Steiner R 1983.
Study characteristics | ||
Methods | Accrual (May 1977 ‐ Jan 1980)
RCT ‐ methodology not described Groups at baseline similar in age and diagnosis, post operative disease free interval and time interval between diagnosis and commencement of treatment. Performance status more favourable in combination group |
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Participants | 119 women with MBC with no prior chemotherapy for ABC, no signs of cardiac failure and the presence of progressive disease in evaluable lesions
116 patients had previous endocrine therapy
100% MBC
100% firstline Randomised numbers not provided Assessable no: 1) n = 53 2) n = 54 |
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Interventions | A vs A + V1 1) Doxorubicin 70 mg/m2 IV on day 1 of a 3/52 cycle 2) Doxorubicin 70 mg/m2 IV on day 1 of a 3/52 cycle + Vincristine 1.4 mg/m2 (max 2mg) on days 1 and 8 **Maximum of 8 courses |
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Outcomes | No survival curves. Survival curves for responders only
No TTP curves Median survival 1) 10mths 2) 14mths OR (CR+PR) 1) 30/53 2) 28/54 Toxicity: Nausea and vomiting 1) 42/53 2) 47/54 Alopecia 1) 44/53 2) 47/54 WCC 1) 3/53 2) 10/54 Toxic death 1) 1/53 (septicaemia) 2) 1/54 (pantocytopenia) |
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Notes | Not ITT ‐ 119 women were entered into the study but 10 were excluded from the analysis. A further 2 women who died soon after randomisation were included in the survival analysis but not in the response analysis. | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Not reported |
Allocation concealment (selection bias) | Unclear risk | Not reported |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Randomisation numbers not provided and insufficient information provided to permit judgement |
Selective reporting (reporting bias) | High risk | Provides survival information for responders only |