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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.
Affiliation
  • Mouysset JL; Department of Medical Oncology, Clinique Rambot Provencale, Aix en Provence, France.
  • Freier B; Clinical Oncology, Wojewodzki Szpital Specjalistyczny, Wroclaw, Poland.
  • van den Bosch J; Department of Internal Medicine/Oncology, Albert Schweitzer Ziekenhuis locatie Dordwijk, Dordrecht, the Netherlands.
  • Levaché CB; Radiotherapy Service, Medical Oncology, Polyclinique Francheville, Périgueux, France.
  • Bols A; Central Pharmacy, AZ Sint-Jan Brugge-Oostende AV, Brugge, Belgium.
  • Tessen HW; Private Oncology Practice. Goslar, Germany.
  • Belton L; LB Biostatistics, London, UK.
  • Bohac GC; Clinical Research, Amgen Inc., Thousand Oaks, CA, USA.
  • Terwey JH; Medical Development - Oncology, Amgen (Europe) GmbH, Zug, Switzerland.
  • Tonini G; Department of Medical Oncology, Università Campus Bio-Medico, Roma, Italy.
Cancer Manag Res ; 8: 1-10, 2016.
Article in En | MEDLINE | ID: mdl-26855598
ABSTRACT

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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Observational_studies Aspects: Patient_preference Language: En Journal: Cancer Manag Res Year: 2016 Document type: Article Affiliation country: France Country of publication: NEW ZEALAND / NOVA ZELÂNDIA / NUEVA ZELANDA / NZ

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Observational_studies Aspects: Patient_preference Language: En Journal: Cancer Manag Res Year: 2016 Document type: Article Affiliation country: France Country of publication: NEW ZEALAND / NOVA ZELÂNDIA / NUEVA ZELANDA / NZ