SEntine Lymph Node in earLY Ovarian Cancer (SELLY) (SELLY)
Primary Purpose
Sentinel Lymph Node, Ovarian Cancer Stage I
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Sentinel node detection
Sponsored by
About this trial
This is an interventional diagnostic trial for Sentinel Lymph Node focused on measuring ovarian cancer, laparoscopy, sentinel node, lymphadenectomy
Eligibility Criteria
Inclusion Criteria:
- Epithelial ovarian cancer
- Early stage disease limited to the ovary
Exclusion Criteria:
- Evidence of extraovarian disease
- Allergy to the materials used
Sites / Locations
- Giovannni Scambia
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
SENTINEL NODE
Arm Description
Patients with ovarian cancer will receive sentinel node identification and they will be then submitted to complete pelvic and para-aortic lymphadenectomy (as per the present guidelines)
Outcomes
Primary Outcome Measures
Number of participants with procedure-related adverse events
The number of patients with procedure-related adverse events as assessed by CTCAE v4.0
Detection rate
The rate of patients in whom the sentinel node is detected
Secondary Outcome Measures
Negative predictive value
The negative predictive value of sentinel node in assessing nodal status
Full Information
NCT ID
NCT03563781
First Posted
June 10, 2018
Last Updated
June 20, 2023
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
1. Study Identification
Unique Protocol Identification Number
NCT03563781
Brief Title
SEntine Lymph Node in earLY Ovarian Cancer (SELLY)
Acronym
SELLY
Official Title
SEntine Lymph Node in earLY Ovarian Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
November 11, 2017 (Actual)
Primary Completion Date
July 29, 2022 (Actual)
Study Completion Date
May 5, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The present study aims at investigating the feasibility, the detection rate and the negative predictive value of sentinel node in predicting the presence or absence of lymph node metastasis in ovarian cancer patients
Detailed Description
Patients with early stage ovarian cancer have a good prognosis. However, nearly 15% of the initially diagnosed as early stage ovarian cancers, will be upstaged after an appropriate surgical staging due to lymphatic metastasis, despite of preoperative radiological data. Therefore, complete pelvic and para-aortic lymphadenectomy in these patients represents a crucial procedure. On the other hand, nodal dissection may be associated with threatening intra- and post-operative complications.
If feasible and accurate, the sentinel lymph node procedure could be a modality to avoid unnecessary radical lymphadenectomy without missing important information on nodal status.
With the present study we aim at exploring the role of sentinel node dissection in early ovarian cancer patients.
Patients with ovarian cancer macroscopically limited to the ovary (early ovarian cancer) will receive injection of a tracer (patent blue or indocyanine green) which have already been proven safe and extremely effective in several other gynecologic and non-gynecologic malignancies. Then the retroperitoneal spaces will be opened as for a standard lymphadenectomy procedure and the lymph node marked with the tracer will be identified. After dissection of the sentinel node, lymphadenectomy will be completed according to current guidelines.
Operative data, pathological findings and accuracy of sentinel node in predicting nodal status will be registered.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sentinel Lymph Node, Ovarian Cancer Stage I
Keywords
ovarian cancer, laparoscopy, sentinel node, lymphadenectomy
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All patients with early ovarian cancer will receive sentinel node procedure before full lymphadenectomy, in order to assess the accuracy of sentinel node in diagnosing the presence of nodal metastases.
Masking
None (Open Label)
Allocation
N/A
Enrollment
176 (Actual)
8. Arms, Groups, and Interventions
Arm Title
SENTINEL NODE
Arm Type
Other
Arm Description
Patients with ovarian cancer will receive sentinel node identification and they will be then submitted to complete pelvic and para-aortic lymphadenectomy (as per the present guidelines)
Intervention Type
Procedure
Intervention Name(s)
Sentinel node detection
Intervention Description
Patients will receive injection of tracer in the ovarian ligaments to identify the lymphatic drainage of the affected ovary and ultimately the sentinel node. Afterwards, systematic lymphadenectomy will be accomplished according to current guidelines.
Primary Outcome Measure Information:
Title
Number of participants with procedure-related adverse events
Description
The number of patients with procedure-related adverse events as assessed by CTCAE v4.0
Time Frame
6 months
Title
Detection rate
Description
The rate of patients in whom the sentinel node is detected
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Negative predictive value
Description
The negative predictive value of sentinel node in assessing nodal status
Time Frame
24 months
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
This is a gynecologic study therefore only biologically female patients will be included
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Epithelial ovarian cancer
Early stage disease limited to the ovary
Exclusion Criteria:
Evidence of extraovarian disease
Allergy to the materials used
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Giovanni Scambia, MD
Organizational Affiliation
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Official's Role
Principal Investigator
Facility Information:
Facility Name
Giovannni Scambia
City
Rome
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
The IPD will be shared only with those making official request to the study investigator
IPD Sharing Time Frame
The data will become available One year after publication, and they will be available for 6 months.
IPD Sharing Access Criteria
Direct request to the study PI
Citations:
PubMed Identifier
29224846
Citation
Uccella S, Gisone B, Stevenazzi G, Ghezzi F. Laparoscopic sentinel node detection with ICG for early ovarian cancer: Description of a technique and literature review. Eur J Obstet Gynecol Reprod Biol. 2018 Feb;221:193-194. doi: 10.1016/j.ejogrb.2017.12.004. Epub 2017 Dec 6. No abstract available.
Results Reference
result
PubMed Identifier
29194194
Citation
Sadeghi R. Feasibility of Sentinel Node Mapping in Ovarian Tumors: What Is the Evidence? Int J Gynecol Cancer. 2018 Feb;28(2):421-422. doi: 10.1097/IGC.0000000000001158. No abstract available.
Results Reference
result
PubMed Identifier
28375928
Citation
Nyberg RH, Korkola P, Maenpaa JU. Sentinel Node and Ovarian Tumors: A Series of 20 Patients. Int J Gynecol Cancer. 2017 May;27(4):684-689. doi: 10.1097/IGC.0000000000000948.
Results Reference
result
PubMed Identifier
31601646
Citation
Scambia G, Nero C, Uccella S, Vizza E, Ghezzi F, Cosentino F, Chiantera V, Fagotti A. Sentinel-node biopsy in early stage ovarian cancer: a prospective multicentre study (SELLY). Int J Gynecol Cancer. 2019 Nov;29(9):1437-1439. doi: 10.1136/ijgc-2019-000886. Epub 2019 Oct 9.
Results Reference
derived
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SEntine Lymph Node in earLY Ovarian Cancer (SELLY)
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