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. 2003 Jul 1;89(1):55–64. doi: 10.1038/sj.bjc.6601095

Table 2. Methodological assessment by ELCWP score, according to trials characteristics: (A) all trials and (B) evaluable trials for meta-analysis.

    Global score (%) Design (/10) Laboratory methodology (/10) Generalisability (/10) Results analysis (/10)
(A) All trials
             
Total (n=28) All studies 54.6 4.0 6.1 6.7 5.0
  Patient number P-value 0.0015 0.03 0.03 0.03 0.008
  Evaluable for the MA (n=25) 54.6 4.0 6.4 6.7 5.0
  Not evaluable for the MA (n=3) 54.2 5.0 7.8 6.7 5.0
  P-value 0.53 0.28 0.17 0.91 0.50
  Positive (n=11) 51.5 4.0 5.7 6.6 5.0
  Negative (n=17) 54.6 5.0 7.14 6.6 5.0
  P-value 0.27 0.07 0.44 0.48 0.94
  IHC Ab clone 100 (n=5) 59.4 4.0 5.0 6.7 7.5
  IHC Ab clone 124 (n=21) 52.1 4.0 6.1 6.7 5.0
  P-value 0.25 0.81 0.54 0.54 0.08
             
(B) Evaluable trials for meta-analysis
Evaluable for the MA (n=25) All studies 54.6 4.0 6.4 6.7 5.0
  Patient number P-value 0.004 0.09 0.03 0.045 0.01
  Positive (n=11) 51.5 4.0 5.7 6.7 5.0
  Negative (n=14) 57.0 5.0 6.8 7.1 5.6
  P-value 0.35 0.01 0.64 0.53 0.80
  IHC Ab clone 100 (n=5) 59.4 4.0 5.0 6.7 7.5
  IHC Ab clone 124 (n=18) 50.3 4.0 5.7 6.7 5.0
  P-value 0.10 0.07 0.37 0.07 1.0

Score distributions are summarised by median values. Positive=studies identifying Bcl-2 positivity as significant good prognostic factor for survival; negative=studies reporting nonsignificant results, or associating Bcl-2 positivity with poor survival; MA=meta-analysis; IHC=immunohistochemistry. The values in bold were significant.