Transfusion risk in cancer patients with chemotherapy-induced anemia when initiating darbepoetin alfa therapy at a baseline hemoglobin level of

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Transfusion risk in cancer patients with chemotherapy-induced anemia when initiating darbepoetin alfa therapy at a baseline hemoglobin level of : an exploratory analysis of a phase 3 trial. / Canon, Jean-Luc; Vansteenkiste, Johan; Hedenus, Michael; Gascon, Pere; Bokemeyer, Carsten; Ludwig, Heinz; Vermorken, Jan; Legg, Jason; Pujol, Beatriz; Bridges, Ken.

In: MED ONCOL, Vol. 29, No. 3, 01.09.2012, p. 2291-9.

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@article{ff3a77f38fb14e788d0571e64c69e5c1,
title = "Transfusion risk in cancer patients with chemotherapy-induced anemia when initiating darbepoetin alfa therapy at a baseline hemoglobin level of: an exploratory analysis of a phase 3 trial",
abstract = "Darbepoetin alfa (DA) is an erythropoiesis-stimulating agent (ESA) approved for treating chemotherapy-induced anemia (CIA). Safety concerns have prompted changes to the ESA-product information, which now recommends initiating ESAs at hemoglobin (Hb) levels < 10 g/dL (US) or ≤ 10 g/dL (EU). The present exploratory analysis of a DA trial examined how baseline-Hb levels at ESA initiation affect transfusion rates, Hb response, and safety outcomes in CIA patients. Data were retrospectively analyzed from a phase 3 trial of CIA patients randomised to 500 mcg DA every 3 weeks (Q3 W) or to 2.25 mcg/kg DA weekly (QW) for 15 weeks. In the current analysis, data were reanalyzed by baseline-Hb categories of <9 g/dL (n = 126), 9 to <10 g/dL (n = 225), and ≥ 10 g/dL (n = 354). The Q3 W and QW groups were combined. Transfusion rates were highest in the <9 g/dL baseline-Hb group in all time periods examined. The Kaplan-Meier percentage (95% CI) of patients achieving Hb ≥ 10 g/dL was 68% (59, 78) and 88% (82, 92) in the <9 g/dL and 9 to <10 g/dL baseline-Hb groups, respectively. With lower baseline-Hb, incidence of a ≥ 1 g/dL-Hb rise in 14 days progressively decreased. Incidence of venous thromboembolic events was similar in all baseline-Hb groups and similar between patients with or without a ≥ 1 g/dL-Hb rise in 14 days. Overall, transfusion risk increased and Hb response decreased at lower baseline-Hb levels in this exploratory analysis. When following ESA-product information to initiate ESAs at Hb ≤ 10 g/dL, the greatest benefit may be achieved when initiating close to 10 g/dL. Prospective studies are needed to further examine this hypothesis.",
keywords = "Adult, Aged, Aged, 80 and over, Anemia, Antineoplastic Agents, Blood Transfusion, Double-Blind Method, Erythropoietin, Female, Hematinics, Hemoglobins, Humans, Male, Middle Aged, Neoplasms, Risk, Young Adult",
author = "Jean-Luc Canon and Johan Vansteenkiste and Michael Hedenus and Pere Gascon and Carsten Bokemeyer and Heinz Ludwig and Jan Vermorken and Jason Legg and Beatriz Pujol and Ken Bridges",
year = "2012",
month = sep,
day = "1",
doi = "10.1007/s12032-011-0103-x",
language = "English",
volume = "29",
pages = "2291--9",
journal = "MED ONCOL",
issn = "1357-0560",
publisher = "Humana Press",
number = "3",

}

RIS

TY - JOUR

T1 - Transfusion risk in cancer patients with chemotherapy-induced anemia when initiating darbepoetin alfa therapy at a baseline hemoglobin level of

T2 - an exploratory analysis of a phase 3 trial

AU - Canon, Jean-Luc

AU - Vansteenkiste, Johan

AU - Hedenus, Michael

AU - Gascon, Pere

AU - Bokemeyer, Carsten

AU - Ludwig, Heinz

AU - Vermorken, Jan

AU - Legg, Jason

AU - Pujol, Beatriz

AU - Bridges, Ken

PY - 2012/9/1

Y1 - 2012/9/1

N2 - Darbepoetin alfa (DA) is an erythropoiesis-stimulating agent (ESA) approved for treating chemotherapy-induced anemia (CIA). Safety concerns have prompted changes to the ESA-product information, which now recommends initiating ESAs at hemoglobin (Hb) levels < 10 g/dL (US) or ≤ 10 g/dL (EU). The present exploratory analysis of a DA trial examined how baseline-Hb levels at ESA initiation affect transfusion rates, Hb response, and safety outcomes in CIA patients. Data were retrospectively analyzed from a phase 3 trial of CIA patients randomised to 500 mcg DA every 3 weeks (Q3 W) or to 2.25 mcg/kg DA weekly (QW) for 15 weeks. In the current analysis, data were reanalyzed by baseline-Hb categories of <9 g/dL (n = 126), 9 to <10 g/dL (n = 225), and ≥ 10 g/dL (n = 354). The Q3 W and QW groups were combined. Transfusion rates were highest in the <9 g/dL baseline-Hb group in all time periods examined. The Kaplan-Meier percentage (95% CI) of patients achieving Hb ≥ 10 g/dL was 68% (59, 78) and 88% (82, 92) in the <9 g/dL and 9 to <10 g/dL baseline-Hb groups, respectively. With lower baseline-Hb, incidence of a ≥ 1 g/dL-Hb rise in 14 days progressively decreased. Incidence of venous thromboembolic events was similar in all baseline-Hb groups and similar between patients with or without a ≥ 1 g/dL-Hb rise in 14 days. Overall, transfusion risk increased and Hb response decreased at lower baseline-Hb levels in this exploratory analysis. When following ESA-product information to initiate ESAs at Hb ≤ 10 g/dL, the greatest benefit may be achieved when initiating close to 10 g/dL. Prospective studies are needed to further examine this hypothesis.

AB - Darbepoetin alfa (DA) is an erythropoiesis-stimulating agent (ESA) approved for treating chemotherapy-induced anemia (CIA). Safety concerns have prompted changes to the ESA-product information, which now recommends initiating ESAs at hemoglobin (Hb) levels < 10 g/dL (US) or ≤ 10 g/dL (EU). The present exploratory analysis of a DA trial examined how baseline-Hb levels at ESA initiation affect transfusion rates, Hb response, and safety outcomes in CIA patients. Data were retrospectively analyzed from a phase 3 trial of CIA patients randomised to 500 mcg DA every 3 weeks (Q3 W) or to 2.25 mcg/kg DA weekly (QW) for 15 weeks. In the current analysis, data were reanalyzed by baseline-Hb categories of <9 g/dL (n = 126), 9 to <10 g/dL (n = 225), and ≥ 10 g/dL (n = 354). The Q3 W and QW groups were combined. Transfusion rates were highest in the <9 g/dL baseline-Hb group in all time periods examined. The Kaplan-Meier percentage (95% CI) of patients achieving Hb ≥ 10 g/dL was 68% (59, 78) and 88% (82, 92) in the <9 g/dL and 9 to <10 g/dL baseline-Hb groups, respectively. With lower baseline-Hb, incidence of a ≥ 1 g/dL-Hb rise in 14 days progressively decreased. Incidence of venous thromboembolic events was similar in all baseline-Hb groups and similar between patients with or without a ≥ 1 g/dL-Hb rise in 14 days. Overall, transfusion risk increased and Hb response decreased at lower baseline-Hb levels in this exploratory analysis. When following ESA-product information to initiate ESAs at Hb ≤ 10 g/dL, the greatest benefit may be achieved when initiating close to 10 g/dL. Prospective studies are needed to further examine this hypothesis.

KW - Adult

KW - Aged

KW - Aged, 80 and over

KW - Anemia

KW - Antineoplastic Agents

KW - Blood Transfusion

KW - Double-Blind Method

KW - Erythropoietin

KW - Female

KW - Hematinics

KW - Hemoglobins

KW - Humans

KW - Male

KW - Middle Aged

KW - Neoplasms

KW - Risk

KW - Young Adult

U2 - 10.1007/s12032-011-0103-x

DO - 10.1007/s12032-011-0103-x

M3 - SCORING: Journal article

C2 - 22081263

VL - 29

SP - 2291

EP - 2299

JO - MED ONCOL

JF - MED ONCOL

SN - 1357-0560

IS - 3

ER -