Elsevier

Gynecologic Oncology

Volume 130, Issue 1, July 2013, Pages 237-245
Gynecologic Oncology

Review
Lymphatic mapping and sentinel node biopsy in squamous cell carcinoma of the vulva: Systematic review and meta-analysis of the literature

https://doi.org/10.1016/j.ygyno.2013.04.023Get rights and content

Highlights

  • We performed a meta-analysis on the accuracy of sentinel node mapping in vulvar SCC.

  • Pooled groin basis sentinel node detection rate was 84.6% [80.5–88] and pooled groin basis sensitivity was 92% [89–94].

  • SN detection rate and sensitivity were related to mapping method, tumor location, and presence of palpable inguinal nodes.

Abstract

Objectives

We reviewed the available literature on the accuracy of sentinel node (SN) mapping in the inguinal lymph node staging of vulvar squamous cell carcinoma (SCC).

Methods

Medline and SCOPUS were searched by using “sentinel AND vulv*” as key words. Studies evaluating the accuracy of SN mapping in the inguinal lymph node staging of vulvar SCC were included if enough data could be extracted for calculation of detection rate and/or sensitivity. Only studies validated by inguinal lymph node dissection were included for sensitivity meta-analysis.

Results

Forty-nine studies were included in the systematic review. Pooled patient and groin basis SN detection rates were 94.4% [92.4–95.9] and 84.6% [80.5–88], respectively. Pooled patient and groin basis sensitivity were 92% [90–95] and 92% [89–94], respectively (or 8% [5–10] and 8% [6–11] false negative rates). Pooled negative predictive values were 97% [96–98] and 98% [97–99] for patient and groin basis analyses respectively. SN detection rate and sensitivity were related to mapping method (blue dye, radiotracer, or both) and location of the tumor (midline vs. lateral tumors). Patients with palpable inguinal nodes had lower detection rate and sensitivity.

Conclusion

SN mapping is an accurate method for inguinal node staging in vulvar SCC. Combining radiotracer and blue dye methods and excluding patients with palpable inguinal nodes result in the highest detection rate and sensitivity. For midline tumors possible false negative results of SN mapping should be taken into account.

Introduction

Vulvar cancer is a rare gynecological malignancy with an incidence of < 4000 cases/year in the United States [1]. The standard treatment for early stage vulvar cancer is surgical excision of the tumor and inguinal lymphadenectomy which can be unilateral or bilateral depending on the tumor location [2]. However, inguinal lymph node dissection is associated with considerable morbidity and can affect the quality of life of vulvar cancer patients [3]. It is also estimated that only a third of early stage vulvar cancer patients have regional lymph node metastases and the remainder of the patients would not benefit from inguinal lymph node dissection [4].

Sentinel node (SN) mapping is an approach to regional lymph node staging of solid tumors which can decrease the morbidity of lymph node dissection. This technique is currently in use in breast cancer, melanoma, and urological and gynecological malignancies [5], [6], [7]. Vulvar cancer is a suitable malignancy for the SN concept and since 1994 several groups have reported the accuracy of SN mapping for inguinal lymph node staging in this cancer [8]. The interest in SN mapping in vulvar cancer has increased considerably since the publication of GROINSS-V results [9], [10].

In the current study, we reviewed the available literature on SN mapping in vulvar cancer and presented the results in systematic review and meta-analysis formats.

Section snippets

Search strategy

Two authors independently searched Medline and SCOPUS databases by using “sentinel AND vulv*” as key words (last search on March 2013). No language or time restriction was imposed on the search. The reference lists of relevant studies were also searched for possible missing articles.

Inclusion criteria

All studies evaluating SN mapping in vulvar cancer were included if enough data could be extracted for calculation of detection rate and/or sensitivity. For sensitivity, only studies validated by inguinal lymph node

Results

The search process of the study is shown in Fig. 1. The first search yielded 400 potentially relevant studies; 290 studies were irrelevant and were excluded after reviewing the title and abstract. Full texts of the remaining 110 studies were considered for detailed evaluation; 63 studies were excluded in this stage due to incomplete data or being letter to editors, case reports, and review articles. Finally, 47 studies were included in the systematic review [16], [17], [18], [19], [20], [21],

Discussion

According to this systematic review the pooled rate and sensitivity for SLN mapping in vulvar SCC are high: 94.4% and 92% on the patient basis and 84.6% and 92% on the groin basis. However the studies included in the current systematic review were not homogenous (I2 indices for SN detection and sensitivity were 74% and 19%). In order to explain the reason of the heterogeneity across studies we performed subgroup analyses. Several variables were related to SN detection and sensitivity.

Quality of the included studies

Not all included studies in the current systematic review have the same quality. As shown in Table 1, 30 studies either did not recruit patients consecutively or did not report their recruitment protocol at all. Subgroup analysis regarding the level of evidence of the included studies (not shown in Table 2) showed pooled SN detection rate of 92% and 81% for level 2 and 3 studies, respectively. Pooled sensitivities were 94% and 92% for level 2 and 3 studies, respectively. This means that quality

Conclusion

SN mapping is an accurate method for inguinal node staging in vulvar SCC. Combining radiotracer and blue dye methods and excluding patients with palpable inguinal nodes results in the highest detection rate and sensitivity. For midline tumors, we should be cautious since unilateral SN detection can lead to false negative results on the other side. The best decision in this setting would be inguinal lymph node dissection on the detection failure side. Further studies are needed to clarify the

Conflict of interest statement

Authors declare no conflict of interest.

Acknowledgements

This study is a result of a thesis as a joint project in Nuclear Medicine Research Center and Women's Health Research Center of Mashhad University of Medical Sciences. Vice Chancellery of Research of Mashhad University of Medical Sciences financially supported this thesis with the approval number of 911226.

References (72)

  • C. Louis-Sylvestre et al.

    Interpretation of sentinel node identification in vulvar cancer

    Gynecol Obstet Fertil

    (2006)
  • K.Y. Terada et al.

    Outcomes for patients with T1 squamous cell cancer of the vulva undergoing sentinel node biopsy

    Gynecol Oncol

    (2006)
  • S. Johann et al.

    Comparison of outcome and recurrence-free survival after sentinel lymph node biopsy and lymphadenectomy in vulvar cancer

    Gynecol Oncol

    (2008)
  • M. Hampl et al.

    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)
  • J.D. García et al.

    First results in the sentinel lymph node procedure in vulvar squamous cell carcinoma

    Prog Obstet Ginecol

    (2009)
  • J. Radziszewski et al.

    The accuracy of the sentinel lymph node concept in early stage squamous cell vulvar carcinoma

    Gynecol Oncol

    (2010)
  • G. Lindell et al.

    Evaluation of preoperative lymphoscintigraphy and sentinel node procedure in vulvar cancer

    Eur J Obstet Gynecol Reprod Biol

    (2010)
  • R. Guedec-Ghelfi et al.

    Impact of the SPECT/CT in the sentinel lymph node detection. Apropos of 32 cases

    Med Nucl

    (2011)
  • M. Klar et al.

    Sentinel lymph node detection in patients with vulvar carcinoma; feasibility of intra-operative mapping with technetium-99m-labeled nanocolloid

    Eur J Surg Oncol

    (2011)
  • L.M. Crane et al.

    Intraoperative near-infrared fluorescence imaging for sentinel lymph node detection in vulvar cancer: first clinical results

    Gynecol Oncol

    (2011)
  • J. Zekan et al.

    Reliability of sentinel node assay in vulvar cancer: the first Croatian validation trial

    Gynecol Oncol

    (2012)
  • C. Levenback et al.

    Intraoperative lymphatic mapping and sentinel node identification with blue dye in patients with vulvar cancer

    Gynecol Oncol

    (2001)
  • A. Taghizadeh Kermani et al.

    Accuracy of sentinel node biopsy in the staging of non-small cell lung carcinomas: systematic review and meta-analysis of the literature

    Lung Cancer

    (2013)
  • H. Javan et al.

    The accuracy of sentinel node biopsy in breast cancer patients with the history of previous surgical biopsy of the primary lesion: systematic review and meta-analysis of the literature

    Eur J Surg Oncol

    (2012)
  • R.L. Coleman et al.

    Is bilateral lymphadenectomy for midline squamous carcinoma of the vulva always necessary? An analysis from Gynecologic Oncology Group (GOG) 173

    Gynecol Oncol

    (2013)
  • C. Louis-Sylvestre et al.

    Sentinel node localization should be interpreted with caution in midline vulvar cancer

    Gynecol Oncol

    (2005)
  • D.H. Moore

    Reflections on vulvar tumors, lymphatic drainage, and sentinel lymph node biopsy

    Gynecol Oncol

    (2013)
  • A. Jemal et al.

    Cancer statistics, 2010

    CA Cancer J Clin

    (2010)
  • T. Saito et al.

    Management of lymph nodes in the treatment of vulvar cancer

    Int J Clin Oncol

    (2007)
  • M. Pantelic et al.

    Surgical treatment of invasive vulvar cancer

    Med Pregl

    (2012)
  • R. Sadeghi et al.

    Sentinel node mapping in the prostate cancer

    Meta-analysis. Nuklearmedizin

    (2011)
  • M. Ansari et al.

    Sentinel node biopsy in endometrial cancer: systematic review and meta-analysis of the literature

    Eur J Gynaecol Oncol

    (2013)
  • M. Egger et al.

    Bias in meta-analysis detected by a simple, graphical test

    BMJ

    (1997)
  • S. Duval et al.

    Trim and fill: a simple funnel-plot-based method of testing and adjusting for publication bias in meta-analysis

    Biometrics

    (2000)
  • J. Zamora et al.

    Meta-DiSc: a software for meta-analysis of test accuracy data

    BMC Med Res Methodol

    (2006)
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