Risk-Reducing Surgeries for Hereditary Ovarian Cancer

Sponsor
Lei Li (Other)
Overall Status
Recruiting
CT.gov ID
NCT03294343
Collaborator
(none)
600
1
3
72
8.3

Study Details

Study Description

Brief Summary

Based on studies of "Inherited Susceptible Genes Among Epithelial Ovarian Cancer" (NCT03015376, clinicaltrials.gov) and "Cohort Study of Universal Screening for Lynch Syndrome in Chinese Patients of Endometrial Cancer" (NCT03291106, clinicaltrials.gov), we provide risk-reducing surgeries of salpingo-oophorectomy with/without hysterectomy for healthy carriers with mutation genes of hereditary ovarian cancer, which is defined ovarian cancer with relevant pathogenic mutations.

Condition or Disease Intervention/Treatment Phase
  • Procedure: salpingo-oophorectomy only by laparoscopy
  • Procedure: salpingo-oophorectomy with hysterectomy by laparoscopy
  • Other: Follow-up
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
600 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Risk-Reducing Surgeries of Salpingo-oophorectomy With/Without Hysterectomy for Carriers With Mutation Genes of Hereditary Ovarian Cancer
Actual Study Start Date :
Sep 1, 2017
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Sep 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: HBOCS

For carriers with mutation genes of BRCA1, BRCA2 (both belonging to mutation genes of hereditary breast and ovarian cancer syndrome, HBOCS) and ATM, BRIP1, RAD51, RAD51C, and RAD51D (all belonging to mutation genes of other hereditary ovarian cancer syndrome), if they demand for risk-reducing surgeries, counseling, decision-making analysis, then salpingo-oophorectomy only by laparoscopy and long-term follow-up are provided.

Procedure: salpingo-oophorectomy only by laparoscopy
Salpingo-oophorectomy are provided for carriers with mutation genes of BRCA1, BRCA2 (both belonging to mutation genes of hereditary breast and ovarian cancer syndrome, HBOCS) and ATM, BRIP1, RAD51, RAD51C, and RAD51D (all belonging to mutation genes of other hereditary ovarian cancer syndrome). Detailed multi-disciplinary counseling, decision-making analysis before surgeries, and long-term follow-up and health management after surgeries are provided for all participants.

Experimental: Lynch syndromes

for carriers with mutation genes of MLH1, MSH2, MSH6, PMS2, EPCAM (all belonging to mutation genes of Lynch syndromes) and STK11, , if they demand for risk-reducing surgeries, counseling, decision-making analysis, then salpingo-oophorectomy with hysterectomy by laparoscopy and long-term follow-up are provided.

Procedure: salpingo-oophorectomy with hysterectomy by laparoscopy
Salpingo-oophorectomy with hysterectomy are provided for carriers with mutation genes of MLH1, MSH2, MSH6, PMS2, EPCAM (all belonging to mutation genes of Lynch syndromes) and STK11. Detailed multi-disciplinary counseling, decision-making analysis before surgeries, and long-term follow-up and health management after surgeries are provided for all participants.

Other: Refusal to surgery

For carriers with any mutation genes (BRCA1, BRCA2, ATM, BRIP1, RAD51, RAD51C, RAD51D, STK11, MLH1, MSH2, MSH6, PMS2 and EPCAM) but refusal to any risk-reducing surgeries, counseling, decision-making analysis, and then long-term follow-up are provided.

Other: Follow-up
Detailed multi-disciplinary counseling, decision-making analysis and long-term follow-up are provided for carriers with any mutation genes but refusal to any risk-reducing gynecologic surgeries

Outcome Measures

Primary Outcome Measures

  1. Occult cancer or precancerous lesion in histological specimen [5 years]

    Precancerous lesions include serous tubal intraepithelial carcinoma (STIC) and endometrial intraepithelial neoplasia (EIN)

Secondary Outcome Measures

  1. Overall survival [10 years]

    Duration from surgery to death

  2. Incidence of primary peritoneal carcinoma [10 years]

    Incidence of primary peritoneal carcinoma after reception or refusal risk-reducing salpingo-oophorectomy

  3. Incidence of primary uterine cancer [10 years]

    Incidence of primary uterine cancer after reception or refusal risk-reducing hysterectomy

Eligibility Criteria

Criteria

Ages Eligible for Study:
35 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Carriers with known and definite mutation genes of hereditary ovarian cancer.

  • With children and without further requirement of pregnancy.

  • No less than 35 years for carriers with mutation gene of BRCA1.

  • No less than 40 years for carriers with mutation gene of BRCA2.

  • No less than 45 years for carriers with mutation genes of BRIP1, RAD51C, RAD51D and RAD51.

  • No less than 50 years for carriers with mutation genes of ATM, MSH2, MLH1, SH6, PMS2, EPCAM and STK11.

Exclusion Criteria:
  • Without children.

  • Not reaching appreciate ages.

  • With contraindications of laparoscopy.

  • Refusal of risk-reducing surgeries.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Lei Li Beijing China/Beiing China 100000

Sponsors and Collaborators

  • Lei Li

Investigators

  • Principal Investigator: Lei Li, MD, Peking Union Medical College Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lei Li, Professor, Peking Union Medical College Hospital
ClinicalTrials.gov Identifier:
NCT03294343
Other Study ID Numbers:
  • SOHHO
First Posted:
Sep 27, 2017
Last Update Posted:
Dec 26, 2017
Last Verified:
Dec 1, 2017
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 26, 2017