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Tuberculosis in patients with malignant neoplasms of various localizations – the experience of the Central Research Institute of Tuberculosis

https://doi.org/10.54921/2413-0346-2025-13-4-15-21

Abstract

The aim of the study was to analyze the spectrum of clinical forms of respiratory tuberculosis (RTB) in patients with malignant neoplasms (MN), determine the relationship between the oncological course and treatment period, and assess the relative risk of developing RTB within this cohort.
Methods. A single-center cohort study was conducted between 2018 and 2025 at the Central Research Institute of Tuberculosis including 61 patients with verified RTB and MN. A comprehensive diagnostic algorithm was used, including clinical laboratory examination, imaging, TB immunodiagnostics, microbiological, and molecular genetic methods.
Results. In 90.2% of cases, malignant neoplasms had extrathoracic localization; the most common were breast cancer (36.1%), lymphomas (16.5%) and gastrointestinal tumors (14.8%). Among the clinical forms of RTB, infiltrative (29.5%), focal (24.6%) TB and TB of the intrathoracic lymph nodes (13.1%) prevailed. Relapse of TB was registered in 49.2% of patients. In 60.7% of patients, RTB was diagnosed during the period of remission of malignant neoplasms after completion of antitumor therapy. The highest relative risk of developing RTB was associated with combined chemo- and radiation therapy: RR = 2.8 compared with radiation therapy, RR = 2.3 compared with chemotherapy and RR = 2.5 compared with surgical treatment (p< 0.05). Before starting antitumor treatment, not a single patient was consulted by a TB specialist.
Conclusion. Patients with malignant neoplasms, especially that receiving combination anticancer therapy, represent a high-risk group for the development and recurrence of tuberculosis, including during cancer remission. Integration of oncology and phthisiology services, the implementation of mandatory tuberculosis screening before anticancer therapy, and individualized monitoring algorithms are necessary to facilitate early TB diagnosis, timely initiation of treatment and an improved prognosis in patients with comorbidities.

About the Authors

N. L. Karpina
Federal State Budgetary Scientific Institution «Central Research Institute of Tuberculosis»
Russian Federation

Moscow



I. Yu. Shabalina
Federal State Budgetary Scientific Institution «Central Research Institute of Tuberculosis»
Russian Federation

Moscow



M. A. Kolesnikova
Federal State Budgetary Scientific Institution «Central Research Institute of Tuberculosis»
Russian Federation

Moscow



References

1. Состояние онкологической помощи населению России в 2024 году / МНИОИ им. П.А. Герцена – филиал ФГБУ «НМИЦ радиологии» Минздрава России; под ред. Каприна А.Д., Старинского В.В., Шахзадовой А.О. – М., 2025. − 275 с.

2. Allemani C. et al. Global surveillance of trends in cancer survival 2000-14 (CONCORD-3): analysis of individual records for 37 513 025 patients diagnosed with one of 18 cancers from 322 population-based registries in 71 countries // Lancet. – 2018. – Vol. 391, №10125. – P.1023-1075.

3. Bluethmann S.M. et al. Anticipating the «Silver Tsunami»: prevalence trajectories and comorbidity burden among older cancer survivors in the United States // Cancer Epidemiol. Biomarkers Prev. – 2016. – Vol. 25, № 7. – P.1029-1036.

4. Caglayan V. et al. Comparison of QuantiFERON-TB Gold test and tuberculin skin test for the diagnosis of latent tuberculosis infection in hemodialysis patients // Transpl. Infect.Dis. – 2011. – Vol. 13, № 2. – P.183-186.

5. Cathcart J.M. et al. The role of chronic inflammation in the development of lung cancer // Expert Rev. Respir. Med. – 2021. – Vol. 15, № 9. – P. 1099-1115.

6. Cheng M.P., Abou Chakra C.N., Yansouni C.P.et al. Risk of active tuberculosis in patients with cancer: a systematic review and meta-analysis // Clin. Infect. Dis. – 2017. – Vol. 64, № 5. – P.635-644. doi: 10.1093/cid/ciw838.

7. Diel R. et al. Immune-based tests for tuberculosis //Dtsch.Arztebl.Int. – 2019. – Vol. 116, № 12. – P. 195-202.

8. Dobler C.C. Biologic agents and tuberculosis // Microbiol. Spectr. – 2016. – Vol. 4, № 6. doi: 10.1128/microbiolspec.TNMI7-0026-2016.

9. Dobler C.C., Cheung K., Nguyen J., Martin A. Risk of tuberculosis in patients with solid cancers and haematological malignancies: a systematic review and meta-analysis // Eur. Respir. J. – 2017. –Vol. 50, № 2. – P. 1700157. doi: 10.1183/13993003.00157-2017.

10. Dye C. et al. The population dynamics and control of tuberculosis // Science. – 2010. –Vol. 328, № 5980. – P. 856-861.

11. Erkens C.G. et al. Tuberculosis contact investigation in low prevalence countries: a European consensus // Eur.Respir.J. – 2010. – Vol. 36, № 4. – P.925-949.

12. Getahun H. et al. Latent Mycobacterium tuberculosis infection // N. Engl. J. Med. – 2015. – Vol. 372, № 22. – P.2127-2135.

13. Global tuberculosis report 2024. – Geneva: World Health Organization, 2024. https://www.who.int/teams/global-tuberculosis-programme/tb-reports/global-tuberculosis-report-2024

14. Koo S. et al. Risk factors for latent tuberculosis infection in close contacts of active tuberculosis patients in South Korea: a prospective cohort study // BMC Infect.Dis. – 2014. – Vol. 14. – P. 566.

15. Miller K.D. et al. Cancer treatment and survivorship statistics, 2022 // CA Cancer J. Clin. – 2022. – Vol. 72, №5. – P. 409-436.

16. Lobue P.A., Moser K.S. Use of isoniazid for latent tuberculosis infection in a public health clinic // Am. J. Respir. Crit. Care Med. – 2003. – Vol. 168, № 4. – P.443-447.

17. Mazurek G.H. et al. Updated guidelines for using Interferon Gamma Release Assays to detect Mycobacterium tuberculosis infection – United States, 2010 // MMWR Recomm. Rep. – 2010. – Vol. 59 (RR-5). – P. 1-25.

18. Morrison V.A. Immunosuppression associated with novel chemotherapy agents and monoclonal antibodies //Clin. Infect.Dis. – 2014. – Vol. 59, Suppl. 5. – S360-S364.

19. Nachiappan A.C. et al. Pulmonary tuberculosis: role of radiology in diagnosis and management // Radiographics. – 2017. – Vol. 37, № 1. – P. 52-72.

20. National Comprehensive Cancer Network. Prevention and Treatment of Cancer-Related Infections.Version 3. 2023.

21. Sepkowitz K.A. Opportunistic infections in patients with and patients without acquired immunodeficiency syndrome //Clin. Infect. Dis. – 2002. – Vol. 34, №8. – P.1098-1107.

22. Shiels M.S. et al. A prospective study of inflammation and cancer: the PLCO study // Br. J. Cancer. – 2021. – Vol. 124, № 6. – P. 1149-1157.

23. Sung H. et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries // CA Cancer J. Clin. – 2021. – Vol. 71, № 3. – P.209-249.

24. Targeted tuberculin testing and treatment of latent tuberculosis infection // Am. J. Respir. Crit. Care Med. – 2000. – Vol. 161, № 4, Pt. 2. – P. S221-S247.

25. Torres H.A. et al. Tuberculosis infection in patients with cancer and factors affecting the risk of infection: a systematic review and meta-analysis // J. Infect. – 2020. – Vol. 80, № 5. – P. 494-502.

26. Wu C.Y., Hu H.Y., Pu C.Y. et al. Aerodigestive tract, lung and haematological cancers are risk factors for tuberculosis: an 8-year population-based study // Int. J. Tuberc. Lung Dis. – 2011. –Vol. 15, № 1. – P. 125-130.

27. Zhou W., Lu H., Lin J. et al. Coexisting lung cancer and pulmonary tuberculosis: a comprehensive review from incidence to management // Cancer Rep. (Hoboken). – 2025. – Vol. 8, №5. – e70213. doi: 10.1002/cnr2.70213.


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For citations:


Karpina N.L., Shabalina I.Yu., Kolesnikova M.A. Tuberculosis in patients with malignant neoplasms of various localizations – the experience of the Central Research Institute of Tuberculosis. Tuberculosis and socially significant diseases. 2025;13(4):15-21. (In Russ.) https://doi.org/10.54921/2413-0346-2025-13-4-15-21

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