Abstract

AimsRadio(chemo)therapy plays an important role in the treatment of vulvar cancer, either as postoperative treatment or as definitive treatment in patients who present with inoperable disease. Only limited data are available regarding outcome after modern state of the art radio(chemo)therapy and more information regarding prognostic factors are warranted. The aim of this study was to evaluate disease outcomes after radio(chemo)therapy in patients with vulvar cancer with special emphasis on the impact of lichen sclerosis on local control. Materials and methodsAll consecutive patients (n = 109) from the western half of Denmark who were treated with definitive (n = 52) or postoperative (n = 57) radio(chemo)therapy between January 2013 and January 2020 were included. Local control, cause-specific survival and overall survival, as well as morbidity, were analysed using Kaplan–Meier statistics. Prognostic factors for local control were analysed in univariate and multivariate analysis. ResultsAt a median follow-up of 35 (4–95) months, 46 (42.0%) patients were diagnosed with recurrence. Eighty per cent of the recurrences were located to the vulva region, leading to a 5-year local control of 58.9% (confidence interval 47.9–69.9). Cause-specific survival was 62.9% (confidence interval 53.1–72.7), whereas overall survival was 58.0% (confidence interval 47.6–68.5). Grade 3–4 morbidity was diagnosed in 10 (9%) patients. Lichen sclerosis (hazard ratio 3.89; confidence interval 1.93–7.79) was an independent risk factors for local recurrence. Patients without lichen sclerosis had a 5-year local control rate of 83.6% (confidence interval 67.2–99.0) and 62.6% (confidence interval 43.2–82.0) after postoperative and definitive radio(chemo)therapy, respectively. In patients with lichen sclerosis, the local control rate was 44.0% (confidence interval 19.3–69.0) and 17.6% (confidence interval 0–30.0) after postoperative and definitive radio(chemo)therapy, respectively. ConclusionRadio(chemo)therapy plays an important role in the treatment of vulvar cancer. However, despite dose escalation, a substantial proportion of patients experienced local relapse. Pre-existing lichen sclerosis seems to have a significant impact on the risk of recurrence. This should influence surveillance programmes for these patients.

Highlights

  • Vulvar cancer is an uncommon cancer that account for about 5% of all gynaecological malignancies

  • The aim of the present study is to investigate disease outcomes in terms of local control, cause-specific survival and overall survival after definitive or postoperative radio(chemo) therapy

  • All patients were assessed with a clinical examination under general anaesthesia, positron emission tomographycomputed tomography (PET-CT) and magnetic resonance imaging (MRI) scans at diagnosis and were discussed at a multidisciplinary team conference with participation of specialists within oncogynaecology, radiology, pathology and clinical oncology

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Summary

Introduction

Vulvar cancer is an uncommon cancer that account for about 5% of all gynaecological malignancies. There are two main aetiological pathways for vulvar cancer. One pathway is related to previous human papillomavirus (HPV) infection, Author for correspondence: L. The surgical treatment of vulvar cancer includes a wide local excision in operable patients. Due to the risk of regional lymph node metastases in patients with >1 mm invasion depth, sentinel lymph node dissection is recommended in clinical and radiologically node-negative patients with tumour size

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