Role of Pelvic Lymph Node Resection in Vulvar Squamous Cell Cancer: A Subset Analysis of the AGO-CaRE-1 Study.


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
Oct 2021
Historique:
received: 06 11 2020
accepted: 04 02 2021
pubmed: 17 3 2021
medline: 28 9 2021
entrez: 16 3 2021
Statut: ppublish

Résumé

As the population at risk for pelvic nodal involvement remains poorly described, the role of pelvic lymphadenectomy (LAE) in vulvar squamous cell cancer (VSCC) has been a matter of discussion for decades. In the AGO-CaRE-1 study, 1618 patients with International Federation of Gynecology and Obstetrics (FIGO) stage IB or higher primary VSCC treated at 29 centers in Germany between 1998 and 2008 were documented. In this analysis, only patients with pelvic LAE (n = 70) were analyzed with regard to prognosis and correlation between inguinal and pelvic lymph node involvement. The majority of patients had T1b/T2 tumors (n = 47; 67.1%), with a median diameter of 40 mm (2-240 mm); 54/70 patients (77.1%) who received pelvic LAE had positive groin nodes. For 42 of these 54 patients, the number of affected groin nodes had been documented as a median of 3; 14/42 (33.3%) of these patients had histologically confirmed pelvic nodal metastases (median number of affected pelvic nodes 3 [1-12]). In these 14 patients, the median number of affected groin nodes was 7 (1-30), with a groin metastases median maximum diameter of 42.5 mm (12-50). Receiver operating characteristic analysis showed an area under the curve of 0.85, with 83.3% sensitivity and 92.6% specificity for the prediction of pelvic involvement in cases of six or more positive groin nodes. No cases of pelvic nodal involvement without groin metastases were observed. Prognosis in cases of pelvic metastasis was poor, with a median progression-free survival of only 12.5 months. For the majority of node-positive patients with VSCC, pelvic nodal staging appears unnecessary since a relevant risk for pelvic nodal involvement only seems to be present in highly node-positive disease.

Sections du résumé

BACKGROUND BACKGROUND
As the population at risk for pelvic nodal involvement remains poorly described, the role of pelvic lymphadenectomy (LAE) in vulvar squamous cell cancer (VSCC) has been a matter of discussion for decades.
METHODS METHODS
In the AGO-CaRE-1 study, 1618 patients with International Federation of Gynecology and Obstetrics (FIGO) stage IB or higher primary VSCC treated at 29 centers in Germany between 1998 and 2008 were documented. In this analysis, only patients with pelvic LAE (n = 70) were analyzed with regard to prognosis and correlation between inguinal and pelvic lymph node involvement.
RESULTS RESULTS
The majority of patients had T1b/T2 tumors (n = 47; 67.1%), with a median diameter of 40 mm (2-240 mm); 54/70 patients (77.1%) who received pelvic LAE had positive groin nodes. For 42 of these 54 patients, the number of affected groin nodes had been documented as a median of 3; 14/42 (33.3%) of these patients had histologically confirmed pelvic nodal metastases (median number of affected pelvic nodes 3 [1-12]). In these 14 patients, the median number of affected groin nodes was 7 (1-30), with a groin metastases median maximum diameter of 42.5 mm (12-50). Receiver operating characteristic analysis showed an area under the curve of 0.85, with 83.3% sensitivity and 92.6% specificity for the prediction of pelvic involvement in cases of six or more positive groin nodes. No cases of pelvic nodal involvement without groin metastases were observed. Prognosis in cases of pelvic metastasis was poor, with a median progression-free survival of only 12.5 months.
CONCLUSION CONCLUSIONS
For the majority of node-positive patients with VSCC, pelvic nodal staging appears unnecessary since a relevant risk for pelvic nodal involvement only seems to be present in highly node-positive disease.

Identifiants

pubmed: 33723714
doi: 10.1245/s10434-021-09744-y
pii: 10.1245/s10434-021-09744-y
pmc: PMC8460538
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

6696-6704

Informations de copyright

© 2021. The Author(s).

Références

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Auteurs

Linn Woelber (L)

Department of Gynecology and Gynecologic Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. lwoelber@uke.de.

Mareike Bommert (M)

Department of Gynecology and Gynecologic Oncology, Evang. Kliniken Essen-Mitte, Essen, Germany.

Philipp Harter (P)

Department of Gynecology and Gynecologic Oncology, Evang. Kliniken Essen-Mitte, Essen, Germany.

Katharina Prieske (K)

Department of Gynecology and Gynecologic Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Mildred Scheel Cancer Career Center HaTriCS4, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Christine Zu Eulenburg (C)

Department of Epidemiology, UMCG, Universität Groningen, Groningen, The Netherlands.

Julia Jueckstock (J)

Department of Obstetrics and Gynecology, University Hospital, LMU - University of Munich, Munich, Germany.

Felix Hilpert (F)

Oncologic Medical Center at the Jerusalem Hospital Hamburg, Hamburg, Germany.

Nikolaus de Gregorio (N)

Department of Obstetrics and Gynecology, University of Ulm Medical Center, Ulm, Germany.

Severine Iborra (S)

Department of Gynecology and Gynecologic Oncology, University Hospital Aachen, RWTH Aachen, Aachen, Germany.

Jalid Sehouli (J)

Department of Gynecology, Charité University Medicine Berlin, Campus Virchow, Berlin, Germany.

Atanas Ignatov (A)

Department of Obstetrics and Gynecology, University Hospital Magdeburg, Magdeburg, Germany.

Peter Hillemanns (P)

Department of Obstetrics and Gynecology, Hannover Medical School, Hannover, Germany.

Sophie Fuerst (S)

Department of Obstetrics and Gynecology, University Hospital, LMU - University of Munich, Munich, Germany.

Hans-Georg Strauss (HG)

Department of Gynecology, University Hospital Halle, Halle, Germany.

Klaus Baumann (K)

Department of Gynecology, Medical Center Ludwigshafen, Ludwigshafen, Germany.

Matthias Beckmann (M)

Department of Gynecology and Obstetrics, University Hospital Erlangen, Comprehensive Cancer Center Erlangen-EMN, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany.

Alexander Mustea (A)

Department of Gynecology and Gynecologic Oncology, University Medical Center Bonn, Bonn, Germany.

Werner Meier (W)

Department of Obstetrics and Gynecology, Evangelical Hospital Duesseldorf, Duesseldorf, Germany.

Sven Mahner (S)

Department of Obstetrics and Gynecology, University Hospital, LMU - University of Munich, Munich, Germany.

Anna Jaeger (A)

Department of Gynecology and Gynecologic Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

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