Highlights
- •Analysis of the margin relevance in a uniform node-negative vulvar cancer cohort.
- •15.9% (46/289) patients developed recurrence, thereof 34 (11.8%) at the vulva.
- •Vulvar recurrence rates: 12.6% with a margin <8 mm and 10.2% with a margin ≥8 mm.
- •This study fails to confirm the need for a pathological margin distance ≥8 mm.
Abstract
Aim of the study
A tumour-free pathological resection margin of ≥8 mm is considered state-of-the-art.
Available evidence is based on heterogeneous cohorts. This study was designed to clarify
the relevance of the resection margin for loco-regional control in vulvar cancer.
Methods
AGO-CaRE-1 is a large retrospective study. Patients (n = 1618) with vulvar cancer ≥ FIGO stage IB treated at 29 German gynecologic-cancer-centres
1998–2008 were included. This subgroup analysis focuses on solely surgically treated
node-negative patients with complete tumour resection (n = 289).
Results
Of the 289 analysed patients, 141 (48.8%) had pT1b, 140 (48.4%) pT2 and 8 (2.8%) pT3
tumours. One hundred twenty-five (43.3%) underwent complete vulvectomy, 127 (43.9%)
partial vulvectomy and 37 (12.8%) radical local excision. The median minimal resection
margin was 5 mm (1 mm–33 mm); all patients received groin staging, in 86.5% with full
dissection. Median follow-up was 35.1 months. 46 (15.9%) patients developed recurrence,
thereof 34 (11.8%) at the vulva, after a median of 18.3 months. Vulvar recurrence
rates were 12.6% in patients with a margin <8 mm and 10.2% in patients with a margin
≥8 mm. When analysed as a continuous variable, the margin distance had no statistically
significant impact on local recurrence (HR per mm increase: 0.930, 95% CI: 0.849–1.020;
p = 0.125). Multivariate analyses did also not reveal a significant association between
the margin and local recurrence neither when analysed as continuous variable nor categorically
based on the 8 mm cutoff. Results were consistent when looking at disease-free-survival
and time-to-recurrence at any site (HR per mm increase: 0.949, 95% CI: 0.864–1.041;
p = 0.267).
Conclusions
The need for a minimal margin of 8 mm could not be confirmed in the large and homogeneous
node-negative cohort of the AGO-CaRE database.
Keywords
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to European Journal of CancerAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
- Cancer of the vulva.Int J Gynaecol Obstet. 2015; 131: S76-S83
- Trends in the incidence of invasive and in situ vulvar carcinoma.Obstet Gynecol. 2006; 107: 1018-1022
- Sentinel node dissection is safe in the treatment of early-stage vulvar cancer.J Clin Oncol. 2008; 26: 884-889
- Clinical management of primary vulvar cancer.Eur J Cancer. 2011; 47: 2315-2321
- Margin distance and other clinico-pathologic prognostic factors in vulvar carcinoma: a multivariate analysis.Gynecol Oncol. 2007; 104: 636-641
- Vulvar carcinoma. The price of less radical surgery.Cancer. 2002; 95: 2331-2338
- Management of vulvar cancers.Eur J Surg Oncol. 2006; 32: 825-831
- Individualization of treatment for stage I squamous cell vulvar carcinoma.Obstet Gynecol. 1984; 63: 155-162
- Surgical-pathologic variables predictive of local recurrence in squamous cell carcinoma of the vulva.Gynecol Oncol. 1990; 38: 309-314
- Recurrence rate in vulvar carcinoma in relation to pathological margin distance.Int J Gynecol Cancer. 2010; 20: 869-873
- Prognostic value of pathological resection margin distance in squamous cell cancer of the vulva.Ann Surg Oncol. 2011 Dec; 18: 3811-3818
- How important is the pathological margin distance in vulvar cancer?.Eur J Surg Oncol. 2015; 41: 1653-1658
- The importance of the groin node status for the survival of T1 and T2 vulval carcinoma patients.Gynecol Oncol. 1995; 57: 327-334
- Prognostic role of lymph node metastases in vulvar cancer and implications for adjuvant treatment.Int J Gynecol Cancer. 2012; 22: 503-508
- Correlates of sexual function following vulvar excision.Gynecol Oncol. 2007; 105: 600-603
- Sexual dysfunction following vulvectomy.Gynecol Oncol. 2000; 77: 73-77
- Sexual activity and function after surgical treatment in patients with (pre)invasive vulvar lesions.Support Care Cancer. 2015; 24: 419-428
- New aspects of vulvar cancer: changes in localization and age of onset.Gynecol Oncol. 2008; 109: 340-345
- AJCC cancer staging manual.6th ed. 2002
- Adjuvant therapy in lymph node-positive vulvar cancer: the AGO-CaRE-1 study.J Natl Cancer Inst. 2015; 107
- Outcome and patterns of recurrence for International Federation of Gynecology and Obstetrics (FIGO) stages I and II squamous cell vulvar cancer.Obstet Gynecol. 2009; 113: 895-901
- Understanding and preventing local tumour recurrence.Lancet Oncol. 2009; 10: 645-646
- Vulvar field resection: novel approach to the surgical treatment of vulvar cancer based on ontogenetic anatomy.Gynecol Oncol. 2010; 119: 106-113
- Surgical therapy of T1 and T2 vulvar carcinoma: further experience with radical wide excision and selective inguinal lymphadenectomy.Gynecol Oncol. 1995; 57: 215-220
- Human papillomavirus, lichen sclerosus, and squamous cell carcinoma of the vulva: detection and prognostic significance.Gynecol Oncol. 1994; 52: 180-184
- Carcinoma of the vulva: epidemiology and pathogenesis.Obstet Gynecol. 1992; 79: 448-454
- Differentiated vulvar intraepithelial neoplasia is often found in lesions, previously diagnosed as lichen sclerosus, which have progressed to vulvar squamous cell carcinoma.Mod Pathol. 2011; 24: 297-305
- The etiologic role of HPV in vulvar squamous cell carcinoma fine tuned.Cancer Epidemiol Biomarkers Prev. 2009; 18: 2061-2067
- Recurrent squamous cell carcinoma of the vulva: clinicopathologic determinants identifying low risk patients.Cancer. 2000; 88: 1869-1876
- Patterns of recurrence in patients with squamous cell carcinoma of the vulva. A multicenter CTF study.Cancer. 2000; 89: 116-122
- Sites of failure and times to failure in carcinoma of the vulva treated conservatively: a Gynecologic Oncology Group study.Am J Obstet Gynecol. 1996; 174 ([discussion 1132–3]): 1128-1132
- 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: 8-14
Article info
Publication history
Published online: November 09, 2016
Accepted:
September 26,
2016
Received in revised form:
September 8,
2016
Received:
July 16,
2016
Footnotes
☆This study was presented in part at ASCO Annual Meeting 2014.
Identification
Copyright
© 2016 Elsevier Ltd. All rights reserved.