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. 2015 Dec 10;2015(12):CD011134. doi: 10.1002/14651858.CD011134.pub2

Luporini 1979.

Study characteristics
Patient sampling Country
Italy
Study design
retrospective
Setting
Hospital
Dates of data collection
1974 ‐ 1976
Population (n)
204
Inclusion criteria
Large bowel malignancies, radical resection
Exclusion criteria
N/R
Participants Included (n)
198
Patient characteristics and setting Age range
N/R
Smoking status
N/R
Site of primary tumour
Large intestine
Stage of primary tumour
Dukes A ‐ B 11, C1 39, C2 30, CH (liver involvement) 32
Perioperative investigations done to ensure no residual disease
N/R
Chemotherapy/radiotherapy?
Yes
Recurrences (n)
62
Site of recurrences
N/R
Index tests CEA timing
N/R
CEA technique
N/R
CEA threshold
5 µg/L
Definition of positive
N/R
Which CEA value (s) used?
N/R
More data available?
N/R
Target condition and reference standard(s) Follow‐up schedule
N/R
Flow and timing Timing of CEA vs reference standard (days)
Unclear
Comparative  
Notes  
Methodological quality
Item Authors' judgement Risk of bias Applicability concerns
DOMAIN 1: Patient Selection
Was a consecutive or random sample of patients enrolled? Unclear    
Did the study avoid inappropriate exclusions? Unclear    
    Unclear Low
DOMAIN 2: Index Test All CEA thresholds
If a threshold was used, was it pre‐specified? Yes    
Is the same method and instrument used for all CEA measurements? Unclear    
Is there an estimation of reproducibility of the method, for example the % coefficient of variation at specific concentrations? No    
Is there an indication of method accuracy, for example, is there evidence of participation in an external quality assessment and proficiency testing scheme? No    
    Unclear Low
DOMAIN 3: Reference Standard
Is the reference standards likely to correctly classify the target condition? Unclear    
Were the reference standard results interpreted without knowledge of the results of the index tests? No    
    Unclear Low
DOMAIN 4: Flow and Timing
Did all patients receive the same reference standard? Unclear    
Were all patients included in the analysis? Unclear    
Was the index test repeated prior to the reference standard? Unclear    
Was the the timing between index test(s) and reference standard ascertainable? Unclear    
Did all patients receive a reference standard? Unclear    
    Unclear