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. 2022 Aug 22;2022(8):CD010260. doi: 10.1002/14651858.CD010260.pub3

Summary of findings 2. Hysterectomy (simple or radical) with neoadjuvant chemotherapy versus radiotherapy alone for women with locally advanced cervical cancer.

Hysterectomy (simple or radical) with neoadjuvant chemotherapy versus radiotherapy alone for women with locally advanced cervical cancer
Patient or population: women with locally advanced cervical cancer
Settings: outpatient
Intervention: neoadjuvant chemotherapy + radical hysterectomy
Comparison: radiotherapy alone
Outcomes Relative effect
(95% CI) No of participants
(studies) Certainty of the evidence
(GRADE) Comments
Overall survival
Median follow‐up 39–60 months in the 3 trials
HR 0.71 (0.55 to 0.93) 571
(3 RCTs) ⊕⊕⊕⊝
Moderatea
Disease‐ or progression‐free survival
Median follow‐up 39–60 months in the 3 trials
HR 0.75 (0.53 to 1.05) 571
(3 RCTs) ⊕⊕⊕⊝
Moderatea There were varying definitions of disease‐ and progression‐free survival. However, we did not consider this merited further downgrading to low‐certainty evidence.
Quality of life Not reported.
Severe adverse events and toxicity Acute severe toxicity
RR 1.32 (0.47 to 3.71)
118
(1 RCT)
⊕⊕⊝⊝
Lowb
Long‐term severe complications
RR 0.86 (0.49 to 1.50)
409
(1 RCT)
Severe late toxicity
RR 0.60 (0.27 to 1.34)
118
(1 RCT)
CI: confidence interval; HR: hazard ratio; RCT: randomised controlled trial; RR: risk ratio.
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 one level due to concerns regarding the uncertainty of risk of bias in individual trials.
bDowngraded two levels due to incomplete and poor reporting of important adverse events and toxicities and sparseness of data.