Cyclophosphamide, thalidomide, and dexamethasone (CTD) as initial therapy for patients with multiple myeloma unsuitable for autologous transplantation

Author:

Morgan Gareth J.1,Davies Faith E.1,Gregory Walter M.2,Russell Nigel H.3,Bell Sue E.2,Szubert Alexander J.2,Coy Nuria Navarro2,Cook Gordon4,Feyler Sylvia5,Byrne Jenny L.3,Roddie Huw6,Rudin Claudius7,Drayson Mark T.8,Owen Roger G.4,Ross Fiona M.9,Jackson Graham H.10,Child J. Anthony2,

Affiliation:

1. Institute of Cancer Research, Royal Marsden Hospital, London, United Kingdom;

2. Clinical Trials Research Unit, University of Leeds, Leeds, United Kingdom;

3. Nottingham University Hospital, Nottingham, United Kingdom;

4. St James's University Hospital, Leeds, United Kingdom;

5. Calderdale and Huddersfield National Health Service (NHS) Trust, Huddersfield, United Kingdom;

6. Western General Hospital, Edinburgh, United Kingdom;

7. Royal Devon and Exeter Hospital, Exeter, United Kingdom;

8. College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom;

9. Wessex Regional Genetics Laboratory, University of Southampton, Salisbury, United Kingdom; and

10. Department of Haematology, University of Newcastle, Newcastle-upon-Tyne, United Kingdom

Abstract

Abstract As part of the randomized MRC Myeloma IX trial, we compared an attenuated regimen of cyclophosphamide, thalidomide, and dexamethasone (CTDa; n = 426) with melphalan and prednisolone (MP; n = 423) in patients with newly diagnosed multiple myeloma ineligible for autologous stem-cell transplantation. The primary endpoints were overall response rate, progression-free survival, and overall survival (OS). The overall response rate was significantly higher with CTDa than MP (63.8% vs 32.6%; P < .0001), primarily because of increases in the rate of complete responses (13.1% vs 2.4%) and very good partial responses (16.9% vs 1.7%). Progression-free survival and OS were similar between groups. In this population, OS correlated with the depth of response (P < .0001) and favorable interphase fluorescence in situ hybridization profile (P < .001). CTDa was associated with higher rates of thromboembolic events, constipation, infection, and neuropathy than MP. In elderly patients with newly diagnosed multiple myeloma (median age, 73 years), CTDa produced higher response rates than MP but was not associated with improved survival outcomes. We highlight the importance of cytogenetic profiling at diagnosis and effective management of adverse events. This trial was registered at International Standard Randomized Controlled Trials Number as #68454111.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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