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. 2014 May 30;111(22):405–406. doi: 10.3238/arztebl.2014.0405b

Correspondence (letter to the editor): In Reply

Axel Schlitt *
PMCID: PMC4078233  PMID: 24980570

In their contribution, Ivanyi et al. discuss the potential cardiotoxic side effects of the tyrosine kinase inhibitors sunitinib and sorafenib. They describe the side effect of this treatment—namely, restricted left-ventricular ejection fraction (1)—which was reported in what is thus far the only published one full-text study, as a sequela of uncontrolled arterial hypertension, rather than of the treatment itself. The authors cite two studies that have been publish in abstract form.

We thank our correspondents for their comments; in this context we regard the proactive regulation of blood pressure as specious. We refer readers to the study cited in our article (1), product information from Germany regarding both substances, which describes heart failure as a “common” side effect for sorafenib (product information, sorafenib) and “occasional” for sunitinib (product information, sunitinib). Furthermore, we wish to point out that patients who receive treatment with tyrosine kinase inhibitors are described as “stage a heart failure” patients by many authors (2, 3).

In sum, this is consistent with the proposed algorithm of repeated controls (medical history, physical examination, which obviously includes blood pressure measurement, ECG, and echocardiography), which is set out in Figure 3 (4).

Ivanyi et al. subsequently criticize the “confusion of curative and palliative treatments” and the “lack of discrimination between acute, sporadically occurring, and cumulative cardiotoxicities” in our article.

We think that regular monitoring of cardiotoxic side effects is necessary, independent of the therapeutic intention (curative or palliative) or the time of onset, since therapy-related heart failure changes the therapeutic approach, independent of curative or palliative intent. Last, but not least, heart failure adversely affects a patient’s quality of life.

Footnotes

Conflict of interest statement

Prof. Schlitt has received consultancy fees (Advisory Board) from Boehringer Ingelheim. He has received lecture fees and reimbursement of conference fees and travel expenses from Sanofi-Aventis, Servier, Boehringer Ingelheim, and Bayer AG. He has also received trial funding (third-party funds) from GSK, Sanofi-Aventis, Mitsubishi, Endotis, Bayer AG, Boehringer Ingelheim, Novartis, Actelion, and BMS.

References

  • 1.Schmiedinger M, Zielinski CC, Vogl UM, et al. Cardiac toxicity of sunitinib and sorafenib in patients with metastatic renal cell carcinoma. J Clin Oncol. 2008;26:5204–5212. doi: 10.1200/JCO.2007.15.6331. [DOI] [PubMed] [Google Scholar]
  • 2.Chintalgattu V, Patel SS, Khakoo AY. Cardiovascular effects of tyrosine kinase inhibitors used for gastrointestinal stromal tumors. Hematol Oncol Clin North Am. 2009;23:97–107. doi: 10.1016/j.hoc.2008.11.004. [DOI] [PubMed] [Google Scholar]
  • 3.Yancy CW, Jessup M, Bozkurt B, et al. 2013 ACCF/AHA guideline for the management of heart failure: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol. 2013;62:e147–e239. doi: 10.1016/j.jacc.2013.05.019. [DOI] [PubMed] [Google Scholar]
  • 4.Schlitt A, Jordan K, Vordermark D, Schwamborn J, Langer T, Thomssen C. Cardiotoxicity and oncological treatments. Dtsch Arztebl Int. 2014;111:161–168. doi: 10.3238/arztebl.2014.0161. [DOI] [PMC free article] [PubMed] [Google Scholar]

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