Hemoglobin levels and quality of life in patients with symptomatic chemotherapy-induced anemia: the eAQUA study
Creators
- 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/PMC4725626Additional details
Identifiers
Publishing Information
- Journal Title
- Cancer Management and Research
- Journal Volume
- 8
- Journal Page Range
- p. 1-10
- ISSN
- 1179-1322
INIS
- Country of Publication
- New Zealand
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47121516
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- AMINO ACIDS; ANEMIAS; CHEMOTHERAPY; DOSES; DRUGS; ERYTHROPOIESIS; FATIGUE; HEMOGLOBIN; NEOPLASMS; PATIENTS; SAFETY; TRANSFUSIONS
- Descriptors DEC
- BLOOD FORMATION; CARBOXYLIC ACIDS; DISEASES; GLOBINS; HEMIC DISEASES; HETEROCYCLIC ACIDS; HETEROCYCLIC COMPOUNDS; MECHANICAL PROPERTIES; MEDICINE; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; PIGMENTS; PORPHYRINS; PROTEINS; SYMPTOMS; THERAPY
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