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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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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. |
format | Online Article Text |
id | pubmed-4725626 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
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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