Trial on Radical Upfront Surgery in Advanced Ovarian Cancer

Ovarian Cancer Clinical Trial

— TRUST  

Official title:

Trial on Radical Upfront Surgery in Advanced Ovarian Cancer

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02828618
• Other study ID #: AGO-OVAR OP.7/TRUST
• Status: Active, not recruiting
• Phase: N/A
• Start date: July 2016
• Est. completion date: February 2025

Study information

• Verified date: May 2024
• Source: AGO Study Group
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study consists of three parts, whereas Part 1 and Part 2 are performed in Germany only, and Part 3 is a multinational trial. All patients with suspicion of advanced ovarian cancer are detected in the participating study centers in a pre-screening. The study centers will register all patients with suspected ovarian cancer in a screening log. After the patients have given informed consent, they can be enrolled in different parts of the study. TRUST-Trial: This part compares two strategies in the therapy of advanced ovarian cancer. En detail, this part of the trial will evaluate if one of two strategies of timing surgery within the therapeutic procedures may show any significant advances in terms of overall survival over the other.

Description:

Both randomised groups are treated with surgery for complete resection following guideline recommendations and including median laparotomy, complete adhesiolysis, hysterectomy, bilateral salpingo-oophorectomy, omentectomy and (partial) resection of all affected organs (e.g. small or large bowel, peritoneum, spleen, pancreas, peritoneum, urinary tract etc.) as well as pelvic and paraaortic lymphadenectomy if indicated. Patients with significant pleural effusion (>500 mL in the right chest or any pleural effusion in the left chest, assessed either through ultrasound or CT scan) need to undergo video assisted thoracoscopy or open assessment of the pleura prior or during debulking surgery to detect and if possible remove intrathoracic disease. Group 1: Primary debulking surgery Patients allocated to the primary debulking group undergo surgery followed by 6 cycles of platinum and taxane based chemotherapy. Recommended systemic treatment Group 1: It is recommended to start systemic treatment after sufficient regeneration from surgery [45], which will be ideally 2 to 6 weeks (but at the latest 8 weeks) after surgery. The following treatments are recommended: 1. Participation in a prospective randomized trial, as long as participation is possible in case of randomization in either arm of the current study 2. Carboplatin AUC 5-6 / paclitaxel 175 mg/m² q21 / bevacizumab 15mg/KG q21, 6 cycles followed by bevacizumab maintenance therapy for a total of 15 months or until disease progression. 3. Carboplatin AUC 5-6 / paclitaxel 175 mg/m² q21, 6 cycles. Substitution of paclitaxel by docetaxel (75mg/m²) in cases of contraindications to paclitaxel is possible. Maintenance/consolidation therapy inside prospective trials or according to national standard treatments is allowed. Additional treatment outside prospective studies is not recommended. 4. Carboplatin AUC 5 - 6, q21 , 6 cycles in the case of contraindications of combination chemotherapy Group 2: Interval debulking surgery Patients allocated to the interval debulking surgery group undergo biopsy to confirm ovarian cancer and then 3 cycles of neoadjuvant preoperative platinum and taxane based chemotherapy. Then interval debulking surgery is performed followed by 3 cycles of postoperative platinum and taxane based chemotherapy Recommended systemic treatment Group 2: It is recommended to start systemic treatment as soon as possible after biopsy confirmation of ovarian cancer. The following treatments are recommended for neoadjuvant chemotherapy: 1. Participation in a prospective randomized trial, as long as participation is possible in case of randomization in either arm of the current study 2. Carboplatin AUC5-6 / paclitaxel 175 mg/m² q21, 3 cycles. Substitution of paclitaxel by docetaxel (75mg/m²) in cases of contraindications to paclitaxel is possible. 3. Carboplatin AUC 5-6, q21 , 3 cycles in the case of contraindications of combination chemotherapy It is recommended to start postoperative chemotherapy after sufficient regeneration from interval debulking surgery, which will be ideally 2 to 6 weeks after surgery. The following treatments are recommended: 1. Participation in a prospective randomized trial, as long as participation is possible in case of randomization in either arm of the current study 2. Carboplatin AUC 5-6 / paclitaxel 175 mg/m² q21 / bevacizumab 15mg/KG q21, 3 cycles followed by bevacizumab maintenance therapy for a total of 15 months or until disease progression. 3. Carboplatin AUC5-6 / paclitaxel 175 mg/m² q21, 3 cycles. Substitution of paclitaxel by docetaxel (75mg/m²) in cases of contraindications to paclitaxel is possible. Maintenance/consolidation therapy inside prospective trials or according to national standard treatments is allowed. Additional treatment outside prospective studies is not recommended. 4. Carboplatin AUC 5-6, q21 , 3 cycles in the case of contraindications of combination chemotherapy

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 797
• Est. completion date: February 2025
• Est. primary completion date: December 2024
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• suspected or histologically confirmed, newly diagnosed invasive epithelial ovarian cancer FIGO stage IIIB-IV (IV only if resectable metastasis)
• Females aged = 18 years
• Patients who have given their written informed consent
• Good performance status (ECOG 0/1)
• Good ASA score (1/2)
• Preoperative CA 125/CEA ratio = 25 (if CA-125 is elevated)*
• If <25 and/or biopsy with non-serous, non-endometroid histology, esophago-gastro-duodenoscopy (EGD) and colonoscopy mandatory to exclude gastrointestinal primary cancer
• Assessment of an experienced surgeon, that based on all available information, the patient can undergo the procedure and the tumor can potentially be completely resected
• Adequate bone marrow function: Absolute neutrophil count (ANC) = 1.5 x 109/L. This ANC cannot have been induced or supported by granulocyte colony stimulating factors.
• Platelet count = 100 x 109/L.
• Renal function: Serum-Creatinine = 1.5 x institutional upper limit normal (ULN).
• Hepatic function:
• Bilirubin = 1.5 x ULN.
• SGOT = 3 x ULN
• Alkaline phosphatase = 2.5 x ULN.
• Neurologic function: Neuropathy (sensory and motor) less than or equal to CTCAE Grade 1.

Exclusion Criteria:

• Non epithelial ovarian malignancies and borderline tumors
• Secondary invasive neoplasms in the last 5 years (except synchronal endometrial carcinoma FIGO IA G1/2, non melanoma skin cancer, breast cancer T1 N0 M0 G1/2) or with any signs of relapse or activity.
• Recurrent ovarian cancer
• Prior chemotherapy for ovarian cancer or abdominal/pelvic radiotherapy
• Unresectable parenchymal lung metastasis, liver metastasis or bulky lymph-nodes in the mediastinum in CT chest and abdomen/pelvis
• Clinical relevant dysfunctions of blood clotting (including drug induced)
• Any significant medical reasons, age or performance status that will not allow to perform the study procedures (estimation of investigator)
• Pregnancy
• Dementia or significantly altered mental status that would prohibit the understanding and giving of informed consent
• Any reasons interfering with regular follow-up

Related Conditions & MeSH terms

• Carcinoma, Ovarian Epithelial
• Ovarian Cancer
• Ovarian Neoplasms

Intervention

Procedure:
• PDS (Primary Debulkdung Surgery)
PDS with maximum effort to achieve the goal of complete gross resection
• 6 cycles of standard chemotherapy
6 cycles of standard chemotherapy after Primary Debuling Surgery
• Timing of surgery after 3 cycles of standard NACT, IDS
Timing of surgery after 3 cycles of standard NACT
• IDS
IDS with maximum effort to achieve the goal of complete gross resection after NACT

Drug:
• 3 cycles of standard chemotherapy
3 more cycles (for a total of 6) of standard chemotherapy after IDS

Locations

Country	Name	City	State
Austria	Medical University of Vienna	Vienna
Denmark	University Hospital, Rigshospitalet	Copenhagen
France	Institut Bergonié	Bordeaux
France	Hôpital Européen Georges Pompidou (HEGP)	Paris
France	Institute Gustave Roussy	Villejuif
Germany	Charité - Universitätsmedizin Berlin, Campus Virchow Klinikum, Klinik für Gynäkologie	Berlin
Germany	Universitätsklinikum Carl Gustav Carus Dresden, Klinik & Poliklinik f. Frauenheilkunde & Geburtshilfe	Dresden
Germany	Kaiserswerther Diakonie; Florence-Nightingale-Hospital	Dusseldorf
Germany	Kliniken Essen-Mitte, Evang. Huyssens-Stiftung, Klinik für Gynäkologie und gyn. Onkologie	Essen
Germany	Universitätsklinikum Hamburg-Eppendorf, Klinik und Poliklinik für Gynäkologie	Hamburg
Germany	Klinik und Poliklinik für Frauenheilkunde und Geburtshilfe, Klinikum der Universität München	München
Germany	Klinikum rechts der Isar, Frauen- und Poliklinik	München
Germany	Universitätsklinikum Tübingen	Tübingen
Italy	European Institute of Oncology; Gynecologic Cancer Surgery	Milano
Italy	Fondazione IRCCS Istituto Nazionale Tumori - Milan	Milano
Italy	Istituto Nazionale per lo Studio e la Cura dei Tumori di Napoli	Naples
Sweden	Skane University Hospital	Lund
Sweden	Karolinska University Hospital	Solna
United Kingdom	Imperial College London, Hammersmith Hospital, Surgery&Cancer	London
United States	Memorial Sloan Kettering Cancer Center	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
AGO Study Group

Countries where clinical trial is conducted

United States,  Austria,  Denmark,  France,  Germany,  Italy,  Sweden,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	overall survival (OS)	To compare the overall survival (OS) after primary debulking surgery (PDS) versus interval debulking surgery (IDS) following neoadjuvant chemotherapy (NACT) in patients with FIGO (2014) stage IIIB-IVB ovarian, tubal, and peritoneal carcinoma.; The primary endpoint overall survival time is calculated from the date of randomization until the date of death from any cause or date of last contact (censored observation).	Patients will be followed up for a minimum of 5 years after registration/randomisation or until death
Secondary	Progression-free survival (PFS)	Progression-free survival time is calculated from the date of randomization until the date of first progressive disease or death, whichever occurs first or date of last contact (censored observation). Progressive disease is defined as clinical or imaging-detected tumor progression or death in cases without prior documented tumor progression.	Patients will be followed up for a minimum of 5 years after registration/randomisation or until death
Secondary	Progression-free survival 2 (PFS2)	PFS2 time is calculated from the date of randomization until the date of second progressive disease or death, whichever occurs first or date of last contact (censored observation).	Patients will be followed up for a minimum of 5 years after registration/randomisation or until death
Secondary	Time to first subsequent anticancer therapy or death (TFST)	Time to first subsequent anticancer therapy is calculated from the date of randomization until the starting date of the first subsequent anticancer therapy or death, whichever occurs first or date of last contact (censored observation). Maintenance treatments following a cytostatic treatment are not considered separate treatment lines.	Patients will be followed up for a minimum of 5 years after registration/randomisation or until death
Secondary	Time to second subsequent anticancer therapy or death (TSST)	Time to second subsequent anticancer therapy is calculated from the date of randomization until the starting date of the second subsequent anticancer therapy or death, whichever occurs first or date of last contact (censored observation). Maintenance treatments following a cytostatic treatment are not considered separate treatment lines.	Patients will be followed up for a minimum of 5 years after registration/randomisation or until death
Secondary	Quality of life (QoL)	Quality of life (QoL) as measured by EORTC QLQ-C30 (Version 3), EORTC QLQ-OV28, EQ-5D-3L	Patients will be followed up for a minimum of 5 years after registration/randomisation or until death
Secondary	Documentation of surgical complications	Assessment of safety: documentation of surgical complications 28 days after surgery and 1 year after surgery.	Patients will be followed up for 1 year after surgery or until death