Uterine Manipulator Versus No Uterine Manipulator in Endometrial Cancer Trial

NCT05687084RecruitingNAINTERVENTIONAL

Summary

Key Facts

Lead Sponsor

Universita di Verona

Enrollment

1030

Start Date

2023-01-16

Completion Date

2031-12-31

Study Type

INTERVENTIONAL

Official Title

Randomized Controlled Trial on the Oncologic Outcomes of Use Versus Not Use of the Uterine Manipulator in the Surgical Treatment of Apparent Uterine-confined Endometrial Carcinoma

Interventions

Uterine manipulator use

Conditions

Endometrial Neoplasms

Eligibility

Age Range

18 Years – 100 Years

Sex

FEMALE

Inclusion Criteria:

* Diagnosis of Endometrial Cancer of any histology (including carcinosarcoma) and grade
* Planned surgical treatment including hysterectomy and bilateral salpingo-oophorectomy (ovarian preservation in selected patients is not an exclusion criterion)
* Age ≥ 18 years
* No preoperative evidence of extrauterine disease (Clinical stage IIIA, IIIB)
* No preoperative evidence of suspicious lymph nodes (Clinical stage IIIC)
* No preoperative evidence of distant metastasis (Clinical stage IV)
* Approved and signed informed consent

Exclusion Criteria:

* Neoadjuvant therapy
* Synchronous or previous (\< 5 years) invasive cancer, not including non-melanoma skin cancer
* Fertility preservation
* World Health Organization performance score \> 2
* Uterine sarcoma
* Previous pelvic/abdominal radiotherapy, hormone therapy for cancer (\< 5 years), chemotherapy (\< 5 years), pelvic or paraaortic lymphadenectomy, or retroperitoneal surgery
* Inadequate bone marrow function (white blood cells \<3·0×109/L, platelets \<100×109/L)
* Inadequate liver function (bilirubin \>1.5×upper normal limit \[UNL\], aspartate aminotransferase, and alanine aminotransferase \>2.5 × UNL)
* Inadequate kidney function (creatinine clearance \< 60 mL per min calculated according to Cockcroft-Gault 10 or \< 50 mL per min Ethylenediaminetetraacetic acid clearance)
* Intraoperative evidence of stage IV disease

Outcome Measures

Primary Outcomes

Recurrence-free survival

Any recurrence or death related to endometrial cancer (EC) or treatment

Time frame: Each follow-up visit, up to 4 years from the day of surgery

Secondary Outcomes

Cause-specific survival

Any death related to endometrial cancer (EC) or treatment

Time frame: Each follow-up visit, up to 4 years from the day of surgery

Overall survival

Any death for any cause

Time frame: Each follow-up visit, up to 4 years from the day of surgery

Site-specific recurrence-free survival

Any recurrence per site of first recurrence

Time frame: Each follow-up visit, up to 4 years from the day of surgery

Operative time

Time between first incision and skin closure

Time frame: Day of surgery

Intraoperative blood loss

Total blood aspirate during the surgical procedure

Time frame: Day of surgery

30-day post-surgical morbidity

Perioperative (intraoperative and postoperative) complications graded based on the Clavien-Dindo classification

Time frame: 30 days after surgery

Lymphovascular space invasion

Presence of lymphovascular space invasion at definitive pathology

Time frame: Day of surgery

Peritoneal cytology

Presence of positive peritoneal cytology at definitive pathology

Time frame: Day of surgery

Quality of life indexes

The Functional Assessment of Cancer Therapy - General (FACT-G) - A 27-item questionnaire designed to measure four domains of Health-Related Quality of Life in cancer patients: Physical, social, emotional, and functional well-being. Score range 0-108. The higher the score, the better the Quality of Life.

Time frame: Each follow-up visit, up to 4 years from the day of surgery

Locations

UOC Ostetricia e Ginecologia, Azienda Ospedaliera Santa Croce e Carle, Cuneo, Italy

UOC Ostetricia e Ginecologia, Arcispedale Santa Maria Nuova, Reggio Emilia, Italy

AOUI Verona - University of Verona - Department of Obstetrics and Gynecology, Verona, Italy

Uterine Manipulator Versus No Uterine Manipulator in Endometrial Cancer Trial