Breast Cancer Clinical Trial

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

Summary

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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Full Description

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.

View Eligibility Criteria

Eligibility Criteria

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

Study is for people with:

Breast Cancer

Estimated Enrollment:

3000

Study ID:

NCT04294927

Recruitment Status:

Recruiting

Sponsor:

University Medical Center Nijmegen

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There are 5 Locations for this study

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Dana Farber Cancer Institute
Boston Massachusetts, 02215, United States More Info
Karen Lu
Contact
Mayo Clinic
Rochester Minnesota, 55905, United States More Info
Karen Lu
Contact
MD Anderson Cancer Centre
Houston Texas, 77030, United States More Info
Karen Lu
Contact
University of Washington
Seattle Washington, 98195, United States More Info
Elizabeth Swisher
Contact
Monash Health
Melbourne , , Australia More Info
Martha Hickey
Contact
Peter MacCallum Centre
Melbourne , , Australia More Info
Martha Hickey
Contact
Royal Womens Hospital
Melbourne , , Australia More Info
Martha Hickey
Contact
Hopital Universitaire Bruxelles
Brussel , , Belgium More Info
Maxime Fastrez
Contact
Universitair Ziekenhuis Leuven
Leuven , , Belgium More Info
Susanne Housmans
Contact
AC Camargo Cancer Centre
São Paulo , , Brazil More Info
Glauco Baiocchi
Contact
Universita di Bologna
Bologna , , Italy More Info
Myriam Perrone
Contact
San Gerardo Hospital
Monza , , Italy More Info
Robert Fruscio
Contact
Gemelli Hospital
Rome , , Italy More Info
Claudia Marchetti
Contact
Instituto Nacional de Cancerología
Mexico City , , Mexico More Info
David Cantu
Contact
Elisabeth-TweeSteden Ziekenhuis
Tilburg Brabant, , Netherlands More Info
Caroline Vos, MD
Contact
Radboudumc
Nijmegen Gelderland, , Netherlands More Info
Joanne A. de Hullu, MD, PhD
Contact
+31 (0) 24 36 16683
[email protected]
Maastricht University Medical Center
Maastricht Limburg, , Netherlands More Info
Brigitte Slangen, MD, PhD
Contact
Catharina Ziekenhuis
Eindhoven Noord-Brabant, 5623 , Netherlands More Info
Jurgen M.J. Piek, MD, PhD
Contact
[email protected]
Amsterdam University Medical Center
Amsterdam , , Netherlands More Info
Luc van Lonkhuijzen, MD, PhD
Contact
Antoni van Leeuwenhoek
Amsterdam , , Netherlands More Info
Marc van Beurden, MD, PhD
Contact
Medisch Spectrum Twente
Enschede , , Netherlands More Info
Nathalie Reesink-Peters, MD, PhD
Contact
University Medical Center Groningen
Groningen , , Netherlands More Info
Marian Mourits, MD, PhD
Contact
Medical Center Leeuwarden
Leeuwarden , , Netherlands More Info
Mirjam Apperloo, MD, PhD
Contact
Leiden University Medical Center
Leiden , , Netherlands More Info
Katja Gaarenstroom, MD, PhD
Contact
Erasmus Medical Center
Rotterdam , , Netherlands More Info
Marta Piso-Jozwiak, MD, PhD
Contact
University Medical Center Utrecht
Utrecht , , Netherlands More Info
Ronald Zweemer, Prof, MD, PhD
Contact
Maxima Medical Center
Veldhoven , , Netherlands More Info
Sjors Coppus, MD, PhD
Contact
Isala Klinieken
Zwolle , , Netherlands More Info
Arnold-Jan Kruse, MD, PhD
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Akershus University Hospital
Nordbyhagen , , Norway
Oslo University Hospital
Oslo , , Norway More Info
Anne Dorum
Contact
Stavanger Uniersity Hospital
Stavanger , , Norway More Info
Anne Dorum
Contact
Gdynia Oncology Centre
Gdynia , , Poland More Info
Maciej Stukan
Contact
Bonifraterskie Centrum Medyczne
Katowice , , Poland More Info
Monika Bodjys-Szyndlar
Contact
Medical University of Silesia
Katowice , , Poland More Info
Krzysztof Nowosielski
Contact
National Cancer Institute Warsaw
Warsaw , , Poland More Info
Agnieszka Rychlik
Contact
Karolinksa Institutet
Stockholm , , Sweden More Info
Angelique Flöter-Radestad
Contact
Hospital Británico
Montevideo , , Uruguay More Info
Santiago Scasso
Contact

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

3000

Study ID:

NCT04294927

Recruitment Status:

Recruiting

Sponsor:


University Medical Center Nijmegen

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