Evidence - Salpingectomy, laparoscopic, robot-assisted laparoscopy (DaVinci)

  1. Indication for salpingectomy

    • Opportunistic salpingectomy
    • Sterilization
    • Therapeutic salpingectomy
  2. Opportunistic salpingectomy

    Opportunistic salpingectomy, also an oncological prophylactic salpingectomy for ovarian cancer reduction. Approximately 7,000 women are diagnosed with ovarian cancer annually in Germany. In most cases, the cancer is detected at an advanced stage (FIGO III-IV, about 70%), resulting in a poor prognosis. Additionally, there is no good early detection method.

    In 2010, the British Columbia Ovarian Cancer Research (OVCARE) team proposed prophylactic salpingectomy as a strategy for primary prevention of ovarian cancer, based on the following observations:

    • Carcinogenesis: Most ovarian carcinomas, especially high-grade serous carcinoma, originate from the epithelium of the distal fallopian tube and not from the ovary itself.
    • In patients at high risk for ovarian cancer (e.g., patients with BRCA1 and BRCA2 mutations), a risk-reducing bilateral salpingo-oophorectomy was performed, where occult fallopian tube carcinomas and/or premalignant lesions were found in the fallopian tube, which could not be found in the ovary.
    • Premalignant lesions were also found in the fallopian tubes of patients with average risk. Here, a salpingectomy was performed for benign reasons, such as sterilization or hysterectomy.
    • It was shown that the involvement of the fallopian tubes was up to 75 percent in patients diagnosed with ovarian or primary peritoneal serous carcinoma (with and without BRCA mutations), including the presence of fimbrial precancers up to 60 percent.
    • Tubal ligation can also reduce the risk of ovarian cancer, with large retrospective studies showing a greater risk reduction for non-serous histologies (particularly endometrioid and clear cell carcinomas).

    Mechanisms of risk reduction:

    • Removal of the initial site of carcinogenesis (high-grade serous carcinomas)
    • Removal of the tube for the passage of endometriotic or endosalpingiotic cells (clear cell and endometrioid carcinomas)
    • Removal of the tube for the passage of carcinogens (e.g., talc) or inflammation (e.g., pelvic infection) before reaching the ovary.

    The indication for bilateral opportunistic salpingectomy should only be made for patients undergoing pelvic surgery for another reason (e.g., hysterectomy for benign disease, permanent sterilization) and who have completed family planning. In patients at high risk for cancers of the fallopian tube, ovary, and peritoneum (e.g., BRCA gene mutation, Lynch syndrome), a risk-reducing bilateral salpingo-oophorectomy should be considered after a benefit-risk assessment.

    Many studies have examined the perioperative course after an opportunistic salpingectomy:

    • Extension of surgery time by about 10-16 minutes
    • Blood loss: no difference
    • Hospital stay: no difference
    • Perioperative complications (infections, blood draws, rounds, further diagnostics): no difference
    • Menopause: Onset of menopause was the same in both groups. However, one study showed that the Anti-Müllerian hormone was slightly lower in the salpingectomy group.

    Risk reduction of developing ovarian cancer:

    A meta-analysis showed that with a follow-up period of 18-36 years, a prophylactic bilateral salpingectomy versus no salpingectomy reduced the risk by almost 50 percent adjusted to the study population. Overall, the risk of developing ovarian cancer was very low in both groups (0.8 and 0.7 percent, respectively).

     

    Reference:

    1. Center for Cancer Registry Data: Ovarian Cancer (Ovarian Carcinoma). www.krebsdaten.de/Krebs/DE/Content/Krebsarten/Eierstockkrebs/eierstockkrebs_node.html (last accessed on 7 February 2022).
    2. Homepage. OVCARE. Available at: www.ovcare.ca (Accessed on September 08, 2021).
    3. Crum CP, Drapkin R, Kindelberger D, et al. Lessons from BRCA: the tubal fimbria emerges as an origin for pelvic serous cancer. Clin Med Res 2007; 5:35.
    4. Crum CP, Drapkin R, Miron A, et al. The distal fallopian tube: a new model for pelvic serous carcinogenesis. Curr Opin Obstet Gynecol 2007; 19:3.
    5. Piek JM, van Diest PJ, Zweemer RP, et al. Dysplastic changes in prophylactically removed Fallopian tubes of women predisposed to developing ovarian cancer. J Pathol 2001; 195:451.
    6. Tobacman JK, Greene MH, Tucker MA, et al. Intra-abdominal carcinomatosis after prophylactic oophorectomy in ovarian-cancer-prone families. Lancet 1982; 2:795.
    7. Piver MS, Jishi MF, Tsukada Y, Nava G. Primary peritoneal carcinoma after prophylactic oophorectomy in women with a family history of ovarian cancer. A report of the Gilda Radner Familial Ovarian Cancer Registry. Cancer 1993; 71:2751.
    8. Struewing JP, Watson P, Easton DF, et al. Prophylactic oophorectomy in inherited breast/ovarian cancer families. J Natl Cancer Inst Monogr 1995; :33.
    9. Powell CB, Chen LM, McLennan J, et al. Risk-reducing salpingo-oophorectomy (RRSO) in BRCA mutation carriers: experience with a consecutive series of 111 patients using a standardized surgical-pathological protocol. Int J Gynecol Cancer 2011; 21:846.
    10. Powell CB, Swisher EM, Cass I, et al. Long term follow up of BRCA1 and BRCA2 mutation carriers with unsuspected neoplasia identified at risk reducing salpingo-oophorectomy. Gynecol Oncol 2013; 129:364.
    11. Reitsma W, de Bock GH, Oosterwijk JC, et al. Support of the 'fallopian tube hypothesis' in a prospective series of risk-reducing salpingo-oophorectomy specimens. Eur J Cancer 2013; 49:132.
    12. Wethington SL, Park KJ, Soslow RA, et al. Clinical outcome of isolated serous tubal intraepithelial carcinomas (STIC). Int J Gynecol Cancer 2013; 23:1603.
    13. Finch A, Shaw P, Rosen B, et al. Clinical and pathologic findings of prophylactic salpingo-oophorectomies in 159 BRCA1 and BRCA2 carriers. Gynecol Oncol 2006; 100:58.
    14. Medeiros F, Muto MG, Lee Y, et al. The tubal fimbria is a preferred site for early adenocarcinoma in women with familial ovarian cancer syndrome. Am J Surg Pathol 2006; 30:230.
    15. Colgan TJ, Murphy J, Cole DE, et al. Occult carcinoma in prophylactic oophorectomy specimens: prevalence and association with BRCA germline mutation status. Am J Surg Pathol 2001; 25:1283.
    16. Callahan MJ, Crum CP, Medeiros F, et al. Primary fallopian tube malignancies in BRCA-positive women undergoing surgery for ovarian cancer risk reduction. J Clin Oncol 2007; 25:3985.
    17. Gilks CB, Irving J, Köbel M, et al. Incidental nonuterine high-grade serous carcinomas arise in the fallopian tube in most cases: further evidence for the tubal origin of high-grade serous carcinomas. Am J Surg Pathol 2015; 39:357.
    18. Morrison JC, Blanco LZ Jr, Vang R, Ronnett BM. Incidental serous tubal intraepithelial carcinoma and early invasive serous carcinoma in the nonprophylactic setting: analysis of a case series. Am J Surg Pathol 2015; 39:442.
    19. Nishida N, Murakami F, Higaki K. Detection of serous precursor lesions in resected fallopian tubes from patients with benign diseases and a relatively low risk for ovarian cancer. Pathol Int 2016; 66:337.
    20. Rabban JT, Garg K, Crawford B, et al. Early detection of high-grade tubal serous carcinoma in women at low risk for hereditary breast and ovarian cancer syndrome by systematic examination of fallopian tubes incidentally removed during benign surgery. Am J Surg Pathol 2014; 38:729.
    21. Powell CB, Kenley E, Chen LM, et al. Risk-reducing salpingo-oophorectomy in BRCA mutation carriers: role of serial sectioning in the detection of occult malignancy. J Clin Oncol 2005; 23:127.
    22. Kindelberger DW, Lee Y, Miron A, et al. Intraepithelial carcinoma of the fimbria and pelvic serous carcinoma: Evidence for a causal relationship. Am J Surg Pathol 2007; 31:161.
    23. Carlson JW, Miron A, Jarboe EA, et al. Serous tubal intraepithelial carcinoma: its potential role in primary peritoneal serous carcinoma and serous cancer prevention. J Clin Oncol 2008; 26:4160.
    24. Seidman JD, Zhao P, Yemelyanova A. "Primary peritoneal" high-grade serous carcinoma is very likely metastatic from serous tubal intraepithelial carcinoma: assessing the new paradigm of ovarian and pelvic serous carcinogenesis and its implications for screening for ovarian cancer. Gynecol Oncol 2011; 120:470.
    25. Salvador S, Rempel A, Soslow RA, et al. Chromosomal instability in fallopian tube precursor lesions of serous carcinoma and frequent monoclonality of synchronous ovarian and fallopian tube mucosal serous carcinoma. Gynecol Oncol 2008; 110:408.
    26. McLaughlin JR, Risch HA, Lubinski J, et al. Reproductive risk factors for ovarian cancer in carriers of BRCA1 or BRCA2 mutations: a case-control study. Lancet Oncol 2007; 8:26.
    27. Rice MS, Hankinson SE, Tworoger SS. Tubal ligation, hysterectomy, unilateral oophorectomy, and risk of ovarian cancer in the Nurses' Health Studies. Fertil Steril 2014; 102:192.
    28. Sieh W, Salvador S, McGuire V, et al. Tubal ligation and risk of ovarian cancer subtypes: a pooled analysis of case-control studies. Int J Epidemiol 2013; 42:579.
    29. Tone AA, Salvador S, Finlayson SJ, et al. The role of the fallopian tube in ovarian cancer. Clin Adv Hematol Oncol 2012; 10:296.
    30. Garrett LA, Growdon WB, Goodman A, et al. Endometriosis-associated ovarian malignancy: a retrospective analysis of presentation, treatment, and outcome. J Reprod Med 2013; 58:469.
    31. Wiegand KC, Hennessy BT, Leung S, et al. A functional proteogenomic analysis of endometrioid and clear cell carcinomas using reverse phase protein array and mutation analysis: protein expression is histotype-specific and loss of ARID1A/BAF250a is associated with AKT phosphorylation. BMC Cancer 2014; 14:120.
    32. Menon U, Gentry-Maharaj A, Burnell M, et al. Ovarian cancer population screening and mortality after long-term follow-up in the UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS): a randomised controlled trial. Lancet 2021; 397:2182.
    33. McAlpine JN, Hanley GE, Woo MM, et al. Opportunistic salpingectomy: uptake, risks, and complications of a regional initiative for ovarian cancer prevention. Am J Obstet Gynecol 2014; 210:471.e1.
    34. Garcia C, Martin M, Tucker LY, et al. Experience With Opportunistic Salpingectomy in a Large, Community-Based Health System in the United States. Obstet Gynecol 2016; 128:277.
    35. Hanley GE, Kwon JS, Finlayson SJ, et al. Extending the safety evidence for opportunistic salpingectomy in prevention of ovarian cancer: a cohort study from British Columbia, Canada. Am J Obstet Gynecol 2018; 219:172.e1.
    36. Yoon SH, Kim SN, Shim SH, et al. Bilateral salpingectomy can reduce the risk of ovarian cancer in the general population: A meta-analysis. Eur J Cancer 2016; 55:38.
    37. Hanley GE, Kwon JS, McAlpine JN, et al. Examining indicators of early menopause following opportunistic salpingectomy: a cohort study from British Columbia, Canada. Am J Obstet Gynecol 2020; 223:221.e1.
Sterilization

A complete salpingectomy is not a classic method for sterilization, although the complete salpingec

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