Skip to main content
Top
Published in: Annals of Surgical Oncology 5/2017

01-05-2017 | Gynecologic Oncology

Outcome After Sentinel Lymph Node Dissection in Vulvar Cancer: A Subgroup Analysis of the AGO-CaRE-1 Study

Authors: Rüdiger Klapdor, MD, Peter Hillemanns, MD, Linn Wölber, MD, Julia Jückstock, MD, Felix Hilpert, MD, Nikolaus de Gregorio, MD, Severine Iborra, MD, Jalid Sehouli, MD, Anika Habermann, MD, Sophie Teresa Fürst, MD, Hans Georg Strauß, MD, Klaus Baumann, MD, Falk Thiel, MD, Alexander Mustea, MD, Werner Meier, MD, Philipp Harter, MD, Pauline Wimberger, MD, Lars Hanker, MD, Barbara Schmalfeldt, MD, Ulrich Canzler, MD, Tanja Fehm, MD, Alexander Luyten, MD, Martin Hellriegel, MD, Jens Kosse, MD, Christoph Heiss, MD, Peer Hantschmann, MD, Peter Mallmann, MD, Berno Tanner, MD, Jacobus Pfisterer, MD, Barbara Richter, MD, Martin Jäger, MD, Sven Mahner, MD

Published in: Annals of Surgical Oncology | Issue 5/2017

Login to get access

Abstract

Purpose

Analyzing the large patient cohort of the multicenter AGO-CaRE-1 study, we compared isolated sentinel lymph node dissection (SLND) with radical lymph node dissection (LND) of the groin in relation to recurrence rates and survival.

Methods

The AGO-CaRE-1 study retrospectively collected data on treatment patterns and follow-up of vulvar cancer patients [International Federation of Gynecology and Obstetrics (FIGO) stage ≥1B] treated at 29 gynecologic cancer centers between 1998 and 2008. This subgroup analysis evaluated the influence of SLND alone on progression-free survival (PFS) and overall survival (OS).

Results

In 487 (63.1%) of 772 included patients with tumors smaller than 4 cm, an LND was performed and no metastatic lymph nodes were detected (LN0). Another 69/772 (8.9%) women underwent SLND alone, showing a negative SLN (SLN0). Tumors in the LN0 group were larger and showed a deeper invasion (LN0 vs. SLN0 tumor diameter: 20.0 vs. 13.0 mm, p < 0.001; depth of invasion: 4.0 vs. 3.0 mm, p = 0.002). After a median follow-up of 33 months (0–156), no significant differences in relation to isolated groin recurrence rates (SLN0 3.0% vs. LN0 3.4%, p = 0.845) were detected. Similarly, univariate 3-year PFS analysis showed no significant differences between both groups (SLN0 82.7% vs. LN0 77.6%, p = 0.230). A multivariate Cox regression analysis, including tumor diameter, depth of invasion, age, grading, and lymphovascular space invasion was performed: PFS [hazard ratio (HR) 0.970, 95% confidence interval (CI) 0.517–1.821] and OS (HR 0.695, 95% CI 0.261–1.849) did not differ significantly between both cohorts.

Conclusion

This subgroup analysis of the large AGO-CaRE-1 study showed similar results for groin LND and SLND alone with regard to recurrence rates and survival in node-negative patients with tumors <4 cm.
Literature
1.
go back to reference Levenback C, Burke TW, Gershenson DM, Morris M, Malpica A, Ross MI. Intraoperative lymphatic mapping for vulvar cancer. Obstet Gynecol. 1994;84(2):163–7.PubMed Levenback C, Burke TW, Gershenson DM, Morris M, Malpica A, Ross MI. Intraoperative lymphatic mapping for vulvar cancer. Obstet Gynecol. 1994;84(2):163–7.PubMed
2.
go back to reference Gaarenstroom KN, Kenter GG, Trimbos JB, et al. Postoperative complications after vulvectomy and inguinofemoral lymphadenectomy using separate groin incisions. Int J Gynecol Cancer. 2003;13(4):522–7.CrossRefPubMed Gaarenstroom KN, Kenter GG, Trimbos JB, et al. Postoperative complications after vulvectomy and inguinofemoral lymphadenectomy using separate groin incisions. Int J Gynecol Cancer. 2003;13(4):522–7.CrossRefPubMed
3.
go back to reference Van der Zee, Ate GJ, Oonk MH, De Hullu, Joanne A, et al. Sentinel node dissection is safe in the treatment of early-stage vulvar cancer. J Clin Oncol. 2008;26(6):884–89.CrossRefPubMed Van der Zee, Ate GJ, Oonk MH, De Hullu, Joanne A, et al. Sentinel node dissection is safe in the treatment of early-stage vulvar cancer. J Clin Oncol. 2008;26(6):884–89.CrossRefPubMed
4.
go back to reference Wills A, Obermair A. A review of complications associated with the surgical treatment of vulvar cancer. Gynecol Oncol. 2013;131(2):467–79.CrossRefPubMed Wills A, Obermair A. A review of complications associated with the surgical treatment of vulvar cancer. Gynecol Oncol. 2013;131(2):467–79.CrossRefPubMed
5.
go back to reference Burger MP, Hollema H, Emanuels AG, Krans M, Pras E, Bouma J. The importance of the groin node status for the survival of T1 and T2 vulval carcinoma patients. Gynecol Oncol. 1995;57(3):327–34.CrossRefPubMed Burger MP, Hollema H, Emanuels AG, Krans M, Pras E, Bouma J. The importance of the groin node status for the survival of T1 and T2 vulval carcinoma patients. Gynecol Oncol. 1995;57(3):327–34.CrossRefPubMed
6.
go back to reference te Grootenhuis NC, van der Zee A, van Doorn HC, et al. Sentinel nodes in vulvar cancer: long-term follow-up of the GROningen INternational Study on Sentinel nodes in Vulvar cancer (GROINSS-V) I. Gynecol Oncol. 2016;140(1):8–14.CrossRef te Grootenhuis NC, van der Zee A, van Doorn HC, et al. Sentinel nodes in vulvar cancer: long-term follow-up of the GROningen INternational Study on Sentinel nodes in Vulvar cancer (GROINSS-V) I. Gynecol Oncol. 2016;140(1):8–14.CrossRef
7.
go back to reference Levenback CF, Ali S, Coleman RL, et al. Lymphatic mapping and sentinel lymph node biopsy in women with squamous cell carcinoma of the vulva: a gynecologic oncology group study. J Clin Oncol. 2012;30(31):3786–91.CrossRefPubMedPubMedCentral Levenback CF, Ali S, Coleman RL, et al. Lymphatic mapping and sentinel lymph node biopsy in women with squamous cell carcinoma of the vulva: a gynecologic oncology group study. J Clin Oncol. 2012;30(31):3786–91.CrossRefPubMedPubMedCentral
8.
go back to reference de Hullu JA, Hollema H, Piers DA, et al. Sentinel lymph node procedure is highly accurate in squamous cell carcinoma of the vulva. J Clin Oncol. 2000;18(15):2811–6.CrossRefPubMed de Hullu JA, Hollema H, Piers DA, et al. Sentinel lymph node procedure is highly accurate in squamous cell carcinoma of the vulva. J Clin Oncol. 2000;18(15):2811–6.CrossRefPubMed
9.
go back to reference Hampl M, Hantschmann P, Michels W, Hillemanns P. Validation of the accuracy of the sentinel lymph node procedure in patients with vulvar cancer: results of a multicenter study in Germany. Gynecol Oncol. 2008;111(2):282–8.CrossRefPubMed Hampl M, Hantschmann P, Michels W, Hillemanns P. Validation of the accuracy of the sentinel lymph node procedure in patients with vulvar cancer: results of a multicenter study in Germany. Gynecol Oncol. 2008;111(2):282–8.CrossRefPubMed
11.
go back to reference Hassanzade M, Attaran M, Treglia G, Yousefi Z, Sadeghi R. Lymphatic mapping and sentinel node biopsy in squamous cell carcinoma of the vulva: systematic review and meta-analysis of the literature. Gynecol Oncol. 2013;130(1):237–45.CrossRefPubMed Hassanzade M, Attaran M, Treglia G, Yousefi Z, Sadeghi R. Lymphatic mapping and sentinel node biopsy in squamous cell carcinoma of the vulva: systematic review and meta-analysis of the literature. Gynecol Oncol. 2013;130(1):237–45.CrossRefPubMed
12.
go back to reference Mahner S, Jueckstock J, Hilpert F, et al. Adjuvant therapy in lymph node-positive vulvar cancer: the AGO-CaRE-1 Study. J Natl Cancer Inst. 2015;107(3):dju426. Mahner S, Jueckstock J, Hilpert F, et al. Adjuvant therapy in lymph node-positive vulvar cancer: the AGO-CaRE-1 Study. J Natl Cancer Inst. 2015;107(3):dju426.
13.
go back to reference Levenback CF, van der Zee, Ate GJ, Rob L, et al. Sentinel lymph node biopsy in patients with gynecologic cancers. Gynecol Oncol. 2009;114(2):151–6.CrossRefPubMed Levenback CF, van der Zee, Ate GJ, Rob L, et al. Sentinel lymph node biopsy in patients with gynecologic cancers. Gynecol Oncol. 2009;114(2):151–6.CrossRefPubMed
14.
go back to reference Weaver DL, Le UP, Dupuis SL, et al. Metastasis detection in sentinel lymph nodes: comparison of a limited widely spaced (NSABP protocol B-32) and a comprehensive narrowly spaced paraffin block sectioning strategy. Am J Surg Pathol. 2009;33(11):1583–9.CrossRefPubMedPubMedCentral Weaver DL, Le UP, Dupuis SL, et al. Metastasis detection in sentinel lymph nodes: comparison of a limited widely spaced (NSABP protocol B-32) and a comprehensive narrowly spaced paraffin block sectioning strategy. Am J Surg Pathol. 2009;33(11):1583–9.CrossRefPubMedPubMedCentral
15.
go back to reference Robison K, Roque D, McCourt C, et al. Long-term follow-up of vulvar cancer patients evaluated with sentinel lymph node biopsy alone. Gynecol Oncol. 2014;133(3):416–20.CrossRefPubMed Robison K, Roque D, McCourt C, et al. Long-term follow-up of vulvar cancer patients evaluated with sentinel lymph node biopsy alone. Gynecol Oncol. 2014;133(3):416–20.CrossRefPubMed
16.
go back to reference Rodier JF, Janser JC, Routiot T, et al. Sentinel node biopsy in vulvar malignancies: a preliminary feasibility study. Oncol Rep. 1999;6(6):1249–1252.PubMed Rodier JF, Janser JC, Routiot T, et al. Sentinel node biopsy in vulvar malignancies: a preliminary feasibility study. Oncol Rep. 1999;6(6):1249–1252.PubMed
17.
go back to reference Terada KY, Shimizu DM, Jiang CS, Wong JH. Outcomes for patients with T1 squamous cell cancer of the vulva undergoing sentinel node biopsy. Gynecol Oncol. 2006;102(2):200–203.CrossRefPubMed Terada KY, Shimizu DM, Jiang CS, Wong JH. Outcomes for patients with T1 squamous cell cancer of the vulva undergoing sentinel node biopsy. Gynecol Oncol. 2006;102(2):200–203.CrossRefPubMed
18.
go back to reference Moore RG, Robison K, Brown AK, et al. Isolated sentinel lymph node dissection with conservative management in patients with squamous cell carcinoma of the vulva: a prospective trial. Gynecol Oncol. 2008;109(1):65–70.CrossRefPubMed Moore RG, Robison K, Brown AK, et al. Isolated sentinel lymph node dissection with conservative management in patients with squamous cell carcinoma of the vulva: a prospective trial. Gynecol Oncol. 2008;109(1):65–70.CrossRefPubMed
19.
go back to reference Covens A, Vella ET, Kennedy EB, Reade CJ, Jimenez W, Le T. Sentinel lymph node biopsy in vulvar cancer: systematic review, meta-analysis and guideline recommendations. Gynecol Oncol. 2015;137(2):351–61.CrossRefPubMed Covens A, Vella ET, Kennedy EB, Reade CJ, Jimenez W, Le T. Sentinel lymph node biopsy in vulvar cancer: systematic review, meta-analysis and guideline recommendations. Gynecol Oncol. 2015;137(2):351–61.CrossRefPubMed
20.
go back to reference Puig-Tintore LM, Ordi J, Vidal-Sicart S, et al. Further data on the usefulness of sentinel lymph node identification and ultrastaging in vulvar squamous cell carcinoma. Gynecol Oncol. 2003;88(1):29–34.CrossRefPubMed Puig-Tintore LM, Ordi J, Vidal-Sicart S, et al. Further data on the usefulness of sentinel lymph node identification and ultrastaging in vulvar squamous cell carcinoma. Gynecol Oncol. 2003;88(1):29–34.CrossRefPubMed
21.
go back to reference Oonk MH, Hollema H, van der Zee AG. Sentinel node biopsy in vulvar cancer: Implications for staging. Best Pract Res Clin Obstet Gynaecol. 2015;29(6):812–21.CrossRefPubMed Oonk MH, Hollema H, van der Zee AG. Sentinel node biopsy in vulvar cancer: Implications for staging. Best Pract Res Clin Obstet Gynaecol. 2015;29(6):812–21.CrossRefPubMed
22.
go back to reference Oonk MH, van Hemel BM, Hollema H, et al. Size of sentinel-node metastasis and chances of non-sentinel-node involvement and survival in early stage vulvar cancer: results from GROINSS-V, a multicentre observational study. Lancet Oncol. 2010;11(7):646–52.CrossRefPubMed Oonk MH, van Hemel BM, Hollema H, et al. Size of sentinel-node metastasis and chances of non-sentinel-node involvement and survival in early stage vulvar cancer: results from GROINSS-V, a multicentre observational study. Lancet Oncol. 2010;11(7):646–52.CrossRefPubMed
Metadata
Title
Outcome After Sentinel Lymph Node Dissection in Vulvar Cancer: A Subgroup Analysis of the AGO-CaRE-1 Study
Authors
Rüdiger Klapdor, MD
Peter Hillemanns, MD
Linn Wölber, MD
Julia Jückstock, MD
Felix Hilpert, MD
Nikolaus de Gregorio, MD
Severine Iborra, MD
Jalid Sehouli, MD
Anika Habermann, MD
Sophie Teresa Fürst, MD
Hans Georg Strauß, MD
Klaus Baumann, MD
Falk Thiel, MD
Alexander Mustea, MD
Werner Meier, MD
Philipp Harter, MD
Pauline Wimberger, MD
Lars Hanker, MD
Barbara Schmalfeldt, MD
Ulrich Canzler, MD
Tanja Fehm, MD
Alexander Luyten, MD
Martin Hellriegel, MD
Jens Kosse, MD
Christoph Heiss, MD
Peer Hantschmann, MD
Peter Mallmann, MD
Berno Tanner, MD
Jacobus Pfisterer, MD
Barbara Richter, MD
Martin Jäger, MD
Sven Mahner, MD
Publication date
01-05-2017
Publisher
Springer International Publishing
Published in
Annals of Surgical Oncology / Issue 5/2017
Print ISSN: 1068-9265
Electronic ISSN: 1534-4681
DOI
https://doi.org/10.1245/s10434-016-5687-0

Other articles of this Issue 5/2017

Annals of Surgical Oncology 5/2017 Go to the issue