Skip to main content
Top
Published in: Annals of Surgical Oncology 7/2020

01-07-2020 | Urologic Oncology

Pelvic Exenteration for Anal and Urogenital Squamous Cell Carcinoma: Experience and Outcomes from an Exenteration Unit Over 12 Years

Authors: Nicholas Smith, MBBS, FRACS, Peadar S. Waters, MB, BCh, BAO, MD, MCH, MedED, FRCS, Oliver Peacock, BMBS, PhD, FRCS, Joseph C. Kong, MBBS, FRACS, Jacob McCormick, MBBS, FRACS, Satish K. Warrier, MBBS, MS, FRACS, Orla McNally, MBBAO, BCh, FRCSI, MRCOG, FRANZCOG, CGO, Andrew C. Lynch, MBChB, MMedSc, FRACS, Alexander G. Heriot, MA, MB, BChir, MD, MBA, FRCS (Gen.), FRCSEd, FRACS, FACS

Published in: Annals of Surgical Oncology | Issue 7/2020

Login to get access

Abstract

Background

Pelvic exenteration has increasingly been shown to improve disease-free and overall survival for patients with locally advanced pelvic malignancies. Squamous cell carcinoma (SCC) is the second most common pelvic malignancy requiring exenteration.

Objective

The aim of this study was to report the clinical and oncological outcomes from patients treated with pelvic exenteration for anal and urogenital SCC from a single, high-volume unit.

Methods

A review of a prospectively maintained database from 1991 to 2018 at a high-volume specialised institution was performed. Primary endpoints included R0 resection rates, local recurrence and overall survival (OS) rates.

Results

From January 1999 to July 2018, 361 patients underwent pelvic exenteration of which 31 patients were identified with SCC (15 anal SCC, 16 urogenital SCC). The majority of patients were females (n = 24, 77.4%). Median age was 59 (range 35–81). Twenty-seven patients underwent resection with curative intent with an R0 resection rate of 81.5%. Four patients underwent a palliative procedure [R1 = 3 (8%), R2 = 1 (3.3%)]. Mean hospital length of stay was 32 days (range 8–122 days). Disease-free survival was significantly increased in anal SCC with no significant difference in OS compared to urogenital SCC (p = 0.03, p = 0.447 respectively). Advanced pathological T stage was associated with decreased OS (p = 0.023). In the curative intent group the disease-free survival and OS rate was 59.3% and 70% at 24 months, respectively.

Conclusion

Complete R0 resection is achievable in a high proportion of patients. Urogenital SCC is associated with significantly worse disease-free survival, and advanced T-stage was a significant prognostic factor for OS.
Literature
1.
go back to reference Brunschwig A. Complete excision of pelvic viscera in the male for advanced carcinoma of the sigmoid invading the urinary bladder. Ann Surg. 1949;129(4):499–504.CrossRef Brunschwig A. Complete excision of pelvic viscera in the male for advanced carcinoma of the sigmoid invading the urinary bladder. Ann Surg. 1949;129(4):499–504.CrossRef
2.
go back to reference Brown KGM, Solomon MJ, Koh CE. Pelvic exenteration surgery: the evolution of radical surgical techniques for advanced and recurrent pelvic malignancy. Dis Colon Rectum. 2017;60(7):745–54.CrossRef Brown KGM, Solomon MJ, Koh CE. Pelvic exenteration surgery: the evolution of radical surgical techniques for advanced and recurrent pelvic malignancy. Dis Colon Rectum. 2017;60(7):745–54.CrossRef
4.
go back to reference PelvEx Collaborative. Surgical and survival outcomes following pelvic exenteration for locally advanced primary rectal cancer: results from an international collaboration. Ann Surg. 2019;269(2):315–321.CrossRef PelvEx Collaborative. Surgical and survival outcomes following pelvic exenteration for locally advanced primary rectal cancer: results from an international collaboration. Ann Surg. 2019;269(2):315–321.CrossRef
5.
go back to reference Ferenschild FTJ, Vermaas M, Verhoef C, Ansink AC, Kirkels WJ, Eggermont AMM, et al. Total pelvic exenteration for primary and recurrent malignancies. World J Surg. 2009;33(7):1502–8.CrossRef Ferenschild FTJ, Vermaas M, Verhoef C, Ansink AC, Kirkels WJ, Eggermont AMM, et al. Total pelvic exenteration for primary and recurrent malignancies. World J Surg. 2009;33(7):1502–8.CrossRef
6.
go back to reference Grulich AE, Poynten IM, Machalek DA, Jin F, Templeton DJ, Hillman RJ. The epidemiology of anal cancer. Sex Health. 2012;9(6):504–8.CrossRef Grulich AE, Poynten IM, Machalek DA, Jin F, Templeton DJ, Hillman RJ. The epidemiology of anal cancer. Sex Health. 2012;9(6):504–8.CrossRef
7.
go back to reference Barnholtz-Sloan JS, Maldonado JL, Pow-sang J, Giuliano AR. Incidence trends in primary malignant penile cancer. Urol Oncol. 2007. 25(5):361–7. Barnholtz-Sloan JS, Maldonado JL, Pow-sang J, Giuliano AR. Incidence trends in primary malignant penile cancer. Urol Oncol. 2007. 25(5):361–7.
8.
go back to reference Nigro ND, Seydel HG, Considine B, Vaitkevicius VK, Leichman L, Kinzie JJ. Combined preoperative radiation and chemotherapy for squamous cell carcinoma of the anal canal. Cancer. 1983;51(10):1826–9.CrossRef Nigro ND, Seydel HG, Considine B, Vaitkevicius VK, Leichman L, Kinzie JJ. Combined preoperative radiation and chemotherapy for squamous cell carcinoma of the anal canal. Cancer. 1983;51(10):1826–9.CrossRef
9.
go back to reference Schiller DE, Cummings BJ, Rai S, et al. Outcomes of salvage surgery for squamous cell carcinoma of the anal canal. Ann Surg Oncol. 2007;14:2780–9. Schiller DE, Cummings BJ, Rai S, et al. Outcomes of salvage surgery for squamous cell carcinoma of the anal canal. Ann Surg Oncol. 2007;14:2780–9.
10.
go back to reference Eeson G, Foo M, Harrow S, McGregor G, Hay J. Outcomes of salvage surgery for epidermoid carcinoma of the anus following failed combined modality treatment. Am J Surg. 2011;201:628–33.CrossRef Eeson G, Foo M, Harrow S, McGregor G, Hay J. Outcomes of salvage surgery for epidermoid carcinoma of the anus following failed combined modality treatment. Am J Surg. 2011;201:628–33.CrossRef
11.
go back to reference van der Wal BCH, Cleffken BI, Gulec B, Kaufman HS, Choti MA. Results of salvage abdominoperineal resection for recurrent anal carcinoma following combined chemoradiation therapy. J Gastrointest Surg. 2001;5(4):383–7.CrossRef van der Wal BCH, Cleffken BI, Gulec B, Kaufman HS, Choti MA. Results of salvage abdominoperineal resection for recurrent anal carcinoma following combined chemoradiation therapy. J Gastrointest Surg. 2001;5(4):383–7.CrossRef
12.
go back to reference Minhas, S., Kayes, O., Hegarty, P., Kumar, P., Freeman, A. and Ralph, D. What surgical resection margins are required to achieve oncological control in men with primary penile cancer? BJU Int. 2005;96:1040–3.CrossRef Minhas, S., Kayes, O., Hegarty, P., Kumar, P., Freeman, A. and Ralph, D. What surgical resection margins are required to achieve oncological control in men with primary penile cancer? BJU Int. 2005;96:1040–3.CrossRef
13.
go back to reference Yang HY, Park SC, Hyun JH, Seo HK, Oh JH. Outcomes of pelvic exenteration for recurrent or primary locally advanced colorectal cancer. Ann Surg Treat Res. 2015;89(3):131–7.CrossRef Yang HY, Park SC, Hyun JH, Seo HK, Oh JH. Outcomes of pelvic exenteration for recurrent or primary locally advanced colorectal cancer. Ann Surg Treat Res. 2015;89(3):131–7.CrossRef
14.
go back to reference Hall BL, Hamilton BH, Richards K, Bilimoria KY, Cohen ME, Ko CY. Does surgical quality improve in the American College of Surgeons National Surgical Quality Improvement Program: an evaluation of all participating hospitals. Ann Surg. 2009;250(3):363–76.PubMed Hall BL, Hamilton BH, Richards K, Bilimoria KY, Cohen ME, Ko CY. Does surgical quality improve in the American College of Surgeons National Surgical Quality Improvement Program: an evaluation of all participating hospitals. Ann Surg. 2009;250(3):363–76.PubMed
15.
go back to reference Pawlik TM, Skibber JM, Rodriguez-Bigas MA. Pelvic exenteration for advanced pelvic malignancies. Ann Surg Oncol. 2006;13(5):612.CrossRef Pawlik TM, Skibber JM, Rodriguez-Bigas MA. Pelvic exenteration for advanced pelvic malignancies. Ann Surg Oncol. 2006;13(5):612.CrossRef
16.
go back to reference Ogura A, Akiyoshi T, Konishi T, et al. Safety of laparoscopic pelvic exenteration with urinary diversion for colorectal malignancies. World J Surg. 2016;40(5):1236.CrossRef Ogura A, Akiyoshi T, Konishi T, et al. Safety of laparoscopic pelvic exenteration with urinary diversion for colorectal malignancies. World J Surg. 2016;40(5):1236.CrossRef
17.
go back to reference 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. 2013;15(10):1227–31.CrossRef 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. 2013;15(10):1227–31.CrossRef
19.
go back to reference Flam M, John M, Pajak TF, Petrelli N, Myerson R, Doggett S, et al. Role of mitomycin in combination with fluorouracil and radiotherapy, and of salvage chemoradiation in the definitive nonsurgical treatment of epidermoid carcinoma of the anal canal: results of a phase III randomized intergroup study. J Clin Oncol. 1996; 14(9):2527–39.CrossRef Flam M, John M, Pajak TF, Petrelli N, Myerson R, Doggett S, et al. Role of mitomycin in combination with fluorouracil and radiotherapy, and of salvage chemoradiation in the definitive nonsurgical treatment of epidermoid carcinoma of the anal canal: results of a phase III randomized intergroup study. J Clin Oncol. 1996; 14(9):2527–39.CrossRef
20.
go back to reference Ajani JA, Winter KA, Gunderson LL, et al. Inter-group RTOG 98-11: a phase III randomized study of 5-fluoruracil (5-FU), mitomycin, and radiotherapy versus 5-fluorouracil, cisplatin and radiotherapy in carcinoma of the anal canal. J Clin Oncol. 2006;24:180s. Ajani JA, Winter KA, Gunderson LL, et al. Inter-group RTOG 98-11: a phase III randomized study of 5-fluoruracil (5-FU), mitomycin, and radiotherapy versus 5-fluorouracil, cisplatin and radiotherapy in carcinoma of the anal canal. J Clin Oncol. 2006;24:180s.
21.
go back to reference Das P, Bhatia S, Eng C, Ajani JA, Skibber JM, Rodriguez-Bigas MA, Chang GJ, Bhosale P, Delclos ME, Krishnan S, Janjan NA, Crane CH. Predictors and patterns of recurrence after definitive chemoradiation for anal cancer. Int J Radiat Oncol Biol Phys. 2007; 68(3):794–800.CrossRef Das P, Bhatia S, Eng C, Ajani JA, Skibber JM, Rodriguez-Bigas MA, Chang GJ, Bhosale P, Delclos ME, Krishnan S, Janjan NA, Crane CH. Predictors and patterns of recurrence after definitive chemoradiation for anal cancer. Int J Radiat Oncol Biol Phys. 2007; 68(3):794–800.CrossRef
22.
go back to reference Glynne-Jones R, James R, Meadows H, et al. Optimum time to assess complete clinical response (CR) following chemoradiation (CRT) using mitomycin (MMC) or cisplatin (CisP), with or without maintenance CisP/5FU in squamous cell carcinoma of the anus: results of ACT II. 2012 ASCO annual meeting. J Clin Oncol. 2012;30:abstr 4004. Glynne-Jones R, James R, Meadows H, et al. Optimum time to assess complete clinical response (CR) following chemoradiation (CRT) using mitomycin (MMC) or cisplatin (CisP), with or without maintenance CisP/5FU in squamous cell carcinoma of the anus: results of ACT II. 2012 ASCO annual meeting. J Clin Oncol. 2012;30:abstr 4004.
23.
go back to reference UKCCCR. Epidermoid anal cancer: results from the UKCCCR randomised trial of radiotherapy alone versus radiotherapy, fluorouracil, and mitomycin. UKCCCR Anal Cancer Trial Working Party. UK Co-ordinating Committee on Cancer Research. Lancet. 1996;348:1049–54. UKCCCR. Epidermoid anal cancer: results from the UKCCCR randomised trial of radiotherapy alone versus radiotherapy, fluorouracil, and mitomycin. UKCCCR Anal Cancer Trial Working Party. UK Co-ordinating Committee on Cancer Research. Lancet. 1996;348:1049–54.
29.
go back to reference Diver EJ, Rauh-Hain JA, Del Carmen MG. Total pelvic exenteration for gynecologic malignancies. Int J Surg Oncol. 2012;2012:693535.PubMedPubMedCentral Diver EJ, Rauh-Hain JA, Del Carmen MG. Total pelvic exenteration for gynecologic malignancies. Int J Surg Oncol. 2012;2012:693535.PubMedPubMedCentral
30.
go back to reference Ahmadi N, Tan K-K, Solomon MJ, Al-Mozany N, Carter J. Pelvic exenteration for primary and recurrent gynecologic malignancies is safe and achieves acceptable long-term outcomes. J Gynecol Surg. 2014;30(5):255–9.CrossRef Ahmadi N, Tan K-K, Solomon MJ, Al-Mozany N, Carter J. Pelvic exenteration for primary and recurrent gynecologic malignancies is safe and achieves acceptable long-term outcomes. J Gynecol Surg. 2014;30(5):255–9.CrossRef
Metadata
Title
Pelvic Exenteration for Anal and Urogenital Squamous Cell Carcinoma: Experience and Outcomes from an Exenteration Unit Over 12 Years
Authors
Nicholas Smith, MBBS, FRACS
Peadar S. Waters, MB, BCh, BAO, MD, MCH, MedED, FRCS
Oliver Peacock, BMBS, PhD, FRCS
Joseph C. Kong, MBBS, FRACS
Jacob McCormick, MBBS, FRACS
Satish K. Warrier, MBBS, MS, FRACS
Orla McNally, MBBAO, BCh, FRCSI, MRCOG, FRANZCOG, CGO
Andrew C. Lynch, MBChB, MMedSc, FRACS
Alexander G. Heriot, MA, MB, BChir, MD, MBA, FRCS (Gen.), FRCSEd, FRACS, FACS
Publication date
01-07-2020
Publisher
Springer International Publishing
Published in
Annals of Surgical Oncology / Issue 7/2020
Print ISSN: 1068-9265
Electronic ISSN: 1534-4681
DOI
https://doi.org/10.1245/s10434-020-08229-8

Other articles of this Issue 7/2020

Annals of Surgical Oncology 7/2020 Go to the issue