Features of indeterminate results of QuantiFERON-TB Gold In-Tube test in patients with haematological malignancies

Author:

Huang Chen-Cheng12ORCID,Jerry Teng Chieh-Lin345,Wu Ming-Feng67,Lee Ching-Hsiao8,Chen Hui-Chen6,Huang Wei-Chang591011ORCID

Affiliation:

1. Institute of Molecular Biology, College of Life Sciences, National Chung Hsing University, Taichung

2. Division of Chest Medicine, Department of Internal Medicine, Taichung Hospital, Ministry of Health and Welfare, Taichung

3. Division of Haematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital

4. Department of Life Science, Tunghai University, Taichung

5. School of Medicine, Chung Shan Medical University, Taichung

6. Division of Chest Medicine, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung

7. Department of Medical Laboratory Science and Biotechnology, Central Taiwan University of Science and Technology, Taichung

8. Department of Medical Technology, Jen-Teh Junior College of Medicine, Nursing and Management, Miaoli

9. Division of Chest Medicine, Department of Internal Medicine, Taichung Veterans General Hospital, 1650 Taiwan Boulevard Sec. 4, Taichung, 407

10. Department of Medical Technology, Jen-Teh Junior College of Medicine, Nursing and Management Miaoli

11. Ph.D. Program in Translational Medicine, National Chung Hsing University, Taichung Master Program for Health Administration, Department of Industrial Engineering and Enterprise Information, Tunghai University, Taichung

Abstract

Background and aims: The application of QuantiFERON-TB Gold in-Tube (QFT-GIT) in patients with haematological malignancies (HMs) has not been well studied. Therefore, we aimed to investigate the features of patients with HMs whose QFT-GIT results were indeterminate. Methods: This study enrolled patients with HMs for the analysis of QFT-GIT tests and additional 2-year follow-up. The characteristics and predictors of QFT-GIT indeterminate results were identified. Mycobacterium tuberculosis (TB) incidence rate (IR) and incidence rate ratio (IRR) were also investigated. Results: Of 89 participants, 27 (30.3%) had QFT-GIT indeterminate results. The QFT-GIT indeterminate patients were characterized with the diagnosis of leukaemia (63.0% versus 32.3%, p = 0.044), abnormal white blood count (WBC) (88.9% versus 14.5%, p = 0.001), abnormal lymphocyte percentage (81.5% versus 14.5%, p = 0.001) and lower lymphocyte count (×109/l) (0.5 versus 2.2, p = 0.000) when compared with those with determinate results. Meanwhile, abnormal WBC [odds ratios (OR): 15.18, p = 0.003] and lymphocyte percentage (OR: 6.90, p = 0.033) were predictors of indeterminate results. One patient with the QFT-GIT indeterminate status and high interferon-γ level of negative control result developed active TB with a TB IR of 18.5 per 1000 person-years and an IRR of 0.1 (95% confidence interval, 0.01–0.71) when compared with positive QFT-GIT patients without prophylaxis treatment. Conclusion: Abnormal ranges of WBC and lymphocyte differential count percentage were independent predictors useful to determine the optimal timing of implementing QFT-GIT test in patients with HMs.

Funder

The Biotechnology Medical Technology Policy Research Centre, Taiwan

Publisher

SAGE Publications

Subject

Hematology

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