scholarly journals Machine learning for randomised controlled trials: identifying treatment effectheterogeneity with strict control of type I error

2018 ◽  
Author(s):  
Chris C. Holmes ◽  
James A. Watson

AbstractBackgroundIt is widely acknowledged that retrospective exploratory analyses of randomised controlled trials (RCTs) seeking to identify treatment effect heterogeneity (TEH) are prone to bias and false positives. Yet the increasing availability of multiple data modalities on subjects and the desire to learn all we can from trial participants motivates the inclusion of such analyses within RCTs. Coupled to this, widespread advances in AI and machine learning (ML) methods hold great potential to utilise such data to characterise subjects exhibiting heterogeneous treatment response.MethodsWe present new learning strategies for RCT ML discovery methods that ensure strict control of the false positive reporting rate at a pre-specified level. Our approach uses randomised data partitioning and statistical or ML based prediction on held-out data. This can test for both crossover and non-crossover TEH. The former is done via a two-sample hypothesis test measuring overall predictive performance of the ML method. The latter is done via ‘stacking’ the ML predictors alongside a classical statistical model to formally test the added benefit of the ML algorithm. An adaptation of recent statistical theory allows for the construction of a valid aggregate p-value. This learning strategy is agnostic to the choice of ML method.ResultsWe demonstrate our approach with a re-analysis of the SEAQUAMAT trial. We find no evidence for any crossover subgroup who would benefit from a change in treatment from the current standard-of-care, artesunate, but strong evidence for significant noncrossover TEH within the artesunate treatment group. We find that artesunate provides a differential benefit to patients with high numbers of circulating ring stage parasites.ConclusionsOur ML approach combined with the use of computational notebooks and version control can improve the robustness and transparency of RCT exploratory analyses. The methods allow researchers to apply the latest ML techniques safe in the knowledge that any declared associations are statistically significant at a user defined level.

2018 ◽  
Vol 2 (S1) ◽  
pp. e000154
Author(s):  
Aashka Shah ◽  
Devang Rana ◽  
Supriya Malhotra

Aims and Objectives To review and analyse statistically the evidence from existing randomised controlled trials. To compare the efficacy and safety of carbamazepine and phenytoin when used as monotherapy treatments. To assess the effectiveness of the drug at controlling seizures and to evaluate tolerability with regard to side effects of these drugs. Methodology: A systemic review with the comparative evaluation of efficacy and safety of monotherapy with Carbamazepine and Phenytoin in epilepsy was carried out. Seven studies with Randomised Controlled Trials of carbamazepine and phenytoin as monotherapy were taken up for Meta Analysis based on the inclusion and exclusion criteria. Time to withdrawal of allocated treatment (retention time) was chosen as the primary outcome. Secondary outcomes included Time to achieve 12-month remission (seizure-free period), Time to achieve six-month remission (seizure-free period), Time to first seizure post-randomisation, Adverse events (including adverse events relating to treatment withdrawal. The data was entered in the MedCalc Statistical Software version 17.5.5 and analysed. The principal summary measure were the Odd’s Ratio And Hazard Ratio (HR) (at 95% Confidence Interval). Funnel Plot and Forest Plot were plotted. Results: The overall pooled odd‘s ratio for the primary outcome (for 862 participants) was 0.882(fixed effect model) and 0.877(random effect model) (95% confidence interval (CI)0.63 to 1.22, P = 0.3643). The P value was 0.3643 which proved the statistically insignificant difference in the efficacy of the two drugs(0.05 is considered as significant p value). As for the adverse effects ; rash, dysmorphic and idiosyncratic side effects include gum hypertrophy , hirsutism , acne etc. are more frequently associated with phenytoin. Drowsiness, Tiredness, Fatigue and sedation are more associated with carbamazepine as compared to phenytoin. The overall pooled odd’s ratio for “Time to achieve 6 month remission” (for 232 participants) was 1.232(fixed) and 1.272(random) (95% confidence interval (CI) 0.732 to 2.073(fixed), P = 0.0910), indicating an advantage for phenytoin for the 6 month remission outcome. Conclusion: The study concluded that there was no statistically significant difference achieved between the two treatment arms. Hence the neurophysician is compelled to rely on the individual patient characteristics for dispensing the drug. Hence the study provides a robust evidence that the two treatments are equally efficacious.


2019 ◽  
Author(s):  
Arman Eshaghi ◽  
Alexandra Young ◽  
Peter Wijertane ◽  
Ferran Prados ◽  
Douglas L. Arnold ◽  
...  

AbstractMultiple sclerosis (MS) is subdivided into four phenotypes on the basis of medical history and clinical symptoms. These phenotypes are defined retrospectively and lack clear pathobiological underpinning. Since Magnetic Resonance Imaging (MRI) better reflects disease pathology than clinical symptoms, we aimed to explore MRI-driven subtypes of MS based on pathological changes visible on MRI using unsupervised machine learning. In separate train and external validation sets we looked at a total of 21,170 patient-years of data from 15 randomised controlled trials and three observational cohorts to explore MRI-driven subtypes and test whether these subtypes had differential clinical outcomes. We processed MRI data to obtain measures of brain volumes, lesion volumes, and normal appearing white matter T1/T2. We identified three MRI-driven subtypes who were similar in how they accumulated MRI abnormality. Based on the earliest abnormalities suggested by our model they were called: cortex-led, normal appearing white matter-led, and lesion-led subtypes. In the external validation datasets, the lesion-led subtype showed a faster disability progression and higher disease activity than the cortex-led subtype. In all datasets, MRI-driven subtypes were associated with disability progression (βSubtype=0.04, p=0.02; βStage=-0.06, p<0.001), whilst clinical phenotypes and baseline disability were not. Only the lesion-led subtype showed a significant treatment response in three progressive multiple sclerosis randomised controlled trials (−66%, p=0.009) and in three relapsing remitting multiple sclerosis trials (−89%, p=0.04). Our results show that MRI-driven subtyping using machine learning can prospectively enrich clinical trials with patients who are most likely to respond to treatments.


2017 ◽  
Vol 7 (12) ◽  
pp. 55-65
Author(s):  
Apriani ◽  
Hardi Darmawan ◽  
Theodorus

Latar Belakang: Aktivitas fisik anaerobik dapat mengakibatkan terbentuknya radikal bebas sehingga dapat menyebabkan terjadinya stres oksidatif. Untuk mencegah terjadinya stres oksidatif diperlukan antioksidan sintetik. Salah satu contohnya adalah glisodin. Penelitian ini bertujuan untuk mengetahui efektivitas pemberian antioksidan sintetik dan plasebo terhadap kadar SOD pada aktivitas fisik anaerobik.Metode: Penelitian Randomised Controlled Trials, double blind dilaksanakan di Lapangan Olahraga Universitas Sriwijaya Bukit Palembang, sedangkan untuk pemeriksaan kadar SOD di Laboratorium Biologi Molekuler Universitas Sriwijaya Palembang. Jumlah sampel dalam penelitian ini sebanyak 34 sampel yang dibagi menjadi 2 kelompok yaitu kelompok perlakuan dengan pemberian antioksidan sintetik (glisodin) sebanyak 2 kapsul (500 IU) dan kelompok plasebo dengan pemberian 2 kapsul kosong dengan warna, bentuk dan ukuran yang sama dengan glisodin.Hasil: Hasil penelitian melalui paired t-test menunjukkan bahwa rerata kadar SOD (dalam satuan Dalton) sebelum perlakuan pada kelompok glisodin 0,066 ± 0,059 dan sesudah perlakuan 1,135 ± 0,959, denganp value = 0,000, sedangkan pada kelompok plasebo sebelum perlakuan 0,059 ± 0,064 dan sesudah perlakuan 0,343 ± 0,224, dengan p value = 0,000. Hasil penelitian ini menunjukkan bahwa terjadi peningkatan kadar SOD yang signifikan pada kelompok perlakuan setelah diberikan antioksidan sintetik (glisodin).Kesimpulan: Ada perbedaan efektivitas pemberian antioksidan sintetik dan plasebo terhadap kadar SOD pada aktivitas fisik anaerobik.


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