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Mapping Sentinel Lymph Node in Initial Stages of Ovarian Cancer

Not Applicable
Recruiting
Conditions
Ovarian Cancer
Sentinel Lymph Node
Interventions
Procedure: Sentinel node detection
Registration Number
NCT05184140
Lead Sponsor
Hospital Clinic of Barcelona
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:

1. 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.

2. 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.

3. 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.

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
62
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Adnexal mass with high suspicion of malignancySentinel node detectionAn 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.
Primary Outcome Measures
NameTimeMethod
Detection rate of sentinel node techniqueThrough study completion, an average of 2 years

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
NameTimeMethod
Tracer-related adverse events1 month

The number of patients with tracer-related adverse events

False negative rate and negative predictive value2 years

Evaluate the existence of false negatives in metastatic involvement of the SLN and negative predictive value

Detection rate of gamma-camera, gamma-probe and Infrared fluorescence camera2 years

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 technique2 years

Evaluate the time it takes to perform the SLN technique

Tracer specific detection rate2 years

To know the global and specific SLN identification rate, depending on the type of tracer used.

Anatomical location of the sentinel lymph node2 years

The aortic and pelvic region will be divided 13 regions

Anatomopathological ultrastaging examination of the sentinel lymph node2 years

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®).

Trial Locations

Locations (1)

Núria Agustí Garcia

🇪🇸

Barcelona, Spain

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