ULTRA-LAP Trial: Laparoscopic Debulking Surgery (LDS) in Advanced Ovarian Cancer

Ovarian Cancer Clinical Trial

— ULTRA-LAP  

Official title:

ULTRA-LAP Trial: Laparoscopic Debulking Surgery (LDS) in Advanced Ovarian Cancer: a Feasibility Prospective Study

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05862740
• Other study ID #: 5497/AO/22
• Secondary ID: AOP2674
• Status: Recruiting
• Phase: N/A
• Start date: January 2, 2022
• Est. completion date: December 31, 2027

Study information

• Verified date: May 2023
• Source: Azienda Ospedaliera di Padova
• Contact: Matteo Marchetti, Doctor
• Phone: 0039-049-8213445
• Email: matteomarchetti91[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

ULTRA-LAP is a prospective study is to investigate the safety, efficacy and feasibility of laparoscopic debulking surgery (LDS) for the treatment of patients with advanced ovarian cancer.

The outcomes to measure are:

• Safety: the rate of patients experiencing intra- and post-operative early and late morbidities (within the hospitalization and up to 60 days from surgery)

• Efficacy: the rate of patients in which the surgical target set pre-operatively (complete resection) is achieved by laparoscopy.

• Feasibility: the rate of patients who have their procedure completed by laparoscopy

Patients will undergo laparoscopic debulking surgery (LDS) if the surgical target can be met. If it cannot be achieved by laparoscopy the surgeon will convert to laparotomy.

Description:

The investigators intend to perform a prospective feasibility study on patients with primary diagnosis of advanced ovarian cancer (stage II to IV according to FIGO classification) who are referred to the tertiary cancer centre of the study. The latter is the Department of Gynecology and Obstetrics - Division of Women's and Children's Health - University of Padova

• Italy. The statistical sample size calculation identified a minimum of 62 patients. The anticipated enrollment period will be about 4 years.

To confirm the ultimate eligibility to surgery and recruitment in the study, all patients undergo an exploratory laparoscopy (EXL).

The ideal surgical target is complete resection (CR) of all visible disease. Patients who are deemed not amenable to a CR at EXL will start neo-adjuvant chemotherapy. They will be reconsidered for the ULTRA-LAP study at time of interval surgery after 3 cycles of chemotherapy. Criteria for eligibility after neo-adjuvant chemotherapy are the same as per up-front surgery.

All patients recruited in the ULTRA-LAP trial will be discussed at Gynaecologic Oncology Multidisciplinary team (MDT) meeting, where imaging is reviewed and management is agreed. Following MDT decision:

• A Gynaecologic Oncologist will discuss the standard management and the ULTRA-LAP trial at time of out-patient clinic

• The ULTRA-LAP leaflet and consent form will be provided to the patient together with an accurate explanation of the study

• If the patient accepts to enter the study, a study registration form will be filled

• Participation in the study will be confirmed and the forms signed at time of pre-operative assessment and again confirmed at time of in-patient admission ULTRA-LAP trail will include all surgical procedures necessary to accomplish a complete resection (CR) of disease. The most common procedures necessary to obtain a CR are defined by The European Society of Gynaecological Oncology (ESGO), Society of Gynecologic Oncology (SGO) and the The National Institute for Health and Care Excellence (NICE) guidelines. All procedures will be performed by an expert Gynaecologic Oncologist with proven experience and high skills levels in oncological surgery. Once the surgeon realizes that a CR could not be achieved by laparoscopy, but prove to be feasible by laparotomy, the surgery is immediately converted to laparotomy.

Subsequent follow-up:

1. During Recovery:

• The patients are going to be monitored daily and any relevant complications will be registered, graded (according to Clavien-Dindo classification) and treated.

2. Post recovery:

• 1 st follow-up visit: At time of hospital's discharge an examination will be performed and, if necessary, further exams will be prescribed as appropriate.

• 2 nd follow-up visit: following discharge, the next appointment is in the outpatient clinic roughly 15-20 days from the surgery.

• 3 rd and last visit: at 30 days from the surgery a further appointment will be carried.

At each follow-up appointment the following will be registered:

• Occurrence of complications

• Physical examination

• Changes in normal quality of life.

Achievement of a CR will be determined at time of surgery and confirmed by a pre-chemotherapy CT scan. Should discrepancy arise, CT scan will be reviewed at MDT.

All patients will be closely monitored with a rigorous follow-up program every 90 days for the first two years and then every 120 days for the subsequent 2 years. In addition, all patient could contact the department if any unexpected complications happens between follow-up time.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 62
• Est. completion date: December 31, 2027
• Est. primary completion date: December 31, 2026
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with advanced epithelial ovarian cancer (II-IV Stage FIGO) candidates to PDS (primary debulking surgery) or IDS (interval debulking surgery: neoadjuvant chemotherapy followed by IDS).

• Participant is willing and able to give informed consent for participation in the study.

• Female aged 18 years or above.

• Primary diagnosis of advanced epithelial ovarian cancer (tubal and peritoneal cancer included).

Exclusion Criteria:

• Comorbidities non-allowing for radical surgery

• Poor Performance Status (Karnofsky Index < 70)

• Concomitant or past history of malignancy, regardless of treatment status

• Recent or past story of pancreatitis or hepatitis

• Recent or past story of pleural effusion or lung injuries or respiratory failure

• Cardiac major pathologies

Related Conditions & MeSH terms

• Carcinoma, Ovarian Epithelial
• Ovarian Cancer
• Ovarian Neoplasms

Intervention

Procedure:
• Laparoscopic Debulking Surgery in advanced ovarian cancer
Laparoscopic debulking will be conducted until the surgical target is achieved or the operation is converted to laparotomy.
• Standard laparotomic Debulking Surgery in advanced ovarian cancer
Debulking by laparotomy in patients when debulking could not be accomplished by laparoscopy.

Locations

Country	Name	City	State
Italy	Azienda Ospedaliera Universitaria di Padova,	Padova	Padova, Veneto

Sponsors (2)

Lead Sponsor	Collaborator
Azienda Ospedaliera di Padova	University of Padova

Country where clinical trial is conducted

Italy, 

References & Publications (5)

Elattar A, Bryant A, Winter-Roach BA, Hatem M, Naik R. Optimal primary surgical treatment for advanced epithelial ovarian cancer. Cochrane Database Syst Rev. 2011 Aug 10;2011(8):CD007565. doi: 10.1002/14651858.CD007565.pub2. — View Citation

Elstrand MB, Sandstad B, Oksefjell H, Davidson B, Trope CG. Prognostic significance of residual tumor in patients with epithelial ovarian carcinoma stage IV in a 20 year perspective. Acta Obstet Gynecol Scand. 2012 Mar;91(3):308-17. doi: 10.1111/j.1600-04 — View Citation

Fagotti A, Gueli Alletti S, Corrado G, Cola E, Vizza E, Vieira M, Andrade CE, Tsunoda A, Favero G, Zapardiel I, Pasciuto T, Scambia G. The INTERNATIONAL MISSION study: minimally invasive surgery in ovarian neoplasms after neoadjuvant chemotherapy. Int J G — View Citation

Pomel C, Akladios C, Lambaudie E, Rouzier R, Ferron G, Lecuru F, Classe JM, Fourchotte V, Paillocher N, Wattiez A, Montoriol PF, Thivat E, Beguinot M, Canis M. Laparoscopic management of advanced epithelial ovarian cancer after neoadjuvant chemotherapy: a — View Citation

Shih KK, Chi DS. Maximal cytoreductive effort in epithelial ovarian cancer surgery. J Gynecol Oncol. 2010 Jun;21(2):75-80. doi: 10.3802/jgo.2010.21.2.75. Epub 2010 Jun 30. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety: rate of complications/morbidities	Safety will be measured as the rate of patients experiencing intra- and post-operative early and late morbidities (within and after the hospitalization up to 60 days from surgery) and it will be compared to the morbidity rate of patients having similar surgery by laparotomy. Complications are going to be graded according to Clavien-Dindo classification.	60 days
Primary	Efficacy: rate of complete resection (CR) in group 1	Efficacy will be measured as the rate of patients in which the surgical target set pre-operatively is achieved by laparoscopy.	60 days
Primary	Feasibility: rate of procedures completed by laparoscopy	Feasibility will be measured as the rate of patients who have their procedure completed by laparoscopy.	60 days
Secondary	Progression Free Survival (PFS).	the time interval from the surgical treatment to the date of the documented first recurrence of disease, by CA 125 (Carbohydrate Antigen 125) and/or CT scan.	5 years
Secondary	Overall Survival (OS).	time between surgery and death.	5 years