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Sampurna Kundu

Publications and source records attributed to Sampurna Kundu.

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Adjusting SPRT for an Efficient Procedure with Finite Number of Applications of Less Effective Treatment

We propose an adaptive Sequential Probability Ratio Test (SPRT) which allocates a finite number of applications to the less effective treatment. In the classical SPRT framework, patients are assigned to the two competing treatments one by one until the stopping criterion, based on breaching the boundary values which are pre-determined using the Type-I and Type-II error probabilities, is met. This ensures the control of errors at the cost of ethical efficiency as the exposure to the less effective treatment is large. We begin with proposing an adaptive sequential framework for testing two simple hypotheses that analytically ensures finite exposure to the less effective treatment. Our proposed procedure employs a likelihood ratio driven adaptive allocation rule, dynamically concentrating sampling effort on the superior population while preserving asymptotic efficiency (in terms of average sample number), comparable to the classical SPRT. We derive an explicit closed-form expression for the expected number of allocations to the inferior treatment. Extensive simulation studies and real data analyses substantiate the theoretical results, evincing a significant reduction in inferior allocations compared to the classical SPRT. The proposed design thus offers a balanced method between statistical precision and ethical responsibility, aligning inferential reliability with patient safety.

math.ST

To Study Properties of a Known Procedure in Adaptive Sequential Sampling Design

We consider the procedure proposed by Bhandari et al. (2009) in the context of two-treatment clinical trials, with the objective of minimizing the applications of the less effective drug to the least number of patients. Our focus is on an adaptive sequential procedure that is both simple and intuitive. Through a refined theoretical analysis, we establish that the number of applications of the less effective drug is a finite random variable whose all moments are also finite. In contrast, Bhandari et al. (2009) observed that this number increases logarithmically with the total sample size. We attribute this discrepancy to differences in their choice of the initial sample size and the method of analysis employed. We further extend the allocation rule to multi-treatment setup and derive analogous finiteness results, reinforcing the generalizability of our findings. Extensive simulation studies and real-data analyses support theoretical developments, showing stabilization in allocation and reduced patient exposure to inferior treatments as the total sample size grows. These results enhance the long-term ethical strength of the proposed adaptive allocation strategy.

math.ST