SUROVA - Surgery in Ovarian Cancer, Comparing Primary and Interval Cytoreductive Surgery

University of Navarra

Status: Enrolling

Conditions: Epithelial Ovarian Cancer; Fallopian Tube Neoplasms; Peritoneal Neoplasms

Treatments: Drug: Neoadjuvant chemotherapy; Procedure: Cytoreductive surgery; Drug: Adjuvant chemotherapy

Study type: Observational

Funder types: Other

Identifiers

NCT06223763

SUROVA

Details and patient eligibility

About

An international worldwide retrospective cohort observational study comparing primary cytoreductive surgery with neoadjuvant chemotherapy and interval cytoreductive surgery in patients with carcinoma of the ovary, fallopian tubes, and peritoneum.

Full description

SUROVA study tries to compare the outcomes of primary cytoreductive surgery with neoadjuvant chemotherapy and interval cytoreductive surgery in patients with carcinoma of the ovary, fallopian tubes, and peritoneum operated between 2018 and 2019 worldwide.

The objective is to know if the surgical approach influences our patients' survival (OS and PFS). To answer this question, SUROVA is necessary.

While the prospective Trust Trial, with results expected in 2024, is designed to address this question, a limitation of this study is that it is confined to patients treated in high-end hospitals. This limitation could introduce bias in the results, as many patients may lack access to such high-level healthcare facilities. Therefore, the objective is to extend the scope of this study to real life. To achieve this, the investigators are seeking to collect data from patients treated globally during 2018 and 2019, involving both primary and interval cytoreduction.

The investigators hope that the results of this study will be subjected to evaluation at international meetings and published in reputable international journals. Authorship will be based on a rigorous criterion tied to the number of valid cases included in the study. Naturally, the aim is to include as many authors as possible.

The researchers strongly believe that patients would greatly benefit from SUROVA data and that it will address this critical question and provide invaluable insights.

Enrollment: 5,000 estimated patients

Sex: Female

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients > 18 years old.
• Eastern Cooperative Oncology Group (ECOG) Performance Status 0-1 at the time of the surgery.
• Invasive high-grade epithelial ovarian cancer, fallopian tube carcinoma, or primary peritoneal carcinoma in stage International Federation of Gynecology and Obstetrics (FIGO) IIIB-IVB (IVB only if resectable metastases are present), suspected or histologically confirmed and newly diagnosed.
• Patient underwent primary surgery or first course of neoadjuvant chemotherapy between January 1, 2018, and December 31, 2019.
• American Society of Anesthesiologists Physical Status Classification System (ASA) score 1 or 2 at the time of the surgery.
• Surgery performed by laparotomy with an attempt of maximal effort.
• The surgeon must be a certified or non-certified gynecologic oncologist.
• Based on all available information before the surgery (primary or interval), the patient was considered completely resectable.
• Adequate bone marrow function: Absolute neutrophil count (ANC) ≥ 1.5 x 109/L.
• Preoperative imaging (either CT, whole-body MRI, or positron emission tomography (PET)-CT) excluding unresectable disease as per European Society of Gynaecological Oncology (ESGO) criteria.
• Surgical report on residual disease after surgery.

Exclusion criteria

• Non-epithelial malignant ovarian neoplasms 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 before surgery (primary or interval).
• Pregnant women at the time of diagnosis.

Trial design

5,000 participants in 2 patient groups

Primary cytoreductive surgery

Description:

Patients underwent primary cytoreductive surgery between January 1, 2018, and December 31, 2019. After that, they underwent adjuvant therapy.

Treatment:

Procedure: Cytoreductive surgery

Drug: Adjuvant chemotherapy

Interval cytoreductive surgery

Description:

Patients underwent primary first course of neoadjuvant chemotherapy between January 1, 2018, and December 31, 2019. After neoadjuvant chemotherapy, the patient underwent interval cytoreductive surgery and then, adjuvant chemotherapy.

Treatment:

Drug: Neoadjuvant chemotherapy

Procedure: Cytoreductive surgery

Drug: Adjuvant chemotherapy