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Efficacy of tanezumab vs. placebo on pain, function, safety for patients with knee OA
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OSTEOARTHRITIS
Efficacy of tanezumab vs. placebo on pain, function, safety for patients with knee OA .
High Impact
Este estudo foi identificado como tendo um impacto potencialmente elevado. A métrica de Alto Impacto da OE, baseada em IA, estima a influência que um artigo poderá ter, integrando sinais da revista em que foi publicado e do conteúdo científico do próprio artigo. Desenvolvido com recurso ao mais avançado processamento de linguagem natural, o modelo High Impact da OE prevê com maior precisão o desempenho futuro de um estudo em termos de citações do que o fator de impacto da revista por si só. Isto permite o reconhecimento precoce de investigação clinicamente significativa e ajuda os leitores a concentrarem-se nos artigos com maior probabilidade de moldar a prática futura.

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2016;4(24):20 PLoS One. 2016 Jun 13;11(6):e0157105.

4 randomized controlled trials (n=1833 patients) were included in this meta-analysis for the purpose of comparing analgesic efficacy and safety of tanezumab when compared to placebo treatment. Outcomes of interest included changes in Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain, WOMAC physical function, patient global assessment, the incidence of adverse events, and treatment discontinuation due to adverse effects. Results demonstrated that patients who were given tanezumab had significantly improved pain, function, and global assessment scores when compared to the placebo group. However, significant increases in therapy discontinuation due to adverse effects, development of abnormal peripheral sensation, and peripheral neuropathy were also observed.


Detalhes do financiamento da publicação +
Financiamento:
Non-Industry funded
Patrocinador:
State Key Program of National Natural Science Foundation of China, Special Program for Sino-Russian Joint Research Sponsored by the Ministry of Science and Technology, and Key Program Sponsored by the Tianjin Science and Technology Committee
Conflicts:
None disclosed

Risco de viés

8,5/10

Critérios de notificação

17/20

Índice de Fragilidade

N/A

Were the search methods used to find evidence (original research) on the primary question or questions stated?

Was the search for evidence reasonably comprehensive?

Were the criteria used for deciding which studies to include in the overview reported?

Was the bias in the selection of studies avoided?

Were the criteria used for assessing the validity of the included studies reported?

Was the validity of all of the studies referred to in the text assessed with use of appropriate criteria (either in selecting the studies for inclusion or in analyzing the studies that were cited)?

Were the methods used to combine the findings of the relevant studies (to reach a conclusion) reported?

Were the findings of the relevant studies combined appropriately relative to the primary question that the overview addresses?

Were the conclusions made by the author or authors supported by the data and or analysis reported in the overview?

How would you rate the scientific quality of this evidence?

Sim = 1

Incerto = 0,5

Não relevante = 0

Não = 0

A Avaliação dos Critérios de Relato avalia a transparência com que os autores relatam as caraterísticas metodológicas e do ensaio na publicação. A avaliação está dividida em cinco categorias que são apresentadas de seguida.

4/4

Introduction

4/4

Accessing Data

3/4

Analysing Data

4/4

Results

2/4

Discussion

Detsky AS, Naylor CD, O'Rourke K, McGeer AJ, L'Abbé KA. J Clin Epidemiol. 1992;45:255-65

O Índice de Fragilidade é uma ferramenta que auxilia na interpretação de achados significativos, fornecendo uma medida de força para um resultado. O Índice de Fragilidade representa o número de eventos consecutivos que precisam de ser adicionados a um resultado dicotómico para que o resultado deixe de ser significativo. Um número pequeno representa um resultado mais fraco e um número grande representa um resultado mais forte.

Porque é que este estudo era necessário agora?

First-line treatment for pain associated with osteoarthritis of the knee often includes paracetamol, non-steroidal anti-inflammatory drugs, and other select analgesic medication. Although the efficacy of these treatments has been established through research for the majority of patients with knee OA, there still remains the potential risk of hepatotoxicity, gastrointestinal distress, and cardiorenal side effects. Tanezumab, a newly developed monoclonal antibody, has shown a promising effect in selectively inhibiting nerve growth factor (NGF), a critical element in the experience of osteoarthritic pain. A recent study has shown promising therapeutic efficacy when compared to placebo, however, its use in patients with knee OA specifically has been sparse and inconclusive.

Qual era a principal questão de investigação?

What is the efficacy and safety of the use of Tanezumab for pain associated with osteoarthritis of the knee in terms of improvement in pain, function, patient global assessment, and incidence of adverse events?

Caraterísticas do estudo +
Data Source:
PubMed, EMBASE, and the Cochrane Central Register of Controlled Trials (CENTRAL) were searched for potential studies for inclusion up to July 25, 2015. References lists of eligible studies were also manually searched for any additional articles of relevance.
Index Terms:
Index terms included “Tanezumab” and “knee osteoarthritis”; terms were additionally combined with Boolean operators for search strategy.
Study Selection:
4 randomized controlled trials investigating the use of Tanezumab for the treatment of knee osteoarthritis were included in this meta-analysis. Eligible articles were required to possess the following four criteria: (1) patients enrolled had a diagnosis of knee OA according to the American College of Rheumatology with at least a grade of 2 on the Kellgren-Lawrence grading scale, (2) patients received intravenous administration of Tanezumab, (3) comparisons were made to placebo therapy, and (4) outcomes included WOMAC pain, WOMAC function, patient global assessment (PGA), adverse events, incidence of abnormal peripheral sensations, and incidence of peripheral neuropathy. Study screening and selection was performed by two independent investigators, with conflicts resolved by a discussion with a third reviewer.
Data Extraction:
Data extraction was performed by two independent investigators, with discrepancies resolved by a third reviewer. Mean change in WOMAC pain, WOMAC physical function, and PGA were defined as the primary outcomes of this analysis; secondary outcomes included discontinuation due to adverse events, the incidence of serious adverse events, abnormal peripheral sensations, and peripheral neuropathy.
Data Synthesis:
All statistical analyses were performed with Review Manager (version 5.3). Dichotomous outcomes were assessed with calculated relative risk (RR) and associated 95% confidence intervals (CI) and a random-effects model was used to estimate pooled outcomes without the influence of heterogeneity. Heterogeneity was calculated with I^2 statistics, where values above 50% were labeled as significantly heterogeneous. The Quality of Evidence and Risk of Bias assessments were completed with GRADE and the Cochrane Handbook for Systematic Reviewers of Interventions respectively.
Quais foram os resultados importantes?
  • When compared to placebo, tanezumab groups demonstrated a significantly greater reduction in WOMAC pain scores (4 studies, n=1833 patients; SMD= 0.51 [95% CI 0.34-0.69], p<0.00001, I^2= 48%). (GRADE level of evidence: moderate)
  • Tanezumab groups demonstrated a significantly greater reduction in WOMAC physical function scores when compared to placebo (4 studies, n=1833 patients; SMD=0.56 [95% CI 0.38-0.74], p<0.00001, I^2=52%). (GRADE level of evidence: low)
  • Tanezumab groups demonstrated significantly greater improvement in PGA scores when compared to placebo (2 studies; SMD= 0.34 [95% CI 0.22-0.47], p<0.00001, I^2=0%). (GRADE level of evidence: moderate)
  • When compared to placebo, tanezumab demonstrated a significantly higher risk of therapy discontinuation due to adverse events (3 studies; RR=2.89 [95% CI 1.59-5.26], p=0.0005, I^2=0%). (GRADE level of evidence: very low)
  • Differences in incidence of serious adverse events (defined by requiring significant hospital intervention or causing disability, congenital anomaly, or death) were not significant between tanezumab and placebo groups (4 studies; RR=1.06 [95% CI 0.59-1.92], p=0.84, I^2=0%). (GRADE level of evidence: low)
  • Tanezumab groups demonstrated a significant increase in the incidence of abnormal peripheral sensations when compared placebo (4 studies; RR=3.14 [95% CI 2.12-4.66], p<0.00001, I^2=16%). (GRADE level of evidence: low)
  • Tanezumab groups demonstrated a significant increase in the incidence of peripheral neuropathy when compared the placebo group (2 studies; RR=6.05 [95% CI 2.32-15.81], p=0.0002, I^2=0%). (GRADE level of evidence: low)
  • Subgroup analysis revealed that primary outcomes measures were not significantly different between tanezumab and placebo groups when tested for administration frequency (twice or thrice daily) or phase of the trial (phase II vs. phase III).
De que é que me devo lembrar mais?

For patients with osteoarthritis of the knee, treatment with tanezumab resulted in significant improvements in WOMAC pain, WOMAC function, and patient global assessment while maintaining comparable incidence of serious adverse events when compared to placebo therapy. However, tanezumab was associated with a significantly increased risk of therapy discontinuation due to adverse events, particularly due abnormal peripheral sensation and peripheral neuropathy.

Como é que isto afectará o tratamento dos meus doentes?

The results of this meta-analysis suggest that tanezumab may be of clinical benefit for patients with knee osteoarthritis as evidenced by significant improvements in pain, function, and assessment when compared to placebo. Significantly higher risks of therapy discontinuation (due to adverse effects), development of abnormal peripheral sensation and neuropathy were also noted. Further investigation with controlled methodology is recommended for validation of significant benefits. Direct comparisons made between tanezumab therapy and other popular modes of analgesic relief is also recommended to additionally compare the clinical and safety outcomes.

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Como citar isto ACE Report

OrthoEvidence. Efficacy of tanezumab vs. placebo on pain, function, safety for patients with knee OA. OE Journal. 2016;4(24):20. Available from: https://myorthoevidence.com/AceReport/Show/efficacy-of-tanezumab-vs-placebo-on-pain-function-safety-for-patients-with-knee-oa

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