Sentinel lymph node pathological ultrastaging: Final outcome of the Sentix prospective international study in patients with early-stage cervical cancer

. 2024 Sep ; 188 () : 83-89. [epub] 20240627

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články, multicentrická studie

Perzistentní odkaz   https://www.medvik.cz/link/pmid38941963
Odkazy

PubMed 38941963
DOI 10.1016/j.ygyno.2024.06.015
PII: S0090-8258(24)00330-5
Knihovny.cz E-zdroje

OBJECTIVE: To report the outcome of SLN staging in the SENTIX international prospective trial of SLN biopsy in patients with cervical cancer with an intensive ultrastaging protocol and central quality control and to evaluate how the intensity of pathological assessment correlates with metastatic detection rate in SLNs. METHODS: Eligible were patients with stages T1a1/LVSI+ to T1b2 (<4 cm, ≤2 cm for fertility sparing), common tumor types, no suspicious lymph nodes on imaging, and bilateral SLN detection. SLNs were examined intraoperatively and processed by an intensive protocol for ultrastaging (paraffin blocks sectioned completely in 150-μm intervals/levels). SLNs from each site were submitted for central quality control. RESULTS: In the SENTIX SLN study, 647 out of 733 enrolled patients underwent SLN ultrastaging, identifying 12.5% (81/647) with node positive, N1 cases. Intraoperative detection revealed metastases in 56.8% (46/81) of these cases, categorized into macrometastases (83.7%), micrometastases (26.3%), and isolated tumor cells (9.1%). Ultrastaging identified additional metastatic involvement in 43.2% (35/81) of patients, with detailed sectioning revealing metastases (MAC/MIC) at first level in 20 cases (24.7%), at levels 2-4 in 9 cases (11.1%), and at level ≥5 in 6 cases (7.4%). CONCLUSION: SLN ultrastaging detects additional 43% of N1 (MAC/MIC) in patients with negative LNs by imaging and intraoperative pathological assessment. The detection rate of positive SLN correlates with the intensity (number of levels) of ultrastaging. Examination of four levels from paraffin blocks, which detects >90% of patients with N1, is a reasonable compromise for an international standard for ultrastaging. STUDY REGISTRATION: NCT02494063 (ClinicalTrials.gov).

Center for Gynecologic Oncology Academic Medical Centre Amsterdam Netherlands

Department of Gynaecology and Obstetrics University Hospital Pilsen Charles University Prague Czech Republic

Department of Gynecologic Oncology University Hospital of the Canary Islands Las Palmas de Gran Canaria Spain

Department of Gynecological Oncology Fondazione IRCCS Istituto Nazionale dei Tumori di Milano Italy; Gynecologic Oncology Surgical Division Humanitas San Pio 10 Milan 20159 Italy

Department of Gynecology and Obstetrics Faculty of Medicine Masaryk University Brno Czech Republic

Department of Gynecology and Obstetrics University Hospital Leuven Leuven Cancer Institute Leuven Belgium

Department of Obstetrics and Gynaecology Hospital Ceske Budejovice JSC Ceske Budejovice Czech Republic

Department of Obstetrics and Gynecology Faculty Hospital Trencin Trencin Slovakia

Department of Obstetrics and Gynecology Faculty of Medicine and Dentistry Palacky University University Hospital Olomouc Olomouc Czech Republic

Department of Obstetrics and Gynecology KNTB a s Zlin Czech Republic

Department of Obstetrics and Gynecology La Paz University Hospital Madrid Spain

Department of Obstetrics and Gynecology University Hospital Bulovka 1st Faculty of Medicine Charles University Prague Czech Republic

Department of Obstetrics and Gynecology University Hospital Ostrava Ostrava Poruba Czech Republic

Department of Special Operative and Oncologic Gynaecology Asklepios Clinic Hamburg Hamburg Germany

Gynecologic Oncology Center Department of Gynecology Obstetrics and Neonatology 1st Faculty of Medicine Charles University and General University Hospital Prague Prague Czech Republic

Gynecologic Oncology Surgical Division Humanitas San Pio 10 Milan 20159 Italy; Gynecology Unit IRCCS Fondazione San Gerardo dei Tintori 20900 Monza Italy

Institute of Biostatistics and Analyses Faculty of Medicine Masaryk University Brno Czech Republic

Institute of Pathology 1st Faculty of Medicine Charles University and General University Hospital Prague Czech Republic

Unit of Gynecological Oncology Institute Clinic of Gynecology Obstetrics and Neonatology Hospital Clinic of Barcelona Barcelona Spain

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ClinicalTrials.gov
NCT02494063

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