Review
BibTex RIS Cite

Kemoterapi ve Radyoterapiye Bağlı Kardiyovasküler Toksisite

Year 2019, Volume: 13 Issue: 5, 399 - 403, 23.09.2019
https://doi.org/10.12956/tchd.560892

Abstract

Çocukluk
çağı kanserlerinde sağ-kalım sonrası kardiyovasküler hastalık riski kontrol
gruplarına göre 8-10 kat daha fazla bulunmuştur. Bu konuda yapılan çalışmalar
kardiyovasküler hastalıklardan ölüm riskinin tedavi tamamlandıktan 5-10 yıl
sonra belirgin arttığını, tanı üzerinden 30 yıldan uzun süre geçen hastalarda
kardiyak toksisiteye bağlı hastalıkların en önemli mortalite nedeni olduğunu
göstermiştir. Bu nedenle tedavi sırasında ve sonrasında hastaların düzenli
takibi gerekmektedir. Örneğin, antrasiklin tedavisi verilen ve tedavi üzerinden
10 yıldan uzun süre geçen hastaların yaklaşık yarısında, hiçbir semptom
bulunmasa bile subklinik kardiyak hastalık bulunmaktadır. Sağ-kalım sonrası tüm
hastalar dikkate alındığında bu rakam %25’in üzerindedir. Bu sonuçlar subklinik
bulguların yıllar içerisinde kötüleşeceğini göstermektedir. Çocuklarda
kemoterapiye bağlı toksisiteyi ve uzun dönemde toksisitenin nasıl
sonuçlanacağını tahmin etmek her zaman mümkün değildir. Direkt miyokard hasarı
yanında miyokardiyal fonksiyon kaybı yada vasküler hemodinaminin bozulması gibi
kemoterapiye bağlı değişiklikler kardiyovasküler sistemi etkileyebilir. Kardiyovasküler
sistem ayrıca radyasyon hasarına da açıktır. Temel mekanizma interstisyel
fibrozis gelişmesidir. Tedavisi devam eden hastalarda kardiyovasküler sistem
ile ilgili bazal değerlerin elde edilmesi ve erken bulguların saptanabilmesi
amacıyla düzenli aralarla tanısal değerlendirme yapılmalıdır. Tedavisi
tamamlanan hastalarda ise genel kabul görmüş yaklaşım asemptomatik hastalarda bu
değerlendirmenin 5 yılda bir yapılması, semptomatik hastalarda ise semptomlar
başladığında yapılarak bulgulara göre sıklığının belirlenmesi gerektiği
şeklindedir. Ayrıca en düşük etkili dozun belirlenmesi, alternatif doz ve
uygulama metodlarının geliştirilmesi, protokollere kardiyak koruyucu ajanların
eklenmesi, radyoterapi kullanımı ve dozunun azaltılması ile kardiyak
toksisiteye bağlı hastalık insidansının azaltılması üzerine yeni tedavi
protokolleri geliştirilmelidir. Sağ-kalım sonrası obezitenin önlenmesi,
metabolik sendrom ve hipertansiyon ile mücadele, hiperlipideminin önlenmesi,
erken ateroskleroz gelişiminin takibi, aritmi açısından dikkatli olunması,
sigara, alkol kullanımı ve madde alışkanlığı ile mücadele de önemlidir. 

References

  • 1. Cardinale D, Sandri MT, Colombo A, et al. Prognostic value of troponin I in cardiac risk stratification of cancer patients undergoing high-dose chemotherapy. Circulation 2004; 109: 2749-2754.
  • 2. Lipshultz SE, Rifai N, Dalton VM, et al. The effect of dexrazoxane on myocardial injury in doxorubicin-treated children with acute lymphoblastic leukemia. N Engl J Med 2004; 351: 145-153.
  • 3. Nakamae H, Tsumura K, Terada Y, et al. Notable effects of angiotensin II receptor blocker, valsartan on acute cardiotoxic changes after standart chemotherapy with cyclophospahamide, doxorubicin, vincristine and prednisolone. Cancer 2005; 104: 2492-2498.
  • 4. Kalay N, Basar E, Ozdogru I, et al. Protective effects of carvedilol against anthracycline-induced cardiomyopathy. J Am Coll Cardiol 2006; 48: 2258-2262.
  • 5. Cardinale D, Colombo A, Sandri MT, et al. Prevention of high-dose chemotherapy-induced cardiotoxicity in high-risk patients by angiotensin-converting enzyme inhibition. Circulation 2006; 114: 2474-2481.
  • 6. Cadeddu C, Piras A, Mantovani G, et al. Protective effects of the angiotensin II receptor blocker telmisartan on epirubicin-induced inflammation, oxidative stres and early ventricular impairement. Am Heart J 2010; 160: 487 (e1-7).
  • 7. Yeh ET, Bickford CL. Cardiovascular complications of cancer thrapy: Incidence, pathogenesis, diagnosis and management. J Am Coll Cardiol 2009; 53: 2231-2247.
  • 8. Altena R, Perik PJ, van Veldhuisen DJ, et al. Cardiovascular toxicity caused by cancer treatment: Strategies for early detection. Lancet Oncol 2009; 10: 391-399.
  • 9. Lipshultz SE, Scully RE, Lipsitz SR, et al. Assessment of dexrazoxane as a cardioprotectant in doxorubicin-treated children with high-risk acute lymphoblastic leukemia: Long-term follow-up of a prospective, randomised, multicentretrial. Lancet Oncol 2010; 11: 950-961.
  • 10. Georgakopoulos P, Roussou P, Matsakas E, et al. Cardioprotective effect of metoprolol and enalapril in doxorubicin-treated lymphoma patients: A prospective, parallel group, randomized, controlled study with 36-month follow-up. Am J Hematol 2010; 85: 894-896.
  • 11. Tacyildiz N, Ozyoruk D, Ozelci Kavas G, et al. Selenium in the prevention of anthracycline-induced cardiac toxicity in children with cancer. J Oncol 2012; DOI: 10.1155/2012/651630.
  • 12. Lipshultz SE, Adams MJ, Colan SD, et al. Long-term cardiovascular toxicity in children, adolescents and young adults who receive cancer therapy: Pathophysiology, course, monitoring, management, prevention and research directions. A scientific statement from the American Heart Association. Circulation 2013; 128: 1927-1995.
  • 13. Berardi R, Caramanti M, Savini A, et al. State of the art for cardiotoxicity due to chemotherapy and to targeted therapies: A literature review. Crit Rev Oncol Hematol 2013; 88: 75-86.
  • 14. Kaya MG, Ozkan M, Gunebakmaz O, et al. Protective effects of nebivolol against anthracycline-induced cardiomyopathy: A randomized control study. Int J Cardiol 2013; 167: 2306-2310.
  • 15. Truong J, Yan AT, Cramarossa G, et al. Chemotherapy-induced cardiotoxicity: Detection, prevention and management. Can J Cardiol 2014; 30: 869-878.
  • 16. Bhakta N, Liu Q, Yeo F, et al. Cumulative burden of cardiovascular morbidity among pediatric, adolescent and young adult Hodgkin Lymphoma survivors: An analysis from the St. Jude Lifetime Cohort Study. Lancet Oncol 2016; 17: 1325-1334.
Year 2019, Volume: 13 Issue: 5, 399 - 403, 23.09.2019
https://doi.org/10.12956/tchd.560892

Abstract

References

  • 1. Cardinale D, Sandri MT, Colombo A, et al. Prognostic value of troponin I in cardiac risk stratification of cancer patients undergoing high-dose chemotherapy. Circulation 2004; 109: 2749-2754.
  • 2. Lipshultz SE, Rifai N, Dalton VM, et al. The effect of dexrazoxane on myocardial injury in doxorubicin-treated children with acute lymphoblastic leukemia. N Engl J Med 2004; 351: 145-153.
  • 3. Nakamae H, Tsumura K, Terada Y, et al. Notable effects of angiotensin II receptor blocker, valsartan on acute cardiotoxic changes after standart chemotherapy with cyclophospahamide, doxorubicin, vincristine and prednisolone. Cancer 2005; 104: 2492-2498.
  • 4. Kalay N, Basar E, Ozdogru I, et al. Protective effects of carvedilol against anthracycline-induced cardiomyopathy. J Am Coll Cardiol 2006; 48: 2258-2262.
  • 5. Cardinale D, Colombo A, Sandri MT, et al. Prevention of high-dose chemotherapy-induced cardiotoxicity in high-risk patients by angiotensin-converting enzyme inhibition. Circulation 2006; 114: 2474-2481.
  • 6. Cadeddu C, Piras A, Mantovani G, et al. Protective effects of the angiotensin II receptor blocker telmisartan on epirubicin-induced inflammation, oxidative stres and early ventricular impairement. Am Heart J 2010; 160: 487 (e1-7).
  • 7. Yeh ET, Bickford CL. Cardiovascular complications of cancer thrapy: Incidence, pathogenesis, diagnosis and management. J Am Coll Cardiol 2009; 53: 2231-2247.
  • 8. Altena R, Perik PJ, van Veldhuisen DJ, et al. Cardiovascular toxicity caused by cancer treatment: Strategies for early detection. Lancet Oncol 2009; 10: 391-399.
  • 9. Lipshultz SE, Scully RE, Lipsitz SR, et al. Assessment of dexrazoxane as a cardioprotectant in doxorubicin-treated children with high-risk acute lymphoblastic leukemia: Long-term follow-up of a prospective, randomised, multicentretrial. Lancet Oncol 2010; 11: 950-961.
  • 10. Georgakopoulos P, Roussou P, Matsakas E, et al. Cardioprotective effect of metoprolol and enalapril in doxorubicin-treated lymphoma patients: A prospective, parallel group, randomized, controlled study with 36-month follow-up. Am J Hematol 2010; 85: 894-896.
  • 11. Tacyildiz N, Ozyoruk D, Ozelci Kavas G, et al. Selenium in the prevention of anthracycline-induced cardiac toxicity in children with cancer. J Oncol 2012; DOI: 10.1155/2012/651630.
  • 12. Lipshultz SE, Adams MJ, Colan SD, et al. Long-term cardiovascular toxicity in children, adolescents and young adults who receive cancer therapy: Pathophysiology, course, monitoring, management, prevention and research directions. A scientific statement from the American Heart Association. Circulation 2013; 128: 1927-1995.
  • 13. Berardi R, Caramanti M, Savini A, et al. State of the art for cardiotoxicity due to chemotherapy and to targeted therapies: A literature review. Crit Rev Oncol Hematol 2013; 88: 75-86.
  • 14. Kaya MG, Ozkan M, Gunebakmaz O, et al. Protective effects of nebivolol against anthracycline-induced cardiomyopathy: A randomized control study. Int J Cardiol 2013; 167: 2306-2310.
  • 15. Truong J, Yan AT, Cramarossa G, et al. Chemotherapy-induced cardiotoxicity: Detection, prevention and management. Can J Cardiol 2014; 30: 869-878.
  • 16. Bhakta N, Liu Q, Yeo F, et al. Cumulative burden of cardiovascular morbidity among pediatric, adolescent and young adult Hodgkin Lymphoma survivors: An analysis from the St. Jude Lifetime Cohort Study. Lancet Oncol 2016; 17: 1325-1334.
There are 16 citations in total.

Details

Primary Language Turkish
Subjects ​Internal Diseases
Journal Section REVIEW
Authors

İbrahim İlker Çetin 0000-0001-9480-8278

Hazım Alper Gürsu 0000-0002-0707-2678

Publication Date September 23, 2019
Submission Date May 6, 2019
Published in Issue Year 2019 Volume: 13 Issue: 5

Cite

Vancouver Çetin İİ, Gürsu HA. Kemoterapi ve Radyoterapiye Bağlı Kardiyovasküler Toksisite. Turkish J Pediatr Dis. 2019;13(5):399-403.


The publication language of Turkish Journal of Pediatric Disease is English.


Manuscripts submitted to the Turkish Journal of Pediatric Disease will go through a double-blind peer-review process. Each submission will be reviewed by at least two external, independent peer reviewers who are experts in the field, in order to ensure an unbiased evaluation process. The editorial board will invite an external and independent editor to manage the evaluation processes of manuscripts submitted by editors or by the editorial board members of the journal. The Editor in Chief is the final authority in the decision-making process for all submissions. Articles accepted for publication in the Turkish Journal of Pediatrics are put in the order of publication, with at least 7 articles in each issue, taking into account the acceptance dates. If the articles sent to the reviewers for evaluation are assessed as a senior for publication by the reviewers, the section editor and the editor considering all aspects (originality, high scientific quality and citation potential), it receives publication priority in addition to the articles assigned for the next issue.


The aim of the Turkish Journal of Pediatrics is to publish high-quality original research articles that will contribute to the international literature in the field of general pediatric health and diseases and its sub-branches. It also publishes editorial opinions, letters to the editor, reviews, case reports, book reviews, comments on previously published articles, meeting and conference proceedings, announcements, and biography. In addition to the field of child health and diseases, the journal also includes articles prepared in fields such as surgery, dentistry, public health, nutrition and dietetics, social services, human genetics, basic sciences, psychology, psychiatry, educational sciences, sociology and nursing, provided that they are related to this field. can be published.