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Hemoglobin levels and quality of life in patients with symptomatic chemotherapy-induced anemia: the eAQUA study

PURPOSE: To assess hemoglobin (Hb) outcomes and fatigue-related quality-of-life (QoL) (electronic assessment) in patients with solid tumors and symptomatic chemotherapy-induced anemia receiving cytotoxic chemotherapy and darbepoetin alfa (DA) or another erythropoiesis-stimulating agent according to...

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Autores principales: Mouysset, Jean-Loup, Freier, Beata, van den Bosch, Joan, Levaché, Charles Briac, Bols, Alain, Tessen, Hans Werner, Belton, Laura, Bohac, G Chet, Terwey, Jan-Henrik, Tonini, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725626/
https://www.ncbi.nlm.nih.gov/pubmed/26855598
http://dx.doi.org/10.2147/CMAR.S88110
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author Mouysset, Jean-Loup
Freier, Beata
van den Bosch, Joan
Levaché, Charles Briac
Bols, Alain
Tessen, Hans Werner
Belton, Laura
Bohac, G Chet
Terwey, Jan-Henrik
Tonini, Giuseppe
author_facet Mouysset, Jean-Loup
Freier, Beata
van den Bosch, Joan
Levaché, Charles Briac
Bols, Alain
Tessen, Hans Werner
Belton, Laura
Bohac, G Chet
Terwey, Jan-Henrik
Tonini, Giuseppe
author_sort Mouysset, Jean-Loup
collection PubMed
description PURPOSE: To assess hemoglobin (Hb) outcomes and fatigue-related quality-of-life (QoL) (electronic assessment) in patients with solid tumors and symptomatic chemotherapy-induced anemia receiving cytotoxic chemotherapy and darbepoetin alfa (DA) or another erythropoiesis-stimulating agent according to European indication. METHODS: eAQUA was a Phase IV prospective observational study. The primary outcome (assessed in the primary analysis set [PAS]: patients receiving one or more DA dose who had baseline and week 9 assessments for Hb and QoL) was the proportion of patients receiving DA having both Hb increases ≥1 g/dL and improved QoL between baseline and week 9. Functional Assessment of Cancer Therapy-Fatigue (FACT-F) subscale scores were anchored to fatigue visual analog scale scores to determine the minimally important difference for improved QoL. Overall data/data over time are reported for the full analysis set (patients receiving one or more erythropoiesis-stimulating agent dose, n=1,158); week 9 data (ie, data relating to the primary and secondary outcomes) are reported for the PAS (n=510). Baseline and safety data are included for both the full analysis set and PAS. RESULTS: In the PAS, 69% of patients had stage IV disease and 96% were fatigued. The minimally important difference in FACT-F change score for QoL improvement was 3.5. From baseline to week 9, 32% (95% confidence interval: 28%–36%) of patients had both improved QoL and an Hb increase ≥1 g/dL; proportions were similar across the most common tumor types. At week 9, 49% and 58% of patients had improved QoL or Hb increases ≥1 g/dL, respectively; 70% and 76% had QoL or Hb improvements between baseline and study end, respectively. In the PAS, 16% of patients required transfusions and 32% required iron supplementation. Few patients (<1%) reported adverse drug reactions. CONCLUSION: In this study, patients with solid tumors receiving DA per European indication for symptomatic chemotherapy-induced anemia had clinically meaningful improvements in Hb and QoL.
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spelling pubmed-47256262016-02-05 Hemoglobin levels and quality of life in patients with symptomatic chemotherapy-induced anemia: the eAQUA study Mouysset, Jean-Loup Freier, Beata van den Bosch, Joan Levaché, Charles Briac Bols, Alain Tessen, Hans Werner Belton, Laura Bohac, G Chet Terwey, Jan-Henrik Tonini, Giuseppe Cancer Manag Res Original Research PURPOSE: To assess hemoglobin (Hb) outcomes and fatigue-related quality-of-life (QoL) (electronic assessment) in patients with solid tumors and symptomatic chemotherapy-induced anemia receiving cytotoxic chemotherapy and darbepoetin alfa (DA) or another erythropoiesis-stimulating agent according to European indication. METHODS: eAQUA was a Phase IV prospective observational study. The primary outcome (assessed in the primary analysis set [PAS]: patients receiving one or more DA dose who had baseline and week 9 assessments for Hb and QoL) was the proportion of patients receiving DA having both Hb increases ≥1 g/dL and improved QoL between baseline and week 9. Functional Assessment of Cancer Therapy-Fatigue (FACT-F) subscale scores were anchored to fatigue visual analog scale scores to determine the minimally important difference for improved QoL. Overall data/data over time are reported for the full analysis set (patients receiving one or more erythropoiesis-stimulating agent dose, n=1,158); week 9 data (ie, data relating to the primary and secondary outcomes) are reported for the PAS (n=510). Baseline and safety data are included for both the full analysis set and PAS. RESULTS: In the PAS, 69% of patients had stage IV disease and 96% were fatigued. The minimally important difference in FACT-F change score for QoL improvement was 3.5. From baseline to week 9, 32% (95% confidence interval: 28%–36%) of patients had both improved QoL and an Hb increase ≥1 g/dL; proportions were similar across the most common tumor types. At week 9, 49% and 58% of patients had improved QoL or Hb increases ≥1 g/dL, respectively; 70% and 76% had QoL or Hb improvements between baseline and study end, respectively. In the PAS, 16% of patients required transfusions and 32% required iron supplementation. Few patients (<1%) reported adverse drug reactions. CONCLUSION: In this study, patients with solid tumors receiving DA per European indication for symptomatic chemotherapy-induced anemia had clinically meaningful improvements in Hb and QoL. Dove Medical Press 2016-01-21 /pmc/articles/PMC4725626/ /pubmed/26855598 http://dx.doi.org/10.2147/CMAR.S88110 Text en © 2016 Mouysset et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Mouysset, Jean-Loup
Freier, Beata
van den Bosch, Joan
Levaché, Charles Briac
Bols, Alain
Tessen, Hans Werner
Belton, Laura
Bohac, G Chet
Terwey, Jan-Henrik
Tonini, Giuseppe
Hemoglobin levels and quality of life in patients with symptomatic chemotherapy-induced anemia: the eAQUA study
title Hemoglobin levels and quality of life in patients with symptomatic chemotherapy-induced anemia: the eAQUA study
title_full Hemoglobin levels and quality of life in patients with symptomatic chemotherapy-induced anemia: the eAQUA study
title_fullStr Hemoglobin levels and quality of life in patients with symptomatic chemotherapy-induced anemia: the eAQUA study
title_full_unstemmed Hemoglobin levels and quality of life in patients with symptomatic chemotherapy-induced anemia: the eAQUA study
title_short Hemoglobin levels and quality of life in patients with symptomatic chemotherapy-induced anemia: the eAQUA study
title_sort hemoglobin levels and quality of life in patients with symptomatic chemotherapy-induced anemia: the eaqua study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725626/
https://www.ncbi.nlm.nih.gov/pubmed/26855598
http://dx.doi.org/10.2147/CMAR.S88110
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