4.7 Article

The role of maintenance thalidomide therapy in multiple myeloma: MRC Myeloma IX results and meta-analysis

Journal

BLOOD
Volume 119, Issue 1, Pages 7-15

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2011-06-357038

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Funding

  1. MRC Leukemia Data Monitoring and Ethics Committee
  2. MRC Leukaemia Trial Steering Committee
  3. Haematological Oncology Clinical Studies Group
  4. Myeloma United Kingdom
  5. National Institute for Health Research
  6. National Cancer Research Network
  7. Celgene. Anna Georgieva
  8. MRC
  9. Novartis
  10. MRC [G0100132] Funding Source: UKRI
  11. Medical Research Council [G0100132] Funding Source: researchfish

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Thalidomide maintenance has the potential to modulate residual multiple myeloma (MM) after an initial response. This trial compared the effect of thalidomide maintenance and no maintenance on progression-free survival (PFS) and overall survival (OS) in MM patients. After intensive or nonintensive induction therapy, 820 newly diagnosed MM patients were randomized to open-label thalidomide maintenance until progression, or no maintenance. Interphase FISH (iFISH) analysis was performed at study entry. Median PFS was significantly longer with thalidomide maintenance (log-rank P < .001). Median OS was similar between regimens (log-rank P = .40). Patients with favorable iFISH showed improved PFS (P = .004) and a trend toward a late survival benefit. Patients with adverse iFISH receiving thalidomide showed no significant PFS benefit and worse OS (P = .009). Effective relapse therapy enhanced survival after progression, translating into a significant OS benefit. Meta-analysis of this and other studies show a significant late OS benefit (P < .001, 7-year difference hazard ratio = 12.3; 95% confidence interval, 5.5-19.0). Thalidomide maintenance significantly improves PFS and can be associated with improved OS. iFISH testing is important in assessing the clinical impact of maintenance therapy. Overview analysis demonstrated that thalidomide maintenance was associated with a significant late OS benefit. This trial was registered at www.isrctn.orgas #ISRCTN68454111. (Blood. 2012; 119(1): 7-15)

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