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      Superior overall survival of patients with myeloma achieving very good partial response or better to initial treatment with bortezomib, pegylated liposomal doxorubicin, and dexamethasone, predicted after two cycles by a free light chain- and M-protein-based model: extended follow-up of a phase II trial.

      Leukemia & Lymphoma
      Antineoplastic Combined Chemotherapy Protocols, therapeutic use, Boronic Acids, administration & dosage, Dexamethasone, Doxorubicin, analogs & derivatives, Follow-Up Studies, Humans, Immunoglobulin Light Chains, blood, Models, Statistical, Multiple Myeloma, diagnosis, drug therapy, mortality, Myeloma Proteins, metabolism, Polyethylene Glycols, Prognosis, Pyrazines, Survival Analysis, Treatment Outcome

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          Abstract

          In myeloma, achievement of very good partial response (VGPR) post-transplant is associated with prolonged overall (OS) and progression-free survival (PFS). In this study of bortezomib, pegylated liposomal doxorubicin, and dexamethasone (VDD) in 40 patients with newly diagnosed myeloma (median follow-up 45.1 months), 2-/4-year OS estimates were 95.7%/86.5% versus 82.4%/58.2% for patients achieving ≥VGPR versus 

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