Published January 21, 2016 | Version v1
Journal article

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

  • 1. Department of Medical Oncology, Clinique Rambot Provencale, Aix en Provence (France)
  • 2. Clinical Oncology, Wojewodzki Szpital Specjalistyczny, Wroclaw (Poland)
  • 3. Department of Internal Medicine/Oncology, Albert Schweitzer Ziekenhuis locatie Dordwijk, Dordrecht (Netherlands)
  • 4. Radiotherapy Service, Medical Oncology, Polyclinique Francheville, Périgueux (France)
  • 5. Central Pharmacy, AZ Sint-Jan Brugge-Oostende AV, Brugge (Belgium)
  • 6. Private Oncology Practice. Goslar (Germany)
  • 7. LB Biostatistics, London (United Kingdom)
  • 8. Clinical Research, Amgen Inc., Thousand Oaks, CA (United States)
  • 9. Medical Development - Oncology, Amgen (Europe) GmbH, Zug (Switzerland)
  • 10. Department of Medical Oncology, Università Campus Bio-Medico, Roma (Italy)

Description

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. 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. 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. 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

Availability note (English)

Available from http://dx.doi.org/10.2147/CMAR.S88110; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725626

Additional details

Publishing Information

Journal Title
Cancer Management and Research
Journal Volume
8
Journal Page Range
p. 1-10
ISSN
1179-1322

Optional Information

Copyright
Copyright (c) 2016 Mouysset et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution #En Dash# Non Commercial (unported, v3.0) License
Notes
PMCID: PMC4725626; PMID: 26855598; PUBLISHER-ID: cmar-8-001; OAI: oai:pubmedcentral.nih.gov:4725626