Specialization in Gastric Cancer Surgery

March 17, 2023 updated by: Ali GUNER, Karadeniz Technical University

The Impact of Specialization on Clinical Outcomes in Gastric Cancer Surgery

Specialization is having competent and effective knowledge on a subject, and the tendency towards specialization is increasing due to the fact that it increases the success in the follow-up and treatment process of diseases. It has been observed that specialization in cancer surgery provides significant improvement in clinical outcomes in recent years. In this study, the effect of specialization in gastric cancer surgery on clinical outcomes is being investigated.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Specialization is having sufficient and effective knowledge on a subject. Today, in the medical world, specialization is defined as having competent knowledge on a disease, and in recent years, the benefit of specialization has begun to be emphasized. Initially, it was defined as a branching and over the years, internal and surgical departments were divided into sub-areas. In surgical sciences, these fields are determined as traumatology, breast-endocrine surgery and gastrointestinal system surgery. This branching has brought a different perspective and approach to diseases and has made it possible to be more effective in the management of diseases. In recent years, a specialization approach on diseases and organ systems has developed within these branches. In surgery, surgeons specialized on many organs such as pancreatic surgery, colorectal surgery, gastric surgery, breast surgery, ovarian surgery have increased the efficiency in the management of diseases and the survival and disease-free survival rates of the patients have increased, and the postoperative morbidity and mortality rates have decreased.

Gastric cancer is one of the most common malignant cancers. It is the fifth most common cause of cancer-related death worldwide. Despite advances in diagnosis and treatment methods, patients may still be diagnosed late, and patients still have a poor prognosis due to the biology of gastric cancer. Even in properly treated patients, five-year survival rates are around 20-30%. With the development of surgical techniques and disease management, clinical outcomes of the disease have improved and mortality has been reduced. In the studies, the definition of gastric surgeon was created and it was determined that the mortality decreased proportionally with the increase in the patient volume of the surgeon. In gastric cancer surgery, there are mostly studies on the number of surgeon patients and the number of hospital patients. Post-hoc analysis of hospital volume on patients included in the CRITICS study showed a 13.1% increase in survival in high-volume hospitals compared to low-volume hospitals. The number of annual resections ≥21 was determined as the definition of high-volume hospital. In addition, it was determined that there was a decrease in mortality as the number of annual cases increased in high-volume hospitals. In another study, it was seen that there was an improvement in the mortality of medium and high volume hospitals compared to low volume hospitals. The majority of studies in gastric cancer surgery have focused on hospital volume and surgeon volume. There are no data on the specialization of the surgeon other than a study based in Japan.

In this study, it was aimed to evaluate the effect of specialization in gastric cancer surgery on short- and long-term clinical outcomes.

Study Type

Observational

Enrollment (Actual)

537

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Trabzon, Turkey, 61080
        • Karadeniz Technical University, Faculty of Medicine, Farabi Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patients with clinical stage 1-3 gastric adenocarcinoma undergoing surgical treatment for curative purposes

Description

Inclusion Criteria:

  • cStage I/II/III gastric cancer
  • Histologically proven gastric adenocarcinoma
  • Underwent surgery with curative intent

Exclusion Criteria:

  • Under 18 years old
  • Patients with non-adenocarcinoma diagnosis
  • Emergency surgeries
  • The need for a thoracic approach
  • Patients with a history of non-gastric cancer

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
The specialized group

Patients who were operated by a specialized gastric cancer surgeon. Specialized gastric cancer surgeons were defined as surgeons who meet all of the criteria for a specialized gastric cancer surgeon.

  • Who had undergone professional training in gastric cancer surgery in specialized gastric cancer centers (in Japan or Korea),
  • Who identified themselves as primarily gastric surgeons during the study period
  • Whose annual gastric cancer surgery volume is more than 21
  • Who had undergone professional training in gastric cancer surgery in specialized gastric cancer centers (in Japan or Korea),
  • Who identified themselves as primarily gastric surgeons during the study period
  • Whose annual gastric cancer surgery volume is more than 21
Other Names:
  • Gastric cancer surgery
The non-specialized group

Patients who were operated by a non-specialized surgeon. Non-specialized surgeons were defined as general surgeon who does not have the characteristics of a specialized gastric cancer surgeon.

The non-specialized group will be divided into two subgroups (high-volume vs low-volume) for further analysis.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
30-day mortality
Time Frame: 30 days after the operation (postoperative hospital stay ≤ 30 days) or operation to first discharge from hospital (postoperative hospital stay > 30 days)
Death from any cause within 30 days after surgery or at any time if not discharged from hospital
30 days after the operation (postoperative hospital stay ≤ 30 days) or operation to first discharge from hospital (postoperative hospital stay > 30 days)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
3-year overall survival
Time Frame: 3 years after surgery
Death from any cause is defined as an event.
3 years after surgery
90-day mortality
Time Frame: 90 days after the operation (postoperative hospital stay ≤ 90 days) or operation to first discharge from hospital (postoperative hospital stay > 90 days)
Death from any cause within 90 days after surgery or at any time if not discharged from hospital
90 days after the operation (postoperative hospital stay ≤ 90 days) or operation to first discharge from hospital (postoperative hospital stay > 90 days)
Postoperative complication rate
Time Frame: Within 30 days after the operation
Any complications (graded by the Clavien-Dindo classification) occurred in the postoperative period
Within 30 days after the operation
Postoperative major complication rate
Time Frame: Within 30 days after the operation
≥grade-III Clavien-Dindo complications occurred in the postoperative period
Within 30 days after the operation
Readmission
Time Frame: Within 30 days after the operation
Readmission requiring re-hospitalization for any complications after discharge
Within 30 days after the operation
3-year recurrence-free survival
Time Frame: 3 years after surgery
Death from any cause or the recurrence of gastric cancer are an event.
3 years after surgery
Hospital stay
Time Frame: From the date of surgery until the date of hospital discharge, assessed up to 90 days after the operation
Duration of postoperative hospital stays
From the date of surgery until the date of hospital discharge, assessed up to 90 days after the operation

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Failure-to-cure
Time Frame: Within 30 days after the operation
futile surgery due to intraoperative distant metastasis/irresectability, OR microscopically or macroscopically incomplete resection OR 30-day mortality
Within 30 days after the operation
Neoadjuvant treatment usage
Time Frame: Within the three months before surgery
Neoadjuvant treatment usage rates in patients undergoing surgical treatment
Within the three months before surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ali Guner, MD, Karadeniz Technical University Faculty of Medicine

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 14, 2022

Primary Completion (Actual)

September 15, 2022

Study Completion (Actual)

March 1, 2023

Study Registration Dates

First Submitted

February 22, 2022

First Submitted That Met QC Criteria

March 10, 2022

First Posted (Actual)

March 15, 2022

Study Record Updates

Last Update Posted (Actual)

March 21, 2023

Last Update Submitted That Met QC Criteria

March 17, 2023

Last Verified

March 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

With a reasonable request, we are open to share IPD.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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