Skip to content

Regional Anesthesia and Breast Cancer Recurrence

Regional Anesthesia and Breast Cancer Recurrence

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00418457
Enrollment
2108
Registered
2007-01-04
Start date
2007-01-31
Completion date
2019-12-31
Last updated
2020-06-16

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

Conditions

Breast Neoplasms

Keywords

Breast Cancer, Anesthesia; regional, cancer recurrence, Anesthesia; inhalational, Analgesia; opioid

Brief summary

In this multi-center trial, Stage 1-3 patients having mastectomies or isolated lumpectomy with axillary node dissection will be randomly assigned to thoracic epidural or paravertebral anesthesia/analgesia, or to general anesthesia and morphine analgesia. Participants will be followed for up to 10 years to determine the rate of cancer recurrence or metastasis.

Detailed description

Surgery is the primary and most effective treatment of breast cancer, but residual disease in the form of scattered micrometastases and tumor cells are usually unavoidable. Whether minimal residual disease results in clinical metastases is a function of host defense and tumor survival and growth. At least three perioperative factors shift the balance toward progression of minimal residual disease: 1. Surgery per se depresses cell-mediated immunity, reduces concentrations of tumor-related anti-angiogenic factors (e.g., angiostatin and endostatin), increases concentrations of pro-angiogenic factors such as VEGF, and releases growth factors that promote local and distant growth of malignant tissue. 2. Anesthesia impairs numerous immune functions, including those of neutrophils, macrophages, dendritic cells, T-cell, and natural killer cells. 3. Opioid analgesics inhibit both cellular and humoral immune function in humans, increase angiogenesis, and promote breast tumor growth in rodents. However, regional analgesia attenuates or prevents each of these adverse effects by largely preventing the neuroendocrine surgical stress response, eliminating or reducing the need for general anesthesia, and minimizing opioid requirement. Animal studies indicate that regional anesthesia and optimum postoperative analgesia independently reduce the metastatic burden in animals inoculated with breast adenocarcinoma cells following surgery. Preliminary data in cancer patients are also consistent: paravertebral analgesia for breast cancer surgery reduced risk of recurrence or metastasis approximately four-fold (95% CI of estimated hazard ratio is 0.71 - 0.06) during a 2.5 to 4-year follow-up period compared to opioid analgesia. The investigators will thus test the hypothesis that recurrence after breast cancer surgery is lower with regional anesthesia/analgesia than with general anesthesia and opioid analgesia. In this multi-center trial, Stage 1-3 patients having mastectomies will be randomly assigned to thoracic epidural or paravertebral anesthesia/analgesia, or to general anesthesia and opioid analgesia. As with all time-to-event trials, interim and final analyses are based on the number of outcome events (recurrences in this case) rather than enrollment. The number of patients required is just an estimate and varies based on actual recurrence rates which in turn depend on patients' stage and grade, and ancillary treatments. There will be three evenly spaced interim analyses and a final analysis at 351 recurrences. Confirming our hypothesis will indicate that a minor modification to anesthetic management, one that can be implemented with little risk or cost, will reduce the risk of cancer recurrence - a complication that is often ultimately lethal.

Interventions

DRUGGeneral anesthesia and opioids

General anesthesia, usually with sevoflurane, and opioid analgesia

DRUGRegional analgesia and propofol

Regional anesthesia and analgesia (either epidural or paravertebral), combined with deep sedation or general anesthesia

Sponsors

The Cleveland Clinic
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Primary breast cancer without known extension beyond the breast and axillary nodes (i.e. believed to be Tumor Stage 1-3, Nodes 0-2) * Scheduled for unilateral or bilateral mastectomy with or without implant (isolated lumpectomy will not qualify) * Isolated lumpectomy with axillary node dissection (anticipated removal of at least five nodes) * Written informed consent, including willingness to be randomized to morphine or regional analgesia

Exclusion criteria

* Previous surgery for breast cancer (except diagnostic biopsies) * Inflammatory breast cancer * Age \< 18 or \> 85 years old * Scheduled free flap reconstruction * ASA Physical Status ≥ 4 * Any contraindication to epidural or paravertebral anesthesia and analgesia (including coagulopathy, abnormal anatomy) * Any contraindication to midazolam, propofol, sevoflurane, fentanyl, or morphine * Other cancer not believed by the attending surgeon to be in long-term remission * Systemic disease believed by the attending surgeon to present ≥ 25% two-year mortality

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants Who Had Breast Cancer Recurrence After Breast Cancer Surgeryup to 10 yearstime to breast cancer recurrence from the end of surgery.

Secondary

MeasureTime frameDescription
Number of Participants That Experienced Post-Surgical Pain6 months and 1 yearBrief Pain Inventory is used to evaluate with values of any pain vs. no pain (binary)
Number of Participants That Experienced Neuropathic Pain After Surgery6 month and 1 yearneuropathic pain is a binary outcome: any pain vs. no pain
SF-12 PCS Score6 month and 1 yearPhysical and Mental Health Composite Scores (PCS & MCS) are computed using the scores of twelve questions and range from 0 to 100, where a zero score indicates the lowest level of health measured by the scales and 100 indicates the highest level of health.
SF-12 MCS Score6 month and 1 yearPhysical and Mental Health Composite Scores (PCS & MCS) are computed using the scores of twelve questions and range from 0 to 100, where a zero score indicates the lowest level of health measured by the scales and 100 indicates the highest level of health.

Countries

Austria, China, Germany, Ireland, Singapore, United States

Participant flow

Participants by arm

ArmCount
General Anesthesia and Opioid
General anesthesia followed by opioid administration General anesthesia and opioids: General anesthesia, usually with sevoflurane, and opioid analgesia
1,065
Regional Analgesia and Propofol
Regional anesthesia and analgesia (either epidural or paravertebral) combined with propofol Regional analgesia and propofol: Regional anesthesia and analgesia (either epidural or paravertebral), combined with deep sedation or general anesthesia
1,043
Total2,108

Baseline characteristics

CharacteristicGeneral Anesthesia and OpioidRegional Analgesia and PropofolTotal
Age, Continuous53 years
STANDARD_DEVIATION 11
53 years
STANDARD_DEVIATION 12
53 years
STANDARD_DEVIATION 11
Ethnicity (NIH/OMB)
Hispanic or Latino
4 Participants3 Participants7 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
989 Participants972 Participants1961 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
72 Participants68 Participants140 Participants
Sex: Female, Male
Female
1065 Participants1043 Participants2108 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
22 / 1,06518 / 1,043
other
Total, other adverse events
0 / 1,0650 / 1,043
serious
Total, serious adverse events
0 / 1,0650 / 1,043

Outcome results

Primary

Number of Participants Who Had Breast Cancer Recurrence After Breast Cancer Surgery

time to breast cancer recurrence from the end of surgery.

Time frame: up to 10 years

ArmMeasureValue (NUMBER)
General Anesthesia and OpioidNumber of Participants Who Had Breast Cancer Recurrence After Breast Cancer Surgery111 participants
Regional Analgesia and PropofolNumber of Participants Who Had Breast Cancer Recurrence After Breast Cancer Surgery102 participants
p-value: 0.8495% CI: [0.74, 1.28]Regression, Cox
Secondary

Number of Participants That Experienced Neuropathic Pain After Surgery

neuropathic pain is a binary outcome: any pain vs. no pain

Time frame: 6 month and 1 year

Population: data was not available/collected for all participants due to lost follow up or miss phone call.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
General Anesthesia and OpioidNumber of Participants That Experienced Neuropathic Pain After Surgery1-year57 Participants
General Anesthesia and OpioidNumber of Participants That Experienced Neuropathic Pain After Surgeryat 6-month89 Participants
Regional Analgesia and PropofolNumber of Participants That Experienced Neuropathic Pain After Surgeryat 6-month87 Participants
Regional Analgesia and PropofolNumber of Participants That Experienced Neuropathic Pain After Surgery1-year57 Participants
p-value: 0.8195% CI: [0.75, 1.28]GEE
Secondary

Number of Participants That Experienced Post-Surgical Pain

Brief Pain Inventory is used to evaluate with values of any pain vs. no pain (binary)

Time frame: 6 months and 1 year

Population: data was not available/collected for all participants due to lost follow up or miss phone call.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
General Anesthesia and OpioidNumber of Participants That Experienced Post-Surgical Painat 6-month456 Participants
General Anesthesia and OpioidNumber of Participants That Experienced Post-Surgical Pain1-year232 Participants
Regional Analgesia and PropofolNumber of Participants That Experienced Post-Surgical Painat 6-month442 Participants
Regional Analgesia and PropofolNumber of Participants That Experienced Post-Surgical Pain1-year239 Participants
p-value: 0.795% CI: [0.85, 1.17]GEE
Secondary

SF-12 MCS Score

Physical and Mental Health Composite Scores (PCS & MCS) are computed using the scores of twelve questions and range from 0 to 100, where a zero score indicates the lowest level of health measured by the scales and 100 indicates the highest level of health.

Time frame: 6 month and 1 year

Population: data was not available/collected for all participants due to lost follow up or miss phone call.

ArmMeasureGroupValue (MEAN)Dispersion
General Anesthesia and OpioidSF-12 MCS Scoreat 6-month48.1 units on a scaleStandard Deviation 8.6
General Anesthesia and OpioidSF-12 MCS Score1-year48 units on a scaleStandard Deviation 9.7
Regional Analgesia and PropofolSF-12 MCS Scoreat 6-month48.7 units on a scaleStandard Deviation 8.1
Regional Analgesia and PropofolSF-12 MCS Score1-year48.7 units on a scaleStandard Deviation 9.4
p-value: 0.04395% CI: [0.02, 1.48]Mixed Models Analysis
Secondary

SF-12 PCS Score

Physical and Mental Health Composite Scores (PCS & MCS) are computed using the scores of twelve questions and range from 0 to 100, where a zero score indicates the lowest level of health measured by the scales and 100 indicates the highest level of health.

Time frame: 6 month and 1 year

Population: data was not available/collected for all participants due to lost follow up or miss phone call.

ArmMeasureGroupValue (MEAN)Dispersion
General Anesthesia and OpioidSF-12 PCS Scoreat 6-month49.7 score on a scaleStandard Deviation 8.1
General Anesthesia and OpioidSF-12 PCS Score1-year52.3 score on a scaleStandard Deviation 6.7
Regional Analgesia and PropofolSF-12 PCS Scoreat 6-month49.8 score on a scaleStandard Deviation 8.2
Regional Analgesia and PropofolSF-12 PCS Score1-year52.1 score on a scaleStandard Deviation 7.3
p-value: 0.9695% CI: [-0.63, 0.6]Mixed Models Analysis

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026