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. 2020 Jul 7;2020(7):CD008946. doi: 10.1002/14651858.CD008946.pub3

Summary of findings 4. IFN‐α + acitretin compared to IFN‐α + PUVA for mycosis fungoides.

IFN‐α + acitretin compared toIFN‐α + PUVA for mycosis fungoides
Patient or population: people with mycosis fungoides
Setting: tertiary care setting
Intervention: IFN‐α + acitretin
Comparison: IFN‐α + PUVA
Number of trials included: 1 (Stadler 1998)
Outcomes Anticipated absolute effects* (95% CI) Relative effect
(95% CI) № of participants
(studies) Certainty of the evidence
(GRADE) Comments
Risk with IFN‐α + PUVA Risk with IFN‐α + acitretin
Improvement of quality of life Not measured
Common adverse effects ‐ Flu‐like symptoms
(Time point of measurement: up to 48 weeks or until complete response)
Study population RR 1.32
(0.92 to 1.88) 82
(1 RCT) ⊕⊕⊝⊝
Low a
525 per 1000 693 per 1000
(483 to 987)
Complete response
(Time point of measurement: up to 48 weeks or until complete response)
Study population RR 0.54
(0.35 to 0.84) 82
(1 RCT) ⊕⊕⊝⊝
Low a
700 per 1000 378 per 1000
(245 to 588)
Objective response rate Not measured
*The risk in the intervention group (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: Confidence interval; RR: Risk ratio
GRADE Working Group grades of evidenceHigh certainty: we are very confident that the true effect lies close to that of the estimate of the effect.
Moderate certainty: we are moderately confident in the effect estimate; the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different.
Low certainty: our confidence in the effect estimate is limited; the true effect may be substantially different from the estimate of the effect.
Very low certainty: we have very little confidence in the effect estimate;the true effect is likely to be substantially different from the estimate of effect.

a Downgraded by two levels to low‐certainty evidence. One level because of low internal validity (risk of bias ‐ high risk of attrition bias) and one level because of low sample size (imprecision)