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Epoetin alfa reduces anemia in breast carcinoma patients with no negative impact on survival

In patients with high-risk breast cancer, addition of the erythropoiesis-stimulating agent ( ESA ) Epoetin alfa to the chemotherapy regimen may help avoid the decrease in hemoglobin levels and resulting anemia often seen in these patients and does not negatively affect relapse-free or overall survival.
However, it can increase the risk of thrombotic events.

To investigate the safety and efficacy of Epoetin alfa, Volker Moebus, at the Klinikum Frankfurt Höchst in Frankfurt, Germany, and colleagues, conducted a second randomized study of patients in the intense dose-dense ( IDD ) chemotherapy arm of the AGO-ETC trial.
Of 643 patients receiving the sequential chemotherapy regimen of Epirubicin, Paclitaxel, and Cyclophosphamide, 324 were randomly assigned to receive the ESA Epoetin alfa and 319 were assigned to the non-ESA group.
Researchers compared change in hemoglobin level, percentage of subjects requiring red blood cell ( RBC ) transfusion, incidence of thrombotic events, and, after a median follow-up of 62 months, overall survival, relapse-free survival and intra-mammary relapse in the two groups.

Researchers found that the patients in the non-ESA group had statistically significant reduction in hemoglobin levels and required more RBC transfusions than those in the ESA treatment group ( 28.1% vs 12.8% ).

ESA treatment had no impact on overall surival, relapse-free survival or intra-mammary relapse.

However, patients treated with Epoetin alfa were approximately twice as likely to experience thrombotic events compared with patients in the non-ESA group ( 7% vs 3% ).

According to authors, ESAs appear to be safe drugs for the treatment of chemotherapy-induced anemia in patients with IDD chemotherapy regimens.

In an accompanying editorial, Chau Dang, Clifford Hudis, and Larry Norton, of the Memorial Sloan-Kettering Cancer Center in NY, write that the study of Moebus et al. provides important evidence that ESAs may be safe in the curative treatment of cancer. However, they cite some limitations of the study, ie, a much larger sample size would be needed to unequivocally conclude that Epoetin alfa had no effect on overall or relapse-free survival; the still unacceptably high transfusion rate ( 13% ) in the ESA group; the high cost of ESAs given that they do not improve overall survival or relapse-free survival, and the approximately two-fold rate of thromboembolic events in the ESA group.

In a second editorial, Brian Leyland-Jones, of Edith Sanford Breast Cancer Research Foundation in SD, attempted to put this article into the context of the significant controversy surrounding this field, in terms of the effect of ESAs on overall survival, tumor progression and risk of thrombosis. He especially focused on trials where ESAs were prescribed within label. He noted that these drugs are powerful pharmacological tools, and in an era dominated by personalized medicine, should be prescribed according to individualized risk-benefit ratio. ( Xagena )

Source: Journal of the National Cancer Institute, 2013