Summary of findings 4. Hysterectomy (simple or radical) with chemoradiotherapy versus chemoradiotherapy alone.
Hysterectomy (simple or radical) with chemoradiotherapy versus chemoradiotherapy alone | ||||
Patient or population: women with locally advanced cervical cancer Settings: outpatient Intervention: chemoradiotherapy + hysterectomy (simple or radical) Comparison: chemoradiotherapy alone | ||||
Outcomes | Relative effect | No of participants | Certainty of the evidence (GRADE) | Comments |
Overall survival Median follow‐up 3.8 years |
Overall survival was inadequately reported and it was not possible to calculate a hazard ratio. Overall survival time in the chemoradiotherapy + hysterectomy group was 6–40 months, median survival time was 23 months, and 3‐year survival rate was 82.7%. Total survival time in the chemoradiotherapy group was 5–41 months, median survival time was 22.5 months and 3‐year survival rate was 81.8%. Trial authors reported differences between arms were not statistically significant (P = 0.56). | 102 (1 RCT) | ⊕⊝⊝⊝ Very lowa,b | — |
Progression or event‐free survival Median follow‐up 3.8 years |
Progression‐free survival was inadequately reported in both trials and it was not possible to calculate a hazard ratio. In 1 trial, progression‐free survival time in the chemoradiotherapy + hysterectomy group was 3–40 months, median survival time was 23 months and 3‐year survival rate was 73.1%. The progression‐free survival time in the chemoradiotherapy alone group was 5–41 months, median survival time was 22 months and 3‐year survival rate was 64.8%. There was no significant difference between arms (P = 0.76). Another trial included 61 women and compared chemoradiotherapy + simple or radical hysterectomy vs chemoradiotherapy alone. There was no difference in 3‐year event‐free (death) survival rate (86% in the chemoradiotherapy + hysterectomy group vs 97% in the chemoradiotherapy alone group; log rank P = 0.15). |
163 (2 RCT) | ⊕⊝⊝⊝ Very lowa,b | — |
Quality of life | — | — | — | Not adequately reported. |
Severe/serious adverse events | — | — | — | Not adequately reported. |
RCT: randomised controlled trial. | ||||
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. |
aDowngraded two levels due to sparse data leading to imprecision. bDowngraded one level due to small number of trials and a lack of representation.