Work

The Correlated Beta Dose Optimisation Approach: Optimal Vaccine Dosing Using Mathematical Modelling and Adaptive Trial Design

Year: 2022
Type: article
Abstract: Mathematical modelling methods and adaptive trial design are likely to be effective for optimising vaccine dose but are not yet commonly used. This may be due to uncertainty with regard to the correct choice of parametric model for dose-efficacy or dose-toxicity. Non-parametric models have previously been suggested to be potentially useful in this situation. We propose a novel approach for locating optimal vaccine dose based on the non-parametric Continuous Correlated Beta Process model and adaptive trial design. We call this the 'Correlated Beta' or 'CoBe' dose optimisation approach. We evaluated the CoBe dose optimisation approach compared to other vaccine dose optimisation approaches using a simulation study. Despite using simpler assumptions than other modelling-based methods, we found that the CoBe dose optimisation approach was able to effectively locate the maximum efficacy dose for both single and prime/boost administration vaccines. The CoBe dose optimisation approach was also effective in finding a dose that maximises vaccine efficacy and minimises vaccine-related toxicity. Further, we found that these modelling methods can benefit from the inclusion of expert knowledge, which has been difficult for previous parametric modelling methods. This work further shows that using mathematical modelling and adaptive trial design is likely to be beneficial to locating optimal vaccine dose, ensuring maximum vaccine benefit and disease burden reduction, ultimately saving lives.
Source: Vaccines
Language: English
Open Access status: gold
Estimated APC paid: $2,303
Awards: G1137608440, G1355184373, G1376763848, G1637947929, G1678426632, G1683766189, G1970415052, Improving scientific and public health decision making by developing technologies to increase use of robust methods to calibrate and analyse complex mathematical models, G2081556041, Infection prevention and control for drug-resistant tuberculosis in South Africa in the era of decentralised care: a whole systems approach, G242513792, G2540431516, G2660122252, G2765903232, G312473268, G3240114319, G3272303642, G3329879854, G3393291838, G3470180491, G3566272965, G3567583227, G3582174166, G3745013358, Defining drivers of TB transmission in the era of universal ART, and implications for finding the walking well, Be part of launching a new scientific field - immunostimulation/ immunodynamic (IS/ID) mathematical modelling to accelerate vaccine development, G3888644941, G3993034709, G4060541036, G4076556769, G4130055316, G4197743543, G4264973107, G431770663, G4360562954, G4530537375, G4572116775, G4672374498, G4689986499, G4728353148, G4750217163, G4789575852, G49588791, G4981557136, G5251925207, G5328177787, London School of Hygiene and Tropical Medicine - to understand which investments in novel clinical advances in TB vaccines would have greatest impact, London Interdisciplinary Doctoral Programme, G5866603881, G5873261844, G6353825571, G6418237272, G6672319158, G7103697278, G7221052363, G7318299752, G7460822696, G7509151980, G7809951108, G8050930789, G8057699476, G8107612341, G8278091538, G8432911371, G8475824479, G8666374500, G8768411689, G8811883060, G8985606845, G927319347, G996267264
OpenAlex ID: W4307623895
FWCI: 0.469
Cites: 58
Cited by: 3
Related to: 10