Robotic vs Laparoscopic and Open Surgery for Abdominopelvic Cancers
Early Oncologic and Perioperative Outcomes of Robotic Surgery Across Seven Abdominopelvic Malignancies
1 other identifier
observational
32,949
1 country
1
Brief Summary
Robotic surgery has become an increasingly common option for treating cancers in the abdomen and pelvis. However, whether robotic surgery leads to better cancer-related outcomes than laparoscopic (keyhole) surgery or open surgery is still uncertain. Results may differ across cancer types, and factors such as how complex the surgery is and how experienced the surgeon is may also influence the outcome. This retrospective cohort study examined adults who underwent curative-intent surgery for one of seven abdominopelvic cancers (pancreatic, gastric, rectal, cervical, endometrial, kidney, or prostate cancer) at a large tertiary hospital in Seoul, South Korea, between January 2012 and December 2021. Patients were classified into three groups according to the surgical approach they received: open, laparoscopic, or robotic surgery. The main outcome was 1-year disease-free survival, defined as the time from surgery to the first occurrence of cancer recurrence, distant metastasis, or death from any cause. Additional outcomes included 1-year mortality, overall mortality during follow-up, major postoperative complications, acute kidney injury, and length of hospital stay. To reduce differences between groups that might affect the comparison, the study used a statistical method called propensity score overlap weighting. Additional analyses adjusted for surgical complexity, surgeon experience including robotic learning curve, and pathological cancer stage to isolate the effect of the surgical platform itself. The purpose of this study was to evaluate whether the association between surgical approach and early oncologic and perioperative outcomes differed across the seven cancer types, and whether any observed advantage of the robotic platform remained after accounting for these factors.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2012
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedFirst Submitted
Initial submission to the registry
September 10, 2026
CompletedFirst Posted
Study publicly available on registry
September 16, 2026
CompletedSeptember 16, 2026
September 1, 2026
11 years
September 10, 2026
September 10, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
1-Year Disease-Free Survival
Time from surgery to the first occurrence of cancer recurrence, distant metastasis, or death from any cause, censored at 1 year. Recurrence and metastasis were confirmed radiologically or pathologically. Patients without an event were censored at the last postoperative surveillance encounter.
1 year after surgery
Secondary Outcomes (5)
1-Year All-Cause Mortality
1 year after surgery
Overall All-Cause Mortality During Follow-up
From date of surgery to date of death or end of follow-up, assessed up to approximately 10 years
Major Postoperative Complications Within 30 Days
Within 30 days after surgery
Postoperative Acute Kidney Injury
Within 7 days after surgery
Hospital Length of Stay
From date of surgery to date of hospital discharge, up to 90 days
Study Arms (3)
Open Surgery
Adults who underwent curative-intent abdominopelvic cancer surgery via open (laparotomy) approach for one of seven cancer types (pancreatic, gastric, rectal, cervical, endometrial, kidney, or prostate cancer) between January 2012 and December 2021.
Laparoscopic Surgery
Adults who underwent curative-intent abdominopelvic cancer surgery via conventional laparoscopic approach for one of six cancer types (pancreatic, gastric, rectal, cervical, endometrial, or kidney cancer) between January 2012 and December 2021. Laparoscopic prostatectomy was not performed at the study institution during the study period.
Robotic Surgery
Adults who underwent curative-intent abdominopelvic cancer surgery via robotic-assisted (da Vinci) approach for one of seven cancer types (pancreatic, gastric, rectal, cervical, endometrial, kidney, or prostate cancer) between January 2012 and December 2021.
Interventions
Participants underwent curative-intent surgery for abdominopelvic malignancies (pancreatic, gastric, rectal, cervical, endometrial, kidney, or prostate cancer) and were followed retrospectively without any experimental intervention. The surgical approach (open, laparoscopic, or robotic) was determined by routine clinical practice, not by study protocol. Data were extracted from the institutional electronic medical record system and linked with national administrative data for outcome ascertainment.
Eligibility Criteria
Adults aged 18 years or older who underwent curative-intent abdominopelvic surgery for one of seven nonmetastatic malignant solid tumors (pancreatic, gastric, rectal, cervical, endometrial, kidney, or prostate cancer) at Asan Medical Center, a large tertiary referral center in Seoul, Republic of Korea, between January 1, 2012, and December 31, 2021.
You may qualify if:
- Age 18 years or older
- Underwent curative-intent abdominopelvic surgery for a nonmetastatic malignant solid tumor of one of the following types: pancreatic, gastric, rectal, cervical, endometrial, kidney, or prostate cancer
- Surgery performed between January 1, 2012, and December 31, 2021
- Available postoperative surveillance data
You may not qualify if:
- Presence of distant metastasis before surgery
- Presentation with recurrent disease from previously treated cancer
- Incomplete or missing key demographic, comorbidity, operative, or outcome data required for analysis
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Asan Medical Center, University of Ulsan College of Medicine
Seoul, Songpa-gu, 05505, South Korea
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ji-Hoon Sim, MD, PhD
Asan Medical Center
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
September 10, 2026
First Posted
September 16, 2026
Study Start
January 1, 2012
Primary Completion
December 31, 2022
Study Completion
December 31, 2025
Last Updated
September 16, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share