4.6 Article

Quality of life during and following sequential treatment of previously untreated patients with multiple myeloma: findings of the Medical Research Council Myeloma IX randomised study

Journal

BRITISH JOURNAL OF HAEMATOLOGY
Volume 182, Issue 6, Pages 816-829

Publisher

WILEY
DOI: 10.1111/bjh.15459

Keywords

multiple myeloma; quality of life; EORTC QLQ-C30; EORTC MY-24; immunomodulatory agent

Categories

Funding

  1. MRC Leukaemia Data Monitoring and Ethics Committee
  2. MRC Leukaemia Trial Steering Committee
  3. UK National Cancer Research Institute Haematological Oncology Clinical Studies Group
  4. Myeloma UK
  5. National Institute for Health Research through the National Cancer Research Network
  6. Medical Research Council (London, UK) [G0100132]
  7. Novartis
  8. Schering Health Care
  9. Chugai
  10. Pharmion
  11. Celgene Corporation
  12. Ortho Biotech
  13. MRC [G0100132] Funding Source: UKRI

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In the Medical Research Council (MRC) Myeloma IX trial (ISRCTN684564111) patients were randomised to sodium clodronate or zoledronic acid and induction treatment: cyclophosphamide, vincristine, doxorubicin and dexamethasone (CVAD) or cyclophosphamide, thalidomide and dexamethasone (CTD) followed by autologous stem cell transplant (ASCT) in the intensive pathway; attenuated CTD or melphalan and prednisolone (MP) in the non-intensive pathway. Subsequent randomisation allocated patients to either thalidomide or observation. The European Organisation for Research and Treatment of Cancer (EORTC) quality of life (QoL) questionnaires, QLQ-C30 and QLQ-MY24, were administered at baseline, 3, 6 and 12 months and annually thereafter, enabling the effect of sequential treatment on patient-reported health-related QoL (HR-QoL) to be investigated. The protocol specified four subscales of interest: Pain, Fatigue, Global Health Status/Quality of Life and Physical Functioning at 3, 6 and 12 months that were compared using linear models. The intensive pathway showed significant differences in favour of CTD for Fatigue at 3 months and Physical Functioning at 12 months. The non-intensive pathway and maintenance phase reported significant differences at 3 months; Pain (improved with attenuated CTD) and Global Health status/Quality of Life (improved with observation). The improved outcomes in MRC Myeloma IX were accompanied by some beneficial and few detrimental effects on HR-QoL.

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