Translocation (11;14) in newly diagnosed multiple myeloma, time to reclassify this standard risk chromosomal aberration?

摘要

Abstract Objectives The most common translocation in multiple myeloma (MM) is t(11;14)(q13;q32), and its importance as prognostic factor has been controversial. The aim was to analyze its prognostic value. Method In this retrospective study of 469 newly diagnosed myeloma patients, outcomes in patients with (11;14) and standard risk (t(11;14)SR) or high risk (t(11;14)HR) cytogenetics were compared to outcomes of patients without t(11;14) and SR (non‐t(11;14)SR) or HR (non‐t(11;14)HR), respectively. Results Overall progression‐free survival (PFS) was shorter in t(11;14)SR than non‐t(11;14)SR (median 28.9 vs 35.3?months); however, the difference was not significant ( P ?=?.2). Overall survival (OS) did not differ significantly between the groups. In the subgroup of patients that did not receive high‐dose treatment, PFS was shorter for t(11;14)SR compared to non‐t(11;14)SR, 10.6 vs 24.6?months ( P ?=?.01). Although OS were shorter for t(11,14)SR compared to non‐t(11;14)SR (5‐year OS 41.7% vs 63.8%), the difference was not significant ( P ?=?.1). In HDT patients, no significant difference was observed for OS or PFS between those with or without t(11;14). Conclusion This study shows that t(11;14) is associated with poorer outcome in MM, particularly in non‐high‐dose‐treated SR patients. It should be considered an intermediate or high‐risk marker in these patients.