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Survival Rates and Quality of Life According to Follow-up Period After Gastrectomy for Gastric Cancer (STOFOLUP)

A Prospective Multi-center Randomized Clinical Trial to Compare Survival Rates and Quality of Life According to Follow-up Period in Patients Who Underwent Radical Gastrectomy for Advanced Gastric Cancer (STOFOLUP Trial)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04740346
Enrollment
886
Registered
2021-02-05
Start date
2021-07-05
Completion date
2026-06-30
Last updated
2021-10-27

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

Conditions

Gastric Cancer, Quality of Life, Recurrence

Brief summary

This study is a multi-center, prospective, randomized controlled study. The aim of this study is to compare survival rates and to observe quality of life and nutritional status according to follow-up period in patients who underwent radical gastrectomy for stage 2 or 3 gastric cancer.

Detailed description

The hypothesis of this study is that the survival rates would be different between the 3 months and 6 months follow-up groups. The investigators expected survival differences of 6% and the anticipated 3-year overall survival is 83% in the 6 months follow-up group based on the previous 3 phase clinical trial. On the basis of this hypothesis, the sample size was calculated as 886 patients. Patients who were diagnosed as stage 2 or 3 gastric cancer after gastrectomy will be assigned to 3 months or 6 months follow-up group. The planned examinations including blood test, X-ray , CT, endoscopy, and nutritional markers will be performed according to the protocol and each patients will be followed up for 3 years after enrollment. The primary endpoint is 3 year overall survival and secondary endpoints are other survivals such as 3-year disease-free survival and gastric cancer specific survival, quality of life, and nutritional parameters.

Interventions

DIAGNOSTIC_TESTComputed tomography, Chest X-ray, and blood test

CT will be performed every 3 months after gastrectomy in the 3-months follow-up group. CT will be performed every 6 months after gastrectomy in the 6 months follow-up group.

Sponsors

Korea Health Industry Development Institute
CollaboratorOTHER_GOV
National Cancer Center, Korea
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients aged 19 years or more * Patients who are diagnosed with pathological stage II or III gastric adenocarcinoma according to the AJCC 8th edition * Patients who can understand all information about the trial and decide for themselves whether to participate in this study

Exclusion criteria

* Vulnerable patients such as pregnant and intellectual disability * Patients who cannot undergo CT owing to poor kidney function or severe adverse effects * Patients who are already in another study and cannot follow the schedule for this trial * Patients who are diagnosed with a cancer other than gastric cancer within five years before the gastrectomy * Patients being treated for a cancer other than gastric cancer

Design outcomes

Primary

MeasureTime frameDescription
3-year overall survival3 years after surgeryDeath from any cause is defined as an event.

Secondary

MeasureTime frameDescription
3-year gastric cancer specific survival rate3 years after surgeryDeath from gastric cancer is the only event.
3-year post-recurrence survival rate3 years after surgeryfrom recurrence detection date to last follow-up date (or death)
Summary score of KOQUSS-40 questionnaire3 years after surgeryKOQUSS-40 consists of 8 domains with 40 questions for quality of life and post-gastrectomy symptoms. We will calculate the KOQUSS-40 summary score of each group and compare them between the two groups. The summary score is defined as the mean of eight symptom domains (Indigestion, dysphagia, reflux, dumping syndrome, bowel habit change, constipation, psychological factors, and worry about cancer). The minimum and maximum values are 0 and 100, and higher scores mean a better quality of life.
Summary score of EORTC QLQ C303 years after surgeryEORTC QLQ C30 consists of 15 domains with 30 questions for quality of life of cancer patients. The 15 domains consist of five functional scales (physical, role, cognitive, emotional, and social functioning), a global QOL scale, three symptom scales (fatigue, nausea and vomiting, and pain), and six single items (appetite loss, diarrhea, dyspnea, constipation, insomnia, financial impact). We will calculate the EORTC QLQ C30 summary score of each group and compare them between the two groups. The summary score is defined as the mean of 13 domains (excluding global QOL scale and financial impact). The minimum and maximum values are 0 and 100, and higher scores mean a better quality of life.
3-year recurrence-free survival rate3 years after surgeryDeath from any cause and gastric cancer recurrence are an event.
Difference of body weight (kg)3 years after surgeryDifference of body weight between preoperative and postoperative 3 year values
Incidence of iron deficiency anemia3 years after surgeryIncidence of iron deficiency anemia for the 3 year follow-up after gastrectomy
Incidence of vitamin B12 deficiency3 years after surgeryIncidence of vitamin B12 deficiency for the 3 year follow-up after gastrectomy
Summary score of EORTC QLQ STO223 years after surgeryEORTC QLQ STO22 consists of 9 domains with 22 questions for stomach cancer patients' symptoms. The 9 domains consist of five symptom scales (dysphagia, pain, reflux symptom, eating restriction, anxiety), four single items (having a dry mouth, taste, body image, and hair loss). We will calculate the EORTC QLQ STO22 summary score of each group and compare them between the two groups. The summary score is defined as the mean of 9 domains. The minimum and maximum values are 0 and 100, and higher scores mean a better quality of life.

Countries

South Korea

Contacts

Primary ContactBang Wool Eom, MD PhD
kneeling79@ncc.re.kr82-31-920-1689

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026