# P-1402. Long-term costs and health outcomes of biomarker-based tests to reduce tuberculosis treatment duration in South India: A modeling study

**Authors:** Palak Shah, Madolyn Dauphinais, Pranay Sinha

PMC · DOI: 10.1093/ofid/ofaf695.1589 · Open Forum Infectious Diseases · 2026-01-11

## TL;DR

This study models how using biomarker tests to shorten tuberculosis treatment can be cost-effective in South India, depending on test accuracy and cost.

## Contribution

The study introduces a Markov model to evaluate the cost-effectiveness of biomarker-guided TB treatment shortening in a high-burden setting.

## Key findings

- Biomarker-guided treatment at four or two months was cost-saving compared to standard therapy for all test types except sequencing.
- Two-month strategies were cost-effective if test cost ≤$105 and NPV ≥0.77, while four-month strategies required NPV ≥0.75 and test cost ≤$96.
- Serology and lateral flow tests had >80% probability of being cost-effective across most scenarios.

## Abstract

While effective, tuberculosis (TB) treatment is long and burdensome. Biomarker-guided strategies to shorten therapy have the potential to reduce costs and improve adherence, but the conditions under which such strategies are cost-effective remain unclear.Table 1.Key model inputs and assumptionsTable 2.Model outputs

Key model inputs and assumptions

Model outputs

We developed a Markov model to evaluate the cost-effectiveness of biomarker-guided treatment shortening in South India. Three scenarios were modeled: standard six-month therapy and biomarker-guided completion at four or two months. Outcomes included costs, disability-adjusted life years (DALYs), and incremental cost-effectiveness ratios (ICERs). We conducted one- and two-way sensitivity analyses varying test cost and negative predictive value (NPV), and generated cost-effectiveness acceptability curves (CEACs).Two-way sensitivity analysis of test cost and negative predictive value1A) Analysis with treatment completion at two months at $571.50 willingness to pay threshold; 1B) Analysis with treatment completion at four months at $571.50 willingness to pay thresholdCost-effectiveness acceptability curves for biomarker testing relative to standard therapy.2A) Serology testing at two months; 2B) lateral flow testing at two months; 2C) Serology testing at four months; 2D) lateral flow testing at four months

Two-way sensitivity analysis of test cost and negative predictive value

1A) Analysis with treatment completion at two months at $571.50 willingness to pay threshold; 1B) Analysis with treatment completion at four months at $571.50 willingness to pay threshold

Cost-effectiveness acceptability curves for biomarker testing relative to standard therapy.

2A) Serology testing at two months; 2B) lateral flow testing at two months; 2C) Serology testing at four months; 2D) lateral flow testing at four months

At a willingness-to-pay threshold of $571.50 per DALY averted, biomarker-guided treatment at four or two months was cost-saving compared to standard therapy for all test types except sequencing. For two-month strategies, ICERs ranged from dominance (nucleic-acid amplification test, lateral flow, and serology) to $675/DALY averted (sequencing). At four months, all non-sequencing tests dominated standard care. In one-way sensitivity analysis, results were most sensitive to test cost and NPV. Two-way analysis revealed that two-month strategies were cost-effective if NPV≥0.77 and test cost ≤$105; four-month strategies were cost-effective if NPV ≥0.75 and test cost ≤$96. CEACs showed serology and lateral flow tests had >80% probability of being cost-effective across most simulated scenarios at both time points.

Biomarker-guided treatment shortening can be highly cost-effective in high-burden settings, particularly if test costs are low and NPVs high. These findings can inform target product profiles for TB biomarkers.

All Authors: No reported disclosures

## Linked entities

- **Diseases:** tuberculosis (MONDO:0018076)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12791945/full.md

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Source: https://tomesphere.com/paper/PMC12791945