Skip to content

Rectosigmoid Lesion Excision vs. Resection: A Non-Inferiority Randomized Comparison in Advanced Ovarian Cancer

A Prospective Randomized Controlled Non-Inferiority Study Comparing the Efficacy of Lesion Excision Versus Rectosigmoid Resection in Pelvic Cytoreductive Surgery for Advanced Ovarian Cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07616310
Acronym
RSEnTrail
Enrollment
300
Registered
2026-06-01
Start date
2024-01-10
Completion date
2028-12-31
Last updated
2026-06-01

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

Conditions

Ovarian Cancer (OvCa)

Keywords

Rectosigmoid Resection, Rectosigmoid Lesion Excision

Brief summary

Colorectum is the most common site of metastasis in ovarian cancer. Regarding intestinal surgery, there is controversy over whether to choose bowel resection or tumor removal, and currently, there are no prospective randomized controlled studies comparing the oncological safety of these two surgical approaches. This study is a prospective randomized trial aimed at comparing the efficacy of rectosigmoid resection versus rectosigmoid-preserving lesion excision in advanced ovarian cancer surgery.

Detailed description

Gastrointestinal surgeries, such as intestinal resection and anastomosis, ileostomy and/or colostomy, have become an important step in more than 50% of advanced ovarian cancer tumor cell reduction surgeries. Among them, the sigmoid colon rectum is the main intestinal site affected by ovarian cancer metastasis. To achieve R0 tumor reduction surgery, partial sigmoid colon rectum resection is often performed simultaneously. However, approximately 2.3-6.8% of patients undergoing this surgery have intestinal anastomotic leakage, 17-18% of patients require prophylactic or permanent colostomy, and 40% of patients will experience changes in bowel habits and other rectal anterior low resection syndrome after surgery, which reduces the quality of life of the patients. Numerous studies have found that the rectosigmoid colon involvement in ovarian cancer mainly occurs in the serosa, followed by the muscular layer, and finally the mucosa. Moreover, in 80% of cases, the involvement is limited to the seromuscular layer. Therefore, some studies have suggested that for seromuscular layer infiltration, resection of the rectosigmoid colon during cytoreductive surgery may not be necessary, and partial resection of the intestinal wall or tumor enucleation can be considered. Although tumor enucleation can preserve the rectosigmoid colon when it is involved, some studies have raised concerns about its oncological safety. These studies argue that not resecting the rectosigmoid colon may leave microscopic tumor residues, leading to a decrease in survival rates. In contrast, recent retrospective clinical studies have supported that, compared with intestinal resection, tumor enucleation of the rectosigmoid colon does not affect the prognosis of advanced ovarian cancer. Regarding intestinal metastasis of ovarian cancer, the current National Comprehensive Cancer Network(NCCN) guidelines for ovarian cancer state that preoperative neoadjuvant chemotherapy does not improve survival and therefore do not recommend it. Instead, the guidelines suggest direct surgical treatment. As for the surgical approach, the guidelines only require achieving R0 resection of the intestinal tumor, without specifying whether it is intestinal segment resection or tumor enucleation. Therefore, both rectosigmoid colon resection and tumor enucleation while preserving the rectosigmoid colon are common surgical methods in clinical practice. The investigator analyzed 130 cases of advanced ovarian cancer treated surgically in the investigator's hospital from 2015 to 2021, comparing the rectosigmoid colon resection group with the tumor enucleation group while preserving the rectosigmoid colon. The investigator found no difference in progression-free survival between the two groups, a conclusion consistent with published studies. As there are currently no prospective randomized controlled studies comparing the oncological safety of these two surgical approaches, this study is a prospective randomized study comparing the efficacy of rectosigmoid resection and rectosigmoid-sparing tumor debulking in advanced ovarian cancer surgery. It was designed and led by the Second Affiliated Hospital of Zhejiang University School of Medicine, with the participation of multiple domestic hospitals. The study strictly adheres to Good Clinical Practice(GCP) requirements, is strictly managed, and records data truthfully to provide genuine and scientific research data. This study will provide satisfactory cytoreductive surgery and standardized treatment for enrolled patients, ensuring the patients's benefits. The study will provide reliable clinical evidence for the management of the intestinal tract in cytoreductive surgery for advanced ovarian cancer and introduce new surgical methods to improve the prognosis and quality of life of ovarian cancer patients.

Interventions

PROCEDURERectosigmoid Lesion Excision +tumor cell debulking surgery

Surgery for pelvic rectosigmoid tumors

PROCEDURERectosigmoid Resection +tumor cell debulking surgery

Rectosigmoid Resection +tumor cell debulking surgery

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead SponsorOTHER
Tongji Hospital
CollaboratorOTHER
Zhejiang University
CollaboratorOTHER
Zhejiang Provincial People's Hospital
CollaboratorOTHER
Zhejiang Cancer Hospital
CollaboratorOTHER
Huzhou Central Hospital
CollaboratorOTHER
Ningbo Women & Children's Hospital
CollaboratorOTHER
Shaoxing People's Hospital
CollaboratorOTHER
The Central Hospital of Lishui City
CollaboratorOTHER
Women's Hospital School Of Medicine Zhejiang University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Voluntarily participate in this study and sign the informed consent form; * Age 18-70 years old; * Primary debulking surgery for epithelial ovarian cancer (including neoadjuvant chemotherapy), with or without abdominal and distant metastasis (≥ IIB stage); * Colonoscopy negative (no mucosal layer invasion); * Preoperative imaging (enhanced pelvic MRI) assesses the tumor's involvement of the intestinal surface and/or major parts of the mesentery; * Eastern Cooperative Oncology Group (ECOG) score \< 3; * American Society of Anesthesiologists (ASA) score \< 3.

Exclusion criteria

* Has a history of other malignant tumors or is undergoing other anti-tumor treatments; * Has severe underlying medical conditions that make surgery intolerable; * Epithelial ovarian cancer diagnosed incidentally during emergency surgery; * Participates in other clinical studies simultaneously; * Secondary cytoreductive surgery for epithelial ovarian cancer; * Patients who have received radiotherapy to the abdomen or pelvis before.

Design outcomes

Primary

MeasureTime frameDescription
Progression-free survival(PFS)Two years after the surgeryTwo years progression-free survival rate will be estimated, and 95% confidence intervals will be calculated.

Secondary

MeasureTime frameDescription
Local recurrence rate in the pelvic region(LPR)Two years after the surgeryThe proportion of cases with local recurrence in the pelvic area among the total number of enrolled cases
Overall Survival(OS)Five years since being includedOS is defined as the time from the date of randomization until death
Surgical Complications(SC)Two months after the surgeryIt refers to all the cases where the subjects experienced surgery-related complications, including the type, incidence rate, and severity (graded according to CTCAE V5.0)
Ratio of R0On the day of the surgeryThe proportion of cases that underwent R0 resection (complete resection) among the total number of enrolled cases.
Quality of Life(QoL)Five years after the surgeryAll the subjects will complete the quality of life questionnaire within the specified time until the end event occurs.

Countries

China

Contacts

CONTACTJing Fei
feijing@zju.edu.cn+86 13732238958
CONTACTZhigang Zhang
zzg2011@zju.edu.cn+86 15088621550

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 2, 2026