Samsung Medical Center
Seoul, Seoul-teukbyeolsi, 06351, South Korea
Location status: Recruiting
NCT Number: NCT06330038
There has been ongoing debate about the relationship between cancer recurrence and anesthetic management. Therefore, the investigators will test the hypothesis that the recurrence free survival (RFS) after curative resection of NSCLC is higher in patient who received total intravenous anesthesia (TIVA) than volatile anesthetics in this multi-center randomized trials.
Interested in participating?
Request Info19 year and older
All sexes
Interventional
Phase 4
Seoul, Seoul-teukbyeolsi, 06351, South Korea
Location status: Recruiting
Surgery is the primary treatment for non-small cell lung cancer (NSCLC), but microscopic residual disease may be unavoidable. Preclinical studies have shown that volatile anesthetics might suppress host immunity and promote a pro-malignant environment which supports cancer cell proliferation, migration, and angiogenesis, whereas propofol may preserve cell-mediated immunity and inhibits tumor angiogenesis. However, clinical evidence that propofol-based total intravenous anesthesia (TIVA) can reduce tumor recurrence after curative resection remains inconsistent due to retrospective observational nature of previous studies. Therefore, the investigators will test the hypothesis that the recurrence free survival (RFS) after curative resection of NSCLC is higher in patient who received TIVA than volatile anesthetics in this multi-center randomized trials.
This double-blind, randomized trial will enroll patients at 22 international sites, subject to study registration, institutional review board approval, and patient written informed consent. Eligible patients are adult patients undergoing lung resection surgery with curative intent for NSCLC. At each study site, enrolled subjects will be randomly allocated into the TIVA and GAS group with a 1:1 ratio. A centralized, password-protected, and encrypted web-based electronic case report form will be used for randomization and data upload. This pragmatic trial does not standardize any aspect of patient care. However, potential confounders will be balanced between the study arms.
The primary outcome will be recurrence free survival (RFS). Secondary outcomes will be overall survival and complications within postoperative 7 days. Enrollment of 5384 patients will provide 80% power to detect a 3% treatment effect (hazard ratio of 0.83) at alpha 0.05 for RFS at 3 years.
Confirmation of the study hypothesis would demonstrate that a relatively minor and low cost alteration in anesthetic management has the potential to reduce cancer recurrence risk in NSCLC, an ultimately fatal complication. Rejection of the hypothesis would end the ongoing debate about the relationship between cancer recurrence and anesthetic management.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Propofol will be used for the induction and maintenance of general anesthesia.
Other names: Propofol 1% or 2% inj.
Inhaled anesthetics will be used for the maintenance of general anesthesia.
Other names: Sevoflurane, Desflurane, Isoflurane
Time frame: Within 3 year after curative resection for NSCLC
Time from surgery to the earliest date of local recurrence/metastasis or death from any cause, whichever comes first
Time frame: Within 3 year after curative resection for NSCLC
Time from index surgery to death due to any causes
Time frame: within 7 days post-surgery or at discharge if earlier
Rate of complications which will be assessed with Clavien-Dindo classification and postoperative complications defined by the Society of Thoracic Surgeons (STS) general thoracic surgery databases
Contact information is provided by the study sponsor or research team.
Samsung Medical Center
Other
Recurrence Free Survival After Curative Resection of Non-small Cell Lung Cancer Between Inhalational Gas Anesthesia and Propofol-based Total IntraVenous Anesthesia: a Multicenter, Randomized, Clinical Trial
Acronym: GASTIVA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07222566
Advanced Non-Small Cell Lung Cancer, Bronchial Neoplasms
Bullhead City, Arizona, United States
View Trial DetailsNCT04585750
Adnexal Diseases, Advanced Malignant Neoplasm
Irvine, California, United States
View Trial DetailsNCT07629960
Advanced Solid Tumor, Bronchial Neoplasms
Fairfax, Virginia, United States
View Trial DetailsNCT06561685
Adenocarcinoma, Advanced Solid Tumor
Santa Monica, California, United States
View Trial Details