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Mapping Sentinel Lymph Node in Initial Stages of Ovarian Cancer (MELISA)

Primary Purpose

Ovarian Cancer, Sentinel Lymph Node

Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Sentinel node detection
Sponsored by
Hospital Clinic of Barcelona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Ovarian Cancer focused on measuring Ovarian Cancer, Sentinel Lymph Node

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients with a diagnosis of adnexal mass with high suspicion of malignancy and frozen section examination will undergo the lymphatic map with a radiotracer.
  • Patients with intraoperative diagnosis of epithelial ovarian cancer will undergo the SLN exeresis with two tracers.
  • Patients with a delayed diagnosis of epithelial ovarian cancer who are candidates to undergo a re-staging surgery will undergo the SLN exeresis with two tracers.

Exclusion Criteria:

  • Advanced ovarian cancer (FIGO III/IV)
  • Patients <18 years
  • Pregnancy or lactation
  • Previous vascular surgery (cava, aorta, iliac vessels), lymphadenectomy (pelvic or paraortic) or radiotherapy (pelvic or paraortic field)
  • Severe adherent syndrome that prevents tracer injection
  • The SLN technique will not be performed in case of benign ovarian tumor in the frozen section or borderline tumor (since in these cases there is no clinical indication of performing a lymphadenectomy)
  • Non-operable patient
  • Previous adverse events to the radiotracer or ICG

Sites / Locations

  • Núria Agustí GarciaRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Adnexal mass with high suspicion of malignancy

Arm Description

An ovarian lymphatic map will be performed in patients with adnexal masses suspected of malignancy. Sentinel node exeresis and a complete staging surgery (including pelvic and para-aortic lymphadenectomy) will be performed in patients with ovarian cancer confirmation including restaging surgeries.

Outcomes

Primary Outcome Measures

Detection rate of sentinel node technique
Detection of SLN in initial epithelial ovarian cancer by assessing the concordance of the result between the lymph node metastases and the lymphadenectomy

Secondary Outcome Measures

Tracer specific detection rate
To know the global and specific SLN identification rate, depending on the type of tracer used.
Tracer-related adverse events
The number of patients with tracer-related adverse events
False negative rate and negative predictive value
Evaluate the existence of false negatives in metastatic involvement of the SLN and negative predictive value
Anatomical location of the sentinel lymph node
The aortic and pelvic region will be divided 13 regions
Detection rate of gamma-camera, gamma-probe and Infrared fluorescence camera
Evaluate the performance of intraoperative lymphoscintigraphy with gamma-camera, gamma-probe and Infrared fluorescence camera in the visualization of the ovarian lymphatic map.
Surgical time extension performing SLN technique
Evaluate the time it takes to perform the SLN technique
Anatomopathological ultrastaging examination of the sentinel lymph node
Evaluate if ultrastaging of the SLN improves the detection of micrometastases compared to conventional histology. Ultrastaging protocol will be performed, consisting of two consecutive histological sections (4 μm thick) obtained at regular intervals of 150 μm, performing 4 levels of each paraffin block. The first section will be stained with H&E and the second section will be stained immunohistochemically with an AE1-AE3 anti-keratin antibody (Dako®).

Full Information

First Posted
December 4, 2021
Last Updated
March 4, 2023
Sponsor
Hospital Clinic of Barcelona
Collaborators
Berta Diaz-Feijoo, Aureli Torné, Pilar Paredes, Sergi Vidal-Sicart, Ariel Glickman, Pere Fusté, Tiermes Marina, Francisco Campos
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1. Study Identification

Unique Protocol Identification Number
NCT05184140
Brief Title
Mapping Sentinel Lymph Node in Initial Stages of Ovarian Cancer
Acronym
MELISA
Official Title
MELISA Trial: Mapping sEntinel Lymph Node in Initial StAges of Ovarian Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2021 (Actual)
Primary Completion Date
April 1, 2023 (Anticipated)
Study Completion Date
May 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Clinic of Barcelona
Collaborators
Berta Diaz-Feijoo, Aureli Torné, Pilar Paredes, Sergi Vidal-Sicart, Ariel Glickman, Pere Fusté, Tiermes Marina, Francisco Campos

4. Oversight

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
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Epithelial ovarian cancer (EOC) diagnosed in the initial stage (stage I-II) require complete staging surgery to histologically assess the possible existence of peritoneal or lymph node disease. Systematic pelvic and paraaortic lymphadenectomy in stage I-II EOC is essential since confirming the presence of lymph node metastases means re-staging the disease as stage III. This change of stage has important prognostic and therapeutic implications. However, the lymph node involvement rate is around 10-30% (average of 15%). Systematic pelvic and para-aortic lymphadenectomy carries a risk of intraoperative complications, as well as longer operative time, postoperative complications and longer hospital stay. Moreover, by now there is no evidence suggesting a possible therapeutic value. The sentinel lymph node (SLN) detects the first level of lymph node drainage. The absence of metastases in the SLN predicts the absence of tumor infiltration of the rest of lymph nodes of the same anatomical region and allows to safely avoid lymphadenectomy and its associated morbidity. In addition, the exhaustive evaluation of the SLN by ultrastaging and immunohistochemical study allows to increase the detection of microscopic disease. Sentinel lymph node (SLN) biopsy, implemented in clinical practice in other gynecological tumors (breast, vulva, cervix or endometrium), has been studied very little in the initial ovarian epithelial cancer. Unlike other gynecological tumors, there are multiple anatomical and technical aspects that largely explain this lack of information. The double ovarian vascularization that accompanies lymphatic drainage explains this higher complexity. Therefore, at the present time, the detection of SLN in the initial EOC remains an experimental area without applicability in clinical practice. There are multiple doubts and issues to be resolved regarding the different tracers, the site and time injection and the actual accuracy of the SLN versus the lymphadenectomy.
Detailed Description
The objective of this study is to know the lymphatic drainage and, if the lesion is malignant, remove the sentinel lymph nodes to know if it can predict the involvement of the remaining lymph nodes to assess the possible applicability of SLN in clinical practice. Study design: Evaluation of the ovarian lymphatic map: injection of radiotracer (99mTc-nanocolloid albumin) in patients with a diagnosis of adnexal mass with high suspicion of malignancy. Intraoperative lymphogammagraphy will be performed using a portable gammacamera. Patients with a delayed diagnosis of ovarian cancer who are candidates to undergo a re-staging surgery will be included. After the adnexectomy a frozen section will be performed to confirm the diagnosis of malignancy and then the ICG (Indocyanine green) tracer will be injected. Since the spread and persistence of the ICG in the lymph nodes is rapid, this tracer will be injected only after confirmation of EOC. Simultaneous screening with a gammadetector probe and NIR (near-infrared spectrum) camera will be used to proceed to the detection of SLN according to the lymphatic map previously. Ultrastaging of the SLN by applying hematoxylin and eosin staining (H&E) and, in the absence of metastatic disease, evaluation by immunohistochemistry with cytokeratin AE1: AE3.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ovarian Cancer, Sentinel Lymph Node
Keywords
Ovarian Cancer, Sentinel Lymph Node

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Controlled, prospective, descriptive
Masking
None (Open Label)
Allocation
N/A
Enrollment
62 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Adnexal mass with high suspicion of malignancy
Arm Type
Experimental
Arm Description
An ovarian lymphatic map will be performed in patients with adnexal masses suspected of malignancy. Sentinel node exeresis and a complete staging surgery (including pelvic and para-aortic lymphadenectomy) will be performed in patients with ovarian cancer confirmation including restaging surgeries.
Intervention Type
Procedure
Intervention Name(s)
Sentinel node detection
Other Intervention Name(s)
Complete staging surgery
Intervention Description
Injection of the radiotracer to infundibulo-pelvic and utero-ovarian ligament in patients with high suspicion of malignancy adnexal mass. Injection of green indocyanine r to infundibulo-pelvic and utero-ovarian stumps only in case of malignancy after the adnexectomy. Sentinel node exeresis and a complete staging surgery (including pelvic and para-aortic lymphadenectomy) will be performed in patients with ovarian cancer diagnosis.
Primary Outcome Measure Information:
Title
Detection rate of sentinel node technique
Description
Detection of SLN in initial epithelial ovarian cancer by assessing the concordance of the result between the lymph node metastases and the lymphadenectomy
Time Frame
Through study completion, an average of 2 years
Secondary Outcome Measure Information:
Title
Tracer specific detection rate
Description
To know the global and specific SLN identification rate, depending on the type of tracer used.
Time Frame
2 years
Title
Tracer-related adverse events
Description
The number of patients with tracer-related adverse events
Time Frame
1 month
Title
False negative rate and negative predictive value
Description
Evaluate the existence of false negatives in metastatic involvement of the SLN and negative predictive value
Time Frame
2 years
Title
Anatomical location of the sentinel lymph node
Description
The aortic and pelvic region will be divided 13 regions
Time Frame
2 years
Title
Detection rate of gamma-camera, gamma-probe and Infrared fluorescence camera
Description
Evaluate the performance of intraoperative lymphoscintigraphy with gamma-camera, gamma-probe and Infrared fluorescence camera in the visualization of the ovarian lymphatic map.
Time Frame
2 years
Title
Surgical time extension performing SLN technique
Description
Evaluate the time it takes to perform the SLN technique
Time Frame
2 years
Title
Anatomopathological ultrastaging examination of the sentinel lymph node
Description
Evaluate if ultrastaging of the SLN improves the detection of micrometastases compared to conventional histology. Ultrastaging protocol will be performed, consisting of two consecutive histological sections (4 μm thick) obtained at regular intervals of 150 μm, performing 4 levels of each paraffin block. The first section will be stained with H&E and the second section will be stained immunohistochemically with an AE1-AE3 anti-keratin antibody (Dako®).
Time Frame
2 years
Other Pre-specified Outcome Measures:
Title
Evaluation of sentinel lymph node technique
Description
To check the ovarian lymphatic drainage in patients with suspected malignant adnexal masses
Time Frame
Through study completion, an average of 2 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients with a diagnosis of adnexal mass with high suspicion of malignancy and frozen section examination will undergo the lymphatic map with a radiotracer. Patients with intraoperative diagnosis of epithelial ovarian cancer will undergo the SLN exeresis with two tracers. Patients with a delayed diagnosis of epithelial ovarian cancer who are candidates to undergo a re-staging surgery will undergo the SLN exeresis with two tracers. Exclusion Criteria: Advanced ovarian cancer (FIGO III/IV) Patients <18 years Pregnancy or lactation Previous vascular surgery (cava, aorta, iliac vessels), lymphadenectomy (pelvic or paraortic) or radiotherapy (pelvic or paraortic field) Severe adherent syndrome that prevents tracer injection The SLN technique will not be performed in case of benign ovarian tumor in the frozen section or borderline tumor (since in these cases there is no clinical indication of performing a lymphadenectomy) Non-operable patient Previous adverse events to the radiotracer or ICG
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Núria Agustí, MD
Phone
+34 932 27 54 00
Ext
5334
Email
nagusti@clinic.cat
First Name & Middle Initial & Last Name or Official Title & Degree
Pilar Paredes, PhD
Email
pparedes@clinic.cat
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aureli Torné, PhD
Organizational Affiliation
Hospital Clinic of Barcelona
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Berta Díaz-Feijóo, PhD
Organizational Affiliation
Hospital Clinic of Barcelona
Official's Role
Study Director
Facility Information:
Facility Name
Núria Agustí Garcia
City
Barcelona
ZIP/Postal Code
08014
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Núria Agustí Garcia, MD
Phone
+34627654987
Email
nagusti@clinic.cat

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
Links:
URL
https://ijgc.bmj.com/content/ijgc/31/Suppl_3/A278.3.full.pdf
Description
834 Study of the lymphatic map and detection of the sentinel lymph node in ovaric masses with suspected malignancy
URL
http://dx.doi.org/10.1136/ijgc-2022-003420
Description
Sentinel lymph node mapping in early-stage ovarian cancer: surgical technique in 10 steps

Learn more about this trial

Mapping Sentinel Lymph Node in Initial Stages of Ovarian Cancer

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