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Published in: Archives of Gynecology and Obstetrics 5/2018

01-11-2018 | Gynecologic Oncology

Impact of re-excision of residual adjacent vulvar intraepithelial neoplasia (VIN III) and histological tumour-free margin (hTFM) on survival in primary squamous cell carcinoma of vulva

Authors: Khayal Gasimli, Martina Straussner, Iryna Schmeil, Thomas Karn, Ria Winkelmann, Sven Becker, Ahmed El-Balat

Published in: Archives of Gynecology and Obstetrics | Issue 5/2018

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Abstract

Background

hTFM in primary vulvar cancer is an important prognostic factor. Ideally, a diameter of > 8 mm should be achieved after primary surgery. The role of VIN III persistence after primary surgery in vulvar cancer is still unclear. The main objective of the current study was to study the role of residual VIN III re-excision and compare differences in disease-free survival among patients with different hTFM and in primary vulvar cancer.

Methods

Forty-two patients with residual adjacent VIN III after primary surgery for vulvar cancer which were operated between 2000 and 2016 in our clinic were enrolled in this retrospective study. Re-excision rates for residual adjacent VIN III were calculated. According to the histological margin patients were divided into three group: < 3, 3–8 and > 8 mm. Univariate and multivariate analyses were conducted using the Kaplan–Meier method and Cox proportional hazards models, respectively.

Results

The vast majority of patients had pT1b stage (57.1%), grading G2 (71.4%) and lymph node-negative (45.3%) disease at first diagnosis. The re-excision rate was 57.1%. The 5-year disease-free survival (DFS) rates in patients with < 3, 3–8 and > 8 mm hTFM were 50.0, 50.0 and 81.0%, respectively (p = 0.032). The 5-year DFS rates in patients with re-excision and without re-excision for VIN III were 77.3 and 52.9%, respectively (p = 0.060). In univariate analysis was solely hTFM > 8 mm a prognostic factor for DFS (p = 0.017).

Conclusions

hTFM may be a potential prognostic indicator for DFS in vulvar cancer patients. Re-excision for residual adjacent VIN III could not be established as a prognostic factor for DFS after primary surgery in squamous cell cancer of vulva.
Literature
1.
go back to reference Hampl M, Deckers-Figiel S, Hampl JA et al (2008) New aspects of vulvar cancer: changes in localization and age of onset. Gynecol Oncol 109(3):340–345CrossRefPubMed Hampl M, Deckers-Figiel S, Hampl JA et al (2008) New aspects of vulvar cancer: changes in localization and age of onset. Gynecol Oncol 109(3):340–345CrossRefPubMed
2.
go back to reference Al-Ghamdi A, Freedman D, Miller D et al (2002) Vulvar squamous cell carcinoma in young women: a clinicopathologic study of 21 cases. Gynecol Oncol 84(1):94–101CrossRefPubMed Al-Ghamdi A, Freedman D, Miller D et al (2002) Vulvar squamous cell carcinoma in young women: a clinicopathologic study of 21 cases. Gynecol Oncol 84(1):94–101CrossRefPubMed
3.
go back to reference van Seters M, van Beurden M, de Craen AJM (2005) Is the assumed natural history of vulvar intraepithelial neoplasia III based on enough evidence? A systematic review of 3322 published patients. Gynecol Oncol 97(2):645–651CrossRefPubMed van Seters M, van Beurden M, de Craen AJM (2005) Is the assumed natural history of vulvar intraepithelial neoplasia III based on enough evidence? A systematic review of 3322 published patients. Gynecol Oncol 97(2):645–651CrossRefPubMed
4.
go back to reference Reyes MC, Cooper K (2014) An update on vulvar intraepithelial neoplasia: terminology and a practical approach to diagnosis. J Clin Pathol 67(4):290–294CrossRefPubMed Reyes MC, Cooper K (2014) An update on vulvar intraepithelial neoplasia: terminology and a practical approach to diagnosis. J Clin Pathol 67(4):290–294CrossRefPubMed
5.
go back to reference De Vuyst H, Clifford GM, Nascimento MC et al (2009) Prevalence and type distribution of human papillomavirus in carcinoma and intraepithelial neoplasia of the vulva, vagina and anus: a meta-analysis. Int J Cancer 124(7):1626–1636CrossRefPubMed De Vuyst H, Clifford GM, Nascimento MC et al (2009) Prevalence and type distribution of human papillomavirus in carcinoma and intraepithelial neoplasia of the vulva, vagina and anus: a meta-analysis. Int J Cancer 124(7):1626–1636CrossRefPubMed
6.
go back to reference Insinga RP, Liaw K-L, Johnson LG et al (2008) A systematic review of the prevalence and attribution of human papillomavirus types among cervical, vaginal, and vulvar precancers and cancers in the United States. Cancer Epidemiol Biomark Prev Publ Am Assoc Cancer Res Cosponsored Am Soc Prev Oncol 17(7):1611–1622CrossRef Insinga RP, Liaw K-L, Johnson LG et al (2008) A systematic review of the prevalence and attribution of human papillomavirus types among cervical, vaginal, and vulvar precancers and cancers in the United States. Cancer Epidemiol Biomark Prev Publ Am Assoc Cancer Res Cosponsored Am Soc Prev Oncol 17(7):1611–1622CrossRef
7.
go back to reference Helm CW, Hatch K, Austin JM et al (1992) A matched comparison of single and triple incision techniques for the surgical treatment of carcinoma of the vulva. Gynecol Oncol 46(2):150–156CrossRefPubMed Helm CW, Hatch K, Austin JM et al (1992) A matched comparison of single and triple incision techniques for the surgical treatment of carcinoma of the vulva. Gynecol Oncol 46(2):150–156CrossRefPubMed
8.
go back to reference Raimond E, Pelissier A, Etienette Emeriau M et al (2017) Use of negative pressure wound therapy after vulvar carcinoma: case studies. J Wound Care 26(2):72–74CrossRefPubMed Raimond E, Pelissier A, Etienette Emeriau M et al (2017) Use of negative pressure wound therapy after vulvar carcinoma: case studies. J Wound Care 26(2):72–74CrossRefPubMed
9.
go back to reference Likes WM, Stegbauer C, Tillmanns T et al (2007) Correlates of sexual function following vulvar excision. Gynecol Oncol 105(3):600–603CrossRefPubMed Likes WM, Stegbauer C, Tillmanns T et al (2007) Correlates of sexual function following vulvar excision. Gynecol Oncol 105(3):600–603CrossRefPubMed
10.
go back to reference Grimm D, Eulenburg C, Brummer O et al (2016) Sexual activity and function after surgical treatment in patients with (pre)invasive vulvar lesions. Support Care Cancer 24(1):419–428CrossRefPubMed Grimm D, Eulenburg C, Brummer O et al (2016) Sexual activity and function after surgical treatment in patients with (pre)invasive vulvar lesions. Support Care Cancer 24(1):419–428CrossRefPubMed
11.
go back to reference Heaps JM, Fu YS, Montz FJ et al (1990) Surgical-pathologic variables predictive of local recurrence in squamous cell carcinoma of the vulva. Gynecol Oncol 38(3):309–314CrossRefPubMed Heaps JM, Fu YS, Montz FJ et al (1990) Surgical-pathologic variables predictive of local recurrence in squamous cell carcinoma of the vulva. Gynecol Oncol 38(3):309–314CrossRefPubMed
12.
go back to reference Chan JK, Sugiyama V, Pham H et al (2007) Margin distance and other clinico-pathologic prognostic factors in vulvar carcinoma: a multivariate analysis. Gynecol Oncol 104(3):636–641CrossRefPubMed Chan JK, Sugiyama V, Pham H et al (2007) Margin distance and other clinico-pathologic prognostic factors in vulvar carcinoma: a multivariate analysis. Gynecol Oncol 104(3):636–641CrossRefPubMed
13.
go back to reference Woelber L, Griebel L-F, Eulenburg C et al (1990) Role of tumour-free margin distance for loco-regional control in vulvar cancer—a subset analysis of the Arbeitsgemeinschaft Gynäkologische Onkologie CaRE-1 multicenter study. Eur J Cancer Oxf Engl 2016(69):180–188 Woelber L, Griebel L-F, Eulenburg C et al (1990) Role of tumour-free margin distance for loco-regional control in vulvar cancer—a subset analysis of the Arbeitsgemeinschaft Gynäkologische Onkologie CaRE-1 multicenter study. Eur J Cancer Oxf Engl 2016(69):180–188
14.
go back to reference Baiocchi G, Mantoan H, de Brot L et al (2015) How important is the pathological margin distance in vulvar cancer? Eur J Surg Oncol 41(12):1653–1658CrossRefPubMed Baiocchi G, Mantoan H, de Brot L et al (2015) How important is the pathological margin distance in vulvar cancer? Eur J Surg Oncol 41(12):1653–1658CrossRefPubMed
15.
go back to reference Woolderink JM, de Bock GH, de Hullu JA et al (2006) Patterns and frequency of recurrences of squamous cell carcinoma of the vulva. Gynecol Oncol 103(1):293–299CrossRefPubMed Woolderink JM, de Bock GH, de Hullu JA et al (2006) Patterns and frequency of recurrences of squamous cell carcinoma of the vulva. Gynecol Oncol 103(1):293–299CrossRefPubMed
16.
go back to reference Preti M, Ronco G, Ghiringhello B et al (2000) Recurrent squamous cell carcinoma of the vulva: clinicopathologic determinants identifying low risk patients. Cancer 88(8):1869–1876CrossRefPubMed Preti M, Ronco G, Ghiringhello B et al (2000) Recurrent squamous cell carcinoma of the vulva: clinicopathologic determinants identifying low risk patients. Cancer 88(8):1869–1876CrossRefPubMed
17.
go back to reference Sobin L, Gospodarowicz M, Wittekind C (2011) TNM classification of malignant tumours, 7th edn. Wiley-Blackwell, PA Sobin L, Gospodarowicz M, Wittekind C (2011) TNM classification of malignant tumours, 7th edn. Wiley-Blackwell, PA
18.
go back to reference Oonk MHM, Planchamp F, Baldwin P et al (2017) European society of gynaecological oncology guidelines for the management of patients with vulvar cancer. Int J Gynecol Cancer 27(4):832–837CrossRefPubMed Oonk MHM, Planchamp F, Baldwin P et al (2017) European society of gynaecological oncology guidelines for the management of patients with vulvar cancer. Int J Gynecol Cancer 27(4):832–837CrossRefPubMed
19.
go back to reference Woelber L, Kock L, Gieseking F et al (2011) Clinical management of primary vulvar cancer. Eur J Cancer 47(15):2315–2321CrossRefPubMed Woelber L, Kock L, Gieseking F et al (2011) Clinical management of primary vulvar cancer. Eur J Cancer 47(15):2315–2321CrossRefPubMed
20.
go back to reference Nooij LS, van der Slot MA, Dekkers OM et al (1990) Tumour-free margins in vulvar squamous cell carcinoma: does distance really matter? Eur J Cancer Oxf Engl 2016(65):139–149 Nooij LS, van der Slot MA, Dekkers OM et al (1990) Tumour-free margins in vulvar squamous cell carcinoma: does distance really matter? Eur J Cancer Oxf Engl 2016(65):139–149
21.
go back to reference Dittmer C, Fischer D, Diedrich K et al (2012) Diagnosis and treatment options of vulvar cancer: a review. Arch Gynecol Obstet 285(1):183–193CrossRefPubMed Dittmer C, Fischer D, Diedrich K et al (2012) Diagnosis and treatment options of vulvar cancer: a review. Arch Gynecol Obstet 285(1):183–193CrossRefPubMed
22.
go back to reference Del Pino M, Rodriguez-Carunchio L, Ordi J (2013) Pathways of vulvar intraepithelial neoplasia and squamous cell carcinoma. Histopathology 62(1):161–175CrossRefPubMed Del Pino M, Rodriguez-Carunchio L, Ordi J (2013) Pathways of vulvar intraepithelial neoplasia and squamous cell carcinoma. Histopathology 62(1):161–175CrossRefPubMed
23.
go back to reference Sideri M, Jones RW, Wilkinson EJ et al (2005) Squamous vulvar intraepithelial neoplasia: 2004 modified terminology, ISSVD vulvar oncology subcommittee. J Reprod Med 50(11):807–810PubMed Sideri M, Jones RW, Wilkinson EJ et al (2005) Squamous vulvar intraepithelial neoplasia: 2004 modified terminology, ISSVD vulvar oncology subcommittee. J Reprod Med 50(11):807–810PubMed
24.
go back to reference Edwards CL, Tortolero-Luna G, Linares AC et al (1996) Vulvar intraepithelial neoplasia and vulvar cancer. Obstet Gynecol Clin North Am 23(2):295–324PubMed Edwards CL, Tortolero-Luna G, Linares AC et al (1996) Vulvar intraepithelial neoplasia and vulvar cancer. Obstet Gynecol Clin North Am 23(2):295–324PubMed
25.
go back to reference Groenen SMA, Timmers PJ, Burger CW (2010) Recurrence rate in vulvar carcinoma in relation to pathological margin distance. Int J Gynecol Cancer 20(5):869–873CrossRefPubMed Groenen SMA, Timmers PJ, Burger CW (2010) Recurrence rate in vulvar carcinoma in relation to pathological margin distance. Int J Gynecol Cancer 20(5):869–873CrossRefPubMed
26.
go back to reference Modesitt SC, Waters AB, Walton L et al (1998) Vulvar intraepithelial neoplasia III: occult cancer and the impact of margin status on recurrence. Obstet Gynecol 92(6):962–966PubMed Modesitt SC, Waters AB, Walton L et al (1998) Vulvar intraepithelial neoplasia III: occult cancer and the impact of margin status on recurrence. Obstet Gynecol 92(6):962–966PubMed
27.
go back to reference Stehman FB, Bundy BN, Ball H et al (1996) Sites of failure and times to failure in carcinoma of the vulva treated conservatively: a gynecologic oncology group study. Am J Obstet Gynecol 174(4):1128–1132 (discussion 1132–1133) CrossRefPubMed Stehman FB, Bundy BN, Ball H et al (1996) Sites of failure and times to failure in carcinoma of the vulva treated conservatively: a gynecologic oncology group study. Am J Obstet Gynecol 174(4):1128–1132 (discussion 1132–1133) CrossRefPubMed
28.
go back to reference Te Grootenhuis NC, van der Zee AGJ, van Doorn HC et al (2016) 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 140(1):8–14CrossRef Te Grootenhuis NC, van der Zee AGJ, van Doorn HC et al (2016) 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 140(1):8–14CrossRef
Metadata
Title
Impact of re-excision of residual adjacent vulvar intraepithelial neoplasia (VIN III) and histological tumour-free margin (hTFM) on survival in primary squamous cell carcinoma of vulva
Authors
Khayal Gasimli
Martina Straussner
Iryna Schmeil
Thomas Karn
Ria Winkelmann
Sven Becker
Ahmed El-Balat
Publication date
01-11-2018
Publisher
Springer Berlin Heidelberg
Published in
Archives of Gynecology and Obstetrics / Issue 5/2018
Print ISSN: 0932-0067
Electronic ISSN: 1432-0711
DOI
https://doi.org/10.1007/s00404-018-4887-1

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