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Cardiovascular complications among hematopoietic cell transplantation survivors – the role of cardiomarkers


Authors: Ľ. Harvanová 1,2;  V. Lábska 1;  E. Bojtárová 1;  M. Hrubiško 1,2;  A. Bátorová 1;  J. Dúbrava 3;  J. Gergeľ 4;  B. Mladosievičová 5
Authors place of work: Klinika hematológie a transfuziológie LF UK, LF SZU a UN Bratislava 1;  Katedra hematológie a transfuziológie, Slovenská zdravotnícka univerzita, Bratislava, Slovenská republika 2;  Oddelenie funkčnej diagnostiky, UN Bratislava 3;  Oddelenie klinickej biochémie, Medirex, Bratislava 4;  Ústav patologickej fyziológie, LF UK, Bratislava 5
Published in the journal: Klin Onkol 2022; 35(6): 454-460
Category: Original Articles
doi: https://doi.org/10.48095/ccko2022454

Summary

Background: Allogeneic hematopoietic stem cell transplantation (HSCT) offers potentially curative therapy for numerous malignant and nonmalignant diseases. The number of survivors and length of follow-up after successful HSCT is continually increasing. HSCT can induce damage of various organs and tissues – from minimal potentially progressive subclinical changes to life-threatening conditions. The aim of this thesis was to assess the prognostic value of high sensitive cardiac troponin T (hs-cTnT) and N-terminal pro-B-type natriuretic peptide (NT-proBNP) testing and early identification of patients at high risk of a cardiac event after allogeneic HSCT. Patients and methods: Sixty-three patients with the median age of 37 years at the time of allogeneic HSCT for hematologic diseases were studied. Cardiac bio­markers were serially measured before conditioning regimen and at days 1, 14 and 30 after HSCT. Cardiac systolic and diastolic functions were assessed before the conditioning regimen and 1 month after HSCT by echocardiography. Results: The differences in plasma NT-proBNP and hs-cTnT concentrations during the 30 days following HSCT were statistically significant (P < 0.001 vs. P = 0.02). Seven of 63 patients (11.1 %) developed a cardiac event defined as cardiovascular dys­rhythmias, pericarditis with cardiac tamponade and heart failure. By multivariate analysis, the strongest prognostic factor of cardiac event was an increased level of hs-cTnT and NT-proBNP persisted for a period of 14 days after HSCT (P < 0.0001). The area under the curve from hs-cTnT testing plus NT-proBNP testing together (AUC = 0.95) was superior to each dia­gnostic modality alone. Conclusion: Measurements of plasma NT-proBNP and hs-cTnT concentrations might be a useful tool for identification of high-risk patients requiring further cardiological follow up. Measurement of hs-cTnT plus NT-proBNP together was superior to hs-cTnT and NT-proBNP measurements alone.

Keywords:

cardiotoxicity – allogeneic hematopoietic stem cell transplantation – cardiac biomarkers – acute complications


Zdroje

1. Saunders IM, Tan M, Koura D et al. Long-term follow-up of hematopoietic stem cell transplant survivors: a focus on screening, monitoring, and therapeutics. Pharmacotherapy 2020; 40 (8): 808–841. doi: 10.1002/phar.2443.

2. Carver JR, Desai CJ. Cardiovascular toxicity of antitumor drugs: dimension of the problem in adult settings. In: Minotti G. Cardiotoxicity of non-cardiovascular drugs. Wiley 2010: 127–199.

3. Tuzovic M, Mead M, Young PA et al. Cardiac complications in the adult bone marrow transplant patient. Curr Oncol Rep 2019; 21 (3): 28. doi: 10.1007/s11912-019-07 74-6.

4. Vanderwalde AM, Sun CL, Laddaran L et al. Conditional survival and cause-specific mortality after autologous hematopoietic cell transplantation for hematological malignancies. Leukemia 2013; 27 (5): 1139–1145. doi: 10.1038/leu.2012.311.

5. Yoon JH, Kim HJ, Lee EJ et al. Early left ventricular dysfunction in children after hematopoietic stem cell transplantation for acute leukemia: a case control study using speckle tracking echocardiography. Korean Circ J 2015; 45 (1): 51–58. doi: 10.4070/kcj.2015.45.1.51.

6. Armenian SH, Sun CL, Mills G et al. Predictors of late cardiovascular complications in survivors of hematopoietic cell transplantation. Biol Blood Marrow Transplant 2010; 16 (8): 1138–1144. doi: 10.1016/j.bbmt.2010.02.021.

7. Harvanová Ľ. Dia­gnostika kardiotoxicity. In: Harvanová Ľ. Kardiovaskulárne komplikácie pri mnohopočetnom myelóme. Bratislava: Herba 2021: 89–108.

8. Albini A, Pennesi G, Donatelli F et al. Cardiotoxicity of anticancer drugs: the need for cardio-oncology and cardio-oncological prevention. J Natl Canc Inst 2010; 102 (1): 14–25. doi: 10.1093/jnci/djp440.

9. Yeh J, Whited L, Saliba RM et al. Cardiac toxicity after matched allogeneic hematopoietic cell transplant in the posttransplant cyclophosphamide era. Blood Adv 2021; 5 (24): 5599–5607. doi: 10.1182/bloodadvances.2021004 846.

10. Armenian SH, Yang D, Teh JB et al. Prediction of cardiovascular disease among hematopoietic cell transplantation survivors. Blood Adv 2018; 2 (14): 1756–1764. doi: 10.1182/bloodadvances.2018019117.

11. Xu ZL, Xu LP, Zhang YY et al. Incidence and predictors of severe cardiotoxicity in patients with severe aplastic anaemia after haploidentical haematopoietic stem cell transplantation. Bone Marrow Transplant 2019; 54 (10): 1694–1700. doi: 10.1038/s41409-019-0509-1.

12. De Boer RA, Daniels LB, Maisel AS et al. State of the art: newer bio­markers in heart failure. Eur J Heart Fail 2015; 17 (6): 559–569. doi: 10.1002/ejhf.273.

13. Balážová K, Kubincová D. Current possibilities of early detection of cardiotoxicity of cytostatic treatment. Klin Onkol 2020; 33 (3): 208–213. doi: 10.14735/amko2020 208.

14. Pudil R, Mueller C, Čelutkiene J et al. Role of serum bio­markers in cancer patients receiving cardiotoxic cancer therapies: a position statement from the Cardio-Oncology Study Group of the Heart Failure Association and the Cardio-Oncology Council of the European Society of Cardiology. Eur J Heart Fail 2020; 22 (11): 1966–1983. doi: 10.1002/ejhf.2017.

15. Roziakova L, Bojtarova E, Mistrik M et al. Serial measurements of cardiac bio­markers in patients after allogeneic hematopoietic stem cell transplantation. J Exp Clin Cancer Res 2012; 31 (1): 13. doi: 10.1186/1756-9966- 31-13.

16. Bujak M, Frangogiannis NG. The role of IL-1 in the pathogenesis of heart disease. Arch Immunol Ther Exp (Warsz) 2009; 57 (3): 165–176. doi: 10.1007/s00005-009-0024-y.

17. Chovanec J, Chovanec M, Mego M. Levels of NT-proBNP and troponin T in cancer patients – mini-review. Klin Onkol 2020; 33 (3): 171–176. doi: 10.14735/amko2020171.

18. Lipshultz SE, Scully RE, Lipsitz SR et al. Assessment of dexrazoxane as a cardioprotectant in doxorubicin-treated children with high-risk acute lymphoblastic leukaemia: long-term follow-up of a prospective, randomised, multicentre trial. Lancet Oncol 2010; 11 (10): 950–961. doi: 10.1016/S1470-2045 (10) 70204-7.

19. Sandri MT, Salvatici M, Cardinale D et al. N-terminal pro-B-type natriuretic peptide after high-dose chemotherapy: a marker predictive of cardiac dysfunction? Clin Chem 2005; 51 (8): 1405–1410. doi: 10.1373/clinchem. 2005.050153.

20. Coghlan JG, Handler CE, Kottaridis PD. Cardiac assessment of patients for haematopoietic stem cell transplantation. Best Pract Res Clin Haematol 2007; 20 (2): 247–263. doi: 10.1016/j.beha.2006.09.005.

21. Roziakova L, Mistrik M, Batorova A et al. Can we predict clinical cardiotoxicity with cardiac bio­markers in patients after haematopoietic stem cell transplantation? Cardiovasc Toxicol 2015; 15 (3): 210–216. doi: 10.1007/s12012-014-9286-7.

Štítky
Paediatric clinical oncology Surgery Clinical oncology

Článok vyšiel v časopise

Clinical Oncology

Číslo 6

2022 Číslo 6
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