frame
by request 6+ mo after publication available through The Cancer Imaging Archive expected 1-year after publication.
IPD Sharing Access Criteria
Safe-Harbor deidentified data
Citations:
PubMed Identifier
30768363
Citation
Lowe VJ, Duan F, Subramaniam RM, Sicks JD, Romanoff J, Bartel T, Yu JQM, Nussenbaum B, Richmon J, Arnold CD, Cognetti D, Stack BC Jr. Multicenter Trial of [18F]fluorodeoxyglucose Positron Emission Tomography/Computed Tomography Staging of Head and Neck Cancer and Negative Predictive Value and Surgical Impact in the N0 Neck: Results From ACRIN 6685. J Clin Oncol. 2019 Jul 10;37(20):1704-1712. doi: 10.1200/JCO.18.01182. Epub 2019 Feb 15.
Results Reference
result
Links:
URL
https://clinicaltrials.gov/ct2/show/NCT00983697
Description
National Cancer Institute's clinical trials database
URL
http://www.acrin.org/6685_protocol.aspx
Description
For additional information about the ACRIN 6685 study, visit ACRIN.ORG.

Learn more about this trial

FDG-PET/CT in Assessing the Tumor and Planning Neck Surgery in Patients With Newly Diagnosed H&N Cancer

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