González-Calle Veronica, Rodriguez-Otero Paula, Calasanz Maria J, Guijarro Manuela, Martínez-López Joaquin, Rosiñol Laura, Hernández Miguel T, Teruel Ana I, Gironella Mercedes, Oriol Albert, de la Rubia Javier, González-Rodríguez Ana P, Bargay Joan, de Arriba Felipe, Palomera Luis, González-Pérez Marta-Sonia, Sureda Anna, Ocio Enrique, Lahuerta Juan J, Bladé Joan, San Miguel Jesus F, Mateos Maria V, Gutiérrez Norma C
Department of Hematology, Hospital Universitario de Salamanca, Instituto de Investigacion Biomedica de Salamanca (IBSAL), Centro de Investigación del Cancer (IBMCC-USAL, CSIC) CIBERONC Salamanca Spain.
Department of Hematology, Cancer Center Clinica Universidad de Navarra, CCUN, Centro de Investigacion Medica Aplicadas (Cima); Instituto de Investigación Sanitaria de Navarra (IDISNA) CIBERONC Pamplona Spain.
Hemasphere. 2024 Dec 10;8(12):e70031. doi: 10.1002/hem3.70031. eCollection 2024 Dec.
This study examines the impact of cytogenetic abnormalities and their co-segregation on the prognosis of newly diagnosed multiple myeloma patients. The analysis included 1304 patients from four different GEM-PETHEMA clinical trials. Genetic alterations, such as t(4;14), t(14;16), del(17p), +1q, and del(1p), were investigated using FISH on CD38 purified plasma cells. The frequency of genetic alterations detected were as follows: del(17p) in 8%, t(4;14) in 12%, t(14;16) in 3%, +1q in 43%, and del(1p) in 8%. The median follow-up was 61 months, and the median progression-free survival (PFS) and overall survival (OS) were 44 months and not reached, respectively. Consistent with previous reports, the presence of t(4;14) was associated with shorter PFS and OS. In our series, the presence of t(14;16) did not impact survival, maybe due to limitations in sample size. Del(17p) was linked to poor prognosis using a cut-off level of ≥20% positive cells, without any impact of higher cut-off in prognosis, except for patients with clonal fraction ≥80% who had a dismal outcome. Cosegregation of cytogenetic abnormalities patients worsened the prognosis in t(4;14) patients but not in patients with del(17p), which retained its adverse prognosis even as a solitary abnormality. Gain(1q) was associated with significantly shorter PFS and OS, while del(1p) affected PFS but not OS. Nevertheless, when co-segregation was eliminated, the detrimental effect of +1q or del(1p) was no longer observed. In conclusion, this study confirms the prognostic significance of high-risk cytogenetic abnormalities in MM and highlights the importance of considering co-occurrence for accurate prognosis assessment.
本研究探讨细胞遗传学异常及其共分离对新诊断的多发性骨髓瘤患者预后的影响。分析纳入了来自四项不同的GEM-PETHEMA临床试验的1304例患者。使用FISH技术在CD38纯化的浆细胞上研究了诸如t(4;14)、t(14;16)、del(17p)、+1q和del(1p)等基因改变。检测到的基因改变频率如下:del(17p)为8%,t(4;14)为12%,t(14;16)为3%,+1q为43%,del(1p)为8%。中位随访时间为61个月,中位无进展生存期(PFS)和总生存期(OS)分别为44个月和未达到。与先前报道一致,t(4;14)的存在与较短的PFS和OS相关。在我们的系列研究中,t(14;16)的存在未影响生存,可能是由于样本量的限制。当阳性细胞≥20%时,del(17p)与不良预后相关,除克隆比例≥80%的患者预后极差外,更高的截断值对预后无影响。细胞遗传学异常的共分离使t(4;14)患者的预后恶化,但del(17p)患者的预后未受影响,即使作为单一异常,del(17p)仍具有不良预后。+1q与显著缩短的PFS和OS相关,而del(1p)影响PFS但不影响OS。然而,当消除共分离时,不再观察到+1q或del(1p)的有害作用。总之,本研究证实了高危细胞遗传学异常在MM中的预后意义,并强调了考虑共现情况以进行准确预后评估的重要性。