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Precision cancer medicine selection based on genomic profiling for the treatment of recurrent epithelial ovarian cancer: a prospective, randomized, multicenter clinical study

Precision cancer medicine selection based on genomic profiling for the treatment of recurrent epithelial ovarian cancer: a prospective, randomized, multicenter clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15007441
Enrollment
Unknown
Registered
2015-11-23
Start date
2016-01-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

recurrent epithelial ovarian cancer

Interventions

Empirical treatment group:treat according to NCCN Clinical Practice Guidelines for ovarian cancer
treatment according to analyis of sequencing for tumor genomic profiling:Blood and tissue samples collected from the primary surgery are analyzed via sequencing for tumor genomic profiling. Choose opt

Sponsors

Renji Hospital, School of Medicine, Shanghai Jiao Tong University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1) Female patients over 18 years of age; 2) Patients should have received optimal cytoreductive surgery with residual tumor =1.5*10^9/L Platelet count >=100 *10^9/L, ALT (SGPT) <=2-fold of the upper limit of normal, ULN Bilirubin <1.5-fold of the upper limit of normal, Creatinine <1.6 mg/dl; with a normal ejection fraction; 8) Ability andwillingness to give written informed consent.

Exclusion criteria

Exclusion criteria: 1) Non epithelial tumor or borderline tumor; 2) No recurrence patients of postoperative chemotherapy or was performed cytoreductive surgery after chemotherapy ; 3) Second kinds of tumors or other tumors received surgical treatment, the treatment and the surgical treatment will affect the treatment of recurrent ovarian cancer, or affect the prognosis of the patients; 4) The patient has received non platinum chemotherapy treatment 5) To carry out palliative surgical treatment only; 6) The combined disease is not suitable for surgery and / or chemotherapy; 7) Has been treated with radiotherapy, experimental therapy, hormone therapy, chemotherapy or biological agents; 8) Any drug known to have a severe allergic history will be used in clinical trials; 9) Past medical history showed that there were serious complications.

Design outcomes

Primary

MeasureTime frame
Overall survival;

Secondary

MeasureTime frame
Progression-free survival;Objective Response Rate;

Countries

China

Contacts

Public ContactWen Di
diwen163@163.com+86 13701642665

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026