Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06330038

Anesthesia and Non-small Cell Lung Cancer Recurrence

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.

Recruiting

Interested in participating?

Request Info

Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Samsung Medical Center

Seoul, Seoul-teukbyeolsi, 06351, South Korea

Location status: Recruiting

Location contact

Jeayoun Kim, MD, PhD

CONTACT

[email protected]

821039268786

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • American Society of Anesthesiologists physical status (ASA) Ⅰ-Ⅲ
  • The Eastern Cooperative Oncology Group (ECOG) performance status 0-2
  • Lung resection surgery (segmentectomy, lobectomy, bilobectomy, pneumonectomy; video-assisted, robot-assisted, or open) with curative intent for NSCLC (clinical Tumor, Node, Metastasis (TNM) stage Ⅰ- ⅢA).

Exclusion criteria

  • Distant metastasis or malignant tumor in other organs that according to the attending surgeon is not in long-term remission
  • Severe neurologic conditions
  • Severe hepatic disease (Child-Pugh classification C)
  • Renal failure requiring renal replacement therapy
  • History of anesthesia and/or surgery within 1 yr
  • Previous surgery due to lung cancer (except diagnostic biopsies)
  • Contraindications to any study medication (history of allergy, hypersensitivity reaction, or any other contraindication)
  • Planned joint extrapulmonary procedure
  • Surgery under cardiopulmonary bypass or extracorporeal membrane oxygenation
  • Postoperative sedation
  • Pregnancy, or lactation
  • Patient refusal.

Treatment and study plan

Propofol

Drug

Propofol will be used for the induction and maintenance of general anesthesia.

Other names: Propofol 1% or 2% inj.

Inhaled anesthetics

Drug

Inhaled anesthetics will be used for the maintenance of general anesthesia.

Other names: Sevoflurane, Desflurane, Isoflurane

Primary outcomes

  1. Recurrence free survival

    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

Secondary outcomes

  1. Overall survival

    Time frame: Within 3 year after curative resection for NSCLC

    Time from index surgery to death due to any causes

  2. Postoperative complications

    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

Study contacts

Contact information is provided by the study sponsor or research team.

Jeayoun Kim, MD

CONTACT

[email protected]

8234106590

Sponsors and collaborators

Lead sponsor

Samsung Medical Center

Other

Collaborators

  • All India Institute of Medical Sciences
  • Asan Medical Center
  • Beijing Hospital
  • Chungnam National University Hospital
  • DongGuk University
  • Ewha Womans University
  • Inha University Hospital
  • Khon Kaen University
  • King Chulalongkorn Memorial Hospital
  • Konkuk University Medical Center
  • Korea University Guro Hospital
  • Mayo Clinic
  • Memorial Sloan Kettering Cancer Center
  • Seoul National University Hospital
  • Seoul St. Mary's Hospital
  • Severance Hospital
  • The Affiliated Hospital of Qingdao University
  • University Hospitals Coventry and Warwickshire NHS Trust
  • University of Texas Southwestern Medical Center
  • University of Virginia
  • Yale University

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2028
Study completion
2028
First posted
Mar 26, 2024
Registry last updated
Apr 20, 2026

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.