Volume 2025, Issue 1 9818679
Corrigendum
Open Access

Corrigendum to “Herceptin-Mediated Cardiotoxicity: Assessment by Cardiovascular Magnetic Resonance”

First published: 23 July 2025

J. Jiang, B. Liu, and S. Hothi, “Herceptin-Mediated Cardiotoxicity: Assessment by Cardiovascular Magnetic Resonance,” Cardiology Research and Practice (2022), https://doi.org/10.1155/2022/1910841.

In the article, the authors have identified errors in Table 5. The correct Table 5 is shown as follows:

Table 5. CMR characteristics of chemotherapeutic agents.
T1 T2 EGE LGE ECV ↓ LVEF ↑ LV volume ↓ RVEF Cardiotoxicity/cardiac dysfunction
Herceptin ✓ (89) ✓ [69, 81, 82] X (90) ✓ (50) ✓ (73) ✓ (50) 2%–27% (49)
Anthracycline (doxorubicin) ✓ (87) ✓ (87, 91) ✓ (87) X (90) ✓ (92, 93) ✓ (91) ✓ (70, 94) ✓ (70) 3%–26% (53, 54)
Pertuzumab ✓ (56) 6.6% (95)
Lapatinib ✓ (57, 65) 2.7% (96)
Epirubicin ✓ (97) ✓ (97) ✓ (98) ✓ (99) 0.7%–11.4% (100)
  • Note: T1, T1 mapping; T2, T2 mapping; ECV, extracellular volume; ↓ LVEF, reduction in left ventricular ejection fraction; ↓ RVEF, reduction in right ventricular ejection fraction.
  • Abbreviations: EGE, early gadolinium enhancement; LGE, late gadolinium enhancement; LV, left ventricular.
  • The patient cohort in these trials may have been pre-exposed to anthracycline.

We apologize for this error.

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