Abstract |
Multiple myeloma (MM) is a heterogeneous disease with high-risk patients progressing rapidly despite treatment. Various definitions of high-risk MM are used and we reported that gene expression profile (GEP)-defined high risk was a major predictor of relapse. In spite of our best efforts, the majority of GEP70 high-risk patients relapse and we have noted higher relapse rates during drug-free intervals. This prompted us to explore the concept of less intense drug dosing with shorter intervals between courses with the aim of preventing inter-course relapse. Here we report the outcome of the Total Therapy 5 trial, where this concept was tested. This regimen effectively reduced early mortality and relapse but failed to improve progression-free survival and overall survival due to relapse early during maintenance.
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Authors | Y Jethava, A Mitchell, M Zangari, S Waheed, C Schinke, S Thanendrarajan, J Sawyer, D Alapat, E Tian, C Stein, R Khan, C J Heuck, N Petty, D Avery, D Steward, R Smith, C Bailey, J Epstein, S Yaccoby, A Hoering, J Crowley, G Morgan, B Barlogie, F van Rhee |
Journal | Blood cancer journal
(Blood Cancer J)
Vol. 6
Issue 7
Pg. e453
(07 29 2016)
ISSN: 2044-5385 [Electronic] United States |
PMID | 27471869
(Publication Type: Clinical Trial, Journal Article)
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Chemical References |
- Neoplasm Proteins
- Thalidomide
- Bortezomib
- Lenalidomide
- Melphalan
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Topics |
- Adult
- Aged
- Antineoplastic Combined Chemotherapy Protocols
(administration & dosage)
- Bortezomib
(administration & dosage)
- Disease-Free Survival
- Dose-Response Relationship, Drug
- Female
- Gene Expression Profiling
(methods)
- Gene Expression Regulation, Neoplastic
(drug effects)
- Humans
- Lenalidomide
- Male
- Melphalan
(administration & dosage)
- Middle Aged
- Multiple Myeloma
(drug therapy, genetics, pathology)
- Neoplasm Proteins
(biosynthesis, genetics)
- Thalidomide
(administration & dosage, analogs & derivatives)
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