Tsuda 2004.
Methods | Uncontrolled phase I/II study | |
Participants | 14 patients with gynaecological cancer after primary therapy (ovarian cancer n = 5; NED n = 2) | |
Interventions | Subcutaneous individualised short peptide cocktail Adjuvant: Montanide ISA‐51 |
|
Outcomes | Tumour responses Immune responses: humoral, cellular Adverse events: not separately described for ovarian cancer patients |
|
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | High risk | Uncontrolled trial |
Allocation concealment (selection bias) | High risk | Uncontrolled trial |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Information insufficient to permit judgement of ‘low risk’ or ‘high risk’ |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Information insufficient to permit judgement of ‘low risk’ or ‘high risk’ |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Information insufficient to permit judgement of ‘low risk’ or ‘high risk’ |
Selective reporting (reporting bias) | Unclear risk | Information insufficient to permit judgement of ‘low risk’ or ‘high risk’ |
Other bias | Unclear risk | Information insufficient to permit judgement of ‘low risk’ or ‘high risk’ |