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The Effect of Combined General/Regional Anesthesia on Cancer Recurrence in Patients Having Lung Cancer Resections

Primary Purpose

Non-small Cell Lung Cancer

Status
Active
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
General anesthesia with opioid analgesia
Combined general/epidural anesthesia
Sponsored by
The Cleveland Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non-small Cell Lung Cancer focused on measuring Cancer, General anesthesia, Epidural anesthesia

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Tumor thought to be primary non-small cell lung cancer (stage 1-3) as determined according to the IASLC Lung Cancer Staging Project[ref];
  2. Scheduled for potentially curative tumor resection;
  3. Written informed consent, including willingness to be randomized to epidural anesthesia/analgesia plus general anesthesia or to general anesthesia and postoperative opioid analgesia;
  4. ASA physical status 1-3.

Exclusion Criteria:

  1. Any contraindication to epidural anesthesia, (including coagulopathy, abnormal anatomy).
  2. Any contraindication to midazolam, propofol, sevoflurane, fentanyl, morphine, or hydromorphone.
  3. Age <18 or >85 years old.
  4. Other cancer not believed by the attending surgeon to be in long-term remission.

Sites / Locations

  • Shanghai Chest Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Combined general/epidural anesthesia

General anesthesia with opioid analgesia

Arm Description

Combined general/epidural anesthesia and analgesia. General anesthesia may include propofol, isoflurane, sevoflurane, and other drugs. Epidural anesthesia will include bupivacaine and other local anesthetics.

General anesthesia with routine drugs and intravenous PCA opioid analgesia. General anesthesia may include propofol, isoflurane, sevoflurane, and other drugs.

Outcomes

Primary Outcome Measures

Cancer-free survival
Patients who remain alive without known lung cancer recurrence

Secondary Outcome Measures

Pain intensity
Time-weighted average pain scores over initial two days of hospitalization.
SF-12 Health Survey
McGill Pain Questionnaire
Neuropathic Pain Questionnaire
Opioid use
Total opioid use

Full Information

First Posted
June 20, 2016
Last Updated
June 15, 2023
Sponsor
The Cleveland Clinic
Collaborators
Shanghai Chest Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02840227
Brief Title
The Effect of Combined General/Regional Anesthesia on Cancer Recurrence in Patients Having Lung Cancer Resections
Official Title
The Effect of Combined General/Regional Anesthesia on Cancer Recurrence in Patients Having Lung Cancer Resections
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 2013 (undefined)
Primary Completion Date
June 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Cleveland Clinic
Collaborators
Shanghai Chest Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The primary hypothesis is that disease-free survival is improved in patients undergoing resection for tumor thought to be stage I-III primary non-small cell lung cancer in patients with combined general-epidural anesthesia & analgesia as compared to patients receiving general anesthesia and postoperative patient-controlled opioid analgesia. Patients having surgery for resection of potentially curable lung cancer will be randomized to combined general and epidural anesthesia or general anesthesia with opioid analgesia. The primary outcome will be disease-free survival.
Detailed Description
Surgery is the primary treatment of lung cancer, but surgery releases tumor cells into the systemic circulation. Whether this minimal residual disease results in clinical metastases is a function of host defense. At least three perioperative factors shift the balance toward initiation and progression of minimal residual disease. Surgery per se depresses cell-mediated immunity, reduces concentrations of tumor-related anti-angiogenic factors (e.g., angiostatin and endostatin), and increases concentrations of pro-angiogenic factors such as VEGF. Anesthesia impairs numerous immune functions, including neutrophil, macrophages, dendritic cells, T-cell, and NK-cell functions. Opioid analgesics inhibit both cellular and humoral immune function in humans, and promote tumor growth in rodents. The primary hypothesis is that disease-free survival is improved in patients undergoing resection for tumor thought to be stage I-III primary non-small cell lung cancer in patients with combined general-epidural anesthesia & analgesia as compared to patients receiving general anesthesia and postoperative patient-controlled opioid analgesia. Patients having surgery for resection of potentially curable lung cancer will be randomized to combined general and epidural anesthesia or general anesthesia with opioid analgesia. The primary outcome will be disease-free survival. The effect of combined epidural/general anesthesia versus general anesthesia with opioid analgesia on the primary outcome of disease-free survival (time to the earlier or recurrence or death from any cause) will be assessed uni-variably with Kaplan-Meier analyses and multivariably (primary analysis) with a Cox proportional hazards regression model adjusting for known risk factors for recurrence, including tumor stage, size of tumor, age, sex, receipt of chemotherapy before or after surgery, and clinical site. As usual for this type of analysis, stopping criteria will be based on number of outcome events rather than enrollment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-small Cell Lung Cancer
Keywords
Cancer, General anesthesia, Epidural anesthesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
2000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Combined general/epidural anesthesia
Arm Type
Experimental
Arm Description
Combined general/epidural anesthesia and analgesia. General anesthesia may include propofol, isoflurane, sevoflurane, and other drugs. Epidural anesthesia will include bupivacaine and other local anesthetics.
Arm Title
General anesthesia with opioid analgesia
Arm Type
Experimental
Arm Description
General anesthesia with routine drugs and intravenous PCA opioid analgesia. General anesthesia may include propofol, isoflurane, sevoflurane, and other drugs.
Intervention Type
Procedure
Intervention Name(s)
General anesthesia with opioid analgesia
Intervention Description
General anesthesia with routine drugs and intravenous patient controlled opioid analgesia. General anesthesia may include propofol, isoflurane, sevoflurane, and other drugs.
Intervention Type
Procedure
Intervention Name(s)
Combined general/epidural anesthesia
Intervention Description
Combined general/epidural anesthesia and analgesia. General anesthesia may include propofol, isoflurane, sevoflurane, and other drugs. Epidural anesthesia will include bupivacaine and other local anesthetics.
Primary Outcome Measure Information:
Title
Cancer-free survival
Description
Patients who remain alive without known lung cancer recurrence
Time Frame
3 years or as available
Secondary Outcome Measure Information:
Title
Pain intensity
Description
Time-weighted average pain scores over initial two days of hospitalization.
Time Frame
2 days
Title
SF-12 Health Survey
Time Frame
6, 12, 24, and 36 months
Title
McGill Pain Questionnaire
Time Frame
6, 12, 24, and 36 months
Title
Neuropathic Pain Questionnaire
Time Frame
6, 12, 24, and 36 months
Title
Opioid use
Description
Total opioid use
Time Frame
2 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Tumor thought to be primary non-small cell lung cancer (stage 1-3) as determined according to the IASLC Lung Cancer Staging Project[ref]; Scheduled for potentially curative tumor resection; Written informed consent, including willingness to be randomized to epidural anesthesia/analgesia plus general anesthesia or to general anesthesia and postoperative opioid analgesia; ASA physical status 1-3. Exclusion Criteria: Any contraindication to epidural anesthesia, (including coagulopathy, abnormal anatomy). Any contraindication to midazolam, propofol, sevoflurane, fentanyl, morphine, or hydromorphone. Age <18 or >85 years old. Other cancer not believed by the attending surgeon to be in long-term remission.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel I Sessler, MD
Organizational Affiliation
The Cleveland Clinic
Official's Role
Study Chair
Facility Information:
Facility Name
Shanghai Chest Hospital
City
Shanghai
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The Effect of Combined General/Regional Anesthesia on Cancer Recurrence in Patients Having Lung Cancer Resections

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