Antiepidermal growth factor receptor therapy for glioblastoma | ||||||
Patient or population: Adult (aged ≥ 18 years) with histologically confirmed glioblastoma diagnosis, either newly diagnosed or with recurrent disease were included. Intervention: anti‐EGFR therapy (including anti‐EGFR monoclonal antibodies, EGFR tyrosine kinase inhibitors or vaccines) alone or in combination with standard of care Comparison: standard of care or placebo | ||||||
Outcomes | Illustrative comparative risks | Relative effect (95% CI) | No of participants (studies) | Certainty of evidence (GRADE) | Comment | |
Assumed risk | Corresponding risk | |||||
Overall survival | ||||||
Progression‐free survival | ||||||
Adverse effects | ||||||
Quality of life | ||||||
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk(and its 95% CI) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI). CI: confidence interval; EGFR: epidermal growth factor receptor. | ||||||
GRADE Working Group grades of evidence High certainty: further research is very unlikely to change our confidence in the estimate of effect. Moderate certainty: further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate. Low certainty: further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. Very low certainty: we are very uncertain about the estimate. |