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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05184140
Other study ID # HCB/2021/0130
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2021
Est. completion date May 1, 2023

Study information

Verified date March 2023
Source Hospital Clinic of Barcelona
Contact Núria Agustí, MD
Phone +34 932 27 54 00
Email nagusti@clinic.cat
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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 information / eligibility

Status Recruiting
Enrollment 62
Est. completion date May 1, 2023
Est. primary completion date April 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility 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


Intervention

Procedure:
Sentinel node detection
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.

Locations

Country Name City State
Spain Núria Agustí Garcia Barcelona

Sponsors (9)

Lead Sponsor Collaborator
Hospital Clinic of Barcelona Ariel Glickman, Aureli Torné, Berta Diaz-Feijoo, Francisco Campos, Pere Fusté, Pilar Paredes, Sergi Vidal-Sicart, Tiermes Marina

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Other Evaluation of sentinel lymph node technique To check the ovarian lymphatic drainage in patients with suspected malignant adnexal masses Through study completion, an average of 2 years
Primary 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 Through study completion, an average of 2 years
Secondary Tracer specific detection rate To know the global and specific SLN identification rate, depending on the type of tracer used. 2 years
Secondary Tracer-related adverse events The number of patients with tracer-related adverse events 1 month
Secondary False negative rate and negative predictive value Evaluate the existence of false negatives in metastatic involvement of the SLN and negative predictive value 2 years
Secondary Anatomical location of the sentinel lymph node The aortic and pelvic region will be divided 13 regions 2 years
Secondary 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. 2 years
Secondary Surgical time extension performing SLN technique Evaluate the time it takes to perform the SLN technique 2 years
Secondary 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®). 2 years
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