GENe EXpression After Regional or General ANesthesia in Patients Undergoing Breast Cancer Surgery (GENEXAN)
Primary Purpose
Breast Cancer Female
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
General anesthesia
Regional anesthesia
Sponsored by
About this trial
This is an interventional basic science trial for Breast Cancer Female
Eligibility Criteria
Inclusion Criteria:
- Women 18-85 years old
- No undergoing pregnancy
- ASA Score I-IV
- Patients scheduled for breast surgery
- No contraindications (including surgical) to regional (paravertebral) anesthesia
- No previous breast surgery
- No known hereditary or familial cancer syndromes
- No previous cancer anamnesis, radio o chemiotherapy
- Primary breast cancer with Tumor classification 1-3, Nodes 0-2 as determined
- according to the NCI stage definitions (Primary breast cancer without known extension beyond the breast and axillary nodes)
- Free from pain in preoperative period
- Patients who don't use analgesic drugs before surgery
- Patients without cognitive impairment or mental retardation
Exclusion Criteria:
- Women > 18, < 85 years old
- Pregnancy
- ASA Score > IV
- Previous breast surgery
- Contraindications to regional anesthesia
- Known hereditary or familial cancer syndromes
- Previous cancer anamnesis, radio or chemiotherapy
- Tumor classification > 3, Nodes > 2, M > 0 as determined according to the NCI stage
- definitions
- Pain in preoperative period
- Use of analgesic drugs before surgery
- Cognitive impairment or mental retardation
- Patients who did not gave a written informed consent
- Undergoing therapy with alpha (doxazosin) or beta blockers.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
General anesthesia
Regional anesthesia
Arm Description
Breast cancer surgery (Tumor Stage 1-3, Nodes 0-2 as determined according to the NCI stage definitions http://www.cancer.gov/cancertopics/pdq/treatment/breast/HealthProfessional/page3/print)
Breast cancer surgery (Tumor Stage 1-3, Nodes 0-2 as determined according to the NCI stage definitions http://www.cancer.gov/cancertopics/pdq/treatment/breast/HealthProfessional/page3/print)
Outcomes
Primary Outcome Measures
Whole genome expression by microarray
tumor, biopsy, normal wound tissue
Whole genome expression by mircoarray
tumor, wound tissue
Secondary Outcome Measures
Immune progenitors (MDBCs, GMPs, HPSCs), Natural Killer, T regulatory Lymphocytes, PentraxinIII
in blood
cancer recurrence
local or distant metastasis
survival from cancer
death
Immune progenitors (MDBCs, GMPs, HPSCs), Natural Killer, T regulatory Lymphocytes, PentraxinIII
in blood
Immune progenitors (MDBCs, GMPs, HPSCs), Natural Killer, T regulatory Lymphocytes, PentraxinIII
in blood
Immune progenitors (MDBCs, GMPs, HPSCs), Natural Killer, T regulatory Lymphocytes, PentraxinIII
in blood
Full Information
NCT ID
NCT03779685
First Posted
November 29, 2018
Last Updated
August 4, 2020
Sponsor
Azienda Ospedaliera San Gerardo di Monza
1. Study Identification
Unique Protocol Identification Number
NCT03779685
Brief Title
GENe EXpression After Regional or General ANesthesia in Patients Undergoing Breast Cancer Surgery
Acronym
GENEXAN
Official Title
GENe EXpression in Tissues From Operating Field After Regional or General ANesthesia in Patients Undergoing Breast Cancer Surgery. The GENEXAN Randomized Controlled Genomic Trial
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2021 (Anticipated)
Primary Completion Date
March 1, 2021 (Anticipated)
Study Completion Date
March 1, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda Ospedaliera San Gerardo di Monza
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Breast cancer is the most commonly diagnosed cancer in females and the second leading cause of death from cancer in women. It was estimated that 2 million new cases have occurred in 2018 worldwide 1.
Standard anesthetic procedures for the surgery of breast cancer include general and regional anesthesia 2. Growing preclinical and clinical data support the hypothesis that anesthetic choice may affect cancer-related outcomes.
Recurrence in breast cancer was reduced to four-fold in a retrospective study with a 2.5 to 4 year follow up 3. Recurrence and metastasis-free survival, with multivariate analysis, was 94% (95% CI 87,100) versus 82% (74, 91) at 24 months, and 94 (87, 100) versus 77 (68, 87) at 36 months in the paravertebral and general anesthesia patients, respectively, (p=0.013). Currently large confirmatory randomized trials evaluating breast cancer recurrence in patients operated with general or regional anesthesia are yet undergoing 4.
Detailed Description
Background: Exposure to general or regional anesthesia, can modulate differently breast cancer biology through a direct activity on cancer cells or indirectly through modifications in host response (immune system, angiogenesis, nervous system). Alterations occur both systemically and locally on the surgical site and is supposed that can affect cancer-related outcomes after months or years.
It is not known whether the action of this short exposure to anesthetics on the host and cancer biology is driven by epigenetic alterations in gene and protein expression during the immediate to early post-anesthesia period.
An altered gene and protein expression profile may affect the response of the immune system, angiogenesis and the nervous system and induce more or less propitious conditions to tumor progression. Data from studies in animals and humans show that gene expression may change in the brain and heart after only a short exposure to general anesthesia and that changes may persist for several weeks.
Methods: The GENEXAN is a randomized, controlled, monocentric, genomic trial aiming to test the hypothesis that regional (paravertebral) anesthesia, compared to general anesthesia, would elicit a differential gene and protein expression pattern in cancer tissue and normal surgical microenvironment after breast cancer surgery in women.
Discussion: This research will serve to map gene and protein expression profile after surgery with different anesthetics and elucidate which genes specific to biological systems may affect tumor biology in the immediate operative period.
The findings may also address further research depending on the tissue specificity of the up or down-regulated genes.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer Female
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
General anesthesia
Arm Type
Active Comparator
Arm Description
Breast cancer surgery (Tumor Stage 1-3, Nodes 0-2 as determined according to the NCI stage definitions http://www.cancer.gov/cancertopics/pdq/treatment/breast/HealthProfessional/page3/print)
Arm Title
Regional anesthesia
Arm Type
Experimental
Arm Description
Breast cancer surgery (Tumor Stage 1-3, Nodes 0-2 as determined according to the NCI stage definitions http://www.cancer.gov/cancertopics/pdq/treatment/breast/HealthProfessional/page3/print)
Intervention Type
Procedure
Intervention Name(s)
General anesthesia
Intervention Description
Sevoflurane and morphine
Intervention Type
Procedure
Intervention Name(s)
Regional anesthesia
Intervention Description
Paravertebral block
Primary Outcome Measure Information:
Title
Whole genome expression by microarray
Description
tumor, biopsy, normal wound tissue
Time Frame
before tumor excision
Title
Whole genome expression by mircoarray
Description
tumor, wound tissue
Time Frame
during surgery (just after tumor excision)
Secondary Outcome Measure Information:
Title
Immune progenitors (MDBCs, GMPs, HPSCs), Natural Killer, T regulatory Lymphocytes, PentraxinIII
Description
in blood
Time Frame
before tumor excision
Title
cancer recurrence
Description
local or distant metastasis
Time Frame
each 6 months for up to 7 years
Title
survival from cancer
Description
death
Time Frame
each 6 months for up to 7 years
Title
Immune progenitors (MDBCs, GMPs, HPSCs), Natural Killer, T regulatory Lymphocytes, PentraxinIII
Description
in blood
Time Frame
at the end of surgery
Title
Immune progenitors (MDBCs, GMPs, HPSCs), Natural Killer, T regulatory Lymphocytes, PentraxinIII
Description
in blood
Time Frame
at 24 hours
Title
Immune progenitors (MDBCs, GMPs, HPSCs), Natural Killer, T regulatory Lymphocytes, PentraxinIII
Description
in blood
Time Frame
at 168 hours
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Women 18-85 years old
No undergoing pregnancy
ASA Score I-IV
Patients scheduled for breast surgery
No contraindications (including surgical) to regional (paravertebral) anesthesia
No previous breast surgery
No known hereditary or familial cancer syndromes
No previous cancer anamnesis, radio o chemiotherapy
Primary breast cancer with Tumor classification 1-3, Nodes 0-2 as determined
according to the NCI stage definitions (Primary breast cancer without known extension beyond the breast and axillary nodes)
Free from pain in preoperative period
Patients who don't use analgesic drugs before surgery
Patients without cognitive impairment or mental retardation
Exclusion Criteria:
Women > 18, < 85 years old
Pregnancy
ASA Score > IV
Previous breast surgery
Contraindications to regional anesthesia
Known hereditary or familial cancer syndromes
Previous cancer anamnesis, radio or chemiotherapy
Tumor classification > 3, Nodes > 2, M > 0 as determined according to the NCI stage
definitions
Pain in preoperative period
Use of analgesic drugs before surgery
Cognitive impairment or mental retardation
Patients who did not gave a written informed consent
Undergoing therapy with alpha (doxazosin) or beta blockers.
12. IPD Sharing Statement
Plan to Share IPD
No
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GENe EXpression After Regional or General ANesthesia in Patients Undergoing Breast Cancer Surgery
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