Health-Related Quality of Life in Multiple Myeloma Patients Treated with High- or Low-Dose Lenalidomide Maintenance Therapy after Autologous Stem Cell Transplantation—Results from the LenaMain Trial (NCT00891384)

Author:

Boquoi Amelie1,Giagounidis Aristoteles2,Goldschmidt Hartmut34ORCID,Heinsch Michael5,Rummel Mathias J.6,Kröger Nicolaus7,Mai Elias K.8ORCID,Strapatsas Judith1,Haas Rainer1ORCID,Kobbe Guido1

Affiliation:

1. Department of Hematology, Oncology and Clinical Immunology, University Hospital Duesseldorf, 40225 Duesseldorf, Germany

2. Klinik für Onkologie, Hämatologie und Palliativmedizin, Marien Hospital Düsseldorf, Rochusstr. 2, 40479 Düsseldorf, Germany

3. National Center for Tumor Diseases Heidelberg (NCT), 69120 Heidelberg, Germany

4. Department of Internal Medicine V, University of Heidelberg, 69120 Heidelberg, Germany

5. Helios Klinikum Duisburg, 47166 Duisburg, Germany

6. Medizinische Klinik IV, University Hospital, 35392 Giessen, Germany

7. University Hospital Eppendorf, 20251 Hamburg, Germany

8. Department of Medicine V, Hematology, Oncology and Rheumatology, University of Heidelberg, 69120 Heidelberg, Germany

Abstract

Introduction: The LenaMain trial (NCT00891384) reported increased progression-free survival with 25 mg of lenalidomide maintenance compared to 5 mg. Here, we report the patient-reported outcomes. Materials and Methods: Scores obtained from the EORTC Quality of Life Questionnaire C30 were analyzed for longitudinal changes from baseline within the groups as well as cross-sectional scores. Results: Compliance rates were high, with 95.7% at baseline and 70% during maintenance. At study entry, scores were high for functioning and low for symptoms. During maintenance, the median global health status/quality of life (GHS/QoL) was constant, without significant differences over time (median GHS/QoL: 68 at baseline and 58 for Len high and 68 for Len low at 2 years) and between treatment arms (mean change < 2). Similarly, most functional scale domains were constant. Notably, diarrhea increased consistently for both treatment arms (baseline: −1.905 (range: −5.78–1.97); end of year 2: 16.071 (range: 5.72–26.42); p < 0.05). The subgroup analysis showed that neither disease activity, duration of treatment, nor adverse events affected the health-related quality of life (HR-QoL) or utility. Conclusion: High baseline scores were maintained throughout the trial without significant differences between the Len dosages, which supports continuous treatment with a dose tailored to patients’ HR-QoL.

Funder

Celgene/BMS

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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