Blood Cancer Journal · 2019 · 165 citations · 27 references
MedicineHematologyOncologyCytogeneticsHematologic OncologyMolecular OncologyAneuploidyCancer CytogeneticsClinical CytogeneticsHematologic Malignancy TherapyMultiple MyelomaCytogenetic AbnormalitiesCytogenetic Risk StratificationFluorescent In Situ HybridizationLenalidomide TherapyMultiple Myeloma TherapyMultiple Myeloma TreatmentTriplet Therapy Regimens
Gain of chromosome 1q (+1q) is commonly identified in multiple myeloma and has been associated with inferior outcomes. However, the prognostic implication of +1q has not been evaluated in the setting of standard triplet regimens. We retrospectively analyzed 201 consecutive patients with newly diagnosed myeloma who received induction with lenalidomide, bortezomib, and dexamethasone (RVD) and were tested for +1q at diagnosis by fluorescent in-situ hybridization. Patients with +1q (n = 94), compared to those without +1q (n = 107), had shorter median progression-free survival (PFS) (41.9 months vs 65.1 months, p = 0.002, HR = 1.90) and overall survival (median not reached (NR) for either arm, p = 0.003, HR 2.69). In subgroup analyses, patients with co-occurring +1q and t(4;14), t(14;16) or del(17p) or with 4 or more copies of 1q had significantly worse PFS (25.1 months and 34.6 months, p < 0.001 and p = 0.0063, respectively), whereas patients with three copies and no other high-risk cytogenetic abnormalities had no significant difference in PFS. These data suggest that when treated with RVD induction, patients with +1q should be considered at very high risk for early progression in multiple myeloma when ≥4 copies are detected or in the context of other high-risk cytogenetic abnormalities.
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Lenalidomide, Bortezomib, and Dexamethasone with Transplantation for Myeloma
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