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A Comparison of Alternative Network Meta-Analysis Methods in the Presence of Nonproportional Hazards: A Case Study in First-Line Advanced or Metastatic Renal Cell Carcinoma.
Cope, Shannon; Chan, Keith; Campbell, Harlan; Chen, Jenny; Borrill, John; May, Jessica R; Malcolm, William; Branchoux, Sebastien; Kupas, Katrin; Jansen, Jeroen P.
Afiliación
  • Cope S; Evidence Synthesis and Decision Modeling, PRECISIONheor, Vancouver, BC, Canada. Electronic address: shannon.cope@precisionvh.com.
  • Chan K; Evidence Synthesis and Decision Modeling, PRECISIONheor, Vancouver, BC, Canada.
  • Campbell H; Evidence Synthesis and Decision Modeling, PRECISIONheor, Vancouver, BC, Canada.
  • Chen J; Evidence Synthesis and Decision Modeling, PRECISIONheor, Vancouver, BC, Canada.
  • Borrill J; Worldwide Health Economics and Outcomes Research, Bristol Myers Squibb, Uxbridge, England, UK.
  • May JR; Worldwide Health Economics and Outcomes Research, Bristol Myers Squibb, Uxbridge, England, UK.
  • Malcolm W; Worldwide Health Economics and Outcomes Research, Bristol Myers Squibb, Uxbridge, England, UK.
  • Branchoux S; Health Economics and Outcomes Research, Bristol Myers Squibb, Rueil-Malmaison, France.
  • Kupas K; Global Biometric Sciences, Bristol Myers Squibb, Boudry, Switzerland.
  • Jansen JP; Evidence Synthesis and Decision Modeling, PRECISIONheor, Vancouver, BC, Canada.
Value Health ; 26(4): 465-476, 2023 04.
Article en En | MEDLINE | ID: mdl-36503035
ABSTRACT

OBJECTIVES:

Network meta-analysis (NMA) of time-to-event outcomes based on constant hazard ratios can result in biased findings when the proportional hazards (PHs) assumption does not hold in a subset of trials. We aimed to summarize the published non-PH NMA methods for time-to-event outcomes, demonstrate their application, and compare their results.

METHODS:

The following non-PH NMA methods were compared through an illustrative case study in oncology of 4 randomized controlled trials in terms of progression-free survival and overall survival (1) 1-step or (2) 2-step multivariate NMAs based on traditional survival distributions or fractional polynomials, (3) NMAs with restricted cubic splines for baseline hazard, and (4) restricted mean survival NMA.

RESULTS:

For progression-free survival, the PH assumption did not hold across trials and non-PH NMA methods better reflected the relative treatment effects over time. The most flexible models (fractional polynomials and restricted cubic splines) fit better to the data than the other approaches. Estimated hazard ratios obtained with different non-PH NMA methods were similar at 5 years of follow-up but differed thereafter in the extrapolations. Although there was no strong evidence of PH violation for overall survival, non-PH NMA methods captured this uncertainty in the relative treatment effects over time.

CONCLUSIONS:

When the PH assumption is questionable in a subset of the randomized controlled trials, we recommend assessing alternative non-PH NMA methods to estimate relative treatment effects for time-to-event outcomes. We propose a transparent and explicit stepwise model selection process considering model fit, external constraints, and clinical validity. Given inherent uncertainty, sensitivity analyses are suggested.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Células Renales / Neoplasias Renales Tipo de estudio: Clinical_trials / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Value Health Asunto de la revista: FARMACOLOGIA Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Carcinoma de Células Renales / Neoplasias Renales Tipo de estudio: Clinical_trials / Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Value Health Asunto de la revista: FARMACOLOGIA Año: 2023 Tipo del documento: Article
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