search
Back to results

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
Azienda Ospedaliera San Gerardo di Monza
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Breast Cancer Female

Eligibility Criteria

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

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

    First Posted
    November 29, 2018
    Last Updated
    August 4, 2020
    Sponsor
    Azienda Ospedaliera San Gerardo di Monza
    search

    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

    Learn more about this trial

    GENe EXpression After Regional or General ANesthesia in Patients Undergoing Breast Cancer Surgery

    We'll reach out to this number within 24 hrs