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Trial registered on ANZCTR
Registration number
ACTRN12622000180718
Ethics application status
Approved
Date submitted
14/12/2021
Date registered
2/02/2022
Date last updated
2/02/2022
Date data sharing statement initially provided
2/02/2022
Type of registration
Prospectively registered
Titles & IDs
Public title
Survival and Patterns of Care in the Era of Fluorouracil, Leucovorin, Oxaliplatin and Docetaxel (FLOT)-based Chemotherapy for Gastric and Gastroesophageal Adenocarcinoma (SPACE-FLOT):
An international multicentre cohort study
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Scientific title
Survival and Patterns of Care in the Era of FLOT-based Chemotherapy for Gastric and Gastroesophageal Adenocarcinoma (SPACE-FLOT):
An international multicentre cohort study
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Secondary ID [1]
306240
0
Nil known
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Universal Trial Number (UTN)
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Trial acronym
SPACE-FLOT
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Gastroesophageal adenocarcinomas
324686
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Gastroesophageal cancer
324687
0
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Gastric cancer
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Gastric adenocarcinomas
324969
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Condition category
Condition code
Cancer
322132
322132
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0
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Stomach
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Cancer
322133
322133
0
0
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Oesophageal (gullet)
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
To audit the patterns of care and survival outcomes of patients with gastric and gastroesophageal adenocarcinoma who have undergone preoperative FLOT-based chemotherapy and radical surgical resection stratified by pathological response in the resected specimen.
This study is an international (Australia, New Zealand, Singapore, Malaysia, Hong Kong, Vietnam, India, England, Ireland, Sweden, The Netherlands, France, and Canada) retrospective analysis of practice and outcomes between January 1 2017 to Dec 31 2022. Follow-up data collection is out to Dec 31, 2022 as we need a minimum one-year survival data. We aim to collect data for at least 1500 consecutive patients from all participating sites.
Patient data will include:
• Patient demographics, co-morbidities and characteristics
• Treatment history including pre-operative, operative, and post-operative interventions
• Post-operative complications within 30 days post-surgery
• Clinicopathological and molecular features of disease
• Disease outcomes and survival
• Follow-up data until 2 years post-surgery
All data collected from medical records (no active participant involvement)
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Intervention code [1]
322444
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Diagnosis / Prognosis
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Two-year disease-free survival. This will be assessed by accessing and analysing patient electronic medical records.
Disease free survival: Time from histological diagnosis until disease progression (identified clinically, biochemically, and/or radiologically) or death
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Assessment method [1]
329896
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Timepoint [1]
329896
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Two-year disease-free survival: Time from histological diagnosis until disease progression (identified clinically, biochemically, and/or radiologically) or death. The proportion of patients still disease-free and alive at two-years is defined as two-year DFS.
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Secondary outcome [1]
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Two-year overall survival (OS):
Data will be collected through data-linkage to medical records. There will be no active participant involvement
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Assessment method [1]
404197
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Timepoint [1]
404197
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Two-year OS: Time from histological diagnosis until death. The proportion of patients alive at two-years is defined as two-year OS.
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Secondary outcome [2]
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One-year disease-free survival (DFS)
Data will be collected through data-linkage to medical records. There will be no active participant involvement
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Assessment method [2]
405348
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Timepoint [2]
405348
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One-year DFS: Time from histological diagnosis until disease progression (identified clinically, biochemically, and/or radiologically) or death. The proportion of patients still disease-free and alive at one-years is defined as one-year DFS.
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Eligibility
Key inclusion criteria
• Any patient with gastric and gastroesophageal cancer
• Received preoperative FLOT-based chemotherapy and surgical resection between 01/01/2017 to 31/12/2021
• Age less than or equal to 18 years-of-age
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
• Received further neoadjuvant therapy in addition to FLOT chemotherapy
• Stage 4 disease at diagnosis
• Death within 30 days post resection
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Retrospective
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Statistical methods / analysis
Univariate, multivariate, Kaplan Meier and cox regression analysis will be used in this study. This study is powered to address the 5th hypothesis. Based on the FLOT4 trial, 40% of patients did not receive adjuvant FLOT and the two-year DFS was 55%. Adjuvant chemotherapy is estimated to confer a DFS benefit of 15% at two years (i.e., two-year DFS of 40%, based on the adjuvant chemotherapy with surgery versus surgery alone studies in gastric and gastroesophageal cancers).5, 32 This equates to a hazard ratio of approximately 0.73. Based on this, we will deem 15% as a clinically significant difference in DFS. Therefore, to detect a DFS difference of 15% with 80% power at an alpha level of 0.05, assuming an enrolment ratio of 1 to 0.3 (using a conservative real-world estimate of 30% of patients not receiving adjuvant FLOT), the predicted sample size will be FLOT/surgery/FLOT group: 473 patients, and FLOT/surgery/no adjuvant FLOT group: 157 patients. In total, the number of patents required with minimal/no Tumour Regression Grade (TRG) in the resection specimen = 473 + 157 = 630. Based on local data, 40% of all resected gastric and gastroesophageal cancer show minimal/no TRG, the overall total number of patients required for this study: 630/0.4 = 1575 patients.
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/03/2022
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Actual
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Date of last participant enrolment
Anticipated
1/09/2022
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Actual
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Date of last data collection
Anticipated
31/12/2022
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Actual
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Sample size
Target
1575
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
ACT,NSW,QLD,SA,TAS,WA,VIC
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Recruitment hospital [1]
21320
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The Canberra Hospital - Garran
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Recruitment hospital [2]
21321
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Bankstown-Lidcombe Hospital - Bankstown
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Recruitment hospital [3]
21322
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Royal North Shore Hospital - St Leonards
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Recruitment hospital [4]
21323
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Princess Alexandra Hospital - Woolloongabba
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Recruitment hospital [5]
21324
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Royal Brisbane & Womens Hospital - Herston
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Recruitment hospital [6]
21325
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Flinders Medical Centre - Bedford Park
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Recruitment hospital [7]
21326
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Lyell McEwin Hospital - Elizabeth Vale
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Recruitment hospital [8]
21327
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The Royal Adelaide Hospital - Adelaide
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Recruitment hospital [9]
21328
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Austin Health - Austin Hospital - Heidelberg
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Recruitment hospital [10]
21329
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Bendigo Health Care Group - Bendigo Hospital - Bendigo
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Recruitment hospital [11]
21330
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Box Hill Hospital - Box Hill
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Recruitment hospital [12]
21331
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Monash Medical Centre - Clayton campus - Clayton
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Recruitment hospital [13]
21332
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The Northern Hospital - Epping
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Recruitment hospital [14]
21333
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Peter MacCallum Cancer Centre - Melbourne
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Recruitment hospital [15]
21334
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St Vincent's Private Hospital - Fitzroy
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Recruitment hospital [16]
21335
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Western Hospital - Footscray - Footscray
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Recruitment hospital [17]
21336
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Royal Hobart Hospital - Hobart
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Recruitment hospital [18]
21337
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Launceston General Hospital - Launceston
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Recruitment hospital [19]
21338
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Fiona Stanley Hospital - Murdoch
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Recruitment postcode(s) [1]
36210
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2605 - Garran
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Recruitment postcode(s) [2]
36211
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2200 - Bankstown
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Recruitment postcode(s) [3]
36212
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2065 - St Leonards
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Recruitment postcode(s) [4]
36213
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4102 - Woolloongabba
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Recruitment postcode(s) [5]
36214
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4029 - Herston
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Recruitment postcode(s) [6]
36215
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5042 - Bedford Park
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Recruitment postcode(s) [7]
36216
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5112 - Elizabeth Vale
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Recruitment postcode(s) [8]
36217
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5000 - Adelaide
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Recruitment postcode(s) [9]
36218
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3084 - Heidelberg
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Recruitment postcode(s) [10]
36219
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3550 - Bendigo
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Recruitment postcode(s) [11]
36220
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3128 - Box Hill
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Recruitment postcode(s) [12]
36221
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3168 - Clayton
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Recruitment postcode(s) [13]
36222
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3076 - Epping
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Recruitment postcode(s) [14]
36223
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3000 - Melbourne
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Recruitment postcode(s) [15]
36224
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3065 - Fitzroy
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Recruitment postcode(s) [16]
36225
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3011 - Footscray
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Recruitment postcode(s) [17]
36226
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7000 - Hobart
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Recruitment postcode(s) [18]
36227
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7250 - Launceston
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Recruitment postcode(s) [19]
36228
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6150 - Murdoch
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Recruitment outside Australia
Country [1]
24402
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New Zealand
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State/province [1]
24402
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Auckland
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Country [2]
24403
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New Zealand
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State/province [2]
24403
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Christchurch
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Country [3]
24404
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New Zealand
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State/province [3]
24404
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Dunedin
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Country [4]
24405
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United Kingdom
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State/province [4]
24405
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Birmingham
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Country [5]
24406
0
United Kingdom
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State/province [5]
24406
0
Greater Manchester
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Country [6]
24407
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United Kingdom
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State/province [6]
24407
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Newcastle-upon-Tyne
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Country [7]
24408
0
United Kingdom
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State/province [7]
24408
0
Norwich
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Country [8]
24409
0
United Kingdom
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State/province [8]
24409
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London
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Country [9]
24410
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Ireland
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State/province [9]
24410
0
Dublin
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Country [10]
24411
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Sweden
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State/province [10]
24411
0
Stockholm
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Country [11]
24412
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France
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State/province [11]
24412
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Lille
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Country [12]
24413
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Netherlands
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State/province [12]
24413
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Rotterdam
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Country [13]
24414
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Netherlands
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State/province [13]
24414
0
Utrecht
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Country [14]
24415
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China
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State/province [14]
24415
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Hong Kong
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Country [15]
24416
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India
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State/province [15]
24416
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Vellore
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Country [16]
24417
0
Malaysia
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State/province [16]
24417
0
Selangor
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Country [17]
24418
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Singapore
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State/province [17]
24418
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Singapore
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Country [18]
24419
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Viet Nam
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State/province [18]
24419
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Ho Chi Minh City
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Country [19]
24420
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Canada
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State/province [19]
24420
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Toronto
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Country [20]
24421
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Canada
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State/province [20]
24421
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Montreal
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Funding & Sponsors
Funding source category [1]
310380
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Other
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Name [1]
310380
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Peter MacCallum Cancer Centre
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Address [1]
310380
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305 Grattan St, Melbourne, VIC 3000
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Country [1]
310380
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Australia
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Primary sponsor type
Other
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Name
Peter MacCallum Cancer Centre
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Address
305 Grattan St, Melbourne, VIC 3000
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Country
Australia
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Secondary sponsor category [1]
311522
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None
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Name [1]
311522
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Address [1]
311522
0
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Country [1]
311522
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
310032
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Peter MacCallum Cancer Centre HREC
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Ethics committee address [1]
310032
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305 Grattan St, Melbourne, VIC 3000
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Ethics committee country [1]
310032
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Australia
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Date submitted for ethics approval [1]
310032
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23/09/2021
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Approval date [1]
310032
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30/09/2021
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Ethics approval number [1]
310032
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HREC/76492/PMCC
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Summary
Brief summary
Gastric and gastroesophageal cancers are common and carry exceedingly high mortality rates. Of those patients treated with curative intent, the majority have locally advanced disease, and require chemotherapy before and after radical surgery. Since 2017, 5-fluorouracil, leucovorin, oxaliplatin and paclitaxel (FLOT)-based chemotherapy has become the most commonly used perioperative regimen. This study aims to assess the survival patterns of patients receiving this chemotherapy regimen, and to assess whether receiving FLOT-based chemotherapy both before and after surgical management affects survival compared to those who received only pre-operative FLOT-based chemotherapy. Who is it for? You may be eligible for this study if you are aged 18 years and over, have been diagnosed with gastric or gastroesophageal cancer, and received preoperative FLOT-based chemotherapy and surgical resection between 01/01/2017 to 31/12/2021. Study details For all participants, information regarding survival and disease progression (identified clinically, biochemically, and/or radiologically) will be obtained from your electronic medical record, with no study visits or additional testing required. This data will be used to compare the survival and disease progression between those who did and did not receive post-operative FLOT-based chemotherapy. It is hoped that this research may identify whether there is any further survival benefit from providing post-operative FLOT-based chemotherapy, which may help to dictate future management of patients with gastric or gastroesophageal cancer.
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Trial website
https://www.space-flot.com/
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr David Liu
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Address
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Division of Cancer Surgery
Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, VIC 3000
Upper GI Surgery Unit.
Austin Health, 145 Studley Rd, Heidelberg VIC 3084,
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Country
116254
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Australia
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Phone
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+61 402 857 529
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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David Liu
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Address
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Division of Cancer Surgery
Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, VIC 3000
Upper GI Surgery Unit.
Austin Health, 145 Studley Rd, Heidelberg VIC 3084,
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Country
116255
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Australia
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Phone
116255
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+61 402 857 529
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Fax
116255
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Email
116255
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[email protected]
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Contact person for scientific queries
Name
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David Liu
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Address
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Division of Cancer Surgery
Peter MacCallum Cancer Centre, 305 Grattan St, Melbourne, VIC 3000
Upper GI Surgery Unit.
Austin Health, 145 Studley Rd, Heidelberg VIC 3084,
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Country
116256
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Australia
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Phone
116256
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+61 402 857 529
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Fax
116256
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Email
116256
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF