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Management of surgical menopause in female patients with bladder cancer undergoing radical cystectomy

Abstract

Radical cystectomy is the gold-standard treatment for patients with muscle-invasive and very high-risk non-muscle-invasive bladder cancer. In female patients, radical cystectomy has traditionally included removal of the uterus, ovaries, fallopian tubes and anterior vaginal wall. The majority of female patients undergoing radical cystectomy are postmenopausal, but a subset of patients are premenopausal and experience surgical menopause as a result of bilateral oophorectomy. Surgical menopause results from an abrupt loss of sex steroid hormones, resulting in symptoms such as vasomotor instability and sexual dysfunction, while also increasing the long-term risk of osteoporosis, cardiovascular disease and cognitive decline. The importance of ovarian preservation during radical cystectomy is increasingly recognized; however, oophorectomy might still be indicated in selected premenopausal patients for oncological control. In these individuals, awareness and management of surgical menopause among urologists is often limited, resulting in avoidable morbidity. Thus, when surgical menopause is unavoidable, patients should be counselled regarding symptom management, cardiovascular risk and bone protection; and appropriate hormonal and non-hormonal therapeutic strategies should be implemented where indicated.

Key points

  • Surgical menopause occurs following radical cystectomy when bilateral oophorectomy is carried out in a premenopausal woman.

  • Surgical menopause results in an abrupt cessation of ovarian sex hormone production, causing symptoms including hot flushes and sexual dysfunction.

  • Beyond symptomatic effects, surgical menopause is associated with important long-term risks including an increased risk of all-cause mortality, cardiovascular disease, cognitive decline and loss of bone mineral density.

  • Female patients experiencing surgical menopause should receive evidence-based counselling regarding expected symptoms, hormone replacement therapy and appropriate non-hormonal treatment options.

  • Management of surgical menopause should be multidisciplinary, involving urology, gynaecology and/or menopause specialists, and primary care and allied health professionals, to ensure coordinated symptom control, risk reduction and survivorship care.

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Fig. 1: Symptoms and risks associated with surgical menopause.

References

  1. International Agency for Research on Cancer. Global Cancer Observatory https://gco.iarc.fr/today (accessed 22 Jun 2025).

  2. Witjes, F. et al. European Association of Urology guidelines on muscle-invasive and metastatic bladder cancer, 2022 edition (EAU Guidelines Office, 2022).

  3. Siegel, R. L., Miller, K. D. & Jemal, A. Cancer statistics, 2018. CA Cancer J. Clin. 68, 7–30 (2018).

    PubMed  Google Scholar 

  4. Rocca, W. A., Grossardt, B. R., de Andrade, M., Malkasian, G. D. & Melton, L. J. III. Survival patterns after oophorectomy in premenopausal women: a population-based cohort study. Lancet Oncol. 7, 821–828 (2006).

    Article  PubMed  Google Scholar 

  5. Mytton, J., Evison, F., Chilton, P. J. & Lilford, R. J. Removal of all ovarian tissue versus conserving ovarian tissue at time of hysterectomy in premenopausal patients with benign disease: study using routine data and data linkage. BMJ 356, j372 (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  6. Tuesley, K. M. et al. Hysterectomy with and without oophorectomy and all-cause and cause-specific mortality. Am. J. Obstet. Gynecol. 223, 723.e1–723.e16 (2020).

    Article  PubMed  Google Scholar 

  7. Malek, A. M. et al. The association of age at menopause and all-cause and cause-specific mortality by race, postmenopausal hormone use, and smoking status. Prev. Med. Rep. 14, 100955 (2021).

    Google Scholar 

  8. Sussman, R. D. et al. To oophorectomy or not to oophorectomy: practice patterns among urologists treating bladder cancer. Urol. Oncol. 36, 90.e1–90.e7 (2018).

    Article  PubMed  Google Scholar 

  9. British Gynaecological Cancer Society, British Menopause Society. Management of menopausal symptoms following treatment of gynaecological cancer https://thebms.org.uk/publications/bms-guidelines/management-of-menopausal-symptoms-following-treatment-of-gynaecological-cancer/ (British Menopause Society, 2024).

  10. European Society of Human Reproduction and Embryology. Guideline on premature ovarian insufficiency https://www.eshre.eu/Guidelines-and-Legal/Guidelines/Premature-ovarian-insufficiency (European Society of Human Reproduction and Embryology, 2024).

  11. Panay, N. et al. Evidence-based guideline: premature ovarian insufficiency. Climacteric 27, 510–520 (2024).

    Article  CAS  PubMed  Google Scholar 

  12. Garg, A. & Robinson, L. Surgical menopause: a toolkit for healthcare professionals. British Menopause Society https://thebms.org.uk/wp-content/uploads/2024/10/13-BMS-TfC-Surgical-Menopause-SEPT2024-D.pdf (2024).

  13. Australian Menopause Society. Surgical menopause. Australian Menopause Society https://www.menopause.org.au/hp/information-sheets/surgical-menopause (accessed 1 Nov 2025).

  14. Suzuki, Y. et al. Use of estrogen therapy after surgical menopause in women who are premenopausal. Obstet. Gynecol. 139, 756–763 (2022).

    Article  CAS  PubMed  Google Scholar 

  15. Jang, J. H., Arora, N., Kwon, J. S. & Hanley, G. E. Hormone therapy use after premature surgical menopause based on prescription records: a population-based study. J. Obstet. Gynaecol. Can. 42, 1511–1517 (2020).

    Article  PubMed  Google Scholar 

  16. Wu, C., Chen, D., Stout, M. B., Wu, M. & Wang, S. Hallmarks of ovarian aging. Trends Endocrinol. Metab. 36, 418–439 (2025).

    Article  CAS  PubMed  Google Scholar 

  17. Ozdemir, S., Celik, C., Görkemli, H., Kiyici, A. & Kaya, B. Compared effects of surgical and natural menopause on climacteric symptoms, osteoporosis, and metabolic syndrome. Int. J. Gynaecol. Obstet. 106, 57–61 (2009).

    Article  PubMed  Google Scholar 

  18. Gümüşsoy, S., Öztürk, R., Keskin, G. & Özlem Yıldırım, G. Effects of surgical and natural menopause on body image, self-esteem, and dyadic adjustment: a descriptive and comparative study. Clin. Nurs. Res. 32, 712–722 (2023).

    Article  PubMed  Google Scholar 

  19. Xu, M., Yin, X. & Gong, Y. Association of premature natural and surgical menopause with incidence of depression requiring hospitalization: a prospective cohort study. Am. J. Obstet. Gynecol. 232, 543.e1–543 (2025).

    Article  PubMed  Google Scholar 

  20. Longcope, C. Endocrine function of the postmenopausal ovary. J. Soc. Gynecol. Investig. 8, S67–S68 (2001).

    Article  CAS  PubMed  Google Scholar 

  21. Thurston, R. C. & Joffe, H. Vasomotor symptoms and menopause: findings from the Study of Women’s Health across the Nation. Obstet. Gynecol. Clin. North Am. 38, 489–501 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  22. Nebgen, D. R. et al. Care after premenopausal risk-reducing salpingo-oophorectomy in high-risk women: Scoping review and international consensus recommendations. BJOG 130, 1437–1450 (2023).

    Article  PubMed  PubMed Central  Google Scholar 

  23. Price, S. A. L. et al. What happens after menopause (WHAM)? A progress report of a prospective controlled study of women after pre-menopausal risk-reducing bilateral salpingo-oophorectomy. BJOG https://doi.org/10.1111/1471-0528.18304 (2025).

    Article  PubMed  Google Scholar 

  24. Briggs, P., Medical advisory council of the British Menopause Society. BMS consensus statement genitourinary syndrome of menopause (GSM) https://thebms.org.uk/wp-content/uploads/2025/11/09-NEW-BMS-ConsensusStatement-Genitourinary-Syndrome-of-Menopause-GSM-NOV2025-B.pdf (British Menopause Society, 2025).

  25. Portman, D. J. & Gass, M. L. Vulvovaginal atrophy terminology consensus conference: genitourinary syndrome of menopause: new terminology for vulvovaginal atrophy from the International Society for the Study of Women’s Sexual Health and the North American Menopause Society. J. Sex. Med. 11, 2865 (2014).

    Article  PubMed  Google Scholar 

  26. National Institute for Health and Care Excellence. Menopause: identification and management: NICE guideline 23 https://www.nice.org.uk/guidance/ng23 (NICE, accessed 1 Nov 2025).

  27. Santoro, N., Worsley, R., Miller, K. K., Parish, S. J. & Davis, S. R. Role of estrogens and estrogen-like compounds in female sexual function and dysfunction. J. Sex. Med. 13, 305–316 (2016).

    Article  PubMed  Google Scholar 

  28. Tucker, P. E. et al. Prevalence of sexual dysfunction after risk-reducing salpingo-oophorectomy. Gynecol. Oncol. 140, 95–100 (2016).

    Article  PubMed  Google Scholar 

  29. Clements, M. B. et al. Health-related quality of life for patients undergoing radical cystectomy: results of a large prospective cohort. Eur. Urol. 81, 294–304 (2022).

    Article  PubMed  Google Scholar 

  30. Brotto, L. A. The DSM diagnostic criteria for hypoactive sexual desire disorder in women. Arch. Sex. Behav. 39, 221–239 (2010).

    Article  PubMed  Google Scholar 

  31. Leiblum, S. R. et al. Hypoactive sexual desire disorder in postmenopausal women: US results from the Women’s International Study of Health and Sexuality (WISHeS). Menopause 13, 46–56 (2006).

    Article  PubMed  Google Scholar 

  32. Dennerstein, L. et al. Hypoactive sexual desire disorder in menopausal women: a survey of Western European women. J. Sex. Med. 3, 212–222 (2006).

    Article  PubMed  Google Scholar 

  33. Rocca, W. A. et al. Association of premenopausal bilateral oophorectomy with cognitive performance and risk of mild cognitive impairment. JAMA Netw. Open 4, e2131448 (2021).

    Article  PubMed  PubMed Central  Google Scholar 

  34. Terra, L. et al. Long-term effects of premenopausal risk-reducing salpingo-oophorectomy on cognition in women with high familial risk of ovarian cancer: a cross-sectional study. BJOG 130, 968–977 (2023).

    Article  CAS  PubMed  Google Scholar 

  35. Rocca, W. A., Smith, C. Y., Gazzuola Rocca, L., Savica, R. & Mielke, M. M. Association of premenopausal bilateral oophorectomy with Parkinsonism and Parkinson disease. JAMA Netw. Open 5, e2238663 (2022).

    Article  PubMed  PubMed Central  Google Scholar 

  36. Rocca, W. A., Grossardt, B. R., Miller, V. M., Shuster, L. T. & Brown, R. D. Jr. Premature menopause or early menopause and risk of ischemic stroke. Menopause 19, 272–277 (2012).

    Article  PubMed  PubMed Central  Google Scholar 

  37. Fakkert, I. E. et al. Bone mineral density and fractures after surgical menopause: systematic review and meta-analysis. BJOG 124, 1525–1535 (2017).

    Article  CAS  PubMed  Google Scholar 

  38. Honigberg, M. C. et al. Association of premature natural and surgical menopause with incident cardiovascular disease. JAMA 322, 2411–2421 (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  39. Zhu, D. et al. Type of menopause, age of menopause and variations in the risk of incident cardiovascular disease: pooled analysis of individual data from 10 international studies. Hum. Reprod. 35, 1933–1943 (2020).

    Article  PubMed  PubMed Central  Google Scholar 

  40. Colditz, G. A. et al. Menopause and the risk of coronary heart disease in women. N. Engl. J. Med. 316, 1105–1110 (1987).

    Article  CAS  PubMed  Google Scholar 

  41. Bast, J. A. et al. Cardiovascular consequences of premature menopause. Curr. Cardiol. Rep. 27, 126 (2025).

    Article  PubMed  Google Scholar 

  42. Xing, Z. & Kirby, R. S. Age at natural or surgical menopause, all-cause mortality, and lifespan among postmenopausal women in the United States. Menopause 31, 176–185 (2024).

    Article  PubMed  Google Scholar 

  43. Erekson, E. A., Martin, D. K. & Ratner, E. S. Oophorectomy: the debate between ovarian conservation and elective oophorectomy. Menopause 20, 110–114 (2013).

    Article  PubMed  PubMed Central  Google Scholar 

  44. Gupta, N. et al. Practice patterns regarding female reproductive organ-sparing and nerve-sparing radical cystectomy among urologic oncologists in the United States. Clin. Genitourin. Can. 21, e236–e241 (2023).

    Google Scholar 

  45. Farquhar, C. M. et al. The association of hysterectomy and menopause: a prospective cohort study. BJOG 112, 956–962 (2005).

    Article  PubMed  Google Scholar 

  46. Moorman, P. G. et al. Effect of hysterectomy with ovarian preservation on ovarian function. Obstet. Gynecol. 118, 1271–1279 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  47. Salem, H. & El-Mazny, A. A clinicopathologic study of gynecologic organ involvement at radical cystectomy for bladder cancer. Int. J. Gynecol. Obstet. 115, 188–190 (2011).

    Article  Google Scholar 

  48. Whittum, M. et al. Gynecological organ involvement at robot-assisted radical cystectomy in women: is anterior exenteration necessary? Can. Urol. Assoc. J. 12, e398–e402 (2018).

    Article  PubMed  PubMed Central  Google Scholar 

  49. Taylor, B. L. et al. Gynecologic organ involvement during radical cystectomy for bladder cancer: is it time to routinely spare the ovaries? Clin. Gen. Cancer. 17, e209–e215 (2018).

    Google Scholar 

  50. Avulova, S. et al. Prevalence, predictors, and oncologic outcomes of pelvic organ involvement in women undergoing radical cystectomy. Arch. Pathol. Lab. Med. 147, 202–207 (2023).

    Article  PubMed  Google Scholar 

  51. Lobo, N. et al. Gynaecological organ involvement in women undergoing radical cystectomy: a multicentre study. BJU Int. 133, 474–479 (2024).

    Article  PubMed  Google Scholar 

  52. Bukavina, L. et al. Population estimates of ovarian cancer risk in a cohort of patients with bladder cancer. Eur. Urol. Focus 10, 298–302 (2024).

    Article  PubMed  Google Scholar 

  53. Abboud, M. A. et al. Risk of ovarian malignancy in patients undergoing radical cystectomy for bladder cancer. Urology 123, 181–185 (2019).

    Article  PubMed  Google Scholar 

  54. Kahn, R. M. et al. Salpingectomy for the primary prevention of ovarian cancer: a systematic review. JAMA Surg. 158, 1204–1211 (2023).

    Article  PubMed  PubMed Central  Google Scholar 

  55. Patel, S. H. et al. Safety and efficacy of reproductive organ-sparing radical cystectomy in women with variant histology and advanced stage. Clin. Genitourin. Can. 20, 60–68 (2021).

    CAS  Google Scholar 

  56. Lavallée, E. et al. Functional and oncological outcomes of female pelvic organ-preserving robot-assisted radical cystectomy. Eur. Urol. Open Sci. 36, 34–40 (2022).

    Article  PubMed  Google Scholar 

  57. Park, J. S. et al. Comparison of functional and oncological outcomes between uterus-sparing radical cystectomy and standard radical cystectomy in women: A retrospective study. Investig. Clin. Urol. 63, 612–622 (2022).

    Article  PubMed  PubMed Central  Google Scholar 

  58. Zhong, W. et al. Long-term survival after female pelvic organ-sparing radical cystectomy versus standard radical cystectomy: a multi-institutional propensity score-matched analysis. Int. J. Surg. 109, 2742–2750 (2023).

    Article  PubMed  PubMed Central  Google Scholar 

  59. Rautiola, J. et al. Pelvic organ-sparing robot-assisted radical cystectomy in women with bladder cancer. BJU Int. 136, 747–754 (2025).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  60. Van der Heijden, A. et al. European Association of Urology Guidelines on Muscle-invasive and Metastatic Bladder Cancer, 2025 edition (EAU Guidelines Office, 2025).

  61. Holzbeierlein, J. et al. Treatment of non-metastatic muscle-invasive bladder cancer: AUA/ASCO/SUO guideline (2017; amended 2020, 2024). J. Urol. 212, 3–10 (2024).

    Article  PubMed  Google Scholar 

  62. Czerniak, B. Bladder cancer variants — one disease with many faces. Nat. Rev. Urol. 21, 519–520 (2024).

    Article  PubMed  Google Scholar 

  63. Moursy, E. E. S. et al. Orthotopic genital sparing radical cystectomy in pre-menopausal women with muscle-invasive bladder carcinoma: a prospective study. Indian J. Urol. 32, 65–70 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  64. The North American Menopause Society. The 2022 hormone therapy position statement of the North American Menopause Society advisory panel. Menopause 29, 767–794 (2022).

    Article  Google Scholar 

  65. Smith, D. C., Prentice, R., Thompson, D. J. & Herrmann, W. L. Association of exogenous estrogen and endometrial carcinoma. N. Engl. J. Med. 293, 1164–1167 (1975).

    Article  CAS  PubMed  Google Scholar 

  66. Judd, H. L. et al. Effects of hormone replacement therapy on endometrial histology in postmenopausal women: The Postmenopausal Estrogen/Progestin Interventions (PEPI) trial. JAMA 275, 370–375 (1996).

    Article  CAS  Google Scholar 

  67. Anderson, G. L. et al. Conjugated equine oestrogen and breast cancer incidence and mortality in postmenopausal women with hysterectomy: extended follow-up of the Women’s Health Initiative randomised placebo-controlled trial. Lancet Oncol. 13, 476–486 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Goto, T. & Miyamoto, H. The role of estrogen receptors in urothelial cancer. Front. Endocrinol. 16, 643870 (2021).

    Article  Google Scholar 

  69. Hsu, C. H., Chen, J., Wu, C. Y., Cheng, A. L. & Pu, Y. S. Combination chemotherapy of cisplatin, methotrexate, vinblastine, and high-dose tamoxifen for transitional cell carcinoma. Anticancer Res. 21, 711–715 (2011).

    Google Scholar 

  70. Rovinski, D., Ramos, R. B., Fighera, T. M., Casanova, G. K. & Spritzer, P. M. Risk of venous thromboembolism events in postmenopausal women using oral versus non-oral hormone therapy: a systematic review and meta-analysis. Thromb. Res. 168, 83–95 (2018).

    Article  CAS  PubMed  Google Scholar 

  71. National Institute for Health and Care Excellence. NICE prescribing information: intravaginal oestrogen https://cks.nice.org.uk/topics/incontinence-urinary-in-women/prescribing-information/intravaginal-oestrogen/ (NICE, accessed 1 Nov 2025).

  72. Boardman, H. M. et al. Hormone therapy for preventing cardiovascular disease in post-menopausal women. Cochrane Database Syst. Rev. 10, CD002229 (2015).

    Google Scholar 

  73. Kim, J. E. et al. A systematic review and meta-analysis of effects of menopausal hormone therapy on cardiovascular diseases. Sci. Rep. 10, 20631 (2020).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  74. British Menopause Society. Management of menopause for women with cardiovascular disease http://thebms.org.uk/wp-content/uploads/2024/12/22-BMS-TfC-Management-of-menopause-for-women-with-CVD-DEC2024-A.pdf (British Menopause Society, 2024).

  75. Jiang, H. et al. Loss of bone density and bone strength following premenopausal risk-reducing bilateral salpingo-oophorectomy: a prospective controlled study (WHAM Study). Osteoporos. Int. 32, 101–112 (2021).

    Article  CAS  PubMed  Google Scholar 

  76. Rada, G. et al. Non-hormonal interventions for hot flushes in women with a history of breast cancer. Cochrane Database Syst. Rev. 8, CD004923 (2010).

    Google Scholar 

  77. Fraser, G. L. et al. A phase 2b, randomized, placebo-controlled, double-blind, dose-ranging study of the neurokinin 3 receptor antagonist fezolinetant for vasomotor symptoms associated with menopause. Menopause 27, 382–392 (2020).

    Article  PubMed  PubMed Central  Google Scholar 

  78. Edwards, D. & Panay, N. Treating vulvovaginal atrophy/genitourinary syndrome of menopause: how important is vaginal lubricant and moisturizer composition? Climacteric 19, 151–161 (2016).

    Article  CAS  PubMed  Google Scholar 

  79. Filippini, M. et al. CO2-laser therapy and genitourinary syndrome of menopause: a systematic review and meta-analysis. J. Sex. Med. 19, 452–470 (2022).

    Article  PubMed  Google Scholar 

  80. Brotto, L. A. & Altas, M. New management approaches for female sexual dysfunction. Curr. Opin. Obstet. Gynecol. 36, 372–377 (2024).

    Article  PubMed  Google Scholar 

  81. Prendergast, S. A. & Mueller, J. Pelvic floor physical therapy and female sexual dysfunction. Clin. Obstet. Gynecol. 68, 37–43 (2025).

    Article  PubMed  Google Scholar 

  82. Davis, S. R. et al. Global consensus position statement on the use of testosterone therapy for women. J. Clin. Endocrinol. Metab. 104, 4660–4666 (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  83. Parish, S. J. et al. International Society for the Study of Women’s Sexual Health clinical practice guideline for the use of systemic testosterone for hypoactive sexual desire disorder in women. J. Sex. Med. 18, 849–867 (2021).

    Article  CAS  PubMed  Google Scholar 

  84. Medicines & Healthcare products Regulatory Agency. Public Assessment Report: AndroFeme 10 mg/mL cream testosterone. https://mhraproducts4853.blob.core.windows.net/docs/6f5c86bfb5b17ab2f9f219e3ff8d0188a500e085 (accessed 1 Nov 2025).

  85. Barakeh, D., Mdaihly, H. & Karaoui, L. R. Pharmacotherapy of hypoactive sexual desire disorder in premenopausal women. Ann. Pharmacother. 59, 148–161 (2025).

    Article  CAS  PubMed  Google Scholar 

  86. Camacho, P. M. et al. American Association of Clinical Endocrinologists/American College of Endocrinology clinical practice guidelines for the diagnosis and treatment of postmenopausal osteoporosis — 2020 update. Endocr. Pract. 26, 1–46 (2020).

    Article  PubMed  Google Scholar 

  87. Hickey, M. et al. What happens after menopause? (WHAM): A prospective controlled study of cardiovascular and metabolic risk 12 months after premenopausal risk-reducing bilateral salpingo-oophorectomy. Gynecol. Oncol. 162, 88–96 (2021).

    Article  CAS  PubMed  Google Scholar 

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N.L., E.D. and F.P.B. researched data for the article. N.L., E.D. and C.M. contributed substantially to discussion of the content. N.L., E.D., F.P.B., C.M. and J.D.K. wrote the article. All authors reviewed and/or edited the manuscript before submission.

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Day, E., Bizzarri, F.P., Mackenzie, C. et al. Management of surgical menopause in female patients with bladder cancer undergoing radical cystectomy. Nat Rev Urol (2026). https://doi.org/10.1038/s41585-026-01124-z

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