Abstract
Objective
To compare patient characteristics, imaging results, surgical management and prognosis of borderline ovarian tumors (BOT) between pre and postmenopausal patients.
Materials and methods
A retrospective cohort of all cases of histologically verified BOT between 1990–2018, comparing presentation, imaging, surgical procedures and recurrence. Patients were included in the postmenopausal group if they reported 12 months of amenorrhea with or without menopausal symptoms.
Results
During this 28 year study period, 66 operations were performed in which BOT was confirmed. Postmenopausal patients were 37–89 years old and premenopausal patients 18–50 years old, with an average age of 63.9 ± 13.4 and 36.2 ± 8.4 years, respectively (p < 0.001). The majority of patients in both groups were diagnosed due to abdominal pain, followed by incidental diagnosis on routine ultrasound. Imaging and CA-125 levels upon presentation were similar. Almost sixty percent of postmenopausal and 26.3% of premenopausal patients underwent laparotomy (p = 0.01), while those who underwent laparoscopy were 35.7% and 60.5%, respectively (p = 0.03). Most postmenopausal patients underwent bilateral salpingo-oophorectomy (BSO), whereas premenopausal surgeries involved cystectomy. Nearly all study patients were diagnosed in stage one. Malignant transformation occurred in 7.1% of postmenopausal patients. No malignant transformation was found in premenopausal patients.
Conclusion
BOT's present similarly in pre and postmenopausal patients. Postmenopausal patients undergo more extensive surgery, and are diagnosed in early stage disease. Despite a tendency for a more conservative approach in premenopausal patients, prognosis is similar in both groups.
Similar content being viewed by others
References
Hannibal CG, Huusom LD, Kjaerbye-Thygesen A, Tabor A, Kjaer SK. (2011)Trends in incidence of borderline ovarian tumors in Denmark 1978–2006. Acta Obstet Gynecol Scand. 90(4):305–12. Available from: https://www.ncbi.nlm.nih.gov/pubmed/21306323
Seidman JD, Horkayne-Szakaly I, Haiba M, Boice CR, Kurman RJ, Ronnett BM. (2004) The histologic type and stage distribution of ovarian carcinomas of surface epithelial origin. Int J Gynecol Pathol. 23(1):41–4. Available from: https://www.ncbi.nlm.nih.gov/pubmed/14668549
Gilks CB. (2002) Subclassification of ovarian surface epithelial tumors based on correlation of histologic and molecular pathologic data. Inter J Gynecol. 20:200–5.
Harter P, Gershenson D, Lhomme C, Lecuru F, Ledermann J, Provencher DM, et al. (2005) Gynecologic Cancer InterGroup (GCIG) consensus review for ovarian tumors of low malignant potential (borderline ovarian tumors). Int J Gynecol Cancer 24(9):S5–8. Available from: https://www.ncbi.nlm.nih.gov/pubmed/25341581
Tinelli R, Tinelli A, Tinelli FG, Cicinelli E, Malvasi A. (2006) Conservative surgery for borderline ovarian tumors: A review Gynecologic. Oncology. 185–91. Available from: https://www.ncbi.nlm.nih.gov/pubmed/16216320
Skírnisdóttir I, Garmo H, Wilander E, Holmberg L. (2008) Borderline ovarian tumors in Sweden 1960–2005: trends in incidence and age at diagnosis compared to ovarian cancer. Int J cancer. 123(8):1897–901. Available from: https://www.ncbi.nlm.nih.gov/pubmed/18661518
Ness RB, Cramer DW, Goodman MT, Kjaer SK, Mallin K, Mosgaard BJ, et al. (2002) Infertility, fertility drugs, and ovarian cancer: a pooled analysis of case-control studies. Am J Epidemiol. 155(3):217–24. Available from: https://www.ncbi.nlm.nih.gov/pubmed/11821246
Rizzuto I, Behrens RF, Smith LA (2013) Risk of ovarian cancer in women treated with ovarian stimulating drugs for infertility. John Wiley and Sons, Hoboken
Mørch LS, Løkkegaard E, Andreasen AH, Kjær SK, Lidegaard Ø. (2001) Hormone therapy and ovarian borderline tumors: a national cohort study. Cancer Causes Control. 23(1):113–20. Available from: https://www.ncbi.nlm.nih.gov/pubmed/22037908
Yazbek J, Raju KS, Ben-Nagi J, Holland T, Hillaby K, Jurkovic D.(2007) Accuracy of ultrasound subjective “pattern recognition” for the diagnosis of borderline ovarian tumors. Ultrasound Obstet Gynecol. 29(5):489–95. Available from: https://www.ncbi.nlm.nih.gov/pubmed/17444554
Longacre TA, McKenney JK, Tazelaar HD, Kempson RL, Hendrickson MR (2005 Jun) Ovarian serous tumors of low malignant potential (borderline tumors): outcome-based study of 276 patients with long-term (≥5-year) follow-up. Am J Surg Pathol 29(6):707–723
Zanetta G, Rota S, Chiari S, Bonazzi C, Bratina G, Mangioni C (2001 May 15) Behavior of borderline tumors with particular interest to persistence, recurrence, and progression to invasive carcinoma: a prospective study. J Clin Oncol 19(10):2658–2664
Karlsen NMS, Karlsen MA, Høgdall E, Nedergaard L, Christensen IJ, Høgdall C (2016 Jul 1) Relapse and disease specific survival in 1143 Danish women diagnosed with borderline ovarian tumours (BOT). Gynecol Oncol 142(1):50–53
Obermair A, Tang A, Kondalsamy-Chennakesavan S, Ngan H, Zusterzeel P, Quinn M et al (2013 Feb) Nomogram to predict the probability of relapse in patients diagnosed with borderline ovarian tumors. Int J Gynecol Cancer 23(2):264–267
Song T, Lee YY, Choi CH, Kim TJ, Lee JW, Bae DS et al (2014) Risk factors for progression to invasive carcinoma in patients with borderline ovarian tumors. Int J Gynecol Cancer 24(7):1206–1214
Ho C-L, Kurman RJ, Dehari R, Wang T-L, Shih I-M (2004) Mutations of BRAF and KRAS precede the development of ovarian serous borderline tumors. Cancer research, Belgin
Hauptmann S, Friedrich K, Redline R, Avril S (2017) Ovarian borderline tumors in the 2014 WHO classification: evolving concepts and diagnostic criteria Virchows Archiv. Springer, London
Gershenson DM, Bodurka DC, Lu KH, Nathan LC, Milojevic L, Wong KK et al (2015 Aug 20) Impact of age and primary disease site on outcome in women with low-grade serous carcinoma of the ovary or peritoneum: results of a large single-institution registry of a rare tumor. J Clin Oncol 33(24):2675–2682
Harlow SD, Gass M, Hall JE, Lobo R, Maki P, Rebar RW et al (2012 Apr) Executive summary of the Stages of Reproductive Aging Workshop + 10: addressing the unfinished agenda of staging reproductive aging. Menopause 19(4):387–395
Promoting the Health of an Aging Population.(2004) Abstracts of the 57th Annual Scientific Meeting of the Gerontological Society of America. Washington, DC, USA. Gerontologist 44:1–693. Available from: https://www.ncbi.nlm.nih.gov/pubmed/15612100
Ganer Herman H, Shalev A, Ginath S, Kerner R, Keidar R, Bar J, et al. (2015) Clinical characteristics and the risk for malignancy in postmenopausal women with adnexal torsion. Maturitas. 81(1):57–61. Available from: https://www.ncbi.nlm.nih.gov/pubmed/25804950
Zacharakis D, Thomakos N, Biliatis I, Rodolakis A, Simou M, Daskalakis G, et al. (2013) Ultrasonographic markers and preoperative CA-125 to distinguish between borderline ovarian tumors and stage I ovarian cancer. Acta Obstet Gynecol Scand. 92(3):285–92. Available from: https://www.ncbi.nlm.nih.gov/pubmed/23193945
Sobiczewski P, Dańska-Bidzińska A, Rzepka J, Kupryjańczyk J, Gujski M, Bidziński M, et al. (2012) Evaluation of selected ultrasonographic parameters and marker levels in the preoperative differentiation of borderline ovarian tumors and ovarian cancers. Arch Gynecol Obstet. 286(6):1513–9. Available from: https://www.ncbi.nlm.nih.gov/pubmed/22821506
Morotti M, Menada MV, Gillott DJ, Venturini PL, Ferrero S. (2012) The preoperative diagnosis of borderline ovarian tumors: a review of current literature. Arch Gynecol Obstet 285(4):1103–12. Available from: https://www.ncbi.nlm.nih.gov/pubmed/22210294
Nunes N, Ambler G, Foo X, Naftalin J, Widschwendter M, Jurkovic D. (2014). Use of IOTA simple rules for diagnosis of ovarian cancer: Meta-analysis. Ultrasound Obstet Gynecol 44(5):503–14. Available from: https://www.ncbi.nlm.nih.gov/pubmed/24920435
Van Calster B, Van Hoorde K, Valentin L, Testa AC, Fischerova D, Van Holsbeke C et al (2014 Oct) Evaluating the risk of ovarian cancer before surgery using the ADNEX model to differentiate between benign, borderline, early and advanced stage invasive, and secondary metastatic tumours: Prospective multicentre diagnostic study. BMJ 15:349
Ureyen I, Turan T, Cirik DA, Tasci T, Boran N, Bulbul D et al (2014 Oct) Frozen section in borderline ovarian tumors: is it reliable? Eur J Obstet Gynecol Reprod Biol 1(181):115–118
Basaran D, Salman MC, Calis P, Ozek A, Ozgul N, Usubütün A, et al. Diagnostic accuracy of intraoperative consultation (frozen section) in borderline ovarian tumours and factors associated with misdiagnosis. J Obstet Gynaecol 34(5):429–34. Available from: https://www.ncbi.nlm.nih.gov/pubmed/24734941. Accessed July 2014
Oh S, Kim R, Lee Y-K, Kim JW, Park N-H, Song Y-S. Clinicopathological aspects of patients with recurrence of borderline ovarian tumors. Obstet Gynecol Sci. 58(2):98–105. Available from: https://www.ncbi.nlm.nih.gov/pubmed/25798422. Accessed Mar 2015
Shim SH, Kim SN, Jung PS, Dong M, Kim JE, Lee SJ (2016) Impact of surgical staging on prognosis in patients with borderline ovarian tumours: A meta-analysis. Eur J Cancer. 54:84–95. Available from: https://www.ncbi.nlm.nih.gov/pubmed/26735354. Accessed Feb 2016
Ureyen I, Karalok A, Tasci T, Turkmen O, Boran N, Tulunay G, et al. The Factors Predicting Recurrence in Patients With Serous Borderline Ovarian Tumor. Int J Gynecol Cancer [Internet]. 2016 Jan 1 [cited 2020 Apr 16];26(1):66–72. Available from: https://www.ncbi.nlm.nih.gov/pubmed/26512785. Accessed Jan 2016
Trillsch F, Mahner S, Vettorazzi E, Woelber L, Reuss A, Baumann K, et al. Surgical staging and prognosis in serous borderline ovarian tumours (BOT): a subanalysis of the AGO ROBOT study. Br J Cancer. 112(4):660–6. Available from: https://www.ncbi.nlm.nih.gov/pubmed/25562434. Accessed Feb 2015
Black JD, Altwerger GH, Ratner E, Lu L, Silasi DA, Azodi M, et al. (2016) Management of borderline ovarian tumors based on patient and tumor characteristics. Gynecol Obstet Invest 81(2):169–73. Available from: https://www.ncbi.nlm.nih.gov/pubmed/26067608. Accessed Mar 2016
Song T, Lee Y-Y, Choi CH, Kim T-J, Lee J-W, Bae D-S, et al. (2015) Borderline ovarian tumor in women aged ≥ 65 years: impact on recurrence and survival. Eur J Obstet Gynecol Reprod Biol. 184:38–42. Available from: https://www.ncbi.nlm.nih.gov/pubmed/25463633. Accessed Jan 2015
Funding
This study was not funded.
Author information
Authors and Affiliations
Contributions
O. Tal: Manuscript writing, data collection, protocol development, H. Ganer Herman: Data collection, data analysis, manuscript editing, O. Gluck: Data analysis, manuscript editing, T. Levy: Data management, manuscript editing, R. Kerner: Data management, manuscript editing, J. Bar: Data management, manuscript editing, R. Sagiv: Project development, manuscript editing.
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they have no conflict of interest.
Ethical approval
The study was approved by our institutional ethical review board. As this study is based on encrypted data analysis only, informed consent was not needed.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Tal, O., Ganer Herman, H., Gluck, O. et al. Characteristics and prognosis of borderline ovarian tumors in pre and postmenopausal patients. Arch Gynecol Obstet 302, 693–698 (2020). https://doi.org/10.1007/s00404-020-05652-w
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00404-020-05652-w