Impact of Obstructive SAS on Metastatic Potential of Cutaneous Melanoma (MELA-SAS)
Primary Purpose
Melanoma With a Breslow's Thickness ≥ 1mm, Obstructive Sleep Apnea Syndrome
Status
Withdrawn
Phase
Early Phase 1
Locations
France
Study Type
Interventional
Intervention
nocturnal oximetry
Sponsored by
About this trial
This is an interventional screening trial for Melanoma With a Breslow's Thickness ≥ 1mm
Eligibility Criteria
Inclusion Criteria:
- adults hospitalized in the dermatological unit for the initial consult for a melanoma with a Breslow's Thickness ≥ 1mm
Exclusion Criteria:
- pregnant women
- Institutionalized patient
- patients with metastasis in the lymph node or any organ at the time of the first consult
- patients with another neoplasia requiring treatment other than surgery in the last 5 years
- patients with creatinine above 200µmol/ml or clearance below 30ml/min
Sites / Locations
- Grenoble University Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
screening oxymetry
Arm Description
nocturnal oxymetry to screen for sleep apnea
Outcomes
Primary Outcome Measures
Ratio of metastasis confirmed by thoraco-abdominal-pelvic or cerebral CT in patients subgroups with or without sleep apnea syndrome
sleep apnea is defined witn an Apea Hypopnea Index ≥ 5
Secondary Outcome Measures
Ratio of a positive status of the sentinel lymph node confirmed by histological measurements in patients subgroups with or without sleep apnea syndrome
sleep apnea is defined witn an Apea Hypopnea Index ≥ 5
In the subgroup of patients with sleep apnea syndrome, ratio of patients with metastatic evolution according to the CPAP treatment adherence
adherence of CPAP ≥ 4h by night or 3h by night
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02699918
Brief Title
Impact of Obstructive SAS on Metastatic Potential of Cutaneous Melanoma
Acronym
MELA-SAS
Official Title
Impact of Obstructive Sleep Apnea Syndrome on Metastatic Potential of Cutaneous Melanoma : Prospective Study in Patients With High Risk Melanoma
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Withdrawn
Why Stopped
failure in regulatory statements
Study Start Date
December 1, 2015 (undefined)
Primary Completion Date
April 1, 2016 (Anticipated)
Study Completion Date
October 1, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AGIR à Dom
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Hypothesis: to address if diagnosis of obstructive sleep apnea before or during the extending check-up is a risk factor toward metastasis for melanoma stage ≥ tIIaN0M0 Study design: Adult patients with a Breslow's Thickness ≥ 1mm coming to the surgery consultation will have a nocturnal oximetry for screening of obstructive sleep apnea. Patients having an abnormal nocturnal oximetry will be explored by polysomnography in order to detect sleep apnea syndrome. Patients with sleep apnea will be treated.
Standard dermatologic follow-up over a 3 years period with thoraco-abdominal-pelvic and cerebral CT-scan and a lymph-node ultrasound every 6 months will be performed.
Detailed Description
Melanoma is a cutaneous cancer due to a proliferation of melanocytes. For metastatic cases the prognostic is poor (18% survival at 5 years). Few factors predict metastasis. Sleep Apnea Syndrome is involved in mechanism of carcinogenesis and aggressiveness markers of malignant cutaneous melanoma.
Hypothesis: to address if diagnosis of obstructive sleep apnea before or during the extending check-up is a risk factor toward metastasis for melanoma stage ≥ tIIaN0M0 Study design: Adult patients with a Breslow's Thickness ≥ 1mm coming to the surgery consultation will have a nocturnal oximetry for screening of obstructive sleep apnea. Patients having an abnormal nocturnal oximetry will be explored by polysomnography in order to detect sleep apnea syndrome. Patients with sleep apnea will be treated.
Standard dermatologic follow-up over a 3 years period with thoraco-abdominal-pelvic and cerebral CT-scan and a lymph-node ultrasound every 6 months will be performed.
Sample size: based on previous data from the investigators showing that 25% of patients with a Breslow's Thickness ≥ 1mm will have node or visceral metastasis. For an alpha threshold of 5% and a study power of 80%, with 5% of dropouts, with the hypothesis that 40% of apnea syndrome patients will metastasis versus 20% in the control group the study should include 83 patients in each group.
Statistical analysis: an intermediate analysis after 80 included patients will be performed. Peto method will be followed, results will be considered significant with a p≤0.001 and the study will be stopped.
Normality of data will be checked by Kurtosis and Skewness tests, variance equality will be tested with the Leven test. The significance level will be set at 5%.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Melanoma With a Breslow's Thickness ≥ 1mm, Obstructive Sleep Apnea Syndrome
7. Study Design
Primary Purpose
Screening
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
screening oxymetry
Arm Type
Experimental
Arm Description
nocturnal oxymetry to screen for sleep apnea
Intervention Type
Procedure
Intervention Name(s)
nocturnal oximetry
Intervention Description
nocturnal oximetry for screening of sleep apnea syndrome. Patients with abnormal nocturnal oximetry will be further explored by polysomnography.
Primary Outcome Measure Information:
Title
Ratio of metastasis confirmed by thoraco-abdominal-pelvic or cerebral CT in patients subgroups with or without sleep apnea syndrome
Description
sleep apnea is defined witn an Apea Hypopnea Index ≥ 5
Time Frame
3 years period
Secondary Outcome Measure Information:
Title
Ratio of a positive status of the sentinel lymph node confirmed by histological measurements in patients subgroups with or without sleep apnea syndrome
Description
sleep apnea is defined witn an Apea Hypopnea Index ≥ 5
Time Frame
initial care
Title
In the subgroup of patients with sleep apnea syndrome, ratio of patients with metastatic evolution according to the CPAP treatment adherence
Description
adherence of CPAP ≥ 4h by night or 3h by night
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
adults hospitalized in the dermatological unit for the initial consult for a melanoma with a Breslow's Thickness ≥ 1mm
Exclusion Criteria:
pregnant women
Institutionalized patient
patients with metastasis in the lymph node or any organ at the time of the first consult
patients with another neoplasia requiring treatment other than surgery in the last 5 years
patients with creatinine above 200µmol/ml or clearance below 30ml/min
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Louis Pépin, Pr MD
Organizational Affiliation
University Hospital, Grenoble
Official's Role
Principal Investigator
Facility Information:
Facility Name
Grenoble University Hospital
City
Grenoble
Country
France
12. IPD Sharing Statement
Plan to Share IPD
No
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Impact of Obstructive SAS on Metastatic Potential of Cutaneous Melanoma
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