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. 2022 Jul 27;21:15330338221116489. doi: 10.1177/15330338221116489

Electrochemotherapy as an Alternative Treatment Option to Pelvic Exenteration for Recurrent Vulvar Cancer of the Perineum Region

Gregor Vivod 1,2, Nina Kovacevic 1,2,3,, Maja Čemažar 4,5, Gregor Serša 4,6, Tanja Jesenko 2,4, Maša Bošnjak 4,7, Simona Kranjc Brezar 2,4, Sebastjan Merlo 1,2,8
PMCID: PMC9340424  PMID: 35899313

Abstract

Objective: Pelvic exenteration in women with recurrent vulvar carcinoma is associated with high morbidity and mortality and substantial treatment costs. Because pelvic exenteration severely affects the quality of life and can lead to significant complications, other treatment modalities, such as electrochemotherapy, have been proposed. The aim of this study was to evaluate the feasibility and suitability of electrochemotherapy in the treatment of recurrent vulvar cancer. We aimed to analyze the treatment options, treatment outcomes, and complications in patients with recurrent vulvar cancer of the perineum. Methods: A retrospective analysis of patients who had undergone pelvic exenteration for vulvar cancer at the Institute of Oncology Ljubljana over a 16-year period was performed. As an experimental, less mutilating treatment, electrochemotherapy was performed on one patient with recurrent vulvar cancer involving the perineum. Comparative data analysis was performed between the group with pelvic exenteration and the patient with electrochemotherapy, comparing hospital stay, disease recurrence after treatment, survival after treatment in months, and quality of life after treatment. Results: We observed recurrence of disease in 2 patients with initial FIGO stage IIIC disease 3 months and 32 months after pelvic exenteration, and they died of the disease 15 and 38 months after pelvic exenteration. Two patients with FIGO stage IB were alive at 74 and 88 months after pelvic exenteration. One patient with initial FIGO stage IIIC was alive 12 months after treatment with electrochemotherapy with no visible signs of disease progression in the vulvar region, and the lesions had a complete response. The patient treated with electrochemotherapy was hospitalized for 4 days compared with the patients with pelvic exenteration, in whom the average hospital stay was 19.75 (± 1.68) days. Conclusion: Our experience has shown that electrochemotherapy might be a less radical alternative to pelvic exenteration, especially for patients with initially higher FIGO stages.

Keywords: vulvar cancer, electrochemotherapy, pelvic exenteration, recurrent disease, surgery

Introduction

Vulvar cancer is the fourth most common gynecologic cancer, with an incidence of 2.6 per 100 000 women per year. 1 Historically, vulvar cancer has been and continues to be treated with radical vulvectomy and bilateral groin lymph node dissection or sentinel lymph node biopsy. 2 Radiotherapy may be used as adjuvant therapy after initial surgery or as part of primary therapy for locally advanced diseases. According to guidelines, surveillance is recommended every 3 to 6 months for 2 years after initial treatment, then every 6 to 12 months for another 3 to 5 years, and then annually. 3 Recurrent vulvar cancer occurs in an average of 24% of cases after primary treatment after surgery with or without radiation. 3 Most recurrences occur locally near the surgical margins or in the contralateral lymph node groin region. The therapeutic modalities used depend on the localization, extent of recurrence, and prior radiotherapy or concomitant chemoradiotherapy. 4

In oncologic terminology, pelvic exenteration refers to en bloc resection of the viscera and pelvic organs of the female reproductive tract. Pelvic exenteration is classified as anterior, posterior, and total. In anterior pelvic exenteration, the bladder is removed with or without urethra and formation of urinary diversio, ileal conduit, or continent urinary diversion with or without hysterectomy, with or without resection of vagina and perineum. Posterior pelvic exenteration involves the removal of the rectosigmoid colon and, in some patients, the anal canal with primary anastomosis or formation of an end colostomy with or without hysterectomy. 5 Total pelvic exenteration is the removal of the internal reproductive tract, bladder, and rectosigmoid colon. Further subclassification is made regarding muscle levator ani as the point of resection. Supralevator pelvic exenteration is performed above the levator ani muscle (type 1), infralevator pelvic exenteration is performed to preserve or resect the levator ani muscle without vulvectomy (type 2) and pelvic exenteration with vulvectomy (type 3).6,7

Posterior pelvic exenteration with vulvectomy (type 3) is a generally accepted surgical indication for recurrent vulvar cancer previously treated with radio- or chemoradiotherapy.79 Pelvic exenteration has high mortality and morbidity rate. Due to improvements in preoperative planning, surgical techniques, and peri- and postoperative care, morbidity has decreased over the years, but surgical procedures still significantly affect patients' quality of life.1012 Therefore, new therapeutic options are warranted.

Electrochemotherapy is a local ablative therapy in which the application of reversible electrical pulses to the tumor permeabilizes the cell membrane, allowing cytotoxic drugs to penetrate the cells. 13 It is most commonly used to treat superficial tumors such as melanoma, sarcoma, squamous cell carcinoma, basal cell carcinoma, skin metastases from breast cancer, and others.14,15 It can also be used to treat deep-seated tumors such as primary hepatocellular carcinoma, unresectable colorectal liver metastases, or pancreatic cancer.1618 It is conducted following standard operating procedures, and the method is now used in nearly 170 comprehensive cancer centers around the world. 15

There are few papers describing the use of electrochemotherapy in the palliative treatment of gynecologic cancer, especially squamous cell carcinoma of the vulva.19,20 Safety and local efficacy following electrochemotherapy with bleomycin for locoregional cutaneous recurrences of vulvar carcinoma previously treated with chemotherapy, radiotherapy, and surgery or unsuitable for standard treatments have been demonstrated.2124

Because pelvic exenteration severely compromises the quality of life and can lead to significant complications, 25 other treatment modalities such as electrochemotherapy have been proposed.

To evaluate the feasibility and suitability of electrochemotherapy in the treatment of recurrent squamous cell vulvar cancer, we analyzed the treatment options, treatment outcomes, and complications in patients with recurrent squamous cell vulvar cancer of the perineum.

Methods and Materials

Study Design

A retrospective institutional-based analysis was performed for patients who underwent surgery for vulvar cancer from January 1, 2006 to May 31, 2021 (16-year interval) at the Institute of Oncology Ljubljana. The data collection and analysis were approved by the Medical Board of the Institute based on the positive opinion of Institutional Review Board and Ethical Committee (ERIDNPVO-0001/2020). Informed consent was waived due to the retrospective nature of the study based on approval. The patient data were obtained from the Institutional database Web Doctor 4.2.0 (Marand inženiring d.o.o., Ljubljana, Slovenia). The reporting of this study conforms to STROBE guidelines. 26

Patients and Data Collection

In the analysis of surgical procedures, all procedures except pelvic exenterations were excluded during the observed period in patients without the metastatic spread of the disease. Inpatient reports of 4 patients who had undergone pelvic exenteration were analyzed in terms of primary tumor characteristics, treatment history, details of the procedure, hospital stay, recurrence of disease after treatment, survival after treatment in months, and quality of life after treatment. One patient with recurrent vulvar carcinoma involving the perineum was referred to our institution in June 2021. After clinical evaluation and diagnostic imaging, the patient was presented to the Interinstitutional Tumor Board, which decided that electrochemotherapy was a safe and feasible treatment approach before possible posterior pelvic exenteration with abdomino-perineal excision for the purpose of neoadjuvant therapy. The tumor board consisted of medical oncologists, radiotherapists, and gynecologic oncologists. The electrochemotherapy protocol was approved by the Institutional Medical Board and the Slovenian National Ethics Committee (number 0120-262/2021/3). As an experimental, less mutilating treatment, electrochemotherapy was performed on a patient with recurrent vulvar cancer involving the perineum. Electrochemotherapy with bleomycin was performed according to the standard operating procedure. 15 Briefly, the patient was under general anesthesia. Bleomycin was administered at a dose of 15 000 IU/m2 (Bleomicin Medac, Medac GmbH, Germany). Eight minutes after intravenous administration of the drug, electrical pulses were applied to the tumors in a way that all tumor nodules were covered including the safety margin of ∼1 cm. Hexagonal geometry needle electrodes were used and electrical pulses were generated by Cliniporator (Igea S.P.A., Italy). Altogether 10 applications of electric pulses were delivered.

After the procedure, comparative data analysis was performed between the pelvic exenteration group and the electrochemotherapy patient, comparing hospital stay, recurrence of disease after treatment, survival in months, and posttreatment quality of life.

Pelvic computed tomography (CT) and/or magnetic resonance imaging (MRI) and positron emission tomography-computed tomography (PET-CT) scans were performed preoperatively in all included patients to assess the extent of local metastatic disease and to rule out distant metastasis. All patients were previously informed of the purpose of the study, participated voluntarily, and provided signed, written informed consent. In addition, all patient details have been de-identified.

Results

During the study period, 4 cases of pelvic exenteration for recurrence of vulvar cancer in the perineal region were identified in the database. Two patients underwent total pelvic exenteration and 2 underwent posterior pelvic exenteration. Patient and tumor characteristics are shown in Table 1, surgical characteristics in Table 2, and pain and quality of life in Table 3.

Table 1.

Patients and Tumor Characteristics.

Patient Age (year) at PE or ECT FIGO vulvar cancer stage after primary treatment Site of vulvar cancer recurrence Histologic type Previous
irradiation
Type of
treatment of vulvar cancer recurrence
Recurrence of disease after PE or ECT (months) Survival after PE or ECT (months)
1 70 IIIC Perineum, Introitus SCC Yes TPE 3 Died (15)
2 51 IB Perineum, Vagina SCC Yes TPE nr Alive (74)
3 60 IIIC Perineum SCC Yes PPE 32 Died (38)
4 72 IB Perineum SCC Yes PPE nr Alive (88)
5 64 IIIC Perineum SCC Yes ECT nr Alive (12)

Abbreviations: FIGO, International Federation of Gynecology and Obstetrics; PE, pelvic exenteration; TPE, total pelvic exenteration; PPE, posterior pelvic exenteration; ECT, electrochemotherapy; nr, no recurrence; SCC, squamous cell carcinoma.

Table 2.

Surgical Characteristics.

Patient Type of
treatment of vulvar cancer recurrence
Hospital stay (days) Details of surgery Plastic reconstruction Surgical margins after PE or ECT Revisional surgery
1 TPE 21 Removal of bladder with urethra, formation of urinary diversion (an ileal conduit), hysterectomy with resection of the vagina and perineum,
Removal of rectosigmoid colon with formation of an end colostomy
VRAM Free of malignancy No
2 TPE 15 Removal of bladder with urethra,
Formation of urinary diversion (an ileal conduit),
Resection of the vagina and perineum (hysterectomy in the past),
Removal of rectosigmoid colon with formation of an end colostomy
VRAM Free of malignancy No
3 PPE 21 Resection of distal urethra, perineum,
Removal of rectosigmoid colon with formation of an end colostomy
Primary suturing Free of malignancy For rectovaginal fistula
4 PPE 22 Resection of the vagina and perineum (hysterectomy in the past),
Removal of rectosigmoid colon with formation of an end colostomy
VRAM Free of malignancy No
5 ECT 4 ESOPE Free of malignancy No

Abbreviations: PE, pelvic exenteration; TPE, total pelvic exenteration; PPE, posterior pelvic exenteration; ECT, electrochemotherapy; VRAM, vertical rectus abdominis myocutaneous flap; ESOPE, European Standard Operating Procedures for Electrochemotherapy.

Table 3.

Pain and Quality of Life.

Patient Type of
treatment of vulvar cancer recurrence
Pain described on the VAS scale 1 month after PE or ECT Pain described on the VAS scale 6 months after PE or ECT Pain described on the VAS scale 12 months after PE or ECT Short-term complications after PE or ECT Long-term complications after PE or ECT Clavien-Dindo classification CCI
1 TPE 3/10 3/10 5/10 Partial necrosis of VRAM Pain, leakage of ileal conduit III-b 48.5
2 TPE 3/10 2/10 0/10 Colostomy and ileal conduit handling problems No long-term complications I 8.7
3 PPE 2/10 0/10 0/10 Wound infection,
Rectovaginal fistula
Leakage of colostomy III-b 44.9
4 PPE 3/10 2/10 1/10 Necrosis of colostomy No long-term complications III-b 33.7
5 ECT 4/10 0/10 0/10 No short-term complications No long-term complications / /

Abbreviations: PE, pelvic exenteration; TPE, total pelvic exenteration; PPE, posterior pelvic exenteration; ECT, electrochemotherapy; VAS, Visual Analogue Scale; VRAM, vertical rectus abdominis myocutaneous flap; CCI, comprehensive complication index.

All patients had squamous cell carcinomas and all were initially treated with surgery and radiotherapy. After primary treatment, 2 patients were classified as International Federation of Gynecology and Obstetrics (FIGO) vulvar carcinoma stage IIIC, and 2 patients were classified as stage IB. The mean age of patients with pelvic exenteration was 63.3 (± 3.76) years. In all patients, distant metastases were excluded and resections were radical. In all patients with posterior or total pelvic exenteration, a permanent proximal end colostomy was created. In 2 patients with total pelvic exenteration, an ileal conduit was created.

All patients with pelvic exenteration experienced short- or long-term complications, such as handling problems with colostomy and ileal conduit, pain, wound infections, rectovaginal fistulas, partial necrosis of the VRAM, and necrosis of the colostomy. One of the patients required reoperation because of a rectovaginal fistula. Quality of life was significantly impaired after surgery.

We observed recurrence of disease in 2 patients with initial FIGO stage IIIC disease 3 months and 32 months after pelvic exenteration, and they died of the disease 15 and 38 months after pelvic exenteration. Two patients with FIGO stage IB were alive at 74 and 88 months after pelvic exenteration.

The patient with recurrent vulvar cancer involving the perineum was treated with electrochemotherapy at the age of 64 years. After primary treatment with surgery and chemoradiotherapy, the patient was classified as FIGO stage IIIC vulvar cancer. We observed a local recurrence in the perineal region 10 months after primary treatment (Figure 1). Electrochemotherapy treatment of vulvar cancer perineum lesions was performed according to the European Standard Operating Procedures for Electrochemotherapy (ESOPE). 15 Electrochemotherapy was performed under general anesthesia. The patient had no pain (0/10 on the visual analog scale [VAS]), fever, or malaise after treatment and was discharged from the hospital on the third day after the procedure. The patient was hospitalized for 4 days, compared with pelvic exenteration patients, in whom the average hospital stay was 19.75 (± 1.68) days. Two to 3 weeks after electrochemotherapy, the patient complained of pain, which was described as VAS 4/10. The pain was controlled with oral opioid and nonopioid analgesics. Twelve months after treatment with electrochemotherapy, there were no visible signs of disease progression in the vulvar region, and the lesions had a complete response (Figure 1). The patient had no problems with urination and defecation, no pain, and her quality of life was not affected after electrochemotherapy.

Figure 1.

Figure 1.

(A) Local recurrence of vulvar cancer (circled line) in the perineal region 10 months after primary treatment. (B) Complete response 12 months after treatment with electrochemotherapy (circled line).

Discussion

Pelvic exenteration in women with recurrent vulvar cancer in the perineal region is associated with high morbidity and mortality and substantial treatment costs. 12 Because of prior radiation, surgery is often the only treatment option for local recurrent vulvar cancer in the perineal region, that is, exenterative surgical procedures with the formation of a bowel and/or urinary stoma. 27 Centers tend to be reluctant and cautious in performing such pelvic surgeries. Exenterative surgery is chosen only for patients for whom there are no other treatment options and who are considered to benefit maximally from exenteration. 28

Various reconstructive techniques have been proposed to fill the empty space after pelvic exenteration, including procedures using the omentum, absorbable meshes, or silicone expanders. In addition, vertical (VRAM) and transverse (TRAM) rectus abdominis myocutaneous flaps with vascular supply from branches of the deep inferior epigastric vessels have been successfully used for vaginal reconstruction after pelvic exenteration.2932 The formation of bowel or urinary stoma can seriously affect social relations. This inconvenience is more critical in younger patients and in patients with recurrent diseases.33,34 An alternative to 2 separate stomas is double-barreled wet colostomy (DBWC). This is a lateral loop colostomy that contains both urinary and intestinal diversions in the same segment and drains through a single stoma. DBWC has a less negative impact on patient quality of life than 2 separate stomas.35,36

Spreading to the lymph nodes seems to be the most important prognostic factor, which has already been shown in other clinical and clinicopathologic studies. Moreover, there are no long-term survivors among patients with positive lymph nodes after pelvic exenteration.2,3739 Therefore, the management of patients with recurrent local vulvar carcinoma in the perineal region remains a clinical dilemma, especially considering that these patients are often elderly and have many age-related comorbidities.

In our study, we proposed electrochemotherapy as another treatment modality that has been shown to be feasible and suitable for the treatment of recurrent vulvar cancer. Electrochemotherapy is a locoregional antitumor treatment. Two chemotherapeutic agents are currently used in electrochemotherapy, bleomycin, and cisplatin. Due to the wider use of bleomycin in electrochemotherapy protocols for different types of cancers, we decided also to use bleomycin for the treatment of recurrent vulvar cancer. However, based on our experience with electrochemotherapy with cisplatin of cutaneous tumor nodules in patients with malignant melanoma, squamous cell carcinoma, and basal cell carcinoma, cisplatin could also be effectively used for the treatment of superficial tumors.40,41 The efficacy of electrochemotherapy for skin and subcutaneous tumors is well established and represents a valuable alternative or complementary option for patients with superficial tumors. 42 Treatment with electrochemotherapy has been shown to improve patients quality of life of patients and reduce symptoms such as bleeding, pain, odor, itching, and sexual dysfunction. In women with recurrent vulvar cancer, electrochemotherapy appears to be well tolerated and may lead to noticeable tumor control with concomitant symptom relief. 42

Patients treated with electrochemotherapy had a shorter hospital stay and quality of life was not impaired after electrochemotherapy, compared with patients after pelvic exenteration in whom quality of life decreased significantly due to short- and long-term complications. In addition, one study found that women who underwent pelvic exenteration for gynecologic malignancies became more obese and comorbid during the study period, resulting in more complications, longer length of stay, and higher treatment-related costs. These data help define changes and trends in the use and outcomes of pelvic exenteration for gynecologic cancers. 12

Unfortunately, we do not have data on the sexual quality of life of our patients. Little data and information on sexual quality of life have been available in the literature. Approximately 25% of women treated with vagina-sparing pelvic exenteration were sexually active and had low and moderate levels of intercourse pleasure. In this context, it seems reasonable to hypothesize that sparing the vagina as much as possible during supra levator pelvic exenteration might help to satisfy these unmet needs. 10

Despite the relevance of our data, several limitations of the study should be noted. The main limitation of our study is the lack of validated quality of life questionnaires. Our data were collected from clinical records and do not allow definitive conclusions. The other limitation of the study is its retrospective observational nature.

However, because of the rare vulvar cancer recurrence in the perineal region and the even smaller number of physically fit patients willing to undergo such a radical surgical procedure, conducting a prospective randomized study to investigate the benefits of pelvic exenteration is challenging. Therefore, even small retrospective studies are important to verify the value of pelvic exenteration as the ultimate treatment for vulvar cancer. Most authors agree that pelvic exenteration should be performed only when there are no less radical alternatives or the option of radiation therapy. 28

Conclusions

Our experience showed that electrochemotherapy might be a less radical alternative to pelvic exenteration, especially for patients with initially higher FIGO stages.

Footnotes

Funding: The authors acknowledge the financial support from the state budget by the Slovenian Research Agency, program no. P3-0003.

Ethics Statement: The data collection and its analysis were approved by the Institutional Ethical Committee (ERIDNPVO-0001/2020). The electrochemotherapy protocol was approved by the Institutional and Slovenian National Ethical Committee (number 0120-262/2021/3).

Declaration of Conflicting Interests: The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding: The authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by the Javna Agencija za Raziskovalno Dejavnost RS, (grant no. P3-0003.).

References

  • 1.U.S. Cancer Statistics Working Group. U.S. Cancer Statistics Data Visualizations Tool, based on 2020 submission data (1999–2018): U.S. Department of Health and Human Services, Centers for Disease Control and Prevention and National Cancer Institute; www.cdc.gov/cancer/dataviz, June 2021.
  • 2.Hopkins MP, Morley GW. Pelvic exenteration for the treatment of vulvar cancer. Cancer. 1992;70(12):2835‐2838. doi: 10.1002/1097-0142(19921215)70:12. [DOI] [PubMed] [Google Scholar]
  • 3.NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Vulvar Cancer (Squamous Cell Carcinoma). 2022. https://www.nccn.org/professionals/physician_gls/pdf/vulvar.pdf
  • 4.Salom EM, Penalver M. Recurrent vulvar cancer. Curr Treat Options Oncol. 2002;3(2):143‐153. doi: 10.1007/s11864-002-0060-x [DOI] [PubMed] [Google Scholar]
  • 5.Ang C, Bryant A, Barton DP, Pomel C, Naik R. Exenterative surgery for recurrent gynaecological malignancies. Cochrane gynaecological, neuro-oncology and orphan cancer group, ed. Cochrane Database Syst Rev. 2014;(2):1–15. doi: 10.1002/14651858.CD010449.pub2. Published online February 4, 2014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Maggino T, Landoni F, Sartori E, et al. Patterns of recurrence in patients with squamous cell carcinoma of the vulva. A multicenter CTF study. Cancer. 2000;89(1):116‐122. doi: 10.1002/1097-0142(20000701)89:1. [DOI] [PubMed] [Google Scholar]
  • 7.Kaur M, Joniau S, D’Hoore A, et al. Pelvic exenterations for gynecological malignancies: a study of 36 cases. Int J Gynecol Cancer Off J Int Gynecol Cancer Soc. 2012;22(5):889‐896. doi: 10.1097/IGC.0b013e31824eb8cd [DOI] [PubMed] [Google Scholar]
  • 8.Tan KK, Pal S, Lee PJ, Rodwell L, Solomon MJ. Pelvic exenteration for recurrent squamous cell carcinoma of the pelvic organs arising from the cloaca—a single institution’s experience over 16 years. Colorectal Dis Off J Assoc Coloproctology G B Irel. 2013;15(10):1227‐1231. doi: 10.1111/codi.12306 [DOI] [PubMed] [Google Scholar]
  • 9.Magrina JF. Types of pelvic exenterations: a reappraisal. Gynecol Oncol. 1990;37(3):363‐366. doi: 10.1016/0090-8258(90)90368-u [DOI] [PubMed] [Google Scholar]
  • 10.Dessole M, Petrillo M, Lucidi A, et al. Quality of life in women after pelvic exenteration for gynecological malignancies: a multicentric study. Int J Gynecol Cancer Off J Int Gynecol Cancer Soc. 2018;28(2):267‐273. doi: 10.1097/IGC.0000000000000612 [DOI] [PubMed] [Google Scholar]
  • 11.Straubhar AM, Chi AJ, Zhou QC, et al. Pelvic exenteration for recurrent or persistent gynecologic malignancies: clinical and histopathologic factors predicting recurrence and survival in a modern cohort. Gynecol Oncol. 2021;163(2):294‐298. doi: 10.1016/j.ygyno.2021.08.033 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Matsuo K, Mandelbaum RS, Adams CL, Roman LD, Wright JD. Performance and outcome of pelvic exenteration for gynecologic malignancies: a population-based study. Gynecol Oncol. 2019;153(2):368‐375. doi: 10.1016/j.ygyno.2019.02.002 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Cemazar M, Sersa G. Recent advances in electrochemotherapy. Bioelectricity. 2019;1(4):204‐213. doi: 10.1089/bioe.2019.0028 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Sersa G, Ursic K, Cemazar M, Heller R, Bosnjak M, Campana LG. Biological factors of the tumour response to electrochemotherapy: review of the evidence and a research roadmap. Eur J Surg Oncol J Eur Soc Surg Oncol Br Assoc Surg Oncol. 2021;47(8):1836‐1846. doi: 10.1016/j.ejso.2021.03.229 [DOI] [PubMed] [Google Scholar]
  • 15.Gehl J, Sersa G, Matthiessen LW, et al. Updated standard operating procedures for electrochemotherapy of cutaneous tumours and skin metastases. Acta Oncol Stockh Swed. 2018;57(7):874‐882. doi: 10.1080/0284186X.2018.1454602 [DOI] [PubMed] [Google Scholar]
  • 16.Djokic M, Cemazar M, Bosnjak M, et al. A prospective phase II study evaluating intraoperative electrochemotherapy of hepatocellular carcinoma. Cancers (Basel). 2020;12(12):E3778. doi: 10.3390/cancers12123778 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Edhemovic I, Brecelj E, Cemazar M, et al. Intraoperative electrochemotherapy of colorectal liver metastases: a prospective phase II study. Eur J Surg Oncol J Eur Soc Surg Oncol Br Assoc Surg Oncol. 2020;46(9):1628‐1633. doi: 10.1016/j.ejso.2020.04.037 [DOI] [PubMed] [Google Scholar]
  • 18.Casadei R, Ricci C, Ingaldi C, et al. Intraoperative electrochemotherapy in locally advanced pancreatic cancer: indications, techniques and results-a single-center experience. Updat Surg. 2020;72(4):1089‐1096. doi: 10.1007/s13304-020-00782-x [DOI] [PubMed] [Google Scholar]
  • 19.Perrone AM, Galuppi A, Pirovano C, et al. Palliative electrochemotherapy in vulvar carcinoma: preliminary results of the ELECHTRA (electrochemotherapy vulvar cancer) multicenter study. Cancers (Basel). 2019;11(5):E657. doi: 10.3390/cancers11050657 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Tranoulis A, Georgiou D, Founta C, Mehra G, Sayasneh A, Nath R. Use of electrochemotherapy in women with vulvar cancer to improve quality-of-life in the palliative setting: a meta-analysis. Int J Gynecol Cancer Off J Int Gynecol Cancer Soc. 2020;30(1):107‐114. doi: 10.1136/ijgc-2019-000868 [DOI] [PubMed] [Google Scholar]
  • 21.Merlo S, Vivod G, Bebar S, et al. Literature review and our experience with bleomycin-based electrochemotherapy for cutaneous vulvar metastases from endometrial cancer. Technol Cancer Res Treat. 2021;20(20):15330338211010134. doi: 10.1177/15330338211010134 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Corrado G, Cutillo G, Fragomeni SM, et al. Palliative electrochemotherapy in primary or recurrent vulvar cancer. Int J Gynecol Cancer Off J Int Gynecol Cancer Soc. 2020;30(7):927‐931. doi: 10.1136/ijgc-2019-001178 [DOI] [PubMed] [Google Scholar]
  • 23.Perrone AM, Galuppi A, Borghese G, et al. Electrochemotherapy pre-treatment in primary squamous vulvar cancer. Our preliminary experience. J Surg Oncol. 2018;117(8):1813‐1817. doi: 10.1002/jso.25072 [DOI] [PubMed] [Google Scholar]
  • 24.Pellegrino A, Damiani GR, Mangioni C, et al. Outcomes of bleomycin-based electrochemotherapy in patients with repeated loco-regional recurrences of vulvar cancer. Acta Oncol Stockh Swed. 2016;55(5):619‐624. doi: 10.3109/0284186X.2015.1117134 [DOI] [PubMed] [Google Scholar]
  • 25.Wydra D, Emerich J, Sawicki S, Ciach K, Marciniak A. Major complications following exenteration in cases of pelvic malignancy: a 10-year experience. World J Gastroenterol. 2006;12(7):1115‐1119. doi: 10.3748/wjg.v12.i7.1115 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.von Elm E, Altman DG, Egger M, et al. The strengthening the reporting of observational studies in epidemiology (STROBE) statement: guidelines for reporting observational studies. Ann Intern Med. 2007;147(8):573‐577. doi: 10.7326/0003-4819-147-8-200710160-00010 [DOI] [PubMed] [Google Scholar]
  • 27.Onnis A, Marchetti M, Maggino T. Carcinoma of the vulva: critical analysis of survival and treatment of recurrences. Eur J Gynaecol Oncol. 1992;13(6):480‐485. [PubMed] [Google Scholar]
  • 28.de Gregorio N, de Gregorio A, Ebner F, et al. Pelvic exenteration as ultimate ratio for gynecologic cancers: single-center analyses of 37 cases. Arch Gynecol Obstet. 2019;300(1):161‐168. doi: 10.1007/s00404-019-05154-4 [DOI] [PubMed] [Google Scholar]
  • 29.Devulapalli C, Jia Wei AT, DiBiagio JR, et al. Primary versus flap closure of perineal defects following oncologic resection: a systematic review and meta-analysis. Plast Reconstr Surg. 2016;137(5):1602‐1613. doi: 10.1097/PRS.0000000000002107 [DOI] [PubMed] [Google Scholar]
  • 30.Cibula D, Zikan M, Fischerova D, et al. Pelvic floor reconstruction by modified rectus abdominis myoperitoneal (MRAM) flap after pelvic exenterations. Gynecol Oncol. 2017;144(3):558‐563. doi: 10.1016/j.ygyno.2017.01.014 [DOI] [PubMed] [Google Scholar]
  • 31.Horch RE, Hohenberger W, Eweida A, et al. A hundred patients with vertical rectus abdominis myocutaneous (VRAM) flap for pelvic reconstruction after total pelvic exenteration. Int J Colorectal Dis. 2014;29(7):813‐823. doi: 10.1007/s00384-014-1868-0 [DOI] [PubMed] [Google Scholar]
  • 32.Cortinovis U, Sala L, Bonomi S, et al. Rectus abdominis myofascial flap for vaginal reconstruction after pelvic exenteration. Ann Plast Surg. 2018;81(5):576‐583. doi: 10.1097/SAP.0000000000001578 [DOI] [PubMed] [Google Scholar]
  • 33.Janda M, Obermair A, Cella D, Crandon AJ, Trimmel M. Vulvar cancer patients’ quality of life: a qualitative assessment. Int J Gynecol Cancer Off J Int Gynecol Cancer Soc. 2004;14(5):875‐881. doi: 10.1111/j.1048-891X.2004.14524.x [DOI] [PubMed] [Google Scholar]
  • 34.Perrone AM, Ferioli M, Argnani L, et al. Quality of life with vulvar carcinoma treated with palliative electrochemotherapy: the ELECHTRA (ELEctroCHemoTherapy vulvaR cAncer) study. Cancers (Basel). 2021;13(7):1622. doi: 10.3390/cancers13071622 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Gan J, Hamid R. Literature review: double-barrelled wet colostomy (one stoma) versus ileal conduit with colostomy (two stomas). Urol Int. 2017;98(3):249‐254. doi: 10.1159/000450654 [DOI] [PubMed] [Google Scholar]
  • 36.Gachabayov M, Lee H, Tulina I, et al. Double-barreled wet colostomy versus separate urinary and fecal diversion in patients undergoing total pelvic exenteration: a cohort meta-analysis. Surg Technol Int. 2019;35:148‐152. [PubMed] [Google Scholar]
  • 37.Cavanagh D, Shepherd JH. The place of pelvic exenteration in the primary management of advanced carcinoma of the vulva. Gynecol Oncol. 1982;13(3):318‐322. doi: 10.1016/0090-8258(82)90069-5 [DOI] [PubMed] [Google Scholar]
  • 38.Hannes S, Nijboer JM, Reinisch A, Bechstein WO, Habbe N. Abdominoperineal excisions in the treatment regimen for advanced and recurrent vulvar cancers-analysis of a single-centre experience. Indian J Surg. 2015;77(Suppl 3):1270‐1274. doi: 10.1007/s12262-015-1273-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Schmidt W, Villena-Heinsen C, Schmid H, Engel K, Jochum N, Müller A. Recurrence of vulvar cancer—treatment, experiences and results. Geburtshilfe Frauenheilkd. 1992;52(8):462‐466. doi: 10.1055/s-2007-1023789 [DOI] [PubMed] [Google Scholar]
  • 40.Serša G, Štabuc B, Čemažar M, Jančar B, Miklavčič D, Rudolf Z. Electrochemotherapy with cisplatin: potentiation of local cisplatin antitumour effectiveness by application of electric pulses in cancer patients. Eur J Cancer. 1998;34(8):1213‐1218. doi: 10.1016/S0959-8049(98)00025-2 [DOI] [PubMed] [Google Scholar]
  • 41.Sersa G, Stabuc B, Cemazar M, Miklavcic D, Rudolf Z. Electrochemotherapy with cisplatin: clinical experience in malignant melanoma patients. Clin Cancer Res Off J Am Assoc Cancer Res. 2000;6(3):863‐867. [PubMed] [Google Scholar]
  • 42.Campana LG, Miklavčič D, Bertino G, et al. Electrochemotherapy of superficial tumors—current status: basic principles, operating procedures, shared indications, and emerging applications. Semin Oncol. 2019;46(2):173‐191. doi: 10.1053/j.seminoncol.2019.04.002 [DOI] [PubMed] [Google Scholar]

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