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Propofol vs Sevo for Paediatric Tumor Surgery

Primary Purpose

Solid Tumor, Carcinoma, Malignancy

Status
Recruiting
Phase
Phase 4
Locations
Hong Kong
Study Type
Interventional
Intervention
propofol
sevoflurane
Sponsored by
Hong Kong Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Solid Tumor focused on measuring propofol, sevoflurane, cancer surgery, circulating tumor cells, paediatric

Eligibility Criteria

6 Months - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients coming for elective primary solid tumor resection for curative intent in Hong Kong Children's Hospital
  • AND patients > 5kg
  • AND patients within age limit

Exclusion Criteria:

  • Autoimmune / Chronic inflammatory diseases e.g. Systemic Lupus Erythematosus (SLE), Rheumatoid Arthritis (RA) etc.
  • Current Steroid therapy
  • Surgery for tumour removal in the past year
  • Allergy to Propofol
  • intraoperative use of nitrous oxide
  • Patient susceptible to Malignant Hyperthermia
  • Patients / parents / legal guardians showing preference in anaesthetic techniques during recruitment process

Sites / Locations

  • Hong Kong Children's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Sevoflurane group

propofol group

Arm Description

patients in this group will receive inhalation anaesthesia with sevoflurane at Minimal Alveolar Concentration 0.7-1.3 as the main anaesthetic to achieve Bispectral Index 40-60. Other anaesthetic management will be standardised.

patients in this group will receive intravenous propofol using Target Controlled Infusion 'Paedfusor' model 2-5 as the main anaesthetic to achieve Bispectral Index 40-60. Other anaesthetic management will be standardised.

Outcomes

Primary Outcome Measures

difference in Hypoxia Inducible Factor-1 gene expression
pg/mL

Secondary Outcome Measures

difference in levels of Interleukin-6
pg/mL
difference in levels of Tumor Necrosis Factor-alpha
pg/mL
difference in levels of high sensitivity C reaction protein
mg/L
difference in levels of DNA damage (Comet Assay)
%T (percent tail)
difference in levels of Glutathione Peroxidase
μg/mL
difference in levels of Superoxide dismutase
units/ml
difference in levels of urinary 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG)
ng/mL
difference in levels of 8-oxo-7,8-dihydroguanosine (8-oxoGuo)
ng/mL
difference in the quantity of circulating tumor cells (CTC)
cells/100 µL
cancer free survival at 1 and 3 years
percent

Full Information

First Posted
July 7, 2020
Last Updated
March 14, 2022
Sponsor
Hong Kong Children's Hospital
Collaborators
The University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT04475705
Brief Title
Propofol vs Sevo for Paediatric Tumor Surgery
Official Title
The Effects of Propofol Based Intravenous vs Sevoflurane Inhalation Anaesthesia on Inflammation and Circulating Tumor Cells in Paediatric Tumor Surgery - a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 11, 2021 (Actual)
Primary Completion Date
July 2028 (Anticipated)
Study Completion Date
July 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hong Kong Children's Hospital
Collaborators
The University of Hong Kong

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background: Retrospective studies and meta-analyses have shown a reduction in 5-year survival following inhalational based compared to propofol based total intravenous (TIVA) anaesthesia for cancer surgery. To date there have been no prospective trials published which evaluate the effect of anaesthetic technique on circulating tumour cells (CTC), oxidative stress, and recurrence rate following cancer surgery. Children with cancer often require surgery for tumour excision as well as for other diagnostic and therapeutic procedures. To date there has been no prospective randomized controlled trial evaluating the optimal anaesthetic technique for surgery on children with cancer. Aim: This is a pilot study in paediatric patients who require surgery for tumour excision. The aim is to investigate the effect of sevoflurane inhalational versus propofol intravenous anaesthesia on expression of hypoxia-inducible factor 1 (HIF-1), circulating tumour cells, DNA damage and biomarkers of immunity and inflammation in patients before and after tumour surgery. The patients will be followed up for up to 5 years for tumour recurrence after surgery. Method: This will be a single-blinded randomized controlled trial. One hundred children undergoing tumour excision surgery at the Hong Kong Children's Hospital will be recruited and randomized to receive TIVA or inhalational anaesthesia. Baseline, intraoperative and postoperative blood will be taken for tests of immunity and inflammatory markers, DNA damage and circulating tumour cells. Patients would be followed up to 3 years for tumour recurrence and survival.
Detailed Description
Surgical resection is the main modality of treatment for many solid tumors. Despite successful tumor resection, some patients develop local recurrence or metastasis, causing morbidities and mortality. In recent years, there is growing interest in the pathophysiology of recurrence or metastasis. It is believed that the recurrence is caused by the liberation of circulating tumor cells during surgical manipulation of the tumors and the vascular invasive properties of the tumor cells. Perioperative events, such as surgical stress and anaesthesia may have immunomodulating effects, causing growth or inhibition of circulating tumor cells, which affect disease relapse. There is growing evidence that propofol is anti-inflammatory while sevoflurane is pro-inflammatory and their potential roles in cancer recurrence attract researchers' attention. In adults, there is increasing number of researches showing that propofol may improve patient outcomes in terms of disease survival, when compared to sevoflurane. However, such evidence in paediatric population is lacking. This study aims to compare the effects of propofol based intravenous anaesthesia with inhalation anaesthesia with sevoflurane on perioperative biomarkers of inflammation, circulating tumor cells and disease free survival in 3 years. 100 patients will be recruited for this single blinded randomised controlled trial. They will receive general anaesthesia in Hong Kong Children's Hospital for their primary tumor excision surgery. 50 patients will be randomised to sevoflurane group and 50 patients will be randomised to propofol group. They will receive standardised anaesthetic management in terms of death or anaesthesia, pain management, fluid or thermoregulation management. Sevoflurane group subjects will receive inhalational sevoflurane as main anaesthetic, while propofol group subjects will receive intravenous propofol. These patients will have 4 blood tests collected for analysis for biomarkers of inflammation, DNA damage, oxidative stress and circulating tumor cells. baseline: once patients have intravenous access established intraoperative: when the tumor is deemed resected by surgeons immediately postop: after wound closure 24 hours postop Early postoperative period follow up will look for wound recovery, sepsis, and time to start chemotherapy and need for second look operation for wound complication. Patients will also followed up for 3 years for tumor recurrence and disease survival.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Solid Tumor, Carcinoma, Malignancy, Cancer
Keywords
propofol, sevoflurane, cancer surgery, circulating tumor cells, paediatric

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
single blind controlled trial
Masking
Participant
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sevoflurane group
Arm Type
Active Comparator
Arm Description
patients in this group will receive inhalation anaesthesia with sevoflurane at Minimal Alveolar Concentration 0.7-1.3 as the main anaesthetic to achieve Bispectral Index 40-60. Other anaesthetic management will be standardised.
Arm Title
propofol group
Arm Type
Active Comparator
Arm Description
patients in this group will receive intravenous propofol using Target Controlled Infusion 'Paedfusor' model 2-5 as the main anaesthetic to achieve Bispectral Index 40-60. Other anaesthetic management will be standardised.
Intervention Type
Drug
Intervention Name(s)
propofol
Other Intervention Name(s)
Diprivan
Intervention Description
intravenous propofol using Target Controlled Infusion 'Paedfusor' model 2-5 as the main anaesthetic to achieve Bispectral Index 40-60
Intervention Type
Drug
Intervention Name(s)
sevoflurane
Other Intervention Name(s)
ultane, sevorane
Intervention Description
sevoflurane at Minimal Alveolar Concentration 0.7-1.3 as the main anaesthetic to achieve Bispectral Index 40-60.
Primary Outcome Measure Information:
Title
difference in Hypoxia Inducible Factor-1 gene expression
Description
pg/mL
Time Frame
intraoperative to postoperative 24 hours
Secondary Outcome Measure Information:
Title
difference in levels of Interleukin-6
Description
pg/mL
Time Frame
intraoperative to postoperative 24 hours
Title
difference in levels of Tumor Necrosis Factor-alpha
Description
pg/mL
Time Frame
intraoperative to postoperative 24 hours
Title
difference in levels of high sensitivity C reaction protein
Description
mg/L
Time Frame
intraoperative to postoperative 24 hours
Title
difference in levels of DNA damage (Comet Assay)
Description
%T (percent tail)
Time Frame
intraoperative to postoperative 24 hours
Title
difference in levels of Glutathione Peroxidase
Description
μg/mL
Time Frame
intraoperative to postoperative 24 hours
Title
difference in levels of Superoxide dismutase
Description
units/ml
Time Frame
intraoperative to postoperative 24 hours
Title
difference in levels of urinary 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG)
Description
ng/mL
Time Frame
intraoperative to postoperative 24 hours
Title
difference in levels of 8-oxo-7,8-dihydroguanosine (8-oxoGuo)
Description
ng/mL
Time Frame
intraoperative to postoperative 24 hours
Title
difference in the quantity of circulating tumor cells (CTC)
Description
cells/100 µL
Time Frame
intraoperative to postoperative 24 hours
Title
cancer free survival at 1 and 3 years
Description
percent
Time Frame
intraoperative to postoperative 24 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients coming for elective primary solid tumor resection for curative intent in Hong Kong Children's Hospital AND patients > 5kg AND patients within age limit Exclusion Criteria: Autoimmune / Chronic inflammatory diseases e.g. Systemic Lupus Erythematosus (SLE), Rheumatoid Arthritis (RA) etc. Current Steroid therapy Surgery for tumour removal in the past year Allergy to Propofol intraoperative use of nitrous oxide Patient susceptible to Malignant Hyperthermia Patients / parents / legal guardians showing preference in anaesthetic techniques during recruitment process
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sau Man Lee, MBBS
Phone
+85257413327
Email
lsm335@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Vivian Yuen, MBBS
Phone
+85235133752
Email
yuenmyv@ha.org.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sau Man Lee, MBBS
Organizational Affiliation
Hong Kong Children's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hong Kong Children's Hospital
City
Hong Kong
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rowena Lee
Phone
+85257413327
Email
lsm335@ha.org.hk
First Name & Middle Initial & Last Name & Degree
Vivian Yuen
Phone
+85257413131
Email
yuenmyv@ha.org.hk

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
24803747
Citation
Divatia JV, Ambulkar R. Anesthesia and cancer recurrence: What is the evidence? J Anaesthesiol Clin Pharmacol. 2014 Apr;30(2):147-50. doi: 10.4103/0970-9185.129990. No abstract available.
Results Reference
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PubMed Identifier
23242747
Citation
Heaney A, Buggy DJ. Can anaesthetic and analgesic techniques affect cancer recurrence or metastasis? Br J Anaesth. 2012 Dec;109 Suppl 1:i17-i28. doi: 10.1093/bja/aes421.
Results Reference
background
PubMed Identifier
25818339
Citation
Vinay DS, Ryan EP, Pawelec G, Talib WH, Stagg J, Elkord E, Lichtor T, Decker WK, Whelan RL, Kumara HMCS, Signori E, Honoki K, Georgakilas AG, Amin A, Helferich WG, Boosani CS, Guha G, Ciriolo MR, Chen S, Mohammed SI, Azmi AS, Keith WN, Bilsland A, Bhakta D, Halicka D, Fujii H, Aquilano K, Ashraf SS, Nowsheen S, Yang X, Choi BK, Kwon BS. Immune evasion in cancer: Mechanistic basis and therapeutic strategies. Semin Cancer Biol. 2015 Dec;35 Suppl:S185-S198. doi: 10.1016/j.semcancer.2015.03.004. Epub 2015 Mar 25.
Results Reference
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PubMed Identifier
18550576
Citation
Demicheli R, Retsky MW, Hrushesky WJ, Baum M, Gukas ID. The effects of surgery on tumor growth: a century of investigations. Ann Oncol. 2008 Nov;19(11):1821-8. doi: 10.1093/annonc/mdn386. Epub 2008 Jun 10.
Results Reference
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PubMed Identifier
21935924
Citation
Tavare AN, Perry NJ, Benzonana LL, Takata M, Ma D. Cancer recurrence after surgery: direct and indirect effects of anesthetic agents. Int J Cancer. 2012 Mar 15;130(6):1237-50. doi: 10.1002/ijc.26448. Epub 2011 Nov 9.
Results Reference
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PubMed Identifier
23774231
Citation
Benzonana LL, Perry NJ, Watts HR, Yang B, Perry IA, Coombes C, Takata M, Ma D. Isoflurane, a commonly used volatile anesthetic, enhances renal cancer growth and malignant potential via the hypoxia-inducible factor cellular signaling pathway in vitro. Anesthesiology. 2013 Sep;119(3):593-605. doi: 10.1097/ALN.0b013e31829e47fd.
Results Reference
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PubMed Identifier
18075859
Citation
Kushida A, Inada T, Shingu K. Enhancement of antitumor immunity after propofol treatment in mice. Immunopharmacol Immunotoxicol. 2007;29(3-4):477-86. doi: 10.1080/08923970701675085.
Results Reference
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PubMed Identifier
20889943
Citation
Huitink JM, Heimerikxs M, Nieuwland M, Loer SA, Brugman W, Velds A, Sie D, Kerkhoven RM. Volatile anesthetics modulate gene expression in breast and brain tumor cells. Anesth Analg. 2010 Dec;111(6):1411-5. doi: 10.1213/ANE.0b013e3181fa3533. Epub 2010 Oct 1.
Results Reference
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PubMed Identifier
26556730
Citation
Wigmore TJ, Mohammed K, Jhanji S. Long-term Survival for Patients Undergoing Volatile versus IV Anesthesia for Cancer Surgery: A Retrospective Analysis. Anesthesiology. 2016 Jan;124(1):69-79. doi: 10.1097/ALN.0000000000000936.
Results Reference
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Propofol vs Sevo for Paediatric Tumor Surgery

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