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NCT Number: NCT04294927

TUBectomy With Delayed Oophorectomy in High Risk Women to Assess the Safety of Prevention

The aim of the project is to evaluate the risk-reducing salpingectomy with delayed oophorectomy as an alternative for risk-reducing salpingo-oophorectomy in high risk women with respect to ovarian cancer incidence.

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Key information

About this study

In BRCA1/2 gene mutation carriers, a risk-reducing salpingo-oophorectomy (RRSO) is recommended around the age of 40. This recommendation is based on a 10-40% life-time risk of ovarian cancer in this population and disappointing results of ovarian cancer surveillance for early detection. Moreover, the mortality rate of ovarian cancer is high. Effects of RRSO are a decrease in ovarian cancer risk (80-96%) on one hand and immediate onset of menopause and non-cancer related morbidity on the other hand. The fifty percent breast cancer risk reduction after RRSO has become disputable in the last years. Based on multiple studies showing that most high-grade serous ovarian cancers develop at the distal end of the Fallopian tube, an innovative strategy for RRSO has been developed for this study proposal: risk-reducing salpingectomy (RRS) with delayed risk-reducing oophorectomy (RRO). However, the safety of this strategy has not been proven yet. Before implementing this innovative strategy as standard care we need to investigate the long term effects on ovarian cancer incidence.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women with a class 5 (definitely pathogenic) BRCA1, BRCA2, RAD51C, RAD51D or BRIP1 germline mutation in one of the participating centers.
  • Age at inclusion;
  • BRCA1: 25-40 years
  • BRCA2: 25-45 years
  • RAD51C, RAD51D, BRIP1: 25-50 years
  • Childbearing completed
  • Presence of at least one fallopian tube
  • Participants may have a personal history of non-ovarian malignancy
  • Informed consent must be obtained and documented according to national and local regulatory requirements and the local rules followed in the institution.

Exclusion criteria

  • Postmenopausal status (natural menopause or due to treatment)
  • Wish for second stage RRO within two years after RRS
  • Legally incapable
  • Prior bilateral salpingectomy
  • A personal history of ovarian, fallopian tube or peritoneal cancer
  • Current diagnosis or treatment for malignant disease

Treatment and study plan

Risk-reducing salpingectomy with delayed oophorectomy

Procedure
  • BRCA1: RRS at age 25-40 and RRO at a maximum age of 45 (advised between 35 and 45).
  • BRCA2: RRS at age 25-45 and RRO at a maximum age of 50 (advised between age 40 and 50).
  • BRIP1, RAD51C, RAD51D: RRS at age 25-50 and RRO at a maximum age of 55 (advised between 45 and 55)

Risk-reducing salpingo-oophorectomy

Procedure
  • BRCA1 at a maximum age of 40 (advised between age 35 and 40)
  • BRCA2 at a maximum age of 45 (advised between age 40 and 45)
  • BRIP1, RAD51C, RAD51D: at a maximum age of 50 (advised between 45 and 50)

Primary outcomes

  1. High grade serous (ovarian) cancer incidence

    Time frame: Until the age of 45 for BRCA1 and 50 for BRCA2 germline mutation carriers

    High grade serous (ovarian) cancer incidence

Secondary outcomes

  1. Incidence of (pre)malignant findings in tubes/ovaries

    Time frame: 6 weeks after each surgery

    Incidence of (pre)malignant findings in tubes/ovaries at risk-reducing salpingectomy, oophorectomy and salpingo-oophorectomy.

  2. Peri-operative morbidity and mortality

    Time frame: 6 weeks after each surgery

    Peri-operative morbidity and mortality

  3. Incidence of pelvic cancer (other than ovarian cancer)

    Time frame: Up to the age of 70

    Incidence of pelvic cancer (other than ovarian cancer)

  4. Incidence of breast cancer

    Time frame: Up to the age of 70

    Incidence of breast cancer

  5. Uptake of risk reducing oophorectomy

    Time frame: Up to the age of 70

    Uptake of risk reducing oophorectomy after risk reducing salpingectomy

Other outcomes

  1. High grade serous (ovarian) cancer incidence at the age of 70

    Time frame: Up to the age of 70

    Exploratory outcome measure

Study contacts

Contact information is provided by the study sponsor or research team.

Joanne A. de Hullu, MD, PhD

CONTACT

[email protected]

+31 (0) 24 36 16683

Karen H. Lu, MD, PhD

CONTACT

[email protected]

(713) 745-8902

Sponsors and collaborators

Lead sponsor

University Medical Center Nijmegen

Other

Registry information

Official study title

TUBectomy With Delayed Oophorectomy as Alternative for Risk-reducing Salpingo-oophorectomy in High Risk Women to Assess the Safety of Prevention: TUBA-WISP II Study.

Acronym: TUBA-WISP-II

Important dates

Study start
2020
Primary completion
2040
Study completion
2040
First posted
Mar 4, 2020
Registry last updated
Apr 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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