Endocrine oncology

Tyrosine kinase inhibitors for radioiodine refractory differentiated thyroid cancer: A systematic review and meta‐analysis

Clin Endocrinol (Oxf)Published Systematic review and network meta-analysis of randomised trials

Pooled result · PFSResult — go to the resultHazard ratio 0.19 95% CrI 0.14–0.25

Authors' conclusion

The results of this meta-analysis suggest that targeted therapy with TKIs may be beneficial for patients with radioiodine-refractory advanced or metastatic differentiated thyroid cancer. Among the TKIs analyzed, lenvatinib appeared to be the most effective at improving PFS, although it also had the highest incidence of AEs. Further research through direct randomized controlled trials is needed to determine the optimal choice of TKI for treating patients with RAIR-DTC. This study is beneficial for formulating patients' treatment plans and guides clinicians' decision-making.

Study context

Population
Patients with radioiodine refractory differentiated thyroid cancer (RAIR-DTC) in randomized clinical trials (RCTs) of TKI therapy
Participants
1,310 patients7 studies
Comparison
TKI monotherapies vs placebo
Outcome
PFS
Methodological detailsCochrane risk-of-bias tool
  • Cochrane risk-of-bias tool

Pooled result

As reported in the abstract

Hazard ratio

0.19

95% CrI 0.14–0.25

Lenvatinibvs Placebo
HR 0.19 (95% CrI 0.14–0.25)

Further pooled results

OutcomeHR (95% CrI)
OSApatinibvs PlaceboCrI0.42 (0.18–0.97)
OSAnlotinibvs PlaceboCrI0.36 (0.18–0.73)

Overall survival (OS)

Only apatinib and anlotinib showed statistically significant OS benefit vs placebo

Subgroups (BRAF or RAS mutation; papillary or follicular subtype; prior TKI)

TKI treatment may be similarly effective regardless of mutation, subtype or prior TKI treatment

Safety

Higher incidence of grade ≥3 adverse events (AEs) with tyrosine kinase inhibitors (TKIs) vs placebo
Lenvatinib had the highest incidence of AEs

Original publication

Tyrosine kinase inhibitors for radioiodine refractory differentiated thyroid cancer: A systematic review and meta‐analysis. Clin Endocrinol (Oxf). Published 13 February 2024. doi:10.1111/cen.15027

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